(2-Nitro-phenyl)-acetic acid 2-((4aR,4bS,5S,6aS,6bS,9aR,10aS,10bS)-5-hydroxy-4a,6a-dimethyl-2-oxo-8-propyl-2,4a,4b,5,6,6a,9a,10,10a,10b,11,12-dodecahydro-7,9-dioxa-pentaleno[2,1-a]phenanthren-6b-yl)-2-oxo-ethyl ester

ID: ALA2335078

PubChem CID: 71567257

Max Phase: Preclinical

Molecular Formula: C33H39NO9

Molecular Weight: 593.67

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)COC(=O)Cc2ccccc2[N+](=O)[O-])O1

Standard InChI:  InChI=1S/C33H39NO9/c1-4-7-29-42-27-16-23-22-11-10-20-15-21(35)12-13-31(20,2)30(22)25(36)17-32(23,3)33(27,43-29)26(37)18-41-28(38)14-19-8-5-6-9-24(19)34(39)40/h5-6,8-9,12-13,15,22-23,25,27,29-30,36H,4,7,10-11,14,16-18H2,1-3H3/t22-,23-,25-,27+,29?,30+,31-,32-,33+/m0/s1

Standard InChI Key:  QMYOYDIXXSFRAW-ACHGALFESA-N

Molfile:  

     RDKit          2D

 47 52  0  0  0  0  0  0  0  0999 V2000
   20.7187   -5.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5932   -6.6036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4987   -5.1301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0047   -6.6036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7104   -6.1950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2865   -6.1950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5932   -7.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0047   -4.9692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2865   -5.3737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8833   -6.1950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8833   -7.8294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.8991   -4.4244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9734   -5.7988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4864   -6.4550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0047   -7.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1817   -6.6036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1817   -7.4208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2989   -7.8294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7121   -4.4203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4759   -7.8294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.3077   -5.1301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7104   -4.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5932   -4.9692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5808   -5.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4864   -3.7186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.8867   -3.0129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.8110   -7.1899    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   20.8710   -7.1031    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.4182   -5.6989    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   22.7039   -3.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1071   -2.2959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1178   -3.7112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9242   -2.2896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7617   -6.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0134   -5.5387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7994   -5.3150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3861   -5.8838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1721   -5.6600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3359   -2.9932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1523   -2.9873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.5563   -2.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1379   -1.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.3229   -1.5784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9049   -0.8795    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   23.0877   -0.8893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.3049   -0.1669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.3029   -6.7430    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  6  1  0
  3  1  1  0
  4  5  1  0
  5  1  1  0
  6  9  1  0
  7  2  1  0
  8  1  1  0
  9  8  1  0
 10  2  1  0
 11  7  2  0
  3 12  1  1
 13  3  1  0
 14  5  1  0
 15  4  1  0
 16 10  2  0
 17 16  1  0
 18 15  1  0
 19 12  2  0
 20 17  2  0
 21  3  1  0
  1 22  1  1
  9 23  1  1
  2 24  1  1
 25 12  1  0
 26 25  1  0
  5 27  1  6
  4 28  1  1
  6 29  1  6
 14 13  1  0
  4  6  1  0
  7 18  1  0
 11 17  1  0
 26 30  1  0
 30 31  1  0
 30 32  2  0
 31 33  1  0
 13 34  1  0
 21 35  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 33 39  2  0
 39 40  1  0
 40 41  2  0
 41 42  1  0
 42 43  2  0
 43 33  1  0
 44 45  2  0
 44 46  1  0
 43 44  1  0
 13 47  1  1
M  CHG  2  44   1  46  -1
M  END

Associated Targets(Human)

Caco-2 (12174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Clostridium perfringens (1165 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 593.67Molecular Weight (Monoisotopic): 593.2625AlogP: 4.42#Rotatable Bonds: 8
Polar Surface Area: 142.27Molecular Species: NEUTRALHBA: 9HBD: 1
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.95CX LogD: 4.95
Aromatic Rings: 1Heavy Atoms: 43QED Weighted: 0.26Np Likeness Score: 1.26

References

1. Marquez Ruiz JF, Kedziora K, Pigott M, Keogh B, Windle H, Gavin J, Kelleher DP, Gilmer JF..  (2013)  A nitrophenyl-based prodrug type for colorectal targeting of prednisolone, budesonide and celecoxib.,  23  (6): [PMID:23416011] [10.1016/j.bmcl.2013.01.060]

Source