(Q27089028)

Indolo[2,1-b]quinazoline-6,12-dione (English)

3 October 2016

chemical formula

C₁₅H₈N₂O₂

1 reference

Indolo[2,1-b]quinazoline-6,12-dione (English)

3 October 2016

canonical SMILES

C1=CC=C2C(=C1)C(=O)N3C4=CC=CC=C4C(=O)C3=N2

1 reference

Chemical constituents of Clausena lansium

Indolo[2,1-b]quinazoline-6,12-dione (English)

3 October 2016

8 references

Quantitative determination of the dual COX-2/5-LOX inhibitor tryptanthrin in Isatis tinctoria by ESI-LC-MS.

Identification and isolation of the cyclooxygenase-2 inhibitory principle in Isatis tinctoria

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts

A comparative study on the skin penetration of pure tryptanthrin and tryptanthrin in Isatis tinctoria extract by dermal microdialysis coupled with isotope dilution ESI-LC-MS.

Insecticidal and fungicidal compounds from Isatis tinctoria

Alkaloids from the root of Isatis indigotica

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts

Phaius mishmensis

1 reference

Isolation, structure elucidation, and synthesis of cytotoxic tryptanthrin analogues from Phaius mishmensis

Calanthe discolor

2 references

Chemical Constituents of Two Oriental Orchids, Calanthe discolor and C. liukiuensis: Precursor Indole Glycoside of Tryptanthrin and Indirubin

Novel indole S,O-bisdesmoside, calanthoside, the precursor glycoside of tryptanthrin, indirubin, and isatin, with increasing skin blood flow promoting effects, from two Calanthe species (Orchidaceae)

Cissus sicyoides

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Couroupita guianensis

1 reference

The structure and properties of some indolic constituents in Couroupita guianensis aubl

Strobilanthes cusia

1 reference

Isolation of Antifungal Principle Tryptanthrin, from Strobilanthes Cusia O. Kuntze

Persicaria tinctoria

1 reference

Anti-neuroinflammatory effects of tryptanthrin from Polygonum tinctorium Lour. in lipopolysaccharide-stimulated BV2 microglial cells

Cissus discolor

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Identifiers

InChI

InChI=1S/C15H8N2O2/c18-13-10-6-2-4-8-12(10)17-14(13)16-11-7-3-1-5-9(11)15(17)19/h1-8H

1 reference

Indolo[2,1-b]quinazoline-6,12-dione (English)

3 October 2016

2 references

Indolo[2,1-b]quinazoline-6,12-dione (English)

3 October 2016

ChEBI release 2020-09-01

2 references

Tryptanthrine (English)

3 October 2016

https://commonchemistry.cas.org/detail?cas_rn=13220-57-0

9 April 2021

1 reference

tcmdc-125859 (English)

3 October 2016

2 references

Indolo[2,1-b]quinazoline-6,12-dione (English)

3 October 2016

ChEBI ID

9768

mapping relation type

2 references

Tryptanthrine (English)

3 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H8N2O2/c18-13-10-6-2-4-8-12(10)17-14(13)16-11-7-3-1-5-9(11)15(17)19/h1-8H

1 reference

TRYPTANTHRIN (English)

3 October 2016

2 references

inferred from InChIKey

splash10-0002-0980000000-c643780746ecfc6271bf

1 reference

0 references

DSSTox substance ID

DTXSID90157431

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

DTXCID0079922

0 references

NSC number

349447

0 references

Guide to Pharmacology Ligand ID

8224

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

8224

tryptanthrin (English)

Human Metabolome Database ID

3 October 2016

HMDB0253473

2 references

based on heuristic

inferred from InChIKey

3 references

Tryptanthrine (English)

3 October 2016

based on heuristic

inferred from InChIKey

UNII

4Y6E3F2U66

1 reference

0 references

1 reference

Tryptanthrine (English)