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Details

Stereochemistry ACHIRAL
Molecular Formula C20H21FN6O5
Molecular Weight 444.4163
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RALTEGRAVIR

SMILES

CN1C(=O)C(O)=C(N=C1C(C)(C)NC(=O)C2=NN=C(C)O2)C(=O)NCC3=CC=C(F)C=C3

InChI

InChIKey=CZFFBEXEKNGXKS-UHFFFAOYSA-N
InChI=1S/C20H21FN6O5/c1-10-25-26-17(32-10)16(30)24-20(2,3)19-23-13(14(28)18(31)27(19)4)15(29)22-9-11-5-7-12(21)8-6-11/h5-8,28H,9H2,1-4H3,(H,22,29)(H,24,30)

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
RALTEGRAVIR
DASH   EMA EPAR   INN   MART.   MI   VANDF   WHO-DD  
INN  
Official Name English
RALTEGRAVIR [MART.]
Common Name English
RALTEGRAVIR [VANDF]
Common Name English
Raltegravir [WHO-DD]
Common Name English
MK-0518
Code English
RALTEGRAVIR [MI]
Common Name English
RALTEGRAVIR [EMA EPAR]
Common Name English
N-(4-FLUOROBENZYL)-5-HYDROXY-1-METHYL-2-(1-METHYL-1-(((5-METHYL-1,3,4-OXADIAZOL-2-YL)CARBONYL)AMINO)ETHYL)-6-OXO-1,6-DIHYDROPYRIMIDINE-4-CARBOXAMIDE
Systematic Name English
raltegravir [INN]
Common Name English
4-PYRIMIDINECARBOXAMIDE, N-((4-FLUOROPHENYL)METHYL)-1,6-DIHYDRO-5-HYDROXY-1-METHYL-2-(1-METHYL-1-(((5-METHYL-1,3,4-OXADIAZOL-2-YL)CARBONYL)AMINO)ETHYL)-6-OXO-
Systematic Name English
N-(2-(4-(4-FLUOROBENZYLCARBAMOYL)-5-HYDROXY-1-METHYL-6-OXO-1,6- DIHYDROPYRIMIDIN-2-YL)PROPAN-2-YL)-5-METHYL-1,3,4-OXADIAZOLE-2-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C281
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
WHO-ATC J05AX08
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
NDF-RT N0000175887
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
WHO-ATC J05AR16
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
EMA ASSESSMENT REPORTS ISENTRESS (AUHTORIZED: HIV INFECTIONS)
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
LIVERTOX NBK548313
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
WHO-VATC QJ05AX08
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
NDF-RT N0000000127
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
Code System Code Type Description
EVMPD
SUB25667
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
INN
8842
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
CAS
518048-05-0
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
PUBCHEM
54671008
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
NCI_THESAURUS
C72837
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
CHEBI
82960
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
DAILYMED
22VKV8053U
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
MESH
C507898
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
DRUG CENTRAL
2352
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
HSDB
8124
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
LACTMED
Raltegravir
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
MERCK INDEX
m9486
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY Merck Index
USAN
TT-71
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
EPA CompTox
DTXSID2048660
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
DRUG BANK
DB06817
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
SMS_ID
100000091686
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
ChEMBL
CHEMBL254316
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
WIKIPEDIA
RALTEGRAVIR
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
FDA UNII
22VKV8053U
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY
RXCUI
719872
Created by admin on Fri Dec 15 16:02:32 UTC 2023 , Edited by admin on Fri Dec 15 16:02:32 UTC 2023
PRIMARY RxNorm
ACTIVE MOIETY
Structure of RALTEGRAVIR
METABOLITE INACTIVE (PARENT)
Structure of RALTEGRAVIR BETA-D-GLUCURONIDE
SALT/SOLVATE (PARENT)
Structure of RALTEGRAVIR POTASSIUM
NIH
NCATS
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ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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