Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H36N2O3 |
Molecular Weight | 328.49 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCC(=O)NCCCC[C@H](N)C(O)=O
InChI
InChIKey=GYDYJUYZBRGMCC-INIZCTEOSA-N
InChI=1S/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1
Molecular Formula | C18H36N2O3 |
Molecular Weight | 328.49 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
A novel acylase from Streptomyces mobaraensis that efficiently catalyzes hydrolysis/synthesis of capsaicins as well as N-acyl-L-amino acids and N-acyl-peptides. | 2006 Jan 11 |
|
Efficient Nepsilon-lauroyl-L-lysine production by recombinant epsilon-lysine acylase from Streptomyces mobaraensis. | 2009 May 20 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 20:01:03 GMT 2023
by
admin
on
Sat Dec 16 20:01:03 GMT 2023
|
Record UNII |
113171Q70B
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English | ||
|
Brand Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
104151
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | |||
|
52315-75-0
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | |||
|
257-843-4
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | |||
|
113171Q70B
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | |||
|
DTXSID80885998
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | |||
|
113171Q70B
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | |||
|
1426404
Created by
admin on Sat Dec 16 20:01:03 GMT 2023 , Edited by admin on Sat Dec 16 20:01:03 GMT 2023
|
PRIMARY | RxNorm |