ID: ALA11502

Max Phase: Preclinical

Molecular Formula: C26H31ClN4O4S

Molecular Weight: 531.08

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1(C)Oc2ccc(S(=O)(=O)N3CCCCC3)cc2[C@H](N(Cc2ncc[nH]2)c2ccc(Cl)cc2)[C@H]1O

Standard InChI:  InChI=1S/C26H31ClN4O4S/c1-26(2)25(32)24(31(17-23-28-12-13-29-23)19-8-6-18(27)7-9-19)21-16-20(10-11-22(21)35-26)36(33,34)30-14-4-3-5-15-30/h6-13,16,24-25,32H,3-5,14-15,17H2,1-2H3,(H,28,29)/t24-,25+/m0/s1

Standard InChI Key:  RZHDQAKIFAATRF-LOSJGSFVSA-N

Associated Targets(non-human)

Mitochondrial complex V; ATP synthase 114 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: 531.08Molecular Weight (Monoisotopic): 530.1755AlogP: 4.52#Rotatable Bonds: 6
Polar Surface Area: 98.76Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.52CX Basic pKa: 6.21CX LogP: 3.79CX LogD: 3.77
Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.49Np Likeness Score: -0.95

References

1. Atwal KS, Wang P, Rogers WL, Sleph P, Monshizadegan H, Ferrara FN, Traeger S, Green DW, Grover GJ..  (2004)  Small molecule mitochondrial F1F0 ATPase hydrolase inhibitors as cardioprotective agents. Identification of 4-(N-arylimidazole)-substituted benzopyran derivatives as selective hydrolase inhibitors.,  47  (5): [PMID:14971888] [10.1021/jm030291x]

Source