(S)-3-chloro-5-(7-(2-((5-chloro-2-(2,4-dimethylpiperazin-1-yl)pyridin-4-yl)amino)-2-oxoethyl)-3-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-yl)-4-fluoro-2-hydroxybenzamide

ID: ALA5286263

Max Phase: Preclinical

Molecular Formula: C27H27Cl2FN8O4

Molecular Weight: 617.47

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  C[C@H]1CN(C)CCN1c1cc(NC(=O)Cn2cc(-c3cc(C(N)=O)c(O)c(Cl)c3F)c3c(=O)n(C)cnc32)c(Cl)cn1

Standard InChI:  InChI=1S/C27H27Cl2FN8O4/c1-13-9-35(2)4-5-38(13)19-7-18(17(28)8-32-19)34-20(39)11-37-10-16(21-26(37)33-12-36(3)27(21)42)14-6-15(25(31)41)24(40)22(29)23(14)30/h6-8,10,12-13,40H,4-5,9,11H2,1-3H3,(H2,31,41)(H,32,34,39)/t13-/m0/s1

Standard InChI Key:  UUBZSBJVJMKQMU-ZDUSSCGKSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA5286263

    ---

Associated Targets(Human)

BCL6 Tchem B-cell lymphoma 6 protein (838 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KARPAS-422 (454 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: 617.47Molecular Weight (Monoisotopic): 616.1516AlogP: 2.83#Rotatable Bonds: 6
Polar Surface Area: 151.61Molecular Species: ACIDHBA: 10HBD: 3
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 5.83CX Basic pKa: 7.69CX LogP: 1.96CX LogD: 1.89
Aromatic Rings: 4Heavy Atoms: 42QED Weighted: 0.30Np Likeness Score: -1.36

References

1. Mamai A, Chau AM, Wilson BJ, Watson ID, Joseph BB, Subramanian PR, Morshed MM, Morin JA, Prakesch MA, Lu T, Connolly P, Kuntz DA, Pomroy NC, Poda G, Nguyen K, Marcellus R, Strathdee G, Theriault B, Subramaniam R, Mohammed M, Abibi A, Chan M, Winston J, Kiyota T, Undzys E, Aman A, Austin N, Du Jardin M, Packman K, Phillippar U, Attar R, Edwards J, O'Meara J, Uehling DE, Al-Awar R, Privé GG, Isaac MB..  (2023)  Discovery of OICR12694: A Novel, Potent, Selective, and Orally Bioavailable BCL6 BTB Inhibitor.,  14  (2.0): [PMID:36793435] [10.1021/acsmedchemlett.2c00502]

Source