3,9-dibromo-12-(3,4-dihydroxy-6-hydroxymethyl-5-methoxytetrahydro-2H-2-pyranyl)-5,7,12,13-tetrahydrofuro[3,4-c]indolo[2,3-a]carbazole-5,7-dione

ID: ALA3350564

Chembl Id: CHEMBL3350564

PubChem CID: 10723016

Max Phase: Preclinical

Molecular Formula: C27H20Br2N2O8

Molecular Weight: 660.27

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CO[C@H]1[C@H](O)[C@@H](O)[C@H](n2c3ccc(Br)cc3c3c4c(c5c6cc(Br)ccc6[nH]c5c32)C(=O)OC4=O)O[C@@H]1CO

Standard InChI:  InChI=1S/C27H20Br2N2O8/c1-37-24-15(8-32)38-25(23(34)22(24)33)31-14-5-3-10(29)7-12(14)17-19-18(26(35)39-27(19)36)16-11-6-9(28)2-4-13(11)30-20(16)21(17)31/h2-7,15,22-25,30,32-34H,8H2,1H3/t15-,22-,23-,24-,25-/m1/s1

Standard InChI Key:  OYAIAOPGGDONAT-XTRZKMQQSA-N

Alternative Forms

1. Parent:

   

   ALA3350564

   7,19-dibromo-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]-13-oxa-3,23-diazahexacyclo[14.7.0.02,10.04,9.011,15.017,22]tricosa-1,4(9),5,7,10,15,17(22),18,20-nonaene-12,14-dione

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 660.27

Molecular Weight (Monoisotopic): 657.9586

AlogP: 3.89

#Rotatable Bonds: 3

Polar Surface Area: 143.24

Molecular Species: NEUTRAL

HBA: 9

HBD: 4

#RO5 Violations: 1

HBA (Lipinski): 10

HBD (Lipinski): 4

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 12.20

CX Basic pKa: ┄

CX LogP: 3.65

CX LogD: 3.65

Aromatic Rings: 5

Heavy Atoms: 39

QED Weighted: 0.17

Np Likeness Score: 1.01

References

1. Moreau P, Anizon F, Sancelme M, Prudhomme M, Bailly C, Carrasco C, Ollier M, Sevère D, Riou JF, Fabbro D, Meyer T, Aubertin AM..  (1998)  Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle.,  41  (10): [PMID:9572888] [10.1021/jm970843+]

2. Moreau P, Anizon F, Sancelme M, Prudhomme M, Sevère D, Riou JF, Goossens JF, Hénichart JP, Bailly C, Labourier E, Tazzi J, Fabbro D, Meyer T, Aubertin AM..  (1999)  Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives.,  42  (10): [PMID:10346933] [10.1021/jm980702n]

Source

Source(1):

• Scientific Literature