ID: ALA5075185

Max Phase: Preclinical

Molecular Formula: C45H57N7O10S

Molecular Weight: 888.06

Molecule Type: Unknown

Representations

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

Standard InChI:  InChI=1S/C45H57N7O10S/c1-29-40(63-28-48-29)31-11-9-30(10-12-31)24-47-43(57)37-23-34(53)25-52(37)44(58)41(45(2,3)4)51-39(55)27-62-22-20-60-18-17-59-19-21-61-26-38(54)49-33-15-13-32(14-16-33)42(56)50-36-8-6-5-7-35(36)46/h5-16,28,34,37,41,53H,17-27,46H2,1-4H3,(H,47,57)(H,49,54)(H,50,56)(H,51,55)/t34-,37+,41-/m1/s1

Standard InChI Key:  CJLCITMDOZXVCN-RDGUTDORSA-N

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

Properties

Molecular Weight: 888.06

Molecular Weight (Monoisotopic): 887.3888

AlogP: 3.77

#Rotatable Bonds: 22

Polar Surface Area: 232.77

Molecular Species: NEUTRAL

HBA: 13

HBD: 6

#RO5 Violations: 3

HBA (Lipinski): 17

HBD (Lipinski): 7

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 11.95

CX Basic pKa: 3.24

CX LogP: 1.53

CX LogD: 1.53

Aromatic Rings: 4

Heavy Atoms: 63

QED Weighted: 0.05

Np Likeness Score: -0.84

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

Source(1):

• Scientific Literature