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Details

Stereochemistry ABSOLUTE
Molecular Formula C35H47N7O5
Molecular Weight 645.7916
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of L-054522

SMILES

C[C@H]([C@@H](NC(=O)N1CCC(CC1)N2C(=O)NC3=C2C=CC=C3)C(=O)N[C@@H](CCCCN)C(=O)OC(C)(C)C)C4=CNC5=C4C=CC=C5

InChI

InChIKey=WFCIXKAZBUIFTR-PKIMSIDOSA-N
InChI=1S/C35H47N7O5/c1-22(25-21-37-26-12-6-5-11-24(25)26)30(31(43)38-28(14-9-10-18-36)32(44)47-35(2,3)4)40-33(45)41-19-16-23(17-20-41)42-29-15-8-7-13-27(29)39-34(42)46/h5-8,11-13,15,21-23,28,30,37H,9-10,14,16-20,36H2,1-4H3,(H,38,43)(H,39,46)(H,40,45)/t22-,28-,30+/m0/s1

HIDE SMILES / InChI

Molecular Formula C35H47N7O5
Molecular Weight 645.7916
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:23:17 GMT 2023
Edited
by admin
on Sat Dec 16 09:23:17 GMT 2023
Record UNII
7W8X3AXG75
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
L-054522
Code English
L054522
Code English
(.BETA.S)-N-((4-(2,3-DIHYDRO-2-OXO-1H-BENZIMIDAZOL-1-YL)-1-PIPERIDINYL)CARBONYL)-.BETA.-METHYL-D-TRYPTOPHYL-L-LYSINE 1,1-DIMETHYLETHYL ESTER
Systematic Name English
TERT-BUTYL (2S)-6-AMINO-2-(((2R,3S)-3-(1H-INDOL-3-YL)-2-((4-(2-OXO-3H-BENZIMIDAZOL-1-YL)PIPERIDINE-1-CARBONYL)AMINO)BUTANOYL)AMINO)HEXANOATE
Systematic Name English
L-LYSINE, (.BETA.S)-N-((4-(2,3-DIHYDRO-2-OXO-1H-BENZIMIDAZOL-1-YL)-1-PIPERIDINYL)CARBONYL)-.BETA.-METHYL-D-TRYPTOPHYL-, 1,1-DIMETHYLETHYL ESTER
Systematic Name English
L-054,522
Code English
N-(4-(2-OXO-2,3-DIHYDRO-1H-BENZIMIDAZOL-1-YL)PIPERIDIN-1-YLCARBONYL)-(3(S)-METHYL)-D-TRYPTOPHYL-L-LYSINE TERT-BUTYL ESTER
Systematic Name English
Code System Code Type Description
CAS
214348-67-1
Created by admin on Sat Dec 16 09:23:17 GMT 2023 , Edited by admin on Sat Dec 16 09:23:17 GMT 2023
PRIMARY
PUBCHEM
15965425
Created by admin on Sat Dec 16 09:23:17 GMT 2023 , Edited by admin on Sat Dec 16 09:23:17 GMT 2023
PRIMARY
FDA UNII
7W8X3AXG75
Created by admin on Sat Dec 16 09:23:17 GMT 2023 , Edited by admin on Sat Dec 16 09:23:17 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY