1-Isopropyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid 4-ethoxycarbonyl-phenyl ester

ID: ALA120210

PubChem CID: 10069273

Max Phase: Preclinical

Molecular Formula: C24H29NO4

Molecular Weight: 395.50

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CCOC(=O)c1ccc(OC(=O)c2ccc3c(c2)C(C)(C)CCN3C(C)C)cc1

Standard InChI:  InChI=1S/C24H29NO4/c1-6-28-22(26)17-7-10-19(11-8-17)29-23(27)18-9-12-21-20(15-18)24(4,5)13-14-25(21)16(2)3/h7-12,15-16H,6,13-14H2,1-5H3

Standard InChI Key:  FGJIKCQWQSSVPD-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

 29 31  0  0  0  0  0  0  0  0999 V2000
   -0.1708   -4.5417    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5417   -4.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5417   -3.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6750   -2.8917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2500   -2.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9625   -3.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1708   -2.8917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8833   -4.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2417   -1.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2542   -4.5417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3917   -3.3042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5292   -2.0542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8833   -3.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6750   -2.0667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9667   -4.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9625   -2.0500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1708   -5.3667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8042   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5292   -2.8792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1042   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2417   -0.8167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8167   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1000   -2.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5417   -2.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8875   -2.4792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8833   -5.7792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5417   -5.7792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9542   -0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6667   -0.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  2  2  0
  4  6  1  0
  5  3  1  0
  6 15  1  0
  7 13  1  0
  8  1  1  0
  9 12  1  0
 10  2  1  0
 11  4  1  0
 12 18  1  0
 13  8  1  0
 14  4  2  0
 15 10  2  0
 16  9  2  0
 17  1  1  0
 18 23  2  0
 19 22  1  0
 20 11  1  0
 21  9  1  0
 22 20  2  0
 23 20  1  0
 24  7  1  0
 25  7  1  0
 26 17  1  0
 27 17  1  0
 28 21  1  0
 29 28  1  0
  3  7  1  0
  5  6  2  0
 19 12  2  0
M  END

Alternative Forms

1. Parent:

   

   ALA120210

   1-Isopropyl-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid 4-ethoxycarbonyl-phenyl ester

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: 395.50

Molecular Weight (Monoisotopic): 395.2097

AlogP: 4.98

#Rotatable Bonds: 5

Polar Surface Area: 55.84

Molecular Species: NEUTRAL

HBA: 5

HBD: ┄

#RO5 Violations: ┄

HBA (Lipinski): 5

HBD (Lipinski): ┄

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: 3.15

CX LogP: 5.95

CX LogD: 5.95

Aromatic Rings: 2

Heavy Atoms: 29

QED Weighted: 0.53

Np Likeness Score: -0.23

References

1. Dhar A, Liu S, Klucik J, Berlin KD, Madler MM, Lu S, Ivey RT, Zacheis D, Brown CW, Nelson EC, Birckbichler PJ, Benbrook DM..  (1999)  Synthesis, structure-activity relationships, and RARgamma-ligand interactions of nitrogen heteroarotinoids.,  42  (18): [PMID:10479291] [10.1021/jm9900974]

2. Zacheis D, Dhar A, Lu S, Madler MM, Klucik J, Brown CW, Liu S, Clement F, Subramanian S, Weerasekare GM, Berlin KD, Gold MA, Houck JR, Fountain KR, Benbrook DM..  (1999)  Heteroarotinoids inhibit head and neck cancer cell lines in vitro and in vivo through both RAR and RXR retinoic acid receptors.,  42  (21): [PMID:10543887] [10.1021/jm990292i]

Source

Source(1):

• Scientific Literature