CA2145681A1 - Method for antogonizing inositol 1,4,5-triphosphate - Google Patents
Method for antogonizing inositol 1,4,5-triphosphateInfo
- Publication number
- CA2145681A1 CA2145681A1 CA002145681A CA2145681A CA2145681A1 CA 2145681 A1 CA2145681 A1 CA 2145681A1 CA 002145681 A CA002145681 A CA 002145681A CA 2145681 A CA2145681 A CA 2145681A CA 2145681 A1 CA2145681 A1 CA 2145681A1
- Authority
- CA
- Canada
- Prior art keywords
- inositol
- triphosphate
- calcium
- release
- binding
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- MMWCIQZXVOZEGG-HOZKJCLWSA-N [(1S,2R,3S,4S,5R,6S)-2,3,5-trihydroxy-4,6-diphosphonooxycyclohexyl] dihydrogen phosphate Chemical compound O[C@H]1[C@@H](O)[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](O)[C@H]1OP(O)(O)=O MMWCIQZXVOZEGG-HOZKJCLWSA-N 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title description 5
- 230000000694 effects Effects 0.000 claims abstract description 6
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000027455 binding Effects 0.000 abstract description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052791 calcium Inorganic materials 0.000 abstract description 7
- 239000011575 calcium Substances 0.000 abstract description 7
- 239000005557 antagonist Substances 0.000 abstract description 3
- 230000003834 intracellular effect Effects 0.000 abstract description 3
- 230000001766 physiological effect Effects 0.000 abstract 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 12
- 229910001424 calcium ion Inorganic materials 0.000 description 12
- 239000000872 buffer Substances 0.000 description 6
- 102000005962 receptors Human genes 0.000 description 6
- 108020003175 receptors Proteins 0.000 description 6
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 229960002897 heparin Drugs 0.000 description 4
- 229920000669 heparin Polymers 0.000 description 4
- MFINAYNMQPYYKN-UHFFFAOYSA-N 3,4-diaminobenzene-1,2-disulfonic acid Chemical class NC1=CC=C(S(O)(=O)=O)C(S(O)(=O)=O)=C1N MFINAYNMQPYYKN-UHFFFAOYSA-N 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 230000036515 potency Effects 0.000 description 3
- 230000009870 specific binding Effects 0.000 description 3
- 210000001519 tissue Anatomy 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- 108091008585 IP3 receptors Proteins 0.000 description 2
- 102000007640 Inositol 1,4,5-Trisphosphate Receptors Human genes 0.000 description 2
- 230000002490 cerebral effect Effects 0.000 description 2
- 210000002472 endoplasmic reticulum Anatomy 0.000 description 2
- 230000009871 nonspecific binding Effects 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 208000030507 AIDS Diseases 0.000 description 1
- 206010001513 AIDS related complex Diseases 0.000 description 1
- 102000003922 Calcium Channels Human genes 0.000 description 1
- 108090000312 Calcium Channels Proteins 0.000 description 1
- 108010001857 Cell Surface Receptors Proteins 0.000 description 1
- 108091006146 Channels Proteins 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 241001492222 Epicoccum Species 0.000 description 1
- 229920002683 Glycosaminoglycan Polymers 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 102000014384 Type C Phospholipases Human genes 0.000 description 1
- 108010079194 Type C Phospholipases Proteins 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000037037 animal physiology Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000036755 cellular response Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- 230000002102 hyperpolarization Effects 0.000 description 1
- 239000003055 low molecular weight heparin Substances 0.000 description 1
- 229940127215 low-molecular weight heparin Drugs 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 102000006240 membrane receptors Human genes 0.000 description 1
- 210000001589 microsome Anatomy 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 210000003463 organelle Anatomy 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000002464 receptor antagonist Substances 0.000 description 1
- 229940044551 receptor antagonist Drugs 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 230000016160 smooth muscle contraction Effects 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 238000013222 sprague-dawley male rat Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000012134 supernatant fraction Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/795—Polymers containing sulfur
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Oligomers of formula (I) have been demonstrated to be effective antagonists of inositol 1,4,5-triphosphate (IP3) by com-petitively vying with IP3 for binding sites. By competitively inhibiting the activity of IP3, the oligomers of this invention can modulate the release of intracellular calcium and elicit the resultant physiological effects.
