N1-((S)-3-(1H-Indol-3-yl)-1-(((R)-3-methyl-1-((3aR,4R,6R,7aS)-5,5,7a-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)butyl)amino)-1-oxopropan-2-yl)-N4-hydroxyterephthalamide

ID: ALA4547369

PubChem CID: 155553474

Max Phase: Preclinical

Molecular Formula: C34H43BN4O6

Molecular Weight: 614.55

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)c1ccc(C(=O)NO)cc1)B1O[C@@H]2[C@@H]3C[C@H](C[C@]2(C)O1)C3(C)C

Standard InChI:  InChI=1S/C34H43BN4O6/c1-19(2)14-28(35-44-29-25-16-23(33(25,3)4)17-34(29,5)45-35)38-32(42)27(15-22-18-36-26-9-7-6-8-24(22)26)37-30(40)20-10-12-21(13-11-20)31(41)39-43/h6-13,18-19,23,25,27-29,36,43H,14-17H2,1-5H3,(H,37,40)(H,38,42)(H,39,41)/t23-,25+,27+,28+,29-,34+/m1/s1

Standard InChI Key:  QETSGGARENBKCB-FJPRILFMSA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4547369

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 614.55

Molecular Weight (Monoisotopic): 614.3276

AlogP: ┄

#Rotatable Bonds: ┄

Polar Surface Area: ┄

Molecular Species: ┄

HBA: ┄

HBD: ┄

#RO5 Violations: ┄

HBA (Lipinski): ┄

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: ┄

CX LogP: ┄

CX LogD: ┄

Aromatic Rings: ┄

Heavy Atoms: ┄

QED Weighted: ┄

Np Likeness Score: ┄

References

1. Zhou Y, Liu X, Xue J, Liu L, Liang T, Li W, Yang X, Hou X, Fang H..  (2020)  Discovery of Peptide Boronate Derivatives as Histone Deacetylase and Proteasome Dual Inhibitors for Overcoming Bortezomib Resistance of Multiple Myeloma.,  63  (9): [PMID:32267687] [10.1021/acs.jmedchem.9b02161]

Source

Source(1):

• Scientific Literature