Tryptanthrine
- Tryptanthrin
- Indolo[2,1-b]quinazoline-6,12-dione
- 13220-57-0
- Tryptanthrine
- TCMDC-125859
- Create:2005-03-26
- Modify:2025-02-01
- 6,12-dihydro-6,12-dioxoindole(2,1-b)quinazoline
- indolo (2, 1b) quinazoline-6, 12 dione
- indolo(2,1-b)quinazolin-6,12-dione
- tryptanthrin
- tryptanthrine
- Tryptanthrin
- Indolo[2,1-b]quinazoline-6,12-dione
- 13220-57-0
- Tryptanthrine
- TCMDC-125859
- GNF-PF-2691
- MFCD00012073
- Indolo(2,1-b)quinazoline-6,12-dione
- NSC 349447
- CHEBI:9768
- CHEMBL306946
- 4Y6E3F2U66
- NSC349447
- NSC-349447
- C15H8N2O2
- SR-01000521538
- Tryptantherin
- Trypthanthrine
- Indolo[2,1-b]quinazoline-6,12-dione; Couroupitine A; NSC 349447; TryptanthrinTryptanthrine;
- TRIPTANTRIN
- Indolo[2,12-dione
- Tryptanthrin (Standard)
- Oprea1_754264
- 6,12-dihydro-6,12-dioxoindole(2,1-b)quinazoline
- MLS001049121
- UNII-4Y6E3F2U66
- GTPL8224
- SCHEMBL2426211
- HY-N6607R
- DTXSID90157431
- Tryptanthrin, >=98% (HPLC)
- HMS2271H05
- HY-N6607
- BDBM50240612
- NSC827100
- s5686
- STK078931
- AKOS000671350
- CCG-208326
- NSC-827100
- NCGC00160337-01
- NCGC00160337-02
- DA-78676
- DS-15687
- NCI60_003113
- SMR000386951
- SY017117
- CS-0034349
- NS00094832
- SR-01000521538-1
- SR-01000521538-4
- BRD-K76973696-001-12-6
- Q27089028
- Indolo[2 pound not1-b]quinazoline-6 pound not12-dione
249.065140 100
130.028854 49.37
221.069290 24.80
250.067764 20.36
102.034676 9.48
130.0277948016827 100
249.07130331600877 78.96
221.07172573271066 31.63
102.0318840636928 21.20
77.03855392170726 11.57
249.06617736816406 100
130.0288848876953 24.01
221.0712127685547 6.36
130.04002380371094 5.54
65.038818359375 2.72
P264, P270, P301+P317, P330, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)
Patents are available for this chemical structure:
https://patentscope.wipo.int/search/en/result.jsf?inchikey=VQQVWGVXDIPORV-UHFFFAOYSA-N
- CAS Common ChemistryLICENSEThe data from CAS Common Chemistry is provided under a CC-BY-NC 4.0 license, unless otherwise stated.https://creativecommons.org/licenses/by-nc/4.0/
- ChemIDplusChemIDplus Chemical Information Classificationhttps://pubchem.ncbi.nlm.nih.gov/source/ChemIDplus
- DTP/NCILICENSEUnless otherwise indicated, all text within NCI products is free of copyright and may be reused without our permission. Credit the National Cancer Institute as the source.https://www.cancer.gov/policies/copyright-reuse
- EPA DSSToxTryptanthrinehttps://comptox.epa.gov/dashboard/DTXSID90157431CompTox Chemicals Dashboard Chemical Listshttps://comptox.epa.gov/dashboard/chemical-lists/
- European Chemicals Agency (ECHA)LICENSEUse of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: "Source: European Chemicals Agency, http://echa.europa.eu/". Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page.https://echa.europa.eu/web/guest/legal-noticeIndolo[2,1-b]quinazoline-6,12-dionehttps://echa.europa.euIndolo[2,1-b]quinazoline-6,12-dione (EC: 106-491-9)https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/392976
- FDA Global Substance Registration System (GSRS)LICENSEUnless otherwise noted, the contents of the FDA website (www.fda.gov), both text and graphics, are not copyrighted. They are in the public domain and may be republished, reprinted and otherwise used freely by anyone without the need to obtain permission from FDA. Credit to the U.S. Food and Drug Administration as the source is appreciated but not required.https://www.fda.gov/about-fda/about-website/website-policies#linking
- ChEBI
- LOTUS - the natural products occurrence databaseLICENSEThe code for LOTUS is released under the GNU General Public License v3.0.https://lotus.nprod.net/Indolo[2,1-b]quinazoline-6,12-dionehttps://www.wikidata.org/wiki/Q27089028LOTUS Treehttps://lotus.naturalproducts.net/
- ChEMBLLICENSEAccess to the web interface of ChEMBL is made under the EBI's Terms of Use (http://www.ebi.ac.uk/Information/termsofuse.html). The ChEMBL data is made available on a Creative Commons Attribution-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-sa/3.0/).http://www.ebi.ac.uk/Information/termsofuse.htmlChEMBL Protein Target Treehttps://www.ebi.ac.uk/chembl/g/#browse/targets
