Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0L1XR
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| Former ID |
DNC000705
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| Drug Name |
Green tea
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| Synonyms |
Oxotremorine; Oxytremorine; Oxotremorin; Tremorine, oxo-; 70-22-4; 2'-Oxopyrrolidino-1-pyrrolidino-4-butyne; MLS000766260; UNII-5RY0UWH1JL; EINECS 200-728-0; 5RY0UWH1JL; NSC 330497; 1-(4-pyrrolidin-1-ylbut-2-ynyl)pyrrolidin-2-one; BRN 1530948; CHEMBL7634; 1-(4-(Pyrrolidin-1-yl)but-2-ynyl)pyrrolidin-2-one; CHEBI:7851; 2-PYRROLIDINONE, 1-(4-(1-PYRROLIDINYL)-2-BUTYNYL)-; RSDOPYMFZBJHRL-UHFFFAOYSA-N; 2-Pyrrolidinone, 1-[4-(1-pyrrolidinyl)-2-butynyl]-; Tocris-0843; Spectrum_001875; Spectrum_001448; AC1L1ILJ; Spectrum5_001099
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1], [2] | |
| Structure |
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Download2D MOL |
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| Formula |
C12H18N2O
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| Canonical SMILES |
C1CCN(C1)CC#CCN2CCCC2=O
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| InChI |
1S/C12H18N2O/c15-12-6-5-11-14(12)10-4-3-9-13-7-1-2-8-13/h1-2,5-11H2
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| InChIKey |
RSDOPYMFZBJHRL-UHFFFAOYSA-N
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| CAS Number |
CAS 70-22-4
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| PubChem Compound ID | ||||
| PubChem Substance ID |
9688, 459069, 3135307, 5204099, 7979247, 8152842, 11111578, 11113735, 11335585, 11360824, 11364342, 11364805, 11366904, 11367367, 11369466, 11369929, 11372797, 11374542, 11377628, 11378096, 11461796, 11485212, 11489384, 11491414, 11492727, 11495262, 11495689, 15121093, 26732553, 26751921, 29223719, 47365120, 47662212, 47810683, 47885342, 48334423, 50039957, 50104597, 50237746, 53786784, 57322362, 85209959, 85787108, 90341593, 92308793, 103088501, 103156731, 103165591, 103918252, 104306964
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| ChEBI ID |
CHEBI:7851
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| References | Top | |||
|---|---|---|---|---|
| REF 1 | URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 302). | |||
| REF 2 | Squalene epoxidase as hypocholesterolemic drug target revisited. Prog Lipid Res. 2003 Jan;42(1):37-50. | |||
| REF 3 | Evaluation of muscarinic agonist-induced analgesia in muscarinic acetylcholine receptor knockout mice. Mol Pharmacol. 2002 Nov;62(5):1084-93. | |||
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