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

Details

Stereochemistry EPIMERIC
Molecular Formula C15H22N6O5S
Molecular Weight 398.437
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADEMETIONINE

SMILES

C[S+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=NC3=C2N=CN=C3N

InChI

InChIKey=MEFKEPWMEQBLKI-AIRLBKTGSA-N
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27?/m0/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
ADEMETIONINE
INN   MART.   WHO-DD  
INN  
Official Name English
MSI-195
Code English
SAME
Code English
5'-((3S)-(3-AMINO-3-CARBOXYPROPYL)METHYLSULFONIO)-5'-DEOXYADENOSINE INNER SALT
Common Name English
TRANSMETIL
Brand Name English
ademetionine [INN]
Common Name English
S-(5'-DESOXYADENOSIN-5'-YL)-L-METHIONINE
Systematic Name English
ADOMET
Brand Name English
Ademetionine [WHO-DD]
Common Name English
ADENOSYLMETHIONINE
Common Name English
S-ADENOSYLMETHIONINE
MI   VANDF  
Systematic Name English
S-ADENOSYL-L-METHIONINE
Common Name English
S-ADENOSYLMETHIONINE [MI]
Common Name English
SAM-E
Code English
SAM
Common Name English
ADEMETIONINE [MART.]
Common Name English
S-ADENOSYLMETHIONINE [VANDF]
Common Name English
Classification Tree Code System Code
LOINC 78966-9
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
NCI_THESAURUS C275
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
FDA ORPHAN DRUG 111498
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
WHO-ATC A16AA02
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
DSLD 591 (Number of products:14)
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
LOINC 80182-9
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
LIVERTOX 867
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
LOINC 80177-9
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
DSLD 1257 (Number of products:115)
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
Code System Code Type Description
FDA UNII
7LP2MPO46S
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
CAS
29908-03-0
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
DRUG BANK
DB00118
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
CHEBI
33442
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
SMS_ID
100000092113
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
EVMPD
SUB05266MIG
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID6032019
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
CHEBI
67040
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
ECHA (EC/EINECS)
249-946-8
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
ChEMBL
CHEMBL1088977
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
PUBCHEM
34755
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
LACTMED
SAM-e
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
DRUG CENTRAL
2414
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
RXCUI
9504
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY RxNorm
CAS
78548-84-2
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
ALTERNATIVE
CHEBI
15414
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
MERCK INDEX
m1414
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY Merck Index
MESH
D012436
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
WIKIPEDIA
S-Adenosyl methionine
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
NCI_THESAURUS
C100098
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
DAILYMED
7LP2MPO46S
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
INN
5479
Created by admin on Fri Dec 15 18:56:58 UTC 2023 , Edited by admin on Fri Dec 15 18:56:58 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of ADEMETIONINE
METABOLITE (PARENT)
Structure of 5'-METHYLTHIOADENOSINE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966