Description
~ W094/07~07 2 1 4 S ~ 8 I PCT/US93/08168 METHOD FOR ANTAGONIZING INOSITOL 1,4,5-TRISPHOSPHATE
BACKGROUND OF THE INVENTION
This application relates to a series of diamino benzenedisulfonic acid oligomers that have demonstrated an affinity for the receptor sites of inositol 1,4,5-triphosphate (IP3) and are, therefore useful in diminishing the bioactivity of IP3, especially with regard to its effect on the release of intracellular calcium ions.
DESCRIPTION OF THE PRIOR ART
The diamino benzenedisulfonic acid oligomers demonstrating utility as IP3 antagonists according to this invention are described in detail in the European Patent Application published January 22, 1992 under Publication No. 0467185 A2. In that publication, the oligomers of the present invention were described as having utility in the diagnosis and/or treatment of AIDS and AIDS related complex.
SUMMARY OF THE INVENTION
The invention herein disclosed relates to a method of inhibiting the activity of inositol 1,4,5-triphosphate (IP3) by occupying the receptor sites specific to IP3 with a compound of the formula:
BACKGROUND OF THE INVENTION
This application relates to a series of diamino benzenedisulfonic acid oligomers that have demonstrated an affinity for the receptor sites of inositol 1,4,5-triphosphate (IP3) and are, therefore useful in diminishing the bioactivity of IP3, especially with regard to its effect on the release of intracellular calcium ions.
DESCRIPTION OF THE PRIOR ART
The diamino benzenedisulfonic acid oligomers demonstrating utility as IP3 antagonists according to this invention are described in detail in the European Patent Application published January 22, 1992 under Publication No. 0467185 A2. In that publication, the oligomers of the present invention were described as having utility in the diagnosis and/or treatment of AIDS and AIDS related complex.
SUMMARY OF THE INVENTION
The invention herein disclosed relates to a method of inhibiting the activity of inositol 1,4,5-triphosphate (IP3) by occupying the receptor sites specific to IP3 with a compound of the formula:
2~ 8 l -2-S03~Na +
H3C~N~I ~NJ~N ~CH3 S03~Na +
-- --n wherein n is a whole number selected from the range of 5 to 20 inclusive and the pharmaceutically acceptable salts thereof.
., DETAILED DESCRIPTION OF THE INVENTION
Inositol 1,4,5-triphosphate (IP3) is a naturally occurring and active component of animal physiology. It is formed intracellularly upon the activation of cell-surface receptors linked to the enzyme phospholipase C. Once generated in sufficient quantities, IP3 acts to stimulate the release of calcium ions from storage organelles within the cell. In this role IP3 is characterized as a "second messenger". Depending upon the type of cell, the calcium released by IP3 ~unctions to stimulate a variety of physiologic processes such as smooth muscle contraction, histamine secretion and the hyperpolarization of nerve cells. Any compound or agent that can promote or interfere with the function of IP3, will promote or interfere with the generation of calcium ions and thereby elicit predictable pharmacological effects.
The process by which IP3 releases calcium ions begins with the binding of IP3 to a specific receptor protein located on an intracellular calcium storage compartment located typically on the endoplasmic reticulum. This receptor protein has been cloned and has been shown to form a calcium "channel" with unique structural properties when bound to IP3. Therefore, when IP3 binds with its receptor, a calcium channel is opened causing the release of calcium stored in the cell's endoplasmic reticulum. In turn, the released calcium will elicit the appropriate cellular response.
Heretofore, the only verified potent antagonist of the 5 IP3 receptor was heparin, a complex glycosaminoglycan. The diamino benzenedisulfonic acid oligomers of this invention also appear to antagonize the effects of IP3 by competing for the receptor site. In most cases, these compounds are more effective than heparin and demonstrate fewer secondary effects. In addition to providing utility as laboratory "tools" in evaluating the therapeutic potential of other IP3 receptor antagonists, the oligomers of this invention would also be administered to modulate IP3-induced calcium release and have a salutary effect on any number of disorders that are caused or exacerbated by an inordinately productive IP3 second messenger pathway.
