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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H11NO2S
Molecular Weight 149.211
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENICILLAMINE

SMILES

CC(C)(S)[C@@H](N)C(O)=O

InChI

InChIKey=VVNCNSJFMMFHPL-VKHMYHEASA-N
InChI=1S/C5H11NO2S/c1-5(2,9)3(6)4(7)8/h3,9H,6H2,1-2H3,(H,7,8)/t3-/m0/s1

HIDE SMILES / InChI
Molecular Formula C5H11NO2S
Molecular Weight 149.211
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:09:34 UTC 2023
Edited
by admin
on Fri Dec 15 15:09:34 UTC 2023
Record UNII
GNN1DV99GX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PENICILLAMINE
EP   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
PENICILLAMINE [VANDF]
Common Name English
PENICILLAMINE [USP MONOGRAPH]
Common Name English
PENICILLAMINE [USP-RS]
Common Name English
D-PENICILLAMINE
Systematic Name English
PENICILLAMINE [EP MONOGRAPH]
Common Name English
PENICILLAMINE [ORANGE BOOK]
Common Name English
CUPRIMINE
Brand Name English
PENICILLAMINE [JAN]
Common Name English
D-3-MERCAPTOVALINE
Common Name English
PENICILLAMINE [MART.]
Common Name English
PENICILLAMINE [USAN]
Common Name English
PENICILLAMINE [EP IMPURITY]
Common Name English
PENICILLAMINE [HSDB]
Common Name English
penicillamine [INN]
Common Name English
PENICILLAMINE [MI]
Common Name English
NSC-81549
Code English
D-VALINE, 3-MERCAPTO-
Systematic Name English
DEPEN
Brand Name English
Penicillamine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ESSENTIAL MEDICINES LIST 4.2
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
NDF-RT N0000175713
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
NCI_THESAURUS C1971
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 2.4
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
WHO-VATC QM01CC01
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
LIVERTOX NBK548246
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
WHO-ATC M01CC01
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
Code System Code Type Description
CAS
52-67-5
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
DRUG BANK
DB00859
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-148-8
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
DAILYMED
GNN1DV99GX
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
MERCK INDEX
m8467
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY Merck Index
IUPHAR
7264
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
ChEMBL
CHEMBL1430
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
FDA UNII
GNN1DV99GX
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
EPA CompTox
DTXSID6037069
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
NCI_THESAURUS
C729
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
PUBCHEM
5852
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
MESH
D010396
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
LACTMED
Penicillamine
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
WIKIPEDIA
PENICILLAMINE
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
SMS_ID
100000082481
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
NSC
81549
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
HSDB
3378
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
INN
1121
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
CHEBI
7959
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
RS_ITEM_NUM
1501006
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
EVMPD
SUB09667MIG
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
RXCUI
7975
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY RxNorm
EVMPD
SUB127001
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
DRUG CENTRAL
2081
Created by admin on Fri Dec 15 15:09:34 UTC 2023 , Edited by admin on Fri Dec 15 15:09:34 UTC 2023
PRIMARY
Related Record Type Details
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
Structure of PENICILLAMINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of PENICILLAMINE DISULFIDE, (±)-
METABOLITE -> PARENT
Related Record Type Details
Structure of 2-ISOPROPYL-5,5-DIMETHYLTHIAZOLIDINE-4-CARBOXYLIC ACID
IMPURITY -> PARENT
Structure of 3,3'-TRITHIOBIS-D-VALINE
IMPURITY -> PARENT
Related Record Type Details
Structure of PENICILLAMINE
ACTIVE MOIETY
NIH
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