(1S,3'R,6'R,7'S,8'E,15'R)-6-chloro-15'-hydroxy-15'-(hydroxymethyl)-7'-methoxy-12'-methyl-3,4-dihydro-2H,13'H-spiro[naphthalene-1,22'-[20]oxa[1,12]diazatetracyclo[14.7.2.0(3,6).0(19,24)]pentacosa[8,16,18,24]tetraen]-13'-one

ID: ALA4543603

PubChem CID: 155543373

Max Phase: Preclinical

Molecular Formula: C34H43ClN2O5

Molecular Weight: 595.18

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  CO[C@H]1/C=C/CCN(C)C(=O)C[C@](O)(CO)c2ccc3c(c2)N(C[C@@H]2CC[C@H]21)C[C@@]1(CCCc2cc(Cl)ccc21)CO3

Standard InChI:  InChI=1S/C34H43ClN2O5/c1-36-15-4-3-7-30(41-2)27-11-8-24(27)19-37-20-33(14-5-6-23-16-26(35)10-12-28(23)33)22-42-31-13-9-25(17-29(31)37)34(40,21-38)18-32(36)39/h3,7,9-10,12-13,16-17,24,27,30,38,40H,4-6,8,11,14-15,18-22H2,1-2H3/b7-3+/t24-,27+,30-,33-,34-/m0/s1

Standard InChI Key:  FMLLMWXGGMXKST-LFJQUMFESA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4543603

   ---

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: 595.18

Molecular Weight (Monoisotopic): 594.2861

AlogP: 4.84

#Rotatable Bonds: 2

Polar Surface Area: 82.47

Molecular Species: NEUTRAL

HBA: 6

HBD: 2

#RO5 Violations: 1

HBA (Lipinski): 7

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 13.12

CX Basic pKa: 4.69

CX LogP: 4.40

CX LogD: 4.40

Aromatic Rings: 2

Heavy Atoms: 42

QED Weighted: 0.48

Np Likeness Score: 0.72

References

1. Rescourio G, Gonzalez AZ, Jabri S, Belmontes B, Moody G, Whittington D, Huang X, Caenepeel S, Cardozo M, Cheng AC, Chow D, Dou H, Jones A, Kelly RC, Li Y, Lizarzaburu M, Lo MC, Mallari R, Meleza C, Rew Y, Simonovich S, Sun D, Turcotte S, Yan X, Wong SG, Yanez E, Zancanella M, Houze J, Medina JC, Hughes PE, Brown SP..  (2019)  Discovery and in Vivo Evaluation of Macrocyclic Mcl-1 Inhibitors Featuring an α-Hydroxy Phenylacetic Acid Pharmacophore or Bioisostere.,  62  (22): [PMID:31736296] [10.1021/acs.jmedchem.9b01310]

Source

Source(1):

• Scientific Literature