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Details

Stereochemistry ACHIRAL
Molecular Formula C17H20O6
Molecular Weight 320.3371
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of MYCOPHENOLIC ACID

SMILES

COC1=C(C)C2=C(C(=O)OC2)C(O)=C1C\C=C(/C)CCC(O)=O

InChI

InChIKey=HPNSFSBZBAHARI-RUDMXATFSA-N
InChI=1S/C17H20O6/c1-9(5-7-13(18)19)4-6-11-15(20)14-12(8-23-17(14)21)10(2)16(11)22-3/h4,20H,5-8H2,1-3H3,(H,18,19)/b9-4+

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
MYCOPHENOLIC ACID
INN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
MYCOPHENOLATE [VANDF]
Common Name English
4-HEXENOIC ACID, 6-(1,3-DIHYDRO-4-HYDROXY-6-METHOXY-7-METHYL-3-OXO-5-ISOBENZOFURANYL)-4-METHYL-, (E)-
Common Name English
MYCOPHENOLATE
VANDF  
Common Name English
MYCOPHENOLIC ACID [MART.]
Common Name English
NSC-129185
Code English
MYCOPHENOLATE MOFETIL IMPURITY F [EP IMPURITY]
Common Name English
MYCOPHENOLIC ACID [VANDF]
Common Name English
68618
Code English
Mycophenolic acid [WHO-DD]
Common Name English
MYCOPHENOLATE MOFETIL IMPURITY, MYCOPHENOLIC ACID- [USP IMPURITY]
Common Name English
(4E)-6-(4-HYDROXY-6-METHOXY-7-METHYL-3-OXO-1,3-DIHYDRO-2-BENZOFURAN-5-YL)-4-METHYLHEX-4-ENOIC ACID
Systematic Name English
(E)-6-(4-Hydroxy-6-methoxy-7-methyl-3-oxo-5-phthalanyl)-4-methyl-4-hexenoic acid
Common Name English
mycophenolic acid [INN]
Common Name English
MYCOPHENOLIC ACID [MI]
Common Name English
4-HEXENOIC ACID, 6-(1,3-DIHYDRO-4-HYDROXY-6-METHOXY-7-METHYL-3-OXO-5-ISOBENZOFURANYL)-4-METHYL-, (4E)-
Common Name English
MYCOPHENOLIC ACID [ORANGE BOOK]
Common Name English
MYFORTIC
Brand Name English
MYCOPHENOLIC ACID [USAN]
Common Name English
Classification Tree Code System Code
LIVERTOX NBK548945
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
NDF-RT N0000175613
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
NCI_THESAURUS C2087
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
WHO-ATC L04AA06
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
NCI_THESAURUS C574
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
WHO-VATC QL04AA06
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
Code System Code Type Description
DRUG BANK
DB01024
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
EVMPD
SUB09098MIG
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
ECHA (EC/EINECS)
246-119-3
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
DRUG CENTRAL
1860
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
MESH
D009173
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
CAS
24280-93-1
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
IUPHAR
6832
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
SMS_ID
100000090388
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
PUBCHEM
446541
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
LACTMED
Mycophenolate
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
MERCK INDEX
m7682
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY Merck Index
CHEBI
62932
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
DAILYMED
HU9DX48N0T
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
CHEBI
67155
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
FDA UNII
HU9DX48N0T
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
ChEMBL
CHEMBL866
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
CAS
483-60-3
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
RXCUI
265323
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
ALTERNATIVE
CHEBI
168396
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
EPA CompTox
DTXSID4041070
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
NSC
129185
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
INN
2950
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
NCI_THESAURUS
C673
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
RXCUI
7145
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
WIKIPEDIA
MYCOPHENOLIC ACID
Created by admin on Fri Dec 15 15:19:57 UTC 2023 , Edited by admin on Fri Dec 15 15:19:57 UTC 2023
PRIMARY
METABOLITE ACTIVE (PARENT)
Structure of MYCOPHENOLIC ACID ACYL GLUCURONIDE
METABOLITE INACTIVE (PARENT)
Structure of MYCOPHENOLIC ACID GLUCURONIDE
METABOLITE INACTIVE (PARENT)
Structure of MYCOPHENOLIC ACID 7-O-GLUCOSIDE
PRODRUG (METABOLITE ACTIVE)
Structure of MYCOPHENOLATE MOFETIL
SALT/SOLVATE (PARENT)
Structure of MYCOPHENOLATE SODIUM
NIH
NCATS
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