EXPERIMENTALS
Measurement of IP3 Bindinq Cerebella from male Sprague-Dawley rats (200 g) were homogenized in 30 volumes of ice-cold buffer A (50 mM Tris, 1 mM dithiothreitol, 1 mM EDTA, pH 7.7 with HCl) with a polytron (setting 9 for 10 seconds). The tissue is then washed twice by centrifugation (20,000 x g, 15 minutes;
Sorvall 28-S., SS-34 rotor) and resuspended in 30 volumes of ice-cold buffer A.
For the binding assays, 1.5 ml eppendorf tubes containing 50 ~1 of test compound (made up as a lOx stock in water) or water, 50 ~1 [3H] IP3 (17Ci/mmol; Dupont-NEN;
usually made as a 25 nM (lOx) stock solution in buffer), and 350 ~1 of buffer B (buffer A with pH adjusted to 8.4) . on ice. Tubes for non-specific binding also contained 50 ~1 of non-radioactive IP3 (100 ~M stock (lOx); final concentration 10 ~M), with an appropriate reduction in the volume of buffer B. Reactions were initiated by the addition of 50 ~1 tissue to make the final volume 500 ~1, 214~681 ~
followed by vortex mixing. Samples were incubated on ice for 10 minutes and then were centrifuged (14,000 x g) in a microfuge (Eppendorf model 5415) for 5 minutes followed by aspiration of the supernatant fraction. The tissue pellets were solubilized overnight in 100 ~1 of Protosol (Dupont-NEN). After solubilization, 73 ~1 of glacial acetic acid were added to decrease chemiluminescence, and the mixture was transferred to scintillation vials. To these vials was added 7 ml of Ecoscint-A (National Diagnostics) and the radioactivity determined by li~uid scintillation spectrophotometry.
Specific binding was defined as the difference between total binding (radioactivity in the absence of test compound and cold IP3) and non-specific binding (radioactivity in the absence of test compound but in the presence of cold IP3). This number was taken as 100%
specific binding. Data points obtained with the test compounds were fit by a computer program (GraphPad-InPlot) to determine their inhibitory potency. The inhibitory potencies of the test compounds were expressed as the concentration of compound that produces 50~ inhibition of specific binding (the ICso value).
The binding data are presented in Table 1 and demonstrate that compounds within the scope of the present invention effectively compete for [3H] IP3 binding sites in rat cerebellar membranes. The compound identified as MDL
102,869 was the most potent competitor for binding with an IC50 of 50 nM, whereas low molecular weight heparin (5100 MW) had an IC50 of 74 nM. MDL 102,869 is the compound according to the claimed invention wherein n = 15.
The potency for binding also seems to correlate with the ability to antagonize IP3-induced calcium ion release.
Thus, 1 and 3 ~M of MDL 102,869 inhibited calcium ion release by 42 and 100~, respectively (see Fig. 1), whereas WO 94/07507 2 1 4 5 ~ 8 1 PCI/US93/08168 10 llM of heparin inhibited release by 9o%. MDL 101,828, which had an IC50 binding of 104 nM, inhibited IP3-induced calcium ion release by 72% at 3 micro moles. MDL 101,828 is the compound according to the claimed invention wherein n = 9.
BindingInhibition of Ins(1,4,5) P3-CompoundICso (nM)Induced Ca2+-release Heparin (low MW)74 9o% at 10 ~M
MDL 101,828 104 42% at 3 llM
MDL 102,869 50 42% at 1 llM
100% at 3 ~M
The tracing of Fig. 1, dramatically illustrates the IP3 inhibition data set forth in the third column of Table 1.
S03~Na +
O ~ O
~H H 4~H N ~CH3 S03~Na +
--n The y-axis represents the concentration of free calcium ions in arbitrary units. The tracing shows that two successive additions of 0.1 llM of IP3 stimulated similar amounts of calcium ion release from cerebellar microsomes.