- Comparative Toxicogenomics Database (CTD)LICENSEIt is to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of NC State University.http://ctdbase.org/about/legal.jsptryptanthrinehttps://ctdbase.org/detail.go?type=chem&acc=C046243
- IUPHAR/BPS Guide to PHARMACOLOGYLICENSEThe Guide to PHARMACOLOGY database is licensed under the Open Data Commons Open Database License (ODbL) https://opendatacommons.org/licenses/odbl/. Its contents are licensed under a Creative Commons Attribution-ShareAlike 4.0 International License (http://creativecommons.org/licenses/by-sa/4.0/)https://www.guidetopharmacology.org/about.jsp#licenseGuide to Pharmacology Target Classificationhttps://www.guidetopharmacology.org/targets.jsp
- Therapeutic Target Database (TTD)tryptanthrinhttps://idrblab.net/ttd/data/drug/details/D0I9AT
- Crystallography Open Database (COD)LICENSEAll data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License. Users of the data should acknowledge the original authors of the structural data.https://creativecommons.org/publicdomain/zero/1.0/
- Human Metabolome Database (HMDB)LICENSEHMDB is offered to the public as a freely available resource. Use and re-distribution of the data, in whole or in part, for commercial purposes requires explicit permission of the authors and explicit acknowledgment of the source material (HMDB) and the original publication (see the HMDB citing page). We ask that users who download significant portions of the database cite the HMDB paper in any resulting publications.http://www.hmdb.ca/citingIndolo[2,1-b]quinazoline-6,12-dionehttp://www.hmdb.ca/metabolites/HMDB0253473
- Japan Chemical Substance Dictionary (Nikkaji)
- KEGGLICENSEAcademic users may freely use the KEGG website. Non-academic use of KEGG generally requires a commercial licensehttps://www.kegg.jp/kegg/legal.htmlPhytochemical compoundshttp://www.genome.jp/kegg-bin/get_htext?br08003.keg
- KNApSAcK Species-Metabolite Database
- Natural Product Activity and Species Source (NPASS)
- NORMAN Suspect List ExchangeLICENSEData: CC-BY 4.0; Code (hosted by ECI, LCSB): Artistic-2.0https://creativecommons.org/licenses/by/4.0/TrypthanthrineNORMAN Suspect List Exchange Classificationhttps://www.norman-network.com/nds/SLE/
- MassBank of North America (MoNA)LICENSEThe content of the MoNA database is licensed under CC BY 4.0.https://mona.fiehnlab.ucdavis.edu/documentation/license
- Metabolomics Workbench
- NIST Mass Spectrometry Data CenterLICENSEData covered by the Standard Reference Data Act of 1968 as amended.https://www.nist.gov/srd/public-lawTryptanthrinehttp://www.nist.gov/srd/nist1a.cfm
- SpectraBaseIndolo[2,1-b]quinazoline-6,12-dionehttps://spectrabase.com/spectrum/HYioun47xCsIndolo[2,1-b]quinazoline-6,12-dionehttps://spectrabase.com/spectrum/7zqTiSx6nNVTRYPTANTHRINhttps://spectrabase.com/spectrum/33DhgpVkUWfTryptanthrinehttps://spectrabase.com/spectrum/Lvm0gWWi3ozIndolo[2,1-b]quinazoline-6,12-dionehttps://spectrabase.com/spectrum/4bZ3DP0dzMFTryptanthrinehttps://spectrabase.com/spectrum/GCWISK4vUYLTryptanthrinehttps://spectrabase.com/spectrum/Kzy6RUUxAlm
- PharosLICENSEData accessed from Pharos and TCRD is publicly available from the primary sources listed above. Please respect their individual licenses regarding proper use and redistribution.https://pharos.nih.gov/abouttryptanthrinhttps://pharos.nih.gov/ligands/C3DQ9SDFJYBK
- Springer Nature
- Thieme ChemistryLICENSEThe Thieme Chemistry contribution within PubChem is provided under a CC-BY-NC-ND 4.0 license, unless otherwise stated.https://creativecommons.org/licenses/by-nc-nd/4.0/
- Wikidatatryptanthrinhttps://www.wikidata.org/wiki/Q27089028
- Wiley
- PubChem
- Medical Subject Headings (MeSH)LICENSEWorks produced by the U.S. government are not subject to copyright protection in the United States. Any such works found on National Library of Medicine (NLM) Web sites may be freely used or reproduced without permission in the U.S.https://www.nlm.nih.gov/copyright.htmltryptanthrinehttps://www.ncbi.nlm.nih.gov/mesh/67046243
- GHS Classification (UNECE)GHS Classification Treehttp://www.unece.org/trans/danger/publi/ghs/ghs_welcome_e.html
- MolGenieMolGenie Organic Chemistry Ontologyhttps://github.com/MolGenie/ontology/
- PATENTSCOPE (WIPO)SID 403732808https://pubchem.ncbi.nlm.nih.gov/substance/403732808