Digitoxigenin
- Digitoxigenin
- 143-62-4
- Cerberigenin
- Echujetin
- Evonogenin
- Create:2005-06-24
- Modify:2025-01-11
- Digitoxigenin
- Uzarigenin
- Digitoxigenin
- 143-62-4
- Cerberigenin
- Echujetin
- Evonogenin
- Thevetigenin
- Digitoxigenine
- MLS002153810
- S63WOD4VOL
- 3-[(3S,5R,8R,9S,10S,13R,14S,17R)-3,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
- NSC 407806
- CHEBI:42219
- EINECS 205-603-4
- MFCD00003687
- 3beta,14-Dihydroxy-5beta-card-20(22)-enolide
- DIGITOXIGENIN [MI]
- (+)-DIGITOXIGENIN
- NSC-407806
- BRN 0095448
- 3-beta,14-Dioxy-digen-(20:22)-olid
- 3-beta,14-Dioxy-carden-(20:22)-olid
- Cardogenen-(20:22)-diol-(3-beta,14)
- DTXSID80162276
- 3-beta,14-Dioxy-digen-(20:22)-olid [German]
- 5-18-03-00348 (Beilstein Handbook Reference)
- 3-beta,14-Dihydroxy-5-beta-card-20(22)-enolide
- 3-beta,14-Dioxy-carden-(20:22)-olid [German]
- Cardogenen-(20:22)-diol-(3-beta,14) [German]
- 3-beta,14beta-dihydroxy-5-beta-card-20(22)-enolide
- 3.beta.,14-Dihydroxy-5.beta.-card-20(22)-enolide
- delta20:22-3,14,21-Trihydroxynorcholenic acid lactone
- .delta.20:22-3,14,21-Trihydroxynorcholenic acid lactone
- Card-20(22)-enolide, 3,14-dihydroxy-, (3beta,5beta)-
- delta-sup(20:22)-3,14,21-Trihydroxynorcholenicacid lactone
- SMR001233182
- Card-20(22)-enolide, 3,14-dihydroxy-, (3-beta,5-beta)-
- Card-20(22)-enolide, 3,14-dihydroxy-, (3.beta.,5.beta.)-
- delta-sup(20:22)-3,14,21-Trihydroxynorcholenic acid lactone
- 3-.beta.,14-Dioxy-digen-(20:22)-olid
- Cardogenen-(20:22)-diol-(3-.beta.,14)
- 5beta-Card-20(22)-enolide, 3beta,14-dihydroxy-
- DTX
- 5.beta.-Card-20(22)-enolide, 3.beta.,14-dihydroxy
- 5.beta.-Card-20(22)-enolide, 3.beta.,14-dihydroxy-
- 5-beta-CARD-20(22)-ENOLIDE, 3-beta,14-DIHYDROXY-
- .DELTA.-sup(20:22)-3,14,21-Trihydroxynorcholenicacid lactone
- 3b,14-Dihydroxy-5b-card-20(22)-enolide
- MLS002701726
- UNII-S63WOD4VOL
- NSC407806
- 1lnm
- 3-((3S,5R,8R,9S,10S,13R,14S,17R)-3,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta(a)phenanthren-17-yl)-2H-furan-5-one
- 4-(3,14-DIHYDROXY-10,13-DIMETHYL-HEXADECAHYDRO-CYCLOPENTA[A]PHENANTHREN-17-YL)-5H-FURAN-2-ONE
- Digitoxigenin; (+)-Digitoxigenin; NSC 407806; Card-20(22)-enolide, 3,14-dihydroxy-, (3beta,5beta)-; 5beta-Card-20(22)-enolide, 3beta,14-dihydroxy- (6CI,7CI,8CI); Delta20:22-3,14,21-Trihydroxynorcholenic acid lactone
- Prestwick_169
- Prestwick0_000436
- Prestwick1_000436
- Prestwick2_000436
- Prestwick3_000436
- CHEMBL1453
- SCHEMBL61224
- BSPBio_000452
- SPBio_002391
- BPBio1_000498
- DTXCID6084767
- BDBM66977
- cid_4369270
- 3-beta,14-Dihydroxy-5-beta,14-beta-card-20(22)-enolide
- HMS1569G14
- HMS2096G14
- HMS2231J22
- HMS3713G14
- LMST01120001
- AKOS015915862
- CCG-220436
- DB04177
- NCGC00179555-01
- 5beta,20(22)-Cardenolide-3beta,14-diol
- 3b,14b-dihydroxy-5b-carda-20(22)-enolid
- D0541
- NS00009205
- 3beta,14-Dihydroxy-5beta,20(22)-cardenolide
- 5.beta.-Card-20(22)-enolide,14-dihydroxy-
- A12049
- 3-BETA, 14-BETA-CARD-20(22)-ENOLIDE
- 5beta-Card-20(22)-enolide, 3beta,14-dihydroxy
- Q411469
- SR-01000841188
- SR-01000841188-2
- 3,14,21-Trihydroxy-20(22)-norcholenic acid lactone
- BRD-K18518344-001-03-5
- BRD-K18518344-001-15-9
- .delta.20:22-3,21-Trihydroxynorcholenic acid lactone
- 5beta-Card-20(22)-enolide, 3beta,14-dihydroxy-(8CI)
- WLN: L E5 B666TJ A1 E1 F- DT5OV CUTJ IQ OQ
- (3alpha,5beta,8alpha)-3,14-dihydroxycard-20(22)-enolide
- .delta.-sup(20:22)-3,21-Trihydroxynorcholenic acid lactone
- 3,14-Dihydroxycard-20(22)-enolide, (3.beta.,5.beta.)- #
- Card-20(22)-enolide,14-dihydroxy-, (3.beta.,5.beta.)-
- Card-20(22)-enolide, 3,14-dihydroxy-, (3beta,5beta)-(9CI)
- 3-[(3S,5R,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-3,14-bis(oxidanyl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
339.2317 999
357.2424 169
135.1168 25
293.2265 22
321.2217 21
339.2319 999
357.2426 164
321.2218 33
135.1167 22
293.2272 16
P264, P270, P301+P316, P321, P330, P405, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)
Aggregated GHS information provided per 41 reports by companies from 2 notifications to the ECHA C&L Inventory.
Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown.
Patents are available for this chemical structure:
https://patentscope.wipo.int/search/en/result.jsf?inchikey=XZTUSOXSLKTKJQ-CESUGQOBSA-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
- DrugBankLICENSECreative Common's Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/legalcode)https://www.drugbank.ca/legal/terms_of_useDigitoxigeninhttps://www.drugbank.ca/drugs/DB04177
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- EPA DSSToxDigitoxigeninhttps://comptox.epa.gov/dashboard/DTXSID80162276CompTox 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-notice3-β,14-dihydroxy-5-β,14-β-card-20(22)-enolidehttps://echa.europa.eu/substance-information/-/substanceinfo/100.005.0953-β,14-dihydroxy-5-β,14-β-card-20(22)-enolide (EC: 205-603-4)https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/133262
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- ChEBI
- LOTUS - the natural products occurrence databaseLICENSEThe code for LOTUS is released under the GNU General Public License v3.0.https://lotus.nprod.net/Digitoxigeninhttps://www.wikidata.org/wiki/Q411469LOTUS 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
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- 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.jspDigitoxigeninhttps://ctdbase.org/detail.go?type=chem&acc=D004073
- Drug Gene Interaction database (DGIdb)LICENSEThe data used in DGIdb is all open access and where possible made available as raw data dumps in the downloads section.http://www.dgidb.org/downloadsDIGITOXIGENINhttps://www.dgidb.org/drugs/drugbank:DB04177
- Therapeutic Target Database (TTD)DIGITOXIGENINhttps://idrblab.net/ttd/data/drug/details/D08ZNS
- 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/
- Japan Chemical Substance Dictionary (Nikkaji)
- LIPID MAPSLipid Classificationhttps://www.lipidmaps.org/
- 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/DigitoxigeninNORMAN Suspect List Exchange Classificationhttps://www.norman-network.com/nds/SLE/
- 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 Workbench
- Nature Chemical Biology
- Nature Synthesis
- NIST Mass Spectrometry Data CenterLICENSEData covered by the Standard Reference Data Act of 1968 as amended.https://www.nist.gov/srd/public-lawDigitoxigeninhttp://www.nist.gov/srd/nist1a.cfm
- SpectraBaseDigitoxigeninhttps://spectrabase.com/spectrum/IG4Ny2xygst3β,14-dihydroxy-5 β-card-20(22)-enolidehttps://spectrabase.com/spectrum/L2tP5tbUFoIDigitoxigeninhttps://spectrabase.com/spectrum/17V0FAd1hun(+)-Digitoxigeninhttps://spectrabase.com/spectrum/6ZAVtlvg7k3β,14-dihydroxy-5β-card-20(22)-enolidehttps://spectrabase.com/spectrum/EzVizajbBSC17-BETA-(2',5'-DIHYDRO-5'-OXO-3'-FURYL)-5-BETA,14-BETA-ANDROSTAN-3-BETA,14-DIOLhttps://spectrabase.com/spectrum/3zKIWp1tuUnDIGITOXIGENIN,(3-BETA-OH,5-BETA-H)https://spectrabase.com/spectrum/H7t4rINPend(+)-Digitoxigeninhttps://spectrabase.com/spectrum/CGMIfoO1ngw
- Protein Data Bank in Europe (PDBe)
- RCSB Protein Data Bank (RCSB PDB)LICENSEData files contained in the PDB archive (ftp://ftp.wwpdb.org) are free of all copyright restrictions and made fully and freely available for both non-commercial and commercial use. Users of the data should attribute the original authors of that structural data.https://www.rcsb.org/pages/policies
- 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/
- Wikidatadigitoxigeninhttps://www.wikidata.org/wiki/Q411469
- WikipediaCotriptylinehttps://en.wikipedia.org/wiki/CotriptylineDigitoxigeninhttps://en.wikipedia.org/wiki/Digitoxigenin
- 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.htmlDigitoxigeninhttps://www.ncbi.nlm.nih.gov/mesh/68004073
- PubChem
- 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 403033411https://pubchem.ncbi.nlm.nih.gov/substance/403033411