NP-MRD: Showing NP-Card for (3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol (NP0329278)

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Record Information

Version

1.0

Created at

2022-09-12 13:31:38 UTC

Updated at

2022-09-12 13:31:39 UTC

NP-MRD ID

NP0329278

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol

Description

CHEMBL3114760 belongs to the class of organic compounds known as 3-beta-hydroxysteroids. These are steroids carrying a beta-hydroxyl group at the 3-position of the steroid backbone. (3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol is found in Rosa rugosa. Based on a literature review very few articles have been published on CHEMBL3114760.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122215312D          

 24 27  0  0  1  0            999 V2000
    6.6328    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6353    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9511    1.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0463    1.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6113    1.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 18 23  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
    3.4704    1.7247   -0.7164 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0170    0.5152    0.1227 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5563    0.8143    1.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7410   -0.6670   -0.4193 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0893   -1.5877    0.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840   -1.3141   -1.5843 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6152   -0.9771   -1.7449 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9283   -0.8326   -0.3772 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1224   -2.0958    0.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5479    0.4049    0.2161 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9710    0.6323    1.5852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4852    1.0539    1.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2538   -0.0050    0.5933 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5509   -1.0579    1.6288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5112   -0.5233   -0.6060 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3031   -1.5943   -1.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5518   -0.9054   -1.8716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3242   -0.4071   -0.7323 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5137    0.3973   -0.9825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6930    1.1757    0.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5850    0.8739    1.1025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3309    1.9329    1.9253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4965    0.6070    0.0830 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3243    1.8871   -0.6746 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5923    2.3694   -0.8956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338    2.2241   -0.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7848    1.3643   -1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6788    0.7069    1.4654 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1204    0.1686    2.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3919    1.8997    1.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526   -0.3068   -0.7815 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8817   -1.2816    1.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5627   -1.0060   -2.5616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2526   -2.4285   -1.5563 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4886   -0.0325   -2.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1811   -1.7775   -2.3499 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4927   -2.0566    1.3613 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1324   -2.6451    0.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7829   -2.8335   -0.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1293    1.2497   -0.4195 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659   -0.2196    2.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4376    1.5027    2.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9464    1.1679    2.3579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4687    2.0316    0.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6288   -1.3471    2.2165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1618   -0.5284    2.4213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1415   -1.8999    1.2997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5077    0.3368   -1.3450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467   -2.4052   -0.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8154   -2.0697   -2.1288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1343   -1.6210   -2.4564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1608   -0.0631   -2.4736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5381   -1.2655   -0.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2001    0.4557   -1.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4714    1.9021    0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9513   -0.0418    1.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5049    1.6372    2.8670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7639    2.7763   -0.1435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3174    2.1597   -0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9220    1.8251   -1.6296 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 24  1  6
 23 21  1  0
 21 22  1  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15  8  1  0
  8  9  1  1
  8  7  1  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  1  1  0
  2  3  1  0
  2 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 18 23  1  0
 13 15  1  0
 13 23  1  0
 10  8  1  0
 24 58  1  0
 24 59  1  0
 24 60  1  0
 21 56  1  1
 22 57  1  0
 20 55  1  0
 19 54  1  0
 18 53  1  1
 17 51  1  0
 17 52  1  0
 16 49  1  0
 16 50  1  0
 15 48  1  6
  9 37  1  0
  9 38  1  0
  9 39  1  0
  7 35  1  0
  7 36  1  0
  6 33  1  0
  6 34  1  0
  4 31  1  6
  5 32  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
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  3 30  1  0
 10 40  1  6
 11 41  1  0
 11 42  1  0
 12 43  1  0
 12 44  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
M  END


  Mrv1652309122215312D          

 24 27  0  0  1  0            999 V2000
    6.6328    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6353    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9511    1.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0463    1.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6113    1.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 18 23  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0329278

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12[C@@H](O)C=C[C@H]1CC[C@@H]1[C@@]3(C)CC[C@H](O)C(C)(C)[C@@H]3CC[C@@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O2/c1-19(2)15-10-13-21(4)16(20(15,3)12-11-17(19)23)8-6-14-7-9-18(24)22(14,21)5/h7,9,14-18,23-24H,6,8,10-13H2,1-5H3/t14-,15+,16-,17+,18+,20+,21-,22+/m1/s1

> <INCHI_KEY>
JFYPLXOOAASGRS-TUUZUYIFSA-N

> <FORMULA>
C22H36O2

> <MOLECULAR_WEIGHT>
332.528

> <EXACT_MASS>
332.271530399

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
39.94442873933872

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,5S,7R,10R,11R,12S,15R)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-13-ene-5,12-diol

> <JCHEM_LOGP>
4.040763430666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.489433390169243

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.224898512152624

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5881035159310034

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
98.9386

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,7R,10R,11R,12S,15R)-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-13-ene-5,12-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      12.381   2.992   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.049   2.218   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.519   3.664   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.042   1.041   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.558   1.312   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.519  -0.407   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.003  -0.678   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.010   0.499   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.487  -0.949   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.533   1.947   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.541   3.125   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.025   2.854   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.502   1.405   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.509   2.583   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.494   0.228   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.971  -1.221   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.455  -1.492   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.462  -0.314   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.923  -0.264   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.495   1.215   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.770   2.079   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.820   3.618   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.986   1.134   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.874   2.670   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   10                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   15                                             
CONECT    9    8                                                            
CONECT   10    8    2   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   23                                             
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   18   13   24                                             
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₆O₂

Average Mass

332.5280 Da

Monoisotopic Mass

332.27153 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@]12[C@@H](O)C=C[C@H]1CC[C@@H]1[C@@]3(C)CC[C@H](O)C(C)(C)[C@@H]3CC[C@@]21C

InChI Identifier

InChI=1S/C22H36O2/c1-19(2)15-10-13-21(4)16(20(15,3)12-11-17(19)23)8-6-14-7-9-18(24)22(14,21)5/h7,9,14-18,23-24H,6,8,10-13H2,1-5H3/t14-,15+,16-,17+,18+,20+,21-,22+/m1/s1

InChI Key

JFYPLXOOAASGRS-TUUZUYIFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rosa rugosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-beta-hydroxysteroids. These are steroids carrying a beta-hydroxyl group at the 3-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

3-beta-hydroxysteroids

Alternative Parents

Substituents

14-alpha-methylsteroid
3-beta-hydroxysteroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

31141827

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

76317773

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol (NP0329278)

MOL for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

3D MOL for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

3D SDF for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

3D-SDF for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

PDB for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

3D PDB for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

SMILES for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

INCHI for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

Structure for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)

3D Structure for NP0329278 ((3s,3ar,3br,5ar,7s,9ar,9br,11ar)-3a,3b,6,6,9a-pentamethyl-3h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-3,7-diol)