ID: ALA313781

Max Phase: Preclinical

Molecular Formula: C36H48F6O5S2

Molecular Weight: 738.90

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(Sc1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1)Sc1cc(C(C)(C)C)c(OC(=O)C(F)(F)C(F)(F)C(F)(F)C(=O)O)c(C(C)(C)C)c1

Standard InChI:  InChI=1S/C36H48F6O5S2/c1-29(2,3)21-15-19(16-22(25(21)43)30(4,5)6)48-33(13,14)49-20-17-23(31(7,8)9)26(24(18-20)32(10,11)12)47-28(46)35(39,40)36(41,42)34(37,38)27(44)45/h15-18,43H,1-14H3,(H,44,45)

Standard InChI Key:  XBIMURZUBIFAHS-UHFFFAOYSA-N

Associated Targets(Human)

Vascular cell adhesion protein 1 212 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: 738.90Molecular Weight (Monoisotopic): 738.2847AlogP: 11.10#Rotatable Bonds: 9
Polar Surface Area: 83.83Molecular Species: ACIDHBA: 6HBD: 2
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 2.24CX Basic pKa: CX LogP: 12.54CX LogD: 9.02
Aromatic Rings: 2Heavy Atoms: 49QED Weighted: 0.09Np Likeness Score: 0.12

References

1. Meng CQ, Somers PK, Rachita CL, Holt LA, Hoong LK, Zheng XS, Simpson JE, Hill RR, Olliff LK, Kunsch C, Sundell CL, Parthasarathy S, Saxena U, Sikorski JA, Wasserman MA..  (2002)  Novel phenolic antioxidants as multifunctional inhibitors of inducible VCAM-1 expression for use in atherosclerosis.,  12  (18): [PMID:12182856] [10.1016/s0960-894x(02)00516-4]

Source