NP-MRD: Showing NP-Card for 5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol (NP0174932)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 12:17:11 UTC

Updated at

2022-09-03 12:17:11 UTC

NP-MRD ID

NP0174932

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

Description

5-{2-[1-(6-Hydroxy-6-methylheptan-2-yl)-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane. 5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol is found in Solanum glaucophyllum. 5-{2-[1-(6-Hydroxy-6-methylheptan-2-yl)-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171500062D          

 30 32  0  0  0  0            999 V2000
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4950   -4.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4554   -4.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247   -3.8074    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.8396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371   -1.9309    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  4  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 18 25  2  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 74 76  0  0  0  0  0  0  0  0999 V2000
   -5.9841   -0.6899   -0.6593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7579    0.5333   -0.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5115    1.1847   -0.6174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3322    0.6649   -0.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0848   -0.5664    0.3050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9757   -1.1759    0.6014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0815   -2.4788    1.3339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9109   -2.8857    2.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3631   -2.1378    1.8441 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4026   -1.7750    0.3924 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0101   -2.8540   -0.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6716   -0.6627    0.2812 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3794   -0.0596   -1.0200 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0766   -0.4807   -1.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5782   -0.9402   -0.0030 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8985   -1.4973    0.0910 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2022   -2.7316   -0.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9610   -0.4736   -0.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8604    0.8327    0.3150 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8557    1.8203   -0.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2966    1.5637   -0.0041 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8931    0.4070   -0.7080 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6854    1.5327    1.4980 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9655    2.7377   -0.4629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6092    2.5210   -1.3279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9195    3.1881   -0.9754 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8764    2.7889   -1.8973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3988    2.7687    0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7723    1.3372    0.4814 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.7951    0.9283    1.8128 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9263   -1.1286   -0.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3024   -1.2780   -1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4911    1.2499   -0.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0013   -1.0984    0.6546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4047   -3.2806    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9565   -2.4262    2.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0776   -2.8079    3.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6712   -3.9811    1.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3345   -1.1979    2.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2148   -2.7235    2.1933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9287   -2.6503   -1.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1936   -3.8302   -0.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7535   -3.0938   -1.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3953    0.0809    1.0985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0442   -0.2548   -1.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2794    1.0686   -0.9040 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9817   -1.2622   -2.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6369    0.3580   -1.7853 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5113   -0.0267    0.6614 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1527   -1.7104    1.1496 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3301   -2.8468   -0.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8179   -3.6622   -0.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0331   -2.5678   -1.7963 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9894   -0.3604   -1.4520 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9541   -0.9488   -0.0743 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7817    0.7578    1.4283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8483    1.2780    0.0364 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6771    2.0365   -1.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6564    2.8569    0.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2036   -0.4478   -0.0706 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3331    0.1198   -1.6071 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8997    0.7527   -1.1352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.8906    2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7377    1.2423    1.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5914    2.5607    1.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7490    2.5157   -0.9902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5333    2.3551   -2.4138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7888    3.1881   -1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7999    4.2844   -1.0567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8401    3.4026   -2.6634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5159    2.9271    1.0833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1815    3.4474    0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7472    1.1634   -0.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0923    1.6478    2.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 29  2  1  0
  2  1  2  0
 10 15  1  0
  2  3  1  0
 10 12  1  0
 17 51  1  0
 17 52  1  0
 17 53  1  0
 16 50  1  1
 18 54  1  0
 18 55  1  0
 19 56  1  0
 19 57  1  0
 20 58  1  0
 20 59  1  0
 22 60  1  0
 22 61  1  0
 22 62  1  0
 23 63  1  0
 23 64  1  0
 23 65  1  0
 24 66  1  0
 15 49  1  1
 14 47  1  0
 14 48  1  0
 13 45  1  0
 13 46  1  0
 12 44  1  1
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
  5 34  1  0
  4 33  1  0
 25 67  1  0
 25 68  1  0
 26 69  1  1
 27 70  1  0
 28 71  1  0
 28 72  1  0
 29 73  1  6
 30 74  1  0
  1 31  1  0
  1 32  1  0
M  END


  Mrv1533004171500062D          

 30 32  0  0  0  0            999 V2000
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -4.0623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4950   -4.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4554   -4.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247   -3.8074    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    3.8396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    3.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4944    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371   -1.9309    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  4  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 18 25  2  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0174932

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCCC(C)(C)O)C1CCC2C(CCCC12C)=CC=C1CC(O)CC(O)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O3/c1-18(8-6-14-26(3,4)30)23-12-13-24-20(9-7-15-27(23,24)5)10-11-21-16-22(28)17-25(29)19(21)2/h10-11,18,22-25,28-30H,2,6-9,12-17H2,1,3-5H3

> <INCHI_KEY>
GMRQFYUYWCNGIN-UHFFFAOYSA-N

> <FORMULA>
C27H44O3

> <MOLECULAR_WEIGHT>
416.646

> <EXACT_MASS>
416.329045277

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
50.14009183403846

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

> <ALOGPS_LOGP>
5.51

> <JCHEM_LOGP>
4.3507409966666675

> <ALOGPS_LOGS>
-4.80

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.288747760735944

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.392873609845417

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2544418727034898

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
126.53249999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.67e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.315  -7.583   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.791  -9.048   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.850  -8.059   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.779  -7.107   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924   1.777   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.590   2.547   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.590   4.087   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.257   4.857   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.257   6.397   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.590   7.167   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.924   6.397   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.924   4.857   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.258   7.167   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.923   7.167   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.923   4.087   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.429  -3.604   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6                                                            
CONECT   10    2   11   29                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   29                                                  
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   25                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21   17                                                       
CONECT   23   21                                                            
CONECT   24   19                                                            
CONECT   25   18                                                            
CONECT   26   14   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   10   13   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
1 alpha, 25 Dihydroxy 20 epi vitamin D3	MeSH
1 alpha, 25-Dihydroxy-20-epi-vitamin D3	MeSH
1 alpha,25 Dihydroxycholecalciferol	MeSH
1 alpha,25 Dihydroxyvitamin D3	MeSH
1 alpha,25-Dihydroxycholecalciferol	MeSH
1 alpha,25-Dihydroxyvitamin D3	MeSH
1,25 Dihydroxycholecalciferol	MeSH
1,25 Dihydroxyvitamin D3	MeSH
1,25 Dihydroxy 20 epi vitamin D3	MeSH
1,25(OH)2-20EPi-D3	MeSH
1,25-Dihydroxycholecalciferol	MeSH
1,25-Dihydroxyvitamin D3	MeSH
1,25-Dihydroxy-20-epi-vitamin D3	MeSH
20 Epi 1alpha,25 dihydroxycholecaliferol	MeSH
20-Epi-1alpha,25-dihydroxycholecaliferol	MeSH
Abbott brand OF calcitriol	MeSH
Alphapharm brand OF calcitriol	MeSH
Bocatriol	MeSH
Calcijex	MeSH
Calcitriol	MeSH
Calcitriol abbott brand	MeSH
Calcitriol alphapharm brand	MeSH
Calcitriol cryopharma brand	MeSH
Calcitriol galderma brand	MeSH
Calcitriol gry brand	MeSH
Calcitriol jenapharm brand	MeSH
Calcitriol kyramed	MeSH
Calcitriol kyramed brand	MeSH
Calcitriol leo brand	MeSH
Calcitriol medice brand	MeSH
Calcitriol nefro	MeSH
Calcitriol renacare brand	MeSH
Calcitriol roche brand	MeSH
Calcitriol-nefro	MeSH
CalcitriolNefro	MeSH
Cryopharma brand OF calcitriol	MeSH
D3, 1 alpha,25-Dihydroxyvitamin	MeSH
D3, 1,25-Dihydroxyvitamin	MeSH
D3, 1,25-Dihydroxy-20-epi-vitamin	MeSH
Decostriol	MeSH
Galderma brand OF calcitriol	MeSH
Gry brand OF calcitriol	MeSH
Hoffmann la roche brand OF calcitriol	MeSH
Hoffmann-la roche brand OF calcitriol	MeSH
Jenapharm brand OF calcitriol	MeSH
KyraMed brand OF calcitriol	MeSH
KyraMed, calcitriol	MeSH
leo Brand OF calcitriol	MeSH
Medice brand OF calcitriol	MeSH
Osteotriol	MeSH
RenaCare brand OF calcitriol	MeSH
Renatriol	MeSH
Rocaltrol	MeSH
Roche brand OF calcitriol	MeSH
Silkis	MeSH
Sitriol	MeSH
Soltriol	MeSH
Tirocal	MeSH
alpha,25-Dihydroxyvitamin D3, 1	MeSH

Chemical Formula

C₂₇H₄₄O₃

Average Mass

416.6460 Da

Monoisotopic Mass

416.32905 Da

IUPAC Name

5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

Traditional Name

5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

CAS Registry Number

Not Available

SMILES

CC(CCCC(C)(C)O)C1CCC2C(CCCC12C)=CC=C1CC(O)CC(O)C1=C

InChI Identifier

InChI=1S/C27H44O3/c1-18(8-6-14-26(3,4)30)23-12-13-24-20(9-7-15-27(23,24)5)10-11-21-16-22(28)17-25(29)19(21)2/h10-11,18,22-25,28-30H,2,6-9,12-17H2,1,3-5H3

InChI Key

GMRQFYUYWCNGIN-UHFFFAOYSA-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
Solanum glaucophyllum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as vitamin d and derivatives. Vitamin D and derivatives are compounds containing a secosteroid backbone, usually secoergostane or secocholestane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Vitamin D and derivatives

Direct Parent

Vitamin D and derivatives

Alternative Parents

Substituents

Triterpenoid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

a hormone (CALCITRIOL )

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
logP	5.51	ALOGPS
logP	4.35	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.39	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	126.53 m³·mol⁻¹	ChemAxon
Polarizability	50.14 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

2524

PDB ID

Not Available

ChEBI ID

125427

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol (NP0174932)

MOL for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

3D MOL for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

3D SDF for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

3D-SDF for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

PDB for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

3D PDB for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

SMILES for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

INCHI for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

Structure for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)

3D Structure for NP0174932 (5-{2-[1-(6-hydroxy-6-methylheptan-2-yl)-7a-methyl-hexahydro-1h-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol)