2-(3-Benzyl-4-oxo-3,4,5,6,7,8-hexahydro-benzo[4,5]thieno[2,3-d]pyrimidin-2-ylsulfanylmethyl)-oxazole-4-carboxylic acid(2-pyrrolidin-1-yl-ethyl)-amide

ID: ALA4531011

Cas Number: 853136-76-2

PubChem CID: 42792280

Max Phase: Preclinical

Molecular Formula: C28H31N5O3S2

Molecular Weight: 549.72

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  O=C(NCCN1CCCC1)c1coc(CSc2nc3sc4c(c3c(=O)n2Cc2ccccc2)CCCC4)n1

Standard InChI:  InChI=1S/C28H31N5O3S2/c34-25(29-12-15-32-13-6-7-14-32)21-17-36-23(30-21)18-37-28-31-26-24(20-10-4-5-11-22(20)38-26)27(35)33(28)16-19-8-2-1-3-9-19/h1-3,8-9,17H,4-7,10-16,18H2,(H,29,34)

Standard InChI Key:  BCMZCPIZJPKEIR-UHFFFAOYSA-N

Molfile:  

 
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M  END

Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

MEF (1005 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

Calculated Properties

Molecular Weight: 549.72Molecular Weight (Monoisotopic): 549.1868AlogP: 4.49#Rotatable Bonds: 9
Polar Surface Area: 93.26Molecular Species: NEUTRALHBA: 9HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.24CX Basic pKa: 7.99CX LogP: 4.94CX LogD: 4.25
Aromatic Rings: 4Heavy Atoms: 38QED Weighted: 0.24Np Likeness Score: -2.32

References

1. Nguyen J, Chen L, Kumar D, Lee J..  (2016)  Facile synthesis of autophagonizer and evaluation of its activity to induce autophagic cell death in apoptosis-defective cell line.,  26  (19): [PMID:27597252] [10.1016/j.bmcl.2016.08.035]

Source