
Identità
Dolutegravir Sodium
Mhux elenkat · C20H18F2N3NaO5
01Identità
| Lazychem ID | LC-60193 |
|---|---|
| CAS RN | Mhux elenkat |
| PubChem CID | 46216142 |
| Molecular formula | C20H18F2N3NaO5 |
| Molecular weight | 441.4 g/mol |
| IUPAC name | sodium (3S,7R)-13-[(2,4-difluorophenyl)methylcarbamoyl]-7-methyl-9,12-dioxo-4-oxa-1,8-diazatricyclo[8.4.0.03,8]tetradeca-10,13-dien-11-olate |
| InChIKey | UGWJRRXTMKRYNK-VSLILLSYSA-M |
02Struttura u stereokimika

The parsed structure contains 4 rings, includes aromatic atoms, includes aliphatic carbon, has 2 defined stereocentres, contains at least one halogen atom. These statements are calculated from the published structure string.
| Defined stereocentres | 2 |
|---|---|
| Ring count | 4 |
| Secondary amines | 0 |
| Tertiary amines | 0 |
| SMILES | C[C@@H]1CCO[C@@H]2N1C(=O)C3=C(C(=O)C(=CN3C2)C(=O)NCC4=C(C=C(C=C4)F)F)[O-].[Na+] |
|---|---|
| InChI | Mhux elenkat |
03Stereochemistry
The published structure contains 2 defined and 0 unassigned tetrahedral stereocentres. The exact wedge and dash depiction is shown above.
Published same-connectivity configurations
2 recordsThese records have the same connectivity, molecular formula and protonation layer, but a different complete InChIKey stereochemical layer. Only separately structure-linked records are shown.


Dolutegravir Enantiomer Impurity (Na Salt)
CAS 1309575-43-6
UGWJRRXTMKRYNK-OEQYQXMYSA-M
2 defined, 0 unassigned centres
Scope: The mathematical 2^n value is only an upper bound. Symmetry and other stereogenic elements can change the number of distinct stereoisomers. A hypothetical configuration is not published as a compound record without a verified structure identity.
04Status fl-Indja
Exact-compound status is evaluated only against the published name and CAS number. Confirm the current official instrument before a regulatory decision.
05Ismijiet u relazzjonijiet
API u mediċina prinċipali
Mhux elenkat
Ismijiet u relazzjonijiet
06Sorsi
- S01PubChem CID 46216142
Structure and machine-readable chemical identifiers.
