NP-MRD: Showing NP-Card for 17-hydroxycyclooctatin (NP0009763)

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Record Information

Version

2.0

Created at

2021-01-05 19:19:56 UTC

Updated at

2021-07-15 17:04:11 UTC

NP-MRD ID

NP0009763

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-hydroxycyclooctatin

Provided By

NPAtlas

Description

17-Hydroxycyclooctatin, (rel)- belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). 17-hydroxycyclooctatin is found in Streptomyces. 17-hydroxycyclooctatin was first documented in 2011 (PMID: 21314175). Based on a literature review very few articles have been published on 17-hydroxycyclooctatin, (rel)-.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106523D          

 58 60  0  0  0  0            999 V2000
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    3.6598   -0.2805   -0.0457 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9317   -0.7713    0.6629 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8438   -2.1531    0.7231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5013   -0.7003    0.8155 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5896   -0.0260    2.1392 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2951    0.7081    2.3053 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6744    0.7729    0.9041 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0733    2.0394    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    0.8058    1.1007 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5514    0.8367   -0.1877 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4460   -0.3546   -0.2924 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5677    0.0979   -1.1910 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7535   -0.7220   -2.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2704    1.5286   -1.5913 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.4034    2.2609    0.7749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1787    3.3884    0.4176 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
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 12 13  1  0  0  0  0
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 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  0  0  0  0
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 19 21  1  6  0  0  0
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 24  8  1  0  0  0  0
 16 11  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
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M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306242106523D          

 58 60  0  0  0  0            999 V2000
    3.6442   -0.9051   -1.4238 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6598   -0.2805   -0.0457 C   0  0  2  0  0  0  0  0  0  0  0  0
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    5.3143   -2.5334   -0.0706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5906   -1.8144    1.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266    0.7385    2.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7577   -0.7307    2.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6537    0.1165    2.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3979    1.7096    2.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0518    2.4311    0.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    2.8384    0.4518 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0818    1.8988   -0.9099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1100   -0.0707    1.7456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0155    1.6977    1.7449 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5734   -1.2600   -2.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6484    1.5350   -2.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9082    2.9132   -0.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9242    2.3858    1.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5811    4.0743    0.0253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5531   -3.5756    0.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4289   -2.2343    0.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1553   -2.1859    1.2904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3165   -2.6073   -2.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4120   -2.3941   -2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6167   -0.6566   -2.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4211   -2.0814   -0.8457 H   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
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 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
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  6  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24  5  1  0  0  0  0
 24  8  1  0  0  0  0
 16 11  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  2 28  1  6  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  4 31  1  0  0  0  0
  5 32  1  1  0  0  0
  6 33  1  0  0  0  0
  6 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
  9 37  1  0  0  0  0
  9 38  1  0  0  0  0
  9 39  1  0  0  0  0
 10 40  1  0  0  0  0
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 11 42  1  6  0  0  0
 12 43  1  1  0  0  0
 13 44  1  1  0  0  0
 14 45  1  0  0  0  0
 15 46  1  0  0  0  0
 15 47  1  0  0  0  0
 16 48  1  6  0  0  0
 17 49  1  0  0  0  0
 17 50  1  0  0  0  0
 18 51  1  0  0  0  0
 20 52  1  0  0  0  0
 20 53  1  0  0  0  0
 20 54  1  0  0  0  0
 21 55  1  0  0  0  0
 22 56  1  0  0  0  0
 22 57  1  0  0  0  0
 23 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009763

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]([H])(C([H])([H])[H])[C@]1([H])\C2=C([H])\C([H])([H])[C@@](O[H])(C([H])([H])[H])[C@]3([H])[C@]([H])(O[H])C([H])([H])[C@@]([H])(C([H])([H])O[H])[C@@]3([H])C([H])([H])[C@@]2(C([H])([H])[H])C([H])([H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O4/c1-12(10-21)14-4-6-19(2)9-15-13(11-22)8-17(23)18(15)20(3,24)7-5-16(14)19/h5,12-15,17-18,21-24H,4,6-11H2,1-3H3/b16-5-/t12-,13+,14-,15-,17-,18+,19-,20+/m1/s1

> <INCHI_KEY>
ZRHLUTXOIYNCOW-QMDVJOKOSA-N

> <FORMULA>
C20H34O4

> <MOLECULAR_WEIGHT>
338.488

> <EXACT_MASS>
338.245709575

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
38.455883292729

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3R,4R,6R,7S,8S,10Z,12R)-4-(hydroxymethyl)-12-[(2S)-1-hydroxypropan-2-yl]-1,8-dimethyltricyclo[9.3.0.0^{3,7}]tetradec-10-ene-6,8-diol

> <ALOGPS_LOGP>
1.40

> <JCHEM_LOGP>
0.7756051206666674

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.01275050277144

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.384366916336198

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5891445200723133

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
95.6767

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.61e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4R,6R,7S,8S,10Z,12R)-4-(hydroxymethyl)-12-[(2S)-1-hydroxypropan-2-yl]-1,8-dimethyltricyclo[9.3.0.0^{3,7}]tetradec-10-ene-6,8-diol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
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   -1.4474   -2.4978    0.4817 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5338   -1.4551   -1.5076 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6854   -1.2866   -0.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1704   -0.4557    0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5467   -0.5357   -1.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7830   -0.4891   -1.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7353    0.8192   -0.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8307   -0.5048    0.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3143   -2.5334   -0.0706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5906   -1.8144    1.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7577   -0.7307    2.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0518    2.4311    0.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    2.8384    0.4518 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0818    1.8988   -0.9099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1100   -0.0707    1.7456 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8942   -0.5258    0.7127 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1775    2.1433   -1.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9082    2.9132   -0.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9242    2.3858    1.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1265    1.4299    0.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5811    4.0743    0.0253 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4120   -2.3941   -2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6167   -0.6566   -2.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4211   -2.0814   -0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 12 19  1  0
 19 20  1  0
 19 21  1  6
 19 22  1  0
 22 23  1  0
 23 24  2  0
 24  5  1  0
 24  8  1  0
 16 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  6
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  1
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  9 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  1
 13 44  1  1
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  6
 17 49  1  0
 17 50  1  0
 18 51  1  0
 20 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       3.644  -0.905  -1.424  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.660  -0.281  -0.046  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.932  -0.771   0.663  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.844  -2.153   0.723  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.501  -0.700   0.816  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.590  -0.026   2.139  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.295   0.708   2.305  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.674   0.773   0.904  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.073   2.039   0.180  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.810   0.806   1.101  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.551   0.837  -0.188  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.446  -0.355  -0.292  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.568   0.098  -1.191  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.753  -0.722  -2.286  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.270   1.529  -1.591  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.478   2.013  -0.370  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.403   2.261   0.775  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.179   3.388   0.418  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.797  -1.625  -0.722  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.447  -2.498   0.482  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.680  -2.429  -1.487  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.534  -1.455  -1.508  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.685  -1.287  -0.676  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.170  -0.456   0.236  0.00  0.00           C+0
HETATM   25  H   UNK     0       4.547  -0.536  -1.994  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.783  -0.489  -1.979  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.734  -1.986  -1.406  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.735   0.819  -0.079  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.831  -0.505   0.067  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.998  -0.387   1.694  0.00  0.00           H+0
HETATM   31  H   UNK     0       5.314  -2.533  -0.071  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.591  -1.814   1.034  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.427   0.739   2.167  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.758  -0.731   2.986  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.654   0.117   2.994  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.398   1.710   2.740  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.052   2.431   0.487  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.330   2.838   0.452  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.082   1.899  -0.910  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.110  -0.071   1.746  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.016   1.698   1.745  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.806   0.910  -1.005  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.894  -0.526   0.713  0.00  0.00           H+0
HETATM   44  H   UNK     0      -4.557   0.141  -0.651  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.573  -1.260  -2.199  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.178   2.143  -1.662  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.648   1.535  -2.496  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.908   2.913  -0.669  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.924   2.386   1.741  0.00  0.00           H+0
HETATM   50  H   UNK     0      -4.127   1.430   0.865  0.00  0.00           H+0
HETATM   51  H   UNK     0      -3.581   4.074   0.025  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.553  -3.576   0.245  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.429  -2.234   0.801  0.00  0.00           H+0
HETATM   54  H   UNK     0      -2.155  -2.186   1.290  0.00  0.00           H+0
HETATM   55  H   UNK     0      -2.317  -2.607  -2.381  0.00  0.00           H+0
HETATM   56  H   UNK     0      -0.412  -2.394  -2.112  0.00  0.00           H+0
HETATM   57  H   UNK     0      -0.617  -0.657  -2.291  0.00  0.00           H+0
HETATM   58  H   UNK     0       1.421  -2.081  -0.846  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    1    3    5   28                                             
CONECT    3    2    4   29   30                                             
CONECT    4    3   31                                                       
CONECT    5    2    6   24   32                                             
CONECT    6    5    7   33   34                                             
CONECT    7    6    8   35   36                                             
CONECT    8    7    9   10   24                                             
CONECT    9    8   37   38   39                                             
CONECT   10    8   11   40   41                                             
CONECT   11   10   12   16   42                                             
CONECT   12   11   13   19   43                                             
CONECT   13   12   14   15   44                                             
CONECT   14   13   45                                                       
CONECT   15   13   16   46   47                                             
CONECT   16   15   17   11   48                                             
CONECT   17   16   18   49   50                                             
CONECT   18   17   51                                                       
CONECT   19   12   20   21   22                                             
CONECT   20   19   52   53   54                                             
CONECT   21   19   55                                                       
CONECT   22   19   23   56   57                                             
CONECT   23   22   24   58                                                  
CONECT   24   23    5    8                                                  
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    6                                                            
CONECT   34    6                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37    9                                                            
CONECT   38    9                                                            
CONECT   39    9                                                            
CONECT   40   10                                                            
CONECT   41   10                                                            
CONECT   42   11                                                            
CONECT   43   12                                                            
CONECT   44   13                                                            
CONECT   45   14                                                            
CONECT   46   15                                                            
CONECT   47   15                                                            
CONECT   48   16                                                            
CONECT   49   17                                                            
CONECT   50   17                                                            
CONECT   51   18                                                            
CONECT   52   20                                                            
CONECT   53   20                                                            
CONECT   54   20                                                            
CONECT   55   21                                                            
CONECT   56   22                                                            
CONECT   57   22                                                            
CONECT   58   23                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  120    0
END

RDKit          3D

58 60  0  0  0  0  0  0  0  0999 V2000
    3.6442   -0.9051   -1.4238 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6598   -0.2805   -0.0457 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9317   -0.7713    0.6629 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8438   -2.1531    0.7231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5013   -0.7003    0.8155 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5896   -0.0260    2.1392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2951    0.7081    2.3053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6744    0.7729    0.9041 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0733    2.0394    0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    0.8058    1.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5514    0.8367   -0.1877 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4460   -0.3546   -0.2924 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5677    0.0979   -1.1910 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7535   -0.7220   -2.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2704    1.5286   -1.5913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4777    2.0132   -0.3695 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4034    2.2609    0.7749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1787    3.3884    0.4176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7973   -1.6253   -0.7218 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4474   -2.4978    0.4817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6801   -2.4285   -1.4873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5338   -1.4551   -1.5076 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6854   -1.2866   -0.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1704   -0.4557    0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5467   -0.5357   -1.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7830   -0.4891   -1.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7341   -1.9855   -1.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353    0.8192   -0.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8307   -0.5048    0.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9984   -0.3868    1.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3143   -2.5334   -0.0706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5906   -1.8144    1.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266    0.7385    2.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7577   -0.7307    2.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6537    0.1165    2.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3979    1.7096    2.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0518    2.4311    0.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    2.8384    0.4518 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0818    1.8988   -0.9099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1100   -0.0707    1.7456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0155    1.6977    1.7449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8061    0.9097   -1.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8942   -0.5258    0.7127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5572    0.1414   -0.6513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5734   -1.2600   -2.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1775    2.1433   -1.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6484    1.5350   -2.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9082    2.9132   -0.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9242    2.3858    1.7410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1265    1.4299    0.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5811    4.0743    0.0253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5531   -3.5756    0.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4289   -2.2343    0.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1553   -2.1859    1.2904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3165   -2.6073   -2.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4120   -2.3941   -2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6167   -0.6566   -2.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4211   -2.0814   -0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 12 19  1  0
 19 20  1  0
 19 21  1  6
 19 22  1  0
 22 23  1  0
 23 24  2  0
 24  5  1  0
 24  8  1  0
 16 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  6
  3 29  1  0
  3 30  1  0
  4 31  1  0
  5 32  1  1
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  9 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  6
 12 43  1  1
 13 44  1  1
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  6
 17 49  1  0
 17 50  1  0
 18 51  1  0
 20 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
17-Hydroxycyclooctatin	MeSH

