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

Details

Stereochemistry ABSOLUTE
Molecular Formula C8H14N3O6P.2H2O
Molecular Weight 315.2176
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CIDOFOVIR

SMILES

O.O.NC1=NC(=O)N(C[C@@H](CO)OCP(O)(O)=O)C=C1

InChI

InChIKey=FPKARFMSZDBYQF-ILKKLZGPSA-N
InChI=1S/C8H14N3O6P.2H2O/c9-7-1-2-11(8(13)10-7)3-6(4-12)17-5-18(14,15)16;;/h1-2,6,12H,3-5H2,(H2,9,10,13)(H2,14,15,16);2*1H2/t6-;;/m0../s1

HIDE SMILES / InChI

Molecular Formula C8H14N3O6P
Molecular Weight 279.187
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:53:50 UTC 2023
Edited
by admin
on Fri Dec 15 15:53:50 UTC 2023
Record UNII
JIL713Q00N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CIDOFOVIR
EMA EPAR   ORANGE BOOK   USAN   VANDF  
USAN  
Official Name English
CIDOFOVIR [USAN]
Common Name English
CIDOFOVIR [ORANGE BOOK]
Common Name English
PHOSPHONIC ACID, ((2-(4-AMINO-2-OXO-1(2H)-PYRIMIDINYL)-1-(HYDROXYMETHYL)ETHOXY)METHYL)-, DIHYDRATE, (S)-
Common Name English
CIDOFOVIR [VANDF]
Common Name English
VISTIDE
Brand Name English
CIDOFOVIR DIHYDRATE
Common Name English
NSC-742135
Code English
CIDOFOVIR [USP MONOGRAPH]
Common Name English
[[(S)-2-(4-Amino-2-oxo-1(2H)-pyrimidinyl)-1-(hydroxymethyl)ethoxy]methyl]phosphonic acid, dihydrate
Common Name English
HPMPC DIHYDRATE
Common Name English
1-((S)-3-HYDROXY-2-(PHOSPHONOMETHOXY)PROPYL)CYTOSINE DIHYDRATE
Systematic Name English
CIDOFOVIR [EMA EPAR]
Common Name English
CIDOFOVIR [USP-RS]
Common Name English
GS-0504
Code English
Classification Tree Code System Code
NCI_THESAURUS C29575
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
NDF-RT N0000175461
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
LIVERTOX NBK548417
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
WHO-VATC QJ05AB12
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
EMA ASSESSMENT REPORTS VISTIDE (WITHDRAWN: CYTOMEGALOVIRUS RETINITIS)
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
WHO-ATC J05AB12
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
NCI_THESAURUS C281
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
Code System Code Type Description
PUBCHEM
60933
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
NCI_THESAURUS
C1600
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
CAS
149394-66-1
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
CHEBI
530615
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
WIKIPEDIA
CIDOFOVIR
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
NSC
742135
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
DRUG CENTRAL
639
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
DRUG BANK
DB00369
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
MESH
C059262
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
CHEBI
59495
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
FDA UNII
JIL713Q00N
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
RS_ITEM_NUM
1133853
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
EVMPD
SUB26395
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
CHEBI
134514
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
USAN
GG-13
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
EPA CompTox
DTXSID6041002
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
SMS_ID
100000091272
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
CHEBI
3696
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
ChEMBL
CHEMBL152
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
RXCUI
83171
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY RxNorm
DAILYMED
JIL713Q00N
Created by admin on Fri Dec 15 15:53:51 UTC 2023 , Edited by admin on Fri Dec 15 15:53:51 UTC 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
TRANSPORTER -> INHIBITOR
PARENT -> SALT/SOLVATE
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY