NP-MRD: Showing NP-Card for 22-Dehydrocholesterol (NP0066351)

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Record Information

Version

1.0

Created at

2022-04-28 10:37:50 UTC

Updated at

2022-04-28 10:37:50 UTC

NP-MRD ID

NP0066351

Secondary Accession Numbers

None

Natural Product Identification

Common Name

22-Dehydrocholesterol

Description

22Z-dehydrocholesterol belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. Thus, 22Z-dehydrocholesterol is considered to be a sterol. 22-Dehydrocholesterol is found in Aplysia depilans, Haliclona oculata, Hypnea japonica , Physarum polycephalum, Posidonia oceanica and Rhizophlyctis rosea. Based on a literature review very few articles have been published on 22z-dehydrocholesterol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282212372D          

 28 31  0  0  1  0            999 V2000
    6.1708   -0.2182    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
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  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
    4.0148    0.1221    0.0000 C   0  0  1  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
    5.3587   -0.3634    0.0000 C   0  0  0  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
    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  1  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
    2.0195    1.1139    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
    1.5660   -0.1416    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2424   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2640   -1.3314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0469   -2.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -2.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1486   -3.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2767   -2.6340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  1  0  0  0
  8 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 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
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 26  1  6  0  0  0
 14 27  1  1  0  0  0
  2 28  1  1  0  0  0
M  END

     RDKit          3D

 72 75  0  0  0  0  0  0  0  0999 V2000
    7.5973   -0.8733    0.9246 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3092   -0.3281    1.4829 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2528    1.1787    1.2354 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0877   -1.0089    0.8809 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0136   -0.8429   -0.5686 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0710   -0.2705   -1.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8861    0.3153   -0.6299 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8344    1.7777   -1.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6079   -0.3281   -1.0838 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6437   -1.8412   -0.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2120   -2.2772   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5589   -1.0155   -0.9350 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9187   -0.9889   -0.3720 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8134   -1.8142   -1.2676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2339   -1.3969   -1.2387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7317   -0.4326   -0.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1839   -0.0709   -0.5090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4388    1.3785   -0.7519 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5358    1.8688   -0.0437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1886    2.1681   -0.4588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4221    1.6135    0.7376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7864    0.2934    0.4205 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6245   -0.5691    1.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4844    0.4082   -0.3230 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5406    1.3959    0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2209    1.3500   -0.5289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3819    0.0216   -0.2976 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5556   -0.2423    1.1823 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8163   -1.8738    1.3681 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6449   -0.8937   -0.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4089   -0.2021    1.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3378   -0.4580    2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2361    1.6195    1.4369 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4151    1.6439    1.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1007    1.2760    0.1206 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2227   -0.7788    1.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2876   -2.1152    1.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8842   -1.2664   -1.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1973   -0.2449   -2.3758 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9657    0.2580    0.4443 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7692    2.0125   -1.7250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191    1.9411   -1.8458 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7229    2.4898   -0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3875   -0.2130   -2.1548 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195   -2.3474   -1.7172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2016   -2.0923    0.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0238   -2.5557    0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0986   -3.0644   -1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5331   -0.8049   -2.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9067   -1.4716    0.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4872   -1.7151   -2.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6933   -2.8964   -1.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9301   -1.9248   -1.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6392   -0.6492   -1.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6127   -0.4353    0.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6753    1.5708   -1.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5535    1.5622    0.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5591    2.2143   -1.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5061    3.1957   -0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7413    2.3817    1.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1814    1.4386    1.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7852   -1.6578    1.4122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6766   -0.3969    2.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931   -0.3241    2.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7152    0.7191   -1.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9452    2.4226    0.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3745    1.3025    1.3440 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4233    2.1986   -0.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4977    1.4568   -1.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632    0.7730    1.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2606   -0.8204    1.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4952   -0.7434    1.4335 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  1
 27  9  1  0
 27 12  1  0
 24 13  1  0
 22 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  1
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  6 39  1  0
  7 40  1  1
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  6
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  6
 13 50  1  1
 14 51  1  0
 14 52  1  0
 15 53  1  0
 17 54  1  0
 17 55  1  0
 18 56  1  6
 19 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  6
 25 66  1  0
 25 67  1  0
 26 68  1  0
 26 69  1  0
 28 70  1  0
 28 71  1  0
 28 72  1  0
M  END


  Mrv1652304282212372D          

 28 31  0  0  1  0            999 V2000
    6.1708   -0.2182    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
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  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
    4.0148    0.1221    0.0000 C   0  0  1  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
    5.3587   -0.3634    0.0000 C   0  0  0  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
    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  1  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
    2.0195    1.1139    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
    1.5660   -0.1416    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2424   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2640   -1.3314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0469   -2.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -2.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1486   -3.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2767   -2.6340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  1  0  0  0
  8 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 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
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 26  1  6  0  0  0
 14 27  1  1  0  0  0
  2 28  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0066351

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C\C=C/[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h6,8-9,18-19,21-25,28H,7,10-17H2,1-5H3/b8-6-/t19-,21+,22+,23-,24+,25+,26+,27-/m1/s1

> <INCHI_KEY>
UPGTYLFCVNHBTN-MMEGKJBPSA-N

> <FORMULA>
C27H44O

> <MOLECULAR_WEIGHT>
384.648

> <EXACT_MASS>
384.339216037

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
49.24221140834616

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,10S,11S,14R,15R)-2,15-dimethyl-14-[(2R,3Z)-6-methylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol

> <ALOGPS_LOGP>
6.89

> <JCHEM_LOGP>
6.750967374

> <ALOGPS_LOGS>
-6.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.20428950550382

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3972437702926293

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
121.73309999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.38e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,10S,11S,14R,15R)-2,15-dimethyl-14-[(2R,3Z)-6-methylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      11.519  -0.407   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.042   1.041   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.049   2.218   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.533   1.947   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.541   3.125   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.025   2.854   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.502   1.405   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.494   0.228   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.010   0.499   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.003  -0.678   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.487  -0.949   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.971  -1.221   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.455  -1.492   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.462  -0.314   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.986   1.134   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.770   2.079   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.495   1.215   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.923  -0.264   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.978  -1.480   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.452  -1.269   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.493  -2.485   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.088  -3.912   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.858  -5.127   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.277  -6.554   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.383  -4.917   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.558  -2.907   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.791  -1.700   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.558   1.312   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   15                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8    4   10   11                                             
CONECT   10    9    1                                                       
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18   27                                             
CONECT   15   14    7   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   14   19                                                  
CONECT   19   18   20   26                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   19                                                            
CONECT   27   14                                                            
CONECT   28    2                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₄O

Average Mass

384.6480 Da

Monoisotopic Mass

384.33922 Da

IUPAC Name

(1S,2R,5S,10S,11S,14R,15R)-2,15-dimethyl-14-[(2R,3Z)-6-methylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol

Traditional Name

(1S,2R,5S,10S,11S,14R,15R)-2,15-dimethyl-14-[(2R,3Z)-6-methylhept-3-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol

CAS Registry Number

Not Available

SMILES

CC(C)C\C=C/[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h6,8-9,18-19,21-25,28H,7,10-17H2,1-5H3/b8-6-/t19-,21+,22+,23-,24+,25+,26+,27-/m1/s1

InChI Key

UPGTYLFCVNHBTN-MMEGKJBPSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aplysia depilans	LOTUS Database	35616633
Haliclona oculata	LOTUS Database	35616633
Hypnea japonica	-	KNApSAcK
Physarum polycephalum	Amoebozoa	KNApSAcK
Posidonia oceanica	Plant	KNApSAcK
Rhizophlyctis rosea	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholesterols and derivatives

Alternative Parents

Substituents

Cholesterol-skeleton
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
Hydroxysteroid
3-hydroxysteroid
3-hydroxy-delta-5-steroid
Delta-5-steroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Cholesterol and derivatives (LMST01010317 )

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	6.89	ALOGPS
logP	6.75	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Acidic)	18.2	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	121.73 m³·mol⁻¹	ChemAxon
Polarizability	49.24 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	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

62975695

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

52931330

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 22-Dehydrocholesterol (NP0066351)

MOL for NP0066351 (22-Dehydrocholesterol)

3D MOL for NP0066351 (22-Dehydrocholesterol)

3D SDF for NP0066351 (22-Dehydrocholesterol)

3D-SDF for NP0066351 (22-Dehydrocholesterol)

PDB for NP0066351 (22-Dehydrocholesterol)

3D PDB for NP0066351 (22-Dehydrocholesterol)

SMILES for NP0066351 (22-Dehydrocholesterol)

INCHI for NP0066351 (22-Dehydrocholesterol)

Structure for NP0066351 (22-Dehydrocholesterol)

3D Structure for NP0066351 (22-Dehydrocholesterol)