The addition of 1 ~lM of MDL 102,869 stimulated a small increase of calcium ion for unknown reasons. In the presence of 102,869, however, calcium ion release stimulated by 0.1 ~lM of IP3 was inhibited by 42%. This inhibition was overcome by the addition of 1 llM of IP3, consistent with competitive antagonism by MDL 102,869.
H3C~N~I ~NJ~N ~CH3 S03~Na +
-- --n wherein n is a whole number selected from the range of 5 to 20 inclusive and the pharmaceutically acceptable salts thereof.
., DETAILED DESCRIPTION OF THE INVENTION
Inositol 1,4,5-triphosphate (IP3) is a naturally occurring and active component of animal physiology. It is formed intracellularly upon the activation of cell-surface receptors linked to the enzyme phospholipase C. Once generated in sufficient quantities, IP3 acts to stimulate the release of calcium ions from storage organelles within the cell. In this role IP3 is characterized as a "second messenger". Depending upon the type of cell, the calcium released by IP3 ~unctions to stimulate a variety of physiologic processes such as smooth muscle contraction, histamine secretion and the hyperpolarization of nerve cells. Any compound or agent that can promote or interfere with the function of IP3, will promote or interfere with the generation of calcium ions and thereby elicit predictable pharmacological effects.
The process by which IP3 releases calcium ions begins with the binding of IP3 to a specific receptor protein located on an intracellular calcium storage compartment located typically on the endoplasmic reticulum. This receptor protein has been cloned and has been shown to form a calcium "channel" with unique structural properties when bound to IP3. Therefore, when IP3 binds with its receptor, a calcium channel is opened causing the release of calcium stored in the cell's endoplasmic reticulum. In turn, the released calcium will elicit the appropriate cellular response.
Heretofore, the only verified potent antagonist of the 5 IP3 receptor was heparin, a complex glycosaminoglycan. The diamino benzenedisulfonic acid oligomers of this invention also appear to antagonize the effects of IP3 by competing for the receptor site. In most cases, these compounds are more effective than heparin and demonstrate fewer secondary effects. In addition to providing utility as laboratory "tools" in evaluating the therapeutic potential of other IP3 receptor antagonists, the oligomers of this invention would also be administered to modulate IP3-induced calcium release and have a salutary effect on any number of disorders that are caused or exacerbated by an inordinately productive IP3 second messenger pathway.
EXPERIMENTALS
Measurement of IP3 Bindinq Cerebella from male Sprague-Dawley rats (200 g) were homogenized in 30 volumes of ice-cold buffer A (50 mM Tris, 1 mM dithiothreitol, 1 mM EDTA, pH 7.7 with HCl) with a polytron (setting 9 for 10 seconds). The tissue is then washed twice by centrifugation (20,000 x g, 15 minutes;
Sorvall 28-S., SS-34 rotor) and resuspended in 30 volumes of ice-cold buffer A.
For the binding assays, 1.5 ml eppendorf tubes containing 50 ~1 of test compound (made up as a lOx stock in water) or water, 50 ~1 [3H] IP3 (17Ci/mmol; Dupont-NEN;
usually made as a 25 nM (lOx) stock solution in buffer), and 350 ~1 of buffer B (buffer A with pH adjusted to 8.4) . on ice. Tubes for non-specific binding also contained 50 ~1 of non-radioactive IP3 (100 ~M stock (lOx); final concentration 10 ~M), with an appropriate reduction in the volume of buffer B. Reactions were initiated by the addition of 50 ~1 tissue to make the final volume 500 ~1, 214~681 ~
followed by vortex mixing. Samples were incubated on ice for 10 minutes and then were centrifuged (14,000 x g) in a microfuge (Eppendorf model 5415) for 5 minutes followed by aspiration of the supernatant fraction. The tissue pellets were solubilized overnight in 100 ~1 of Protosol (Dupont-NEN). After solubilization, 73 ~1 of glacial acetic acid were added to decrease chemiluminescence, and the mixture was transferred to scintillation vials. To these vials was added 7 ml of Ecoscint-A (National Diagnostics) and the radioactivity determined by li~uid scintillation spectrophotometry.
Specific binding was defined as the difference between total binding (radioactivity in the absence of test compound and cold IP3) and non-specific binding (radioactivity in the absence of test compound but in the presence of cold IP3). This number was taken as 100%
specific binding. Data points obtained with the test compounds were fit by a computer program (GraphPad-InPlot) to determine their inhibitory potency. The inhibitory potencies of the test compounds were expressed as the concentration of compound that produces 50~ inhibition of specific binding (the ICso value).
The binding data are presented in Table 1 and demonstrate that compounds within the scope of the present invention effectively compete for [3H] IP3 binding sites in rat cerebellar membranes. The compound identified as MDL
102,869 was the most potent competitor for binding with an IC50 of 50 nM, whereas low molecular weight heparin (5100 MW) had an IC50 of 74 nM. MDL 102,869 is the compound according to the claimed invention wherein n = 15.
The potency for binding also seems to correlate with the ability to antagonize IP3-induced calcium ion release.
Thus, 1 and 3 ~M of MDL 102,869 inhibited calcium ion release by 42 and 100~, respectively (see Fig. 1), whereas WO 94/07507 2 1 4 5 ~ 8 1 PCI/US93/08168 10 llM of heparin inhibited release by 9o%. MDL 101,828, which had an IC50 binding of 104 nM, inhibited IP3-induced calcium ion release by 72% at 3 micro moles. MDL 101,828 is the compound according to the claimed invention wherein n = 9.
BindingInhibition of Ins(1,4,5) P3-CompoundICso (nM)Induced Ca2+-release Heparin (low MW)74 9o% at 10 ~M
MDL 101,828 104 42% at 3 llM
MDL 102,869 50 42% at 1 llM
100% at 3 ~M
The tracing of Fig. 1, dramatically illustrates the IP3 inhibition data set forth in the third column of Table 1.
S03~Na +
O ~ O
~H H 4~H N ~CH3 S03~Na +
--n The y-axis represents the concentration of free calcium ions in arbitrary units. The tracing shows that two successive additions of 0.1 llM of IP3 stimulated similar amounts of calcium ion release from cerebellar microsomes.
The addition of 1 ~lM of MDL 102,869 stimulated a small increase of calcium ion for unknown reasons. In the presence of 102,869, however, calcium ion release stimulated by 0.1 ~lM of IP3 was inhibited by 42%. This inhibition was overcome by the addition of 1 llM of IP3, consistent with competitive antagonism by MDL 102,869.
Claims (3)
1. The use in the manufacture of a medicament for inhibiting the activity of inositol 1,4,5-trisphosphate by occupying a receptor site specific to inositol 1,4,5-trisphosphate effected with a compound of the formula:
wherein n is a whole number within the range of 5-20 and the pharmaceutically acceptable salts thereof.
wherein n is a whole number within the range of 5-20 and the pharmaceutically acceptable salts thereof.
