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Details

Stereochemistry ACHIRAL
Molecular Formula C24H16BrCl2FN3O5S.Na
Molecular Weight 651.264
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ELSULFAVIRINE SODIUM

SMILES

[Na+].CCC(=O)[N-]S(=O)(=O)C1=CC=C(NC(=O)CC2=C(F)C(OC3=CC(Cl)=CC(=C3)C#N)=C(Br)C=C2)C(Cl)=C1

InChI

InChIKey=UJFARQSHFFWJHD-UHFFFAOYSA-M
InChI=1S/C24H17BrCl2FN3O5S.Na/c1-2-21(32)31-37(34,35)17-4-6-20(19(27)11-17)30-22(33)9-14-3-5-18(25)24(23(14)28)36-16-8-13(12-29)7-15(26)10-16;/h3-8,10-11H,2,9H2,1H3,(H2,30,31,32,33);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C24H17BrCl2FN3O5S
Molecular Weight 629.282
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

R-1206 (also known as Elsulfavirine) is a phenylacetamide derivative patented by Roche Palo Alto LLC as non-nucleoside reverse transcriptase inhibitor (NNRTI) for treating retroviral infections. R-1206 is the prodrug of the active compound VM-1500A, a small molecule selective NNRTI, which prevents HIV replication. The antiviral activity of R-1206 is broad, with activity demonstrated towards various viral strains and clinical isolates of HIV, including those resistant to other NNRTIs. Furthermore, R-1206 was associated with a low probability of cross-resistance or resistance development, and a high genetic barrier to the development of resistant drug mutations. In clinical trials, R-1206 20 and 40 mg demonstrated superiority to efavirenz in terms of the effectiveness to reduce the level of viral load to 400 copies/mL after 12 weeks of therapy. R-1206 20 mg once daily is generally well tolerated in ART-naive HIV-1 infected patients.

Approval Year

PubMed

PubMed

TitleDatePubMed
Elsulfavirine: First Global Approval.
2017 Oct
Patents

Patents

Sample Use Guides

20 mg once daily, taken 15 min before meals
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:36:50 GMT 2023
Edited
by admin
on Sat Dec 16 11:36:50 GMT 2023
Record UNII
HKK2U3V1DT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ELSULFAVIRINE SODIUM
Common Name English
ELPIDA
Brand Name English
BENZENEACETAMIDE, 4-BROMO-3-(3-CHLORO-5-CYANOPHENOXY)-N-(2-CHLORO-4-(((1-OXOPROPYL)AMINO)SULFONYL)PHENYL)-2-FLUORO-, MONOSODIUM SALT
Systematic Name English
R-1206 SODIUM
Code English
BENZENEACETAMIDE, 4-BROMO-3-(3-CHLORO-5-CYANOPHENOXY)-N-(2-CHLORO-4-(((1-OXOPROPYL)AMINO)SULFONYL)PHENYL)-2-FLUORO-, SODIUM SALT (1:1)
Systematic Name English
R1206(SODIUM SALT)
Code English
Code System Code Type Description
FDA UNII
HKK2U3V1DT
Created by admin on Sat Dec 16 11:36:50 GMT 2023 , Edited by admin on Sat Dec 16 11:36:50 GMT 2023
PRIMARY
PUBCHEM
46175184
Created by admin on Sat Dec 16 11:36:50 GMT 2023 , Edited by admin on Sat Dec 16 11:36:50 GMT 2023
PRIMARY
SMS_ID
300000021740
Created by admin on Sat Dec 16 11:36:50 GMT 2023 , Edited by admin on Sat Dec 16 11:36:50 GMT 2023
PRIMARY
CAS
867365-40-0
Created by admin on Sat Dec 16 11:36:50 GMT 2023 , Edited by admin on Sat Dec 16 11:36:50 GMT 2023
PRIMARY
CAS
1946785-27-8
Created by admin on Sat Dec 16 11:36:50 GMT 2023 , Edited by admin on Sat Dec 16 11:36:50 GMT 2023
ALTERNATIVE
Related Record Type Details
PARENT -> SALT/SOLVATE