ID: ALA4471308

Max Phase: Preclinical

Molecular Formula: C63H85N15O11S

Molecular Weight: 1260.53

Molecule Type: Unknown

Representations

Canonical SMILES:  CC(=O)c1c(C)c2cnc(Nc3ccc(N4CCN(Cc5cn(CCOCCOCCOCCOCCNC(=O)CCC(=O)N[C@H](C(=O)N6C[C@H](O)C[C@H]6C(=O)NCc6ccc(-c7scnc7C)cc6)C(C)(C)C)nn5)CC4)cn3)nc2n(C2CCCC2)c1=O

Standard InChI:  InChI=1S/C63H85N15O11S/c1-41-50-36-67-62(71-58(50)78(47-9-7-8-10-47)60(84)55(41)43(3)79)69-52-16-15-48(35-65-52)75-22-20-74(21-23-75)37-46-38-76(73-72-46)24-26-87-28-30-89-32-31-88-29-27-86-25-19-64-53(81)17-18-54(82)70-57(63(4,5)6)61(85)77-39-49(80)33-51(77)59(83)66-34-44-11-13-45(14-12-44)56-42(2)68-40-90-56/h11-16,35-36,38,40,47,49,51,57,80H,7-10,17-34,37,39H2,1-6H3,(H,64,81)(H,66,83)(H,70,82)(H,65,67,69,71)/t49-,51+,57-/m1/s1

Standard InChI Key:  MQNKDGVIMBTCAK-MXDFUXOPSA-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: 1260.53

Molecular Weight (Monoisotopic): 1259.6274

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. Su S, Yang Z, Gao H, Yang H, Zhu S, An Z, Wang J, Li Q, Chandarlapaty S, Deng H, Wu W, Rao Y..  (2019)  Potent and Preferential Degradation of CDK6 via Proteolysis Targeting Chimera Degraders.,  62  (16): [PMID:31330105] [10.1021/acs.jmedchem.9b00871]

Source

Source(1):

• Scientific Literature