ID: ALA4089687

Max Phase: Preclinical

Molecular Formula: C29H23Cl2N5O2S

Molecular Weight: 576.51

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N/C(=N/C(=N\S(=O)(=O)c1ccc(Cl)cc1)N1CC(c2ccccc2)C(c2ccc(Cl)cc2)=N1)c1ccccc1

Standard InChI:  InChI=1S/C29H23Cl2N5O2S/c30-23-13-11-21(12-14-23)27-26(20-7-3-1-4-8-20)19-36(34-27)29(33-28(32)22-9-5-2-6-10-22)35-39(37,38)25-17-15-24(31)16-18-25/h1-18,26H,19H2,(H2,32,33,35)

Standard InChI Key:  QGGBJCCFQMWVFN-UHFFFAOYSA-N

Associated Targets(non-human)

Cannabinoid CB1 receptor 739 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cannabinoid CB2 receptor 862 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: 576.51Molecular Weight (Monoisotopic): 575.0950AlogP: 5.95#Rotatable Bonds: 5
Polar Surface Area: 100.48Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 6.59CX LogP: 6.35CX LogD: 6.29
Aromatic Rings: 4Heavy Atoms: 39QED Weighted: 0.23Np Likeness Score: -0.84

References

1. Iyer MR, Cinar R, Katz A, Gao M, Erdelyi K, Jourdan T, Coffey NJ, Pacher P, Kunos G..  (2017)  Design, Synthesis, and Biological Evaluation of Novel, Non-Brain-Penetrant, Hybrid Cannabinoid CB1R Inverse Agonist/Inducible Nitric Oxide Synthase (iNOS) Inhibitors for the Treatment of Liver Fibrosis.,  60  (3): [PMID:28085283] [10.1021/acs.jmedchem.6b01504]

Source