ID: ALA4575646

Max Phase: Preclinical

Molecular Formula: C23H27NO3S2

Molecular Weight: 429.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCC[S+]([O-])CCc1cc(-c2ccc(S(C)(=O)=O)cc2)n(-c2ccccc2)c1C

Standard InChI:  InChI=1S/C23H27NO3S2/c1-4-15-28(25)16-14-20-17-23(19-10-12-22(13-11-19)29(3,26)27)24(18(20)2)21-8-6-5-7-9-21/h5-13,17H,4,14-16H2,1-3H3

Standard InChI Key:  DNBQXSBMDAHGHH-UHFFFAOYSA-N

Associated Targets(non-human)

Cyclooxygenase-1 661 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cyclooxygenase-2 1939 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 429.61Molecular Weight (Monoisotopic): 429.1432AlogP: 4.56#Rotatable Bonds: 8
Polar Surface Area: 62.13Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.36CX LogD: 3.36
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.49Np Likeness Score: -0.95

References

1. Reale A, Brogi S, Chelini A, Paolino M, Di Capua A, Giuliani G, Cappelli A, Giorgi G, Chemi G, Grillo A, Valoti M, Sautebin L, Rossi A, Pace S, La Motta C, Di Cesare Mannelli L, Lucarini E, Ghelardini C, Anzini M..  (2019)  Synthesis, biological evaluation and molecular modeling of novel selective COX-2 inhibitors: sulfide, sulfoxide, and sulfone derivatives of 1,5-diarylpyrrol-3-substituted scaffold.,  27  (19): [PMID:31427145] [10.1016/j.bmc.2019.115045]

Source