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Details

Stereochemistry RACEMIC
Molecular Formula C8H16N2O4S2
Molecular Weight 268.354
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HOMOCYSTINE, DL-

SMILES

N[C@H](CCSSCC[C@@H](N)C(O)=O)C(O)=O

InChI

InChIKey=ZTVZLYBCZNMWCF-PHDIDXHHSA-N
InChI=1S/C8H16N2O4S2/c9-5(7(11)12)1-3-15-16-4-2-6(10)8(13)14/h5-6H,1-4,9-10H2,(H,11,12)(H,13,14)/t5-,6-/m1/s1

HIDE SMILES / InChI

Molecular Formula C8H16N2O4S2
Molecular Weight 268.354
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.7 mM [Ki]
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:10:23 GMT 2023
Edited
by admin
on Fri Dec 15 15:10:23 GMT 2023
Record UNII
Q5T8GG4YC6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HOMOCYSTINE, DL-
Systematic Name English
NSC-43122
Code English
DL-4,4'-DITHIOBIS(2-AMINOBUTYRIC ACID)
Common Name English
L-HOMOCYSTINE DL-FORM [MI]
Common Name English
NSC-11337
Code English
DL-HOMOCYSTINE
Systematic Name English
NSC-226570
Code English
BIS(.GAMMA.-AMINO-.GAMMA.-CARBOXYPROPYL)DISULFIDE
Systematic Name English
BUTYRIC ACID, 4,4'-DITHIOBIS(2-AMINO-, DL-
Common Name English
Code System Code Type Description
CAS
462-10-2
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
NSC
43122
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
PUBCHEM
12358918
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
CAS
870-93-9
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
MERCK INDEX
m6043
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY Merck Index
NSC
226570
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
NSC
11337
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
FDA UNII
Q5T8GG4YC6
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID101014691
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
ECHA (EC/EINECS)
212-803-5
Created by admin on Fri Dec 15 15:10:24 GMT 2023 , Edited by admin on Fri Dec 15 15:10:24 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE