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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H15N3O
Molecular Weight 145.2028
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of L-LYSINAMIDE

SMILES

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

InChI

InChIKey=HKXLAGBDJVHRQG-YFKPBYRVSA-N
InChI=1S/C6H15N3O/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H2,9,10)/t5-/m0/s1

HIDE SMILES / InChI

Molecular Formula C6H15N3O
Molecular Weight 145.2028
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Influence of gradual introduction of hydrophobic groups (stearic acid) in denatured atelocollagen on fibroblasts behavior in vitro.
2007 Mar 1
Keratin transamidation.
2008 Jun 1
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:20:29 GMT 2023
Edited
by admin
on Sat Dec 16 08:20:29 GMT 2023
Record UNII
13E91O1V3F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
L-LYSINAMIDE
Systematic Name English
HEXANAMIDE, 2,6-DIAMINO-, (2S)-
Systematic Name English
LYSINE AMIDE
Common Name English
H-LYS-NH2
Common Name English
HEXANAMIDE, 2,6-DIAMINO-, (S)-
Systematic Name English
Code System Code Type Description
CHEBI
6263
Created by admin on Sat Dec 16 08:20:29 GMT 2023 , Edited by admin on Sat Dec 16 08:20:29 GMT 2023
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FDA UNII
13E91O1V3F
Created by admin on Sat Dec 16 08:20:29 GMT 2023 , Edited by admin on Sat Dec 16 08:20:29 GMT 2023
PRIMARY
CAS
32388-19-5
Created by admin on Sat Dec 16 08:20:29 GMT 2023 , Edited by admin on Sat Dec 16 08:20:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID50186101
Created by admin on Sat Dec 16 08:20:29 GMT 2023 , Edited by admin on Sat Dec 16 08:20:29 GMT 2023
PRIMARY
PUBCHEM
439605
Created by admin on Sat Dec 16 08:20:29 GMT 2023 , Edited by admin on Sat Dec 16 08:20:29 GMT 2023
PRIMARY