Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C48H73ClN2O6 |
| Molecular Weight | 809.556 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 9 / 9 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=C2[C@H]3CC[C@@H]4[C@@]5(C)CC[C@H](OC(=O)CC(C)(C)C(O)=O)C(C)(C)[C@@H]5CC[C@@]4(C)[C@]3(C)CC[C@]2(CC1=O)[C@@H](O)CN(CCN(C)C)CC6=CC=C(Cl)C=C6
InChI
InChIKey=MEOWKUXNVNJAMY-PZFKGGKESA-N
InChI=1S/C48H73ClN2O6/c1-30(2)40-34(52)26-48(37(53)29-51(25-24-50(10)11)28-31-12-14-32(49)15-13-31)23-22-46(8)33(41(40)48)16-17-36-45(7)20-19-38(57-39(54)27-43(3,4)42(55)56)44(5,6)35(45)18-21-47(36,46)9/h12-15,30,33,35-38,53H,16-29H2,1-11H3,(H,55,56)/t33-,35+,36-,37+,38+,45+,46-,47-,48+/m1/s1
Approval Year
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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1443460-91-0
Created by
admin on Mon Mar 31 21:49:50 GMT 2025 , Edited by admin on Mon Mar 31 21:49:50 GMT 2025
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PRIMARY | |||
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G9C7884M8M
Created by
admin on Mon Mar 31 21:49:50 GMT 2025 , Edited by admin on Mon Mar 31 21:49:50 GMT 2025
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PRIMARY | |||
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GSK-2838232
Created by
admin on Mon Mar 31 21:49:50 GMT 2025 , Edited by admin on Mon Mar 31 21:49:50 GMT 2025
|
PRIMARY | Biological Activity of GSK2838232: GSK2838232 inhibits HIV reverse transcriptase activity across a broad panel of HIV-1 isolates, extracted from patent WO/2013090664A1, compound 51. | ||
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71580991
Created by
admin on Mon Mar 31 21:49:50 GMT 2025 , Edited by admin on Mon Mar 31 21:49:50 GMT 2025
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PRIMARY |
ACTIVE MOIETY
