ID: ALA5267110

Max Phase: Preclinical

Molecular Formula: C47H49N9O11

Molecular Weight: 915.96

Associated Items:

Representations

Canonical SMILES:  Cc1c(Cc2cccc(NCc3cn(CCOCCOCCOCCOCCNc4cccc5c4C(=O)N(C4CCC(=O)NC4=O)C5=O)nn3)c2)c(=O)oc2cc(Oc3ncccn3)ccc12

Standard InChI:  InChI=1S/C47H49N9O11/c1-30-35-10-9-34(66-47-49-13-4-14-50-47)27-40(35)67-46(61)37(30)26-31-5-2-6-32(25-31)51-28-33-29-55(54-53-33)16-18-63-20-22-65-24-23-64-21-19-62-17-15-48-38-8-3-7-36-42(38)45(60)56(44(36)59)39-11-12-41(57)52-43(39)58/h2-10,13-14,25,27,29,39,48,51H,11-12,15-24,26,28H2,1H3,(H,52,57,58)

Standard InChI Key:  MODNGVAZDNEDDO-UHFFFAOYSA-N

Associated Targets(Human)

MAP2K2 Tclin Cereblon/MAP2K1/MAP2K2 (13 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

Properties

Molecular Weight: 915.96Molecular Weight (Monoisotopic): 915.3552AlogP: 4.06#Rotatable Bonds: 24
Polar Surface Area: 240.46Molecular Species: NEUTRALHBA: 18HBD: 3
#RO5 Violations: 2HBA (Lipinski): 20HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.59CX Basic pKa: 3.09CX LogP: 3.42CX LogD: 3.42
Aromatic Rings: 6Heavy Atoms: 67QED Weighted: 0.04Np Likeness Score: -0.95

References

1. Wang C, Wang H, Zheng C, Li B, Liu Z, Zhang L, Yuan L, Xu P..  (2023)  Discovery of Coumarin-Based MEK1/2 PROTAC Effective in Human Cancer Cells.,  14  (1.0): [PMID:36655129] [10.1021/acsmedchemlett.2c00446]

Source