2. The use of a compound according to claim 1 wherein n is 9.
3. The use of a compound according to claim 1 wherein n is 15.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95239392A | 1992-09-28 | 1992-09-28 | |
| US07/952,393 | 1992-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2145681A1 true CA2145681A1 (en) | 1994-04-14 |
Family
ID=25492868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002145681A Abandoned CA2145681A1 (en) | 1992-09-28 | 1993-08-30 | Method for antogonizing inositol 1,4,5-triphosphate |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0661982A1 (en) |
| JP (1) | JPH08502068A (en) |
| KR (1) | KR950703347A (en) |
| AU (1) | AU670962B2 (en) |
| CA (1) | CA2145681A1 (en) |
| HU (1) | HUT70192A (en) |
| IL (1) | IL107066A (en) |
| MX (1) | MX9305933A (en) |
| NO (1) | NO951163L (en) |
| NZ (1) | NZ256178A (en) |
| TW (1) | TW260663B (en) |
| WO (1) | WO1994007507A1 (en) |
| ZA (1) | ZA936978B (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2978995A (en) * | 1994-06-30 | 1996-01-25 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. | Methods for treating cell proliferative disorders by modulating signal transduction |
| US5780483A (en) * | 1995-02-17 | 1998-07-14 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| JPH11503110A (en) | 1995-02-17 | 1999-03-23 | スミスクライン・ビーチャム・コーポレイション | IL-8 receptor antagonist |
| US6083920A (en) * | 1995-12-21 | 2000-07-04 | Ayurcore, Inc. | Compositions for modulating intracellular inositol trisphosphate concentration |
| US6005008A (en) * | 1996-02-16 | 1999-12-21 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| US6211373B1 (en) | 1996-03-20 | 2001-04-03 | Smithkline Beecham Corporation | Phenyl urea antagonists of the IL-8 receptor |
| US6262113B1 (en) | 1996-03-20 | 2001-07-17 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| AU3409197A (en) * | 1996-06-27 | 1998-01-14 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
| TR199802695T2 (en) | 1996-06-27 | 1999-04-21 | Smithkline Beecham Corporation | IL-8 Resett�r kar��tlar� |
| DE60127703D1 (en) * | 2000-11-09 | 2007-05-16 | Contrimmune Biotechnology Inc | USE OF XESTOSPONGIN C TO TREAT OR PREVENT HIV INFECTION |
| JP2014531425A (en) | 2011-09-02 | 2014-11-27 | ザ トラスティーズ オブ コロンビア ユニヴァーシティ イン ザ シティ オブ ニューヨーク | CaMKII, IP3R, calcineurin, p38, and MK2 / 3 inhibitors for treating metabolic disorders of obesity |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB781479A (en) * | 1953-08-27 | 1957-08-21 | Ciba Ltd | New polyureas and process for making them |
| US5276182A (en) * | 1990-07-09 | 1994-01-04 | The Dow Chemical Company | Process for preparing polyurea oligomers |
-
1993
- 1993-08-30 JP JP6509054A patent/JPH08502068A/en active Pending
- 1993-08-30 CA CA002145681A patent/CA2145681A1/en not_active Abandoned
- 1993-08-30 AU AU48417/93A patent/AU670962B2/en not_active Ceased
- 1993-08-30 HU HU9500891A patent/HUT70192A/en unknown
- 1993-08-30 EP EP93921252A patent/EP0661982A1/en not_active Ceased
- 1993-08-30 WO PCT/US1993/008168 patent/WO1994007507A1/en not_active Application Discontinuation
- 1993-08-30 KR KR1019950701166A patent/KR950703347A/en not_active Ceased
- 1993-08-30 NZ NZ256178A patent/NZ256178A/en unknown
- 1993-09-21 ZA ZA936978A patent/ZA936978B/en unknown
- 1993-09-22 TW TW082107787A patent/TW260663B/zh active
- 1993-09-22 IL IL107066A patent/IL107066A/en not_active IP Right Cessation
- 1993-09-27 MX MX9305933A patent/MX9305933A/en unknown
-
1995
- 1995-03-27 NO NO951163A patent/NO951163L/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO951163D0 (en) | 1995-03-27 |
| TW260663B (en) | 1995-10-21 |
| EP0661982A1 (en) | 1995-07-12 |
| HU9500891D0 (en) | 1995-05-29 |
| AU670962B2 (en) | 1996-08-08 |
| ZA936978B (en) | 1994-04-18 |
| HUT70192A (en) | 1995-09-28 |
| AU4841793A (en) | 1994-04-26 |
| NZ256178A (en) | 1997-03-24 |
| NO951163L (en) | 1995-03-27 |
| IL107066A0 (en) | 1993-12-28 |
| IL107066A (en) | 1998-01-04 |
| KR950703347A (en) | 1995-09-20 |
| WO1994007507A1 (en) | 1994-04-14 |
| MX9305933A (en) | 1994-04-29 |
| JPH08502068A (en) | 1996-03-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued | ||
| FZDE | Discontinued |
Effective date: 19990518 |