(R,E)-3-(3-methoxyphenyl)-N-(3-phenyl-2-(4-(trifluoromethyl)phenylsulfonamido)propyl)acrylamide

ID: ALA5282208

Max Phase: Preclinical

Molecular Formula: C26H25F3N2O4S

Molecular Weight: 518.56

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1cccc(/C=C/C(=O)NC[C@@H](Cc2ccccc2)NS(=O)(=O)c2ccc(C(F)(F)F)cc2)c1

Standard InChI:  InChI=1S/C26H25F3N2O4S/c1-35-23-9-5-8-20(17-23)10-15-25(32)30-18-22(16-19-6-3-2-4-7-19)31-36(33,34)24-13-11-21(12-14-24)26(27,28)29/h2-15,17,22,31H,16,18H2,1H3,(H,30,32)/b15-10+/t22-/m1/s1

Standard InChI Key:  YQXARSVRDPJIEQ-RCJYHZQCSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA5282208

    ---

Associated Targets(Human)

CTSL Tclin Cathepsin L (3852 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTSS Tchem Cathepsin S (3285 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTSB Tchem Cathepsin B (3822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTSK Tchem Cathepsin K (3011 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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

Calculated Properties

Molecular Weight: 518.56Molecular Weight (Monoisotopic): 518.1487AlogP: 4.43#Rotatable Bonds: 10
Polar Surface Area: 84.50Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.11CX Basic pKa: CX LogP: 4.98CX LogD: 4.98
Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.39Np Likeness Score: -0.87

References

1. Huang H, Zhang Y, Xu X, Liu Y, Zhao J, Ma L, Lei J, Ge W, Li N, Ma E, Li Y, Yuan L..  (2023)  Design and synthesis of dual cathepsin L and S inhibitors and antimetastatic activity evaluation in pancreatic cancer cells.,  80  [PMID:36427655] [10.1016/j.bmcl.2022.129087]

Source