Mitraphylline
- Mitraphylline
- 509-80-8
- Mitraphilline
- Mitraphyllin
- Rubradinine
- Create:2005-06-24
- Modify:2025-01-18
- methyl (19alpha)-19-methyl-2-oxoformosanan-16-carboxylate
- mitraphylline
- Mitraphylline
- 509-80-8
- Mitraphilline
- Mitraphyllin
- Rubradinine
- Ajmalicine oxindole B
- Rubradinin
- UNII-1H9SRL2456
- 1H9SRL2456
- EINECS 208-106-0
- Methyl 19alpha-methyl-2-oxoformosanan-16-carboxylate
- CHEBI:6957
- DTXSID50198926
- methyl (1S,4aS,5aS,6R,10aR)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate
- Methyl (19alpha)-19-methyl-2-oxoformosanan-16-carboxylate
- SPIRO(3H-INDOLE-3,6'(4'AH)-(1H)PYRANO(3,4-F)INDOLIZINE)-4'-CARBOXYLIC ACID, 1,2,5',5'A,7',8',10',10'A-OCTAHYDRO-1'-METHYL-2-OXO-, METHYL ESTER, (1'S,3R,4'AS,5'AS,10'AR)-
- MLS000728610
- Ajmalcinine oxindole B
- Mitraphylline (Standard)
- CHEMBL2135897
- HY-N6946R
- DTXCID10121417
- Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (19.alpha.)-
- HMS2267P09
- HY-N6946
- Mitraphyllin - exact weight protocol
- CCG-36401
- NSC717700
- AKOS040760558
- NSC-717700
- DA-55509
- MS-25901
- SMR000470795
- CS-0081397
- NS00032179
- C09227
- E87144
- AL-651/20569001
- MITRAPHYLLINE (CONSTITUENT OF CAT'S CLAW)
- Q10859059
- MITRAPHYLLINE (CONSTITUENT OF CAT'S CLAW) [DSC]
- Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (19alpha)-
- (1'S,3R,4a'S,5a'S,10a'R)-methyl 1'-methyl-2-oxo-1',4a',5',5a',7',8',10',10a'-octahydrospiro[indoline-3,6'-pyrano[3,4-f]indolizine]-4'-carboxylate
369.18124 999
160.07527 332
337.15479 97
309.15915 85
178.08629 51
369.18207 999
369.23773 33
337.15421 10
369.1203 8
369.28851 6
391.16579512230095 100
149.02073493195795 19.36
241.13215345495118 16.97
263.11346864930573 8.70
335.08941880340336 8.41
160.0783421746476 100
369.18558059349056 40.92
142.0665421842375 18.06
178.0901199010922 12.35
309.1650042940841 11.25
- Cat's Claw (part of)
- Mitragyna speciosa leaf (part of)
P264, P270, P301+P316, P321, P330, P405, 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=JMIAZDVHNCCPDM-DAFCLMLCSA-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
- EPA DSSToxMitraphyllinehttps://comptox.epa.gov/dashboard/DTXSID50198926CompTox 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-noticeMethyl 19α-methyl-2-oxoformosanan-16-carboxylatehttps://echa.europa.eu/substance-information/-/substanceinfo/100.007.370Methyl 19α-methyl-2-oxoformosanan-16-carboxylate (EC: 208-106-0)https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/35924
- 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/Mitraphyllinehttps://www.wikidata.org/wiki/Q10859059LOTUS 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.html
- 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
- 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.html
- Natural Product Activity and Species Source (NPASS)Methyl (1S,4As,5As,6R,10Ar)-1-Methyl-2'-Oxospiro[1,4A,5,5A,7,8,10,10A-Octahydropyrano[3,4-F]Indolizine-6,3'-1H-Indole]-4-Carboxylatehttps://bidd.group/NPASS/compound.php?compoundID=NPC298851
- MassBank Europe
- 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 WorkbenchMethyl (1S,4As,5As,6R,10Ar)-1-Methyl-2'-Oxospiro[1,4A,5,5A,7,8,10,10A-Octahydropyrano[3,4-F]Indolizine-6,3'-1H-Indole]-4-Carboxylatehttps://www.metabolomicsworkbench.org/data/StructureData.php?RegNo=126911
- SpectraBaseMITRAPHYLLINEhttps://spectrabase.com/spectrum/90Gdx5BUiSIMITRAPHYLLINEhttps://spectrabase.com/spectrum/I9YkL81NLZOMitraphyllinehttps://spectrabase.com/spectrum/AXsROUPBkGDMitraphyllinehttps://spectrabase.com/spectrum/Hdf4pL0JRsQ
- 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/
- Wikidatamitraphyllinehttps://www.wikidata.org/wiki/Q10859059
- WikipediaMitraphyllinehttps://en.wikipedia.org/wiki/Mitraphylline
- 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.htmlmitraphyllinehttps://www.ncbi.nlm.nih.gov/mesh/67509328
- GHS Classification (UNECE)GHS Classification Treehttp://www.unece.org/trans/danger/publi/ghs/ghs_welcome_e.html
- NORMAN Suspect List ExchangeLICENSEData: CC-BY 4.0; Code (hosted by ECI, LCSB): Artistic-2.0https://creativecommons.org/licenses/by/4.0/NORMAN Suspect List Exchange Classificationhttps://www.norman-network.com/nds/SLE/
- MolGenieMolGenie Organic Chemistry Ontologyhttps://github.com/MolGenie/ontology/
- PATENTSCOPE (WIPO)SID 446632280https://pubchem.ncbi.nlm.nih.gov/substance/446632280