Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C20H24N2O3S |
| Molecular Weight | 372.481 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)[C@@H]2SC3=CC=CC=C3N(CCN(C)C)C(=O)[C@@H]2O
InChI
InChIKey=NZHUXMZTSSZXSB-MOPGFXCFSA-N
InChI=1S/C20H24N2O3S/c1-21(2)12-13-22-16-6-4-5-7-17(16)26-19(18(23)20(22)24)14-8-10-15(25-3)11-9-14/h4-11,18-19,23H,12-13H2,1-3H3/t18-,19+/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Anaphylatoxin C3a induces rapid protein phosphorylation in guinea pig platelets. | 1994 Sep-Oct |
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| Inhibitory effects of TA-993, a new 1,5-benzothiazepine derivative, on platelet aggregation. | 1996 Apr |
|
| Clinical pharmacokinetics and pharmacodynamics of buspirone, an anxiolytic drug. | 1999 Apr |
|
| An in vitro model for predicting in vivo inhibition of cytochrome P450 3A4 by metabolic intermediate complex formation. | 2000 Sep |
Patents
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| Code System | Code | Type | Description | ||
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91638
Created by
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SUB112491
Created by
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C037769
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91602-22-1
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100000142066
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42399-40-6
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admin on Fri Dec 15 16:17:11 GMT 2023 , Edited by admin on Fri Dec 15 16:17:11 GMT 2023
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255-795-9
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DTXSID00881093
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admin on Fri Dec 15 16:17:11 GMT 2023 , Edited by admin on Fri Dec 15 16:17:11 GMT 2023
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849UT193YJ
Created by
admin on Fri Dec 15 16:17:11 GMT 2023 , Edited by admin on Fri Dec 15 16:17:11 GMT 2023
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PRIMARY |
PARENT (METABOLITE)
SALT/SOLVATE (PARENT)
SUBSTANCE RECORD
