ID: ALA4074172

Max Phase: Preclinical

Molecular Formula: C21H16F4N8O2

Molecular Weight: 488.41

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1nc(-c2nn(Cc3ccccc3F)c3ncccc23)nc(N)c1N1C[C@@H](C(F)(F)F)OC1=O

Standard InChI:  InChI=1S/C21H16F4N8O2/c22-12-6-2-1-4-10(12)8-33-19-11(5-3-7-28-19)14(31-33)18-29-16(26)15(17(27)30-18)32-9-13(21(23,24)25)35-20(32)34/h1-7,13H,8-9H2,(H4,26,27,29,30)/t13-/m0/s1

Standard InChI Key:  UZOAYOOSFZPFTB-ZDUSSCGKSA-N

Associated Targets(non-human)

Gucy1a1 Guanylate cyclase soluble subunit alpha-1 (85 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: 488.41Molecular Weight (Monoisotopic): 488.1332AlogP: 3.13#Rotatable Bonds: 4
Polar Surface Area: 138.07Molecular Species: NEUTRALHBA: 9HBD: 2
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.49CX LogP: 3.52CX LogD: 3.52
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.42Np Likeness Score: -1.21

References

1. Follmann M, Ackerstaff J, Redlich G, Wunder F, Lang D, Kern A, Fey P, Griebenow N, Kroh W, Becker-Pelster EM, Kretschmer A, Geiss V, Li V, Straub A, Mittendorf J, Jautelat R, Schirok H, Schlemmer KH, Lustig K, Gerisch M, Knorr A, Tinel H, Mondritzki T, Trübel H, Sandner P, Stasch JP..  (2017)  Discovery of the Soluble Guanylate Cyclase Stimulator Vericiguat (BAY 1021189) for the Treatment of Chronic Heart Failure.,  60  (12): [PMID:28557445] [10.1021/acs.jmedchem.7b00449]

Source