ID: ALA3672880

Max Phase: Preclinical

Molecular Formula: C25H22FN3O7S

Molecular Weight: 527.53

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(Cc1ccc(C(=O)Oc2ccc(C(=N)N)cc2F)s1)C(=O)Nc1ccc(C(=O)O)c(C(=O)O)c1

Standard InChI:  InChI=1S/C25H22FN3O7S/c1-25(2,24(35)29-13-4-6-15(21(30)31)16(10-13)22(32)33)11-14-5-8-19(37-14)23(34)36-18-7-3-12(20(27)28)9-17(18)26/h3-10H,11H2,1-2H3,(H3,27,28)(H,29,35)(H,30,31)(H,32,33)

Standard InChI Key:  PPLWQAMMKNZODE-UHFFFAOYSA-N

Associated Targets(Human)

Enteropeptidase 772 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trypsin I 2306 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 527.53Molecular Weight (Monoisotopic): 527.1162AlogP: 3.99#Rotatable Bonds: 9
Polar Surface Area: 179.87Molecular Species: ZWITTERIONHBA: 7HBD: 5
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 6#RO5 Violations (Lipinski): 2
CX Acidic pKa: 2.88CX Basic pKa: 10.94CX LogP: 2.99CX LogD: 1.10
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.12Np Likeness Score: -1.03

References

1.  (2015)  Heteroarylcarboxylic acid ester derivative, 
2.  (2016)  Heteroarylcarboxylic acid ester derivative, 

Source

Source(1):