(2S,4R)-1-((S)-2-(2-((6-(2-((4-((2-Aminophenyl)carbamoyl)-phenyl)amino)-2-oxoethoxy)hexyl)oxy)acetamido)-3,3-dimethylbutanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide

ID: ALA5091190

PubChem CID: 166635752

Max Phase: Preclinical

Molecular Formula: C45H57N7O8S

Molecular Weight: 856.06

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ncsc1-c1ccc(CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H](NC(=O)COCCCCCCOCC(=O)Nc2ccc(C(=O)Nc3ccccc3N)cc2)C(C)(C)C)cc1

Standard InChI:  InChI=1S/C45H57N7O8S/c1-29-40(61-28-48-29)31-15-13-30(14-16-31)24-47-43(57)37-23-34(53)25-52(37)44(58)41(45(2,3)4)51-39(55)27-60-22-10-6-5-9-21-59-26-38(54)49-33-19-17-32(18-20-33)42(56)50-36-12-8-7-11-35(36)46/h7-8,11-20,28,34,37,41,53H,5-6,9-10,21-27,46H2,1-4H3,(H,47,57)(H,49,54)(H,50,56)(H,51,55)/t34-,37+,41-/m1/s1

Standard InChI Key:  XBGNSTADRHNHPM-RDGUTDORSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA5091190

    ---

Associated Targets(Human)

HDAC1 Tclin VHL/Histone deacetylase 1 (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC3 Tclin VHL/Histone deacetylase 3 (77 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC2 Tclin VHL/Histone deacetylase 2 (81 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: 856.06Molecular Weight (Monoisotopic): 855.3989AlogP: 5.29#Rotatable Bonds: 20
Polar Surface Area: 214.31Molecular Species: NEUTRALHBA: 11HBD: 6
#RO5 Violations: 4HBA (Lipinski): 15HBD (Lipinski): 7#RO5 Violations (Lipinski): 4
CX Acidic pKa: 12.06CX Basic pKa: 3.24CX LogP: 3.09CX LogD: 3.09
Aromatic Rings: 4Heavy Atoms: 61QED Weighted: 0.05Np Likeness Score: -0.83

References

1. Smalley JP, Baker IM, Pytel WA, Lin LY, Bowman KJ, Schwabe JWR, Cowley SM, Hodgkinson JT..  (2022)  Optimization of Class I Histone Deacetylase PROTACs Reveals that HDAC1/2 Degradation is Critical to Induce Apoptosis and Cell Arrest in Cancer Cells.,  65  (7.0): [PMID:35293758] [10.1021/acs.jmedchem.1c02179]

Source