ID: ALA4212823

Max Phase: Preclinical

Molecular Formula: C28H38FN3O4

Molecular Weight: 499.63

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCc1cccc(-c2c(F)cccc2C(O)(CCCNC(=O)OC)[C@@H]2CCCN(C(=O)CCN)C2)c1

Standard InChI:  InChI=1S/C28H38FN3O4/c1-3-20-8-4-9-21(18-20)26-23(11-5-12-24(26)29)28(35,14-7-16-31-27(34)36-2)22-10-6-17-32(19-22)25(33)13-15-30/h4-5,8-9,11-12,18,22,35H,3,6-7,10,13-17,19,30H2,1-2H3,(H,31,34)/t22-,28?/m1/s1

Standard InChI Key:  AMFATTWGQOSGRT-WZOMIXFGSA-N

Associated Targets(Human)

REN Tclin Renin (5251 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: 499.63Molecular Weight (Monoisotopic): 499.2846AlogP: 3.97#Rotatable Bonds: 10
Polar Surface Area: 104.89Molecular Species: BASEHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.86CX Basic pKa: 9.12CX LogP: 3.22CX LogD: 1.51
Aromatic Rings: 2Heavy Atoms: 36QED Weighted: 0.43Np Likeness Score: -0.77

References

1. Lawhorn BG, Tran T, Hong VS, Morgan LA, Le BT, Harpel MR, Jolivette L, Diaz E, Schwartz B, Gross JW, Tomaszek T, Semus S, Concha N, Smallwood A, Holt DA, Kallander LS..  (2017)  Discovery of renin inhibitors containing a simple aspartate binding moiety that imparts reduced P450 inhibition.,  27  (21): [PMID:28985999] [10.1016/j.bmcl.2017.09.046]

Source