ID: ALA1743616

Max Phase: Preclinical

Molecular Formula: C16H20ClN5O

Molecular Weight: 297.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.O=c1c2ccccc2nnn1CCCCCCn1ccnc1

Standard InChI:  InChI=1S/C16H19N5O.ClH/c22-16-14-7-3-4-8-15(14)18-19-21(16)11-6-2-1-5-10-20-12-9-17-13-20;/h3-4,7-9,12-13H,1-2,5-6,10-11H2;1H

Standard InChI Key:  HXQIAXDXLMKVIH-UHFFFAOYSA-N

Associated Targets(non-human)

Thromboxane-A synthase 658 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: 297.36Molecular Weight (Monoisotopic): 297.1590AlogP: 2.25#Rotatable Bonds: 7
Polar Surface Area: 65.60Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.54CX LogP: 3.39CX LogD: 3.35
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.63Np Likeness Score: -1.91

References

1. Wright WB, Tomcufcik AS, Chan PS, Marsico JW, Press JB..  (1987)  Thromboxane synthetase inhibitors and antihypertensive agents. 4. N-[(1H-imidazol-1-yl)alkyl] derivatives of quinazoline-2,4(1H,3H)-diones, quinazolin-4(3H)-ones, and 1,2,3-benzotriazin-4(3H)-ones.,  30  (12): [PMID:3681898] [10.1021/jm00395a016]

Source