U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C9H14N5O4P
Molecular Weight 287.2123
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TENOFOVIR ANHYDROUS

SMILES

C[C@H](CN1C=NC2=C1N=CN=C2N)OCP(O)(O)=O

InChI

InChIKey=SGOIRFVFHAKUTI-ZCFIWIBFSA-N
InChI=1S/C9H14N5O4P/c1-6(18-5-19(15,16)17)2-14-4-13-7-8(10)11-3-12-9(7)14/h3-4,6H,2,5H2,1H3,(H2,10,11,12)(H2,15,16,17)/t6-/m1/s1

HIDE SMILES / InChI

Molecular Formula C9H14N5O4P
Molecular Weight 287.2123
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:49:08 UTC 2023
Edited
by admin
on Fri Dec 15 15:49:08 UTC 2023
Record UNII
W4HFE001U5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TENOFOVIR ANHYDROUS
Common Name English
tenofovir [INN]
Common Name English
TENOFOVIR [MI]
Common Name English
Tenofovir [WHO-DD]
Common Name English
GS-1275
Code English
PHOSPHONIC ACID, P-(((1R)-2-(6-AMINO-9H-PURIN-9-YL)-1-METHYLETHOXY)METHYL)-
Systematic Name English
(R)-9-(2-PHOSPHONOMETHOXYPROPYL)ADENINE
Systematic Name English
Classification Tree Code System Code
NDF-RT N0000175459
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
NDF-RT N0000175656
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
NDF-RT N0000009947
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
NDF-RT N0000175462
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
NDF-RT N0000175459
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
NDF-RT N0000175459
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
Code System Code Type Description
WIKIPEDIA
Microbicides for sexually transmitted diseases
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
MERCK INDEX
m10559
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY Merck Index
PUBCHEM
464205
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
EPA CompTox
DTXSID9040132
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
INN
7913
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
SMS_ID
100000085232
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
RXCUI
1546017
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY RxNorm
EVMPD
SUB25192
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
ALTERNATIVE
NCI_THESAURUS
C170540
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
FDA UNII
W4HFE001U5
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
EVMPD
SUB04721MIG
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
DRUG BANK
DB00300
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
DAILYMED
W4HFE001U5
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
CAS
147127-20-6
Created by admin on Fri Dec 15 15:49:09 UTC 2023 , Edited by admin on Fri Dec 15 15:49:09 UTC 2023
PRIMARY
Related Record Type Details
TRANSPORTER -> SUBSTRATE
May cause renal toxicity
SALT/SOLVATE -> PARENT
TRANSPORTER -> SUBSTRATE
SOLVATE->ANHYDROUS
TRANSPORTER -> SUBSTRATE
TARGET ORGANISM->INHIBITOR
EC50
TARGET -> INHIBITOR
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METABOLITE ACTIVE -> PARENT
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PRODRUG -> METABOLITE ACTIVE
Activated in liver cells.
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ACTIVE MOIETY