(5S,8R,9R,10S,12R,13S,14R,17S)-4,4,8,10,14-Pentamethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-12,17-diol

ID: ALA4091525

PubChem CID: 137652714

Max Phase: Preclinical

Molecular Formula: C22H36O2

Molecular Weight: 332.53

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC1(C)C=CC[C@]2(C)[C@H]3C[C@@H](O)[C@@H]4[C@@H](O)CC[C@@]4(C)[C@]3(C)CC[C@@H]12

Standard InChI:  InChI=1S/C22H36O2/c1-19(2)9-6-10-20(3)16(19)8-12-21(4)17(20)13-15(24)18-14(23)7-11-22(18,21)5/h6,9,14-18,23-24H,7-8,10-13H2,1-5H3/t14-,15+,16-,17+,18-,20-,21+,22+/m0/s1

Standard InChI Key:  FAADRZJYAMPNQC-CLIKDFRBSA-N

Molfile:  

     RDKit          2D

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   10.5876  -19.8877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1792  -19.1751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7663  -19.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0376  -16.7126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9000  -17.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3168  -17.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0376  -17.5376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6126  -17.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9000  -18.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3376  -16.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8251  -16.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5876  -16.6251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8168  -17.8001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3168  -18.7751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1792  -17.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3126  -17.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6126  -19.1751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4750  -18.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4750  -17.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9000  -17.1126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6042  -18.3501    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0376  -18.3626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3168  -17.1126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8959  -19.5876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3334  -15.4751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0335  -15.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0803  -15.6781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  2  1  0
  5  8  1  0
  6  7  1  0
  7  4  1  0
  8 12  1  0
  9  5  1  0
 10  4  1  0
 11  4  1  0
 12 10  1  0
  2  9  1  0
 13  7  1  0
 14  6  1  0
 15  5  1  0
 16 11  1  0
 17 14  1  0
 18 19  2  0
 19 15  1  0
  5 20  1  1
  8 21  1  6
  7 22  1  6
  6 23  1  1
 13 16  1  0
  8  6  1  0
  9 17  1  0
  2 18  1  0
  9 24  1  6
 10 25  1  1
  4 26  1  1
 11 27  1  1
M  END

Alternative Forms

  1. Parent:

    ALA4091525

    ---

Associated Targets(Human)

HSD11B1 Tclin 11-beta-hydroxysteroid dehydrogenase 1 (5910 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hsd11b1 11-beta-hydroxysteroid dehydrogenase 1 (1542 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: 332.53Molecular Weight (Monoisotopic): 332.2715AlogP: 4.55#Rotatable Bonds:
Polar Surface Area: 40.46Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 3.69CX LogD: 3.69
Aromatic Rings: Heavy Atoms: 24QED Weighted: 0.64Np Likeness Score: 3.07

References

1. Shao LD, Bao Y, Shen Y, Su J, Leng Y, Zhao QS..  (2017)  Synthesis of selective 11β-HSD1 inhibitors based on dammarane scaffold.,  135  [PMID:28458137] [10.1016/j.ejmech.2017.04.059]

Source