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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H26N4O4
Molecular Weight 374.4341
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Frunexian

SMILES

C[C@@H](NC(=O)N1[C@@H]([C@@H](CC2=CC(N)=NC=C2)C1=O)C(O)=O)C3CCCCC3

InChI

InChIKey=NYPSZHLKEMYZKK-XFJVYGCCSA-N
InChI=1S/C19H26N4O4/c1-11(13-5-3-2-4-6-13)22-19(27)23-16(18(25)26)14(17(23)24)9-12-7-8-21-15(20)10-12/h7-8,10-11,13-14,16H,2-6,9H2,1H3,(H2,20,21)(H,22,27)(H,25,26)/t11-,14-,16+/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H26N4O4
Molecular Weight 374.4341
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 16:11:22 UTC 2023
Edited
by admin
on Sat Dec 16 16:11:22 UTC 2023
Record UNII
BKE5CVP3FS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Frunexian
INN   USAN  
Official Name English
frunexian [INN]
Common Name English
(2S,3R)-3-[(2-aminopyridin-4-yl)methyl]-1-{[(1R)-1-cyclohexylethyl]carbamoyl}-4-oxoazetidine-2-carboxylic acid
Systematic Name English
2-azetidinecarboxylic acid, 3-[(2-amino-4-pyridinyl)methyl]-1-[[[(1R)-1-cyclohexylethyl]amino]carbonyl]-4-oxo-, (2S,3R)-
Common Name English
FRUNEXIAN [USAN]
Common Name English
EP-7041
Code English
Code System Code Type Description
PUBCHEM
118291958
Created by admin on Sat Dec 16 16:11:22 UTC 2023 , Edited by admin on Sat Dec 16 16:11:22 UTC 2023
PRIMARY
CAS
1803270-60-1
Created by admin on Sat Dec 16 16:11:22 UTC 2023 , Edited by admin on Sat Dec 16 16:11:22 UTC 2023
PRIMARY
USAN
KL-139
Created by admin on Sat Dec 16 16:11:22 UTC 2023 , Edited by admin on Sat Dec 16 16:11:22 UTC 2023
PRIMARY
NCI_THESAURUS
C199054
Created by admin on Sat Dec 16 16:11:22 UTC 2023 , Edited by admin on Sat Dec 16 16:11:22 UTC 2023
PRIMARY
FDA UNII
BKE5CVP3FS
Created by admin on Sat Dec 16 16:11:22 UTC 2023 , Edited by admin on Sat Dec 16 16:11:22 UTC 2023
PRIMARY
INN
12623
Created by admin on Sat Dec 16 16:11:22 UTC 2023 , Edited by admin on Sat Dec 16 16:11:22 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
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ACTIVE MOIETY