Chemical Formula

C₂₀H₃₄O₄

Average Mass

338.4880 Da

Monoisotopic Mass

338.24571 Da

IUPAC Name

(1R,3R,4R,6R,7S,8S,10Z,12R)-4-(hydroxymethyl)-12-[(2S)-1-hydroxypropan-2-yl]-1,8-dimethyltricyclo[9.3.0.0^{3,7}]tetradec-10-ene-6,8-diol

Traditional Name

(1R,3R,4R,6R,7S,8S,10Z,12R)-4-(hydroxymethyl)-12-[(2S)-1-hydroxypropan-2-yl]-1,8-dimethyltricyclo[9.3.0.0^{3,7}]tetradec-10-ene-6,8-diol

CAS Registry Number

Not Available

SMILES

C[C@H](CO)[C@H]1CC[C@]2(C)C[C@@H]3[C@H](CO)C[C@@H](O)[C@H]3[C@@](C)(O)C\C=C1/2

InChI Identifier

InChI=1S/C20H34O4/c1-12(10-21)14-4-6-19(2)9-15-13(11-22)8-17(23)18(15)20(3,24)7-5-16(14)19/h5,12-15,17-18,21-24H,4,6-11H2,1-3H3/b16-5-/t12-,13+,14-,15-,17-,18+,19-,20+/m1/s1

InChI Key

ZRHLUTXOIYNCOW-QMDVJOKOSA-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
Streptomyces	NPAtlas	21314175

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Substituents

Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Hydrocarbon derivative
Primary alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

sesquiterpenoid (CHEBI:67808 )

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	1.4	ALOGPS
logP	0.78	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	14.38	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.68 m³·mol⁻¹	ChemAxon
Polarizability	38.46 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA003572

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26343769

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

52937079

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kawamura A, Iacovidou M, Hirokawa E, Soll CE, Trujillo M: 17-Hydroxycyclooctatin, a fused 5-8-5 ring diterpene, from Streptomyces sp. MTE4a. J Nat Prod. 2011 Mar 25;74(3):492-5. doi: 10.1021/np100921m. Epub 2011 Feb 11. [PubMed:21314175 ]

Showing NP-Card for 17-hydroxycyclooctatin (NP0009763)

MOL for NP0009763 (17-hydroxycyclooctatin)

3D MOL for NP0009763 (17-hydroxycyclooctatin)

3D SDF for NP0009763 (17-hydroxycyclooctatin)

3D-SDF for NP0009763 (17-hydroxycyclooctatin)

PDB for NP0009763 (17-hydroxycyclooctatin)

3D PDB for NP0009763 (17-hydroxycyclooctatin)

SMILES for NP0009763 (17-hydroxycyclooctatin)

INCHI for NP0009763 (17-hydroxycyclooctatin)

Structure for NP0009763 (17-hydroxycyclooctatin)

3D Structure for NP0009763 (17-hydroxycyclooctatin)