SYP-11277

ID: ALA2392659

Max Phase: Preclinical

Molecular Formula: C23H18Cl2F3N3O4

Molecular Weight: 528.31

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CO/C=C(/C(=O)OC)c1ccccc1COc1cc(C(F)(F)F)nc(Nc2ccc(Cl)cc2Cl)n1

Standard InChI:  InChI=1S/C23H18Cl2F3N3O4/c1-33-12-16(21(32)34-2)15-6-4-3-5-13(15)11-35-20-10-19(23(26,27)28)30-22(31-20)29-18-8-7-14(24)9-17(18)25/h3-10,12H,11H2,1-2H3,(H,29,30,31)/b16-12+

Standard InChI Key:  YYXSCUSVVALMNW-FOWTUZBSSA-N

Associated Targets(Human)

HL-60 67320 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Tetranychus cinnabarinus 1124 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: 528.31Molecular Weight (Monoisotopic): 527.0626AlogP: 6.29#Rotatable Bonds: 8
Polar Surface Area: 82.57Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 10.90CX Basic pKa: 0.49CX LogP: 6.93CX LogD: 6.93
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.21Np Likeness Score: -1.08

References

1. Chai BS, Liu CL, Li HC, Zhang H, Liu SW, Huang G, Chang JB..  (2011)  The discovery of SYP-10913 and SYP-11277: novel strobilurin acaricides.,  67  (9): [PMID:21452169] [10.1002/ps.2164]
2. Chai B, Wang S, Yu W, Li H, Song C, Xu Y, Liu C, Chang J..  (2013)  Synthesis of novel strobilurin-pyrimidine derivatives and their antiproliferative activity against human cancer cell lines.,  23  (12): [PMID:23664877] [10.1016/j.bmcl.2013.04.045]

Source