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

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H21Cl2N3O9
Molecular Weight 494.28
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of KAITOCEPHALIN

SMILES

N[C@H]([C@H](O)[C@]1(CC[C@H](C[C@H](NC(=O)C2=CC(Cl)=C(O)C(Cl)=C2)C(O)=O)N1)C(O)=O)C(O)=O

InChI

InChIKey=AJQRDRIPQOAJCM-BWOKQULHSA-N
InChI=1S/C18H21Cl2N3O9/c19-8-3-6(4-9(20)12(8)24)14(26)22-10(15(27)28)5-7-1-2-18(23-7,17(31)32)13(25)11(21)16(29)30/h3-4,7,10-11,13,23-25H,1-2,5,21H2,(H,22,26)(H,27,28)(H,29,30)(H,31,32)/t7-,10+,11-,13+,18-/m1/s1

HIDE SMILES / InChI

Molecular Formula C18H21Cl2N3O9
Molecular Weight 494.28
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:53:29 GMT 2023
Edited
by admin
on Sat Dec 16 09:53:29 GMT 2023
Record UNII
9B96C79PCS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
KAITOCEPHALIN
Common Name English
PF-1191
Code English
2,5-PYRROLIDINEDIPROPANOIC ACID, .ALPHA.2-AMINO-2-CARBOXY-.ALPHA.5-((3,5-DICHLORO-4-HYDROXYBENZOYL)AMINO)-.BETA.2-HYDROXY-, (.ALPHA.2R,.ALPHA.5S,.BETA.2S,2R,5R)-
Systematic Name English
(-)-KAITOCEPHALIN
Common Name English
Code System Code Type Description
FDA UNII
9B96C79PCS
Created by admin on Sat Dec 16 09:53:29 GMT 2023 , Edited by admin on Sat Dec 16 09:53:29 GMT 2023
PRIMARY
EPA CompTox
DTXSID801316521
Created by admin on Sat Dec 16 09:53:29 GMT 2023 , Edited by admin on Sat Dec 16 09:53:29 GMT 2023
PRIMARY
PUBCHEM
11329395
Created by admin on Sat Dec 16 09:53:29 GMT 2023 , Edited by admin on Sat Dec 16 09:53:29 GMT 2023
PRIMARY
WIKIPEDIA
Kaitocephalin
Created by admin on Sat Dec 16 09:53:29 GMT 2023 , Edited by admin on Sat Dec 16 09:53:29 GMT 2023
PRIMARY
CAS
198710-92-8
Created by admin on Sat Dec 16 09:53:29 GMT 2023 , Edited by admin on Sat Dec 16 09:53:29 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY