NP-MRD: Showing NP-Card for (1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate (NP0280837)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 06:50:42 UTC

Updated at

2022-09-09 06:50:42 UTC

NP-MRD ID

NP0280837

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate

Description

(1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]Octadec-9-en-8-yl acetate belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. (1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate is found in Dysidea arenaria. Based on a literature review very few articles have been published on (1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]Octadec-9-en-8-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092208502D          

 35 39  0  0  1  0            999 V2000
    4.9852    1.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1730    1.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8927    2.6190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6412    1.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1264   -2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2545   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7609   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5781   -2.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0845   -3.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9017   -2.9945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7736   -3.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6334   -1.5975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185   -2.3768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2336   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1094    0.5816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 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
 17 19  1  0  0  0  0
 11 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  1  0  0  0
  7 25  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
  5 34  1  0  0  0  0
 26 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END

     RDKit          3D

 81 85  0  0  0  0  0  0  0  0999 V2000
   -5.3147   -4.1648   -1.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0419   -2.7749   -1.6253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6717   -2.2973   -2.6000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1206   -1.9704   -0.9857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9034   -0.6702   -1.4155 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4870   -0.4349   -1.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5978    0.2062   -1.0942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2337    0.4044   -1.5671 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1578   -0.4155   -2.7621 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6887   -0.4484   -2.6346 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0112    0.2361   -1.3240 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3341   -0.0677   -0.8040 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7160   -1.5198   -0.6732 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7129    0.6042    0.4916 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2350    0.4258    0.6467 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6408    1.1088    1.9565 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1215    0.9790    2.1851 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5859   -0.4442    2.2738 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9221    1.7367    1.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7835   -0.0614   -0.5403 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5312   -1.5313   -0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5605    0.6944    0.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8549    0.9376    1.0925 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4526    2.1326    0.4411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051    0.7728    0.2531 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2879    0.4499    0.7345 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2627   -0.8657    1.5062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3533   -0.6845    2.5611 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7042    1.5123    1.7123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8454    2.3630    1.2543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0108    1.6005    0.7164 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9779    1.3298    1.7015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6572    0.3092    0.0601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2268    0.4057   -0.4219 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1067    1.6312   -1.1008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2520   -4.5333   -1.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3198   -4.1835   -0.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4210   -4.7702   -1.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5824   -0.4736   -2.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2100   -0.8187   -2.8144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0908    1.4857   -1.7755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2765   -1.4274   -2.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1525    0.1396   -3.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9628   -1.4930   -2.7031 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1062    0.1488   -3.4724 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9449    1.3419   -1.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0765    0.3628   -1.5502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6106   -1.8891    0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2817   -2.1913   -1.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8305   -1.5790   -0.8559 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3092    0.1247    1.3944 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5485    1.6735    0.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5041   -0.6397    0.8000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7763    0.8908   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0421    0.7473    2.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4272    2.1904    1.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3213    1.4420    3.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0259   -0.9331    3.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6513   -0.4407    2.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5038   -0.9842    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9809    1.7663    1.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9650    1.2252    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6011    2.7813    1.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8635   -2.1754   -1.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5849   -1.6475   -0.2499 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9055   -1.8668    0.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9707    0.0378    1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0928    1.6623    0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9863    1.1433    2.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8319   -1.6969    0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2405   -1.0978    1.9581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -0.7382    3.4443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9957    1.0938    2.7144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8558    2.2100    1.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5181    3.2045    0.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2182    2.9090    2.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5335    2.2539   -0.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6912    2.0259    1.7097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2909    0.1508   -0.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7761   -0.5819    0.7024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6700    1.6606   -1.9114 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 34  1  0
 34 35  1  6
 34 33  1  0
 33 31  1  0
 31 32  1  0
 31 30  1  0
 30 29  1  0
 29 26  1  0
 26 27  1  1
 27 28  1  0
 26 25  1  0
 25 24  1  6
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  1  1
 20 11  1  0
 20  8  1  0
 25  7  1  0
 23 25  1  0
 26 34  1  0
 18 58  1  0
 18 59  1  0
 18 60  1  0
 17 57  1  0
 19 61  1  0
 19 62  1  0
 19 63  1  0
 16 55  1  0
 16 56  1  0
 15 53  1  0
 15 54  1  0
 14 51  1  0
 14 52  1  0
 12 47  1  6
 13 48  1  0
 13 49  1  0
 13 50  1  0
 11 46  1  6
 10 44  1  0
 10 45  1  0
  9 42  1  0
  9 43  1  0
  8 41  1  6
  6 40  1  0
  5 39  1  6
  1 36  1  0
  1 37  1  0
  1 38  1  0
 35 81  1  0
 33 79  1  0
 33 80  1  0
 31 77  1  6
 32 78  1  0
 30 75  1  0
 30 76  1  0
 29 73  1  0
 29 74  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 23 69  1  1
 22 67  1  0
 22 68  1  0
 21 64  1  0
 21 65  1  0
 21 66  1  0
M  END


  Mrv1652309092208502D          

 35 39  0  0  1  0            999 V2000
    4.9852    1.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1730    1.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8927    2.6190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6412    1.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1264   -2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2545   -1.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7609   -2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5781   -2.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0845   -3.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9017   -2.9945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7736   -3.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6334   -1.5975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4185   -2.3768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1382   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3261   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0458   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2336   -0.5346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1094    0.5816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 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
 17 19  1  0  0  0  0
 11 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  1  0  0  0
  7 25  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
  5 34  1  0  0  0  0
 26 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0280837

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](OC(C)=O)[C@@]4(O)C[C@@H](O)CC[C@]4(CO)[C@]33O[C@@H]3C[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O6/c1-17(2)7-6-8-18(3)21-9-10-22-23-13-24(34-19(4)31)28(33)14-20(32)11-12-27(28,16-30)29(23)25(35-29)15-26(21,22)5/h13,17-18,20-22,24-25,30,32-33H,6-12,14-16H2,1-5H3/t18-,20+,21-,22+,24-,25-,26-,27-,28+,29+/m1/s1

> <INCHI_KEY>
HDUDIWVTPSZRBL-PLIUQPHZSA-N

> <FORMULA>
C29H46O6

> <MOLECULAR_WEIGHT>
490.681

> <EXACT_MASS>
490.329439201

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
56.637981424138054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0^{1,17}.0^{2,7}.0^{11,15}]octadec-9-en-8-yl acetate

> <JCHEM_LOGP>
3.205561026666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.823345445215608

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.105569043754127

> <JCHEM_PKA_STRONGEST_BASIC>
-2.728569924406264

> <JCHEM_POLAR_SURFACE_AREA>
99.52000000000001

> <JCHEM_REFRACTIVITY>
133.4602

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0^{1,17}.0^{2,7}.0^{11,15}]octadec-9-en-8-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       9.306   3.169   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.790   3.440   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.266   4.889   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.797   2.263   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.320   0.815   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.836   0.544   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.359  -0.905   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.875  -1.176   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.091  -0.231   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.366  -1.095   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.938  -2.574   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.883  -3.790   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.303  -5.217   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.408  -3.579   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.354  -4.795   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.879  -4.585   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.824  -5.800   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.350  -5.590   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.244  -7.227   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.399  -2.624   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.070  -4.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.406  -3.802   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.890  -3.531   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.782  -2.982   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.367  -2.082   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.851  -1.811   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.374  -3.259   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.381  -4.437   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.858  -2.988   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.342  -2.717   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.819  -1.269   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.303  -0.998   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.811  -0.092   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.327  -0.363   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.804   1.086   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   25                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   20                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   11    8   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23   25                                                       
CONECT   25   24    7   23   26                                             
CONECT   26   25   27   29   34                                             
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33    5   26   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-Dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0,.0,.0,]octadec-9-en-8-yl acetic acid	Generator

Chemical Formula

C₂₉H₄₆O₆

Average Mass

490.6810 Da

Monoisotopic Mass

490.32944 Da

IUPAC Name

(1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0^{1,17}.0^{2,7}.0^{11,15}]octadec-9-en-8-yl acetate

Traditional Name

(1R,2R,5S,7R,8R,11R,14R,15R,17R)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2R)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0^{1,17}.0^{2,7}.0^{11,15}]octadec-9-en-8-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](OC(C)=O)[C@@]4(O)C[C@@H](O)CC[C@]4(CO)[C@]33O[C@@H]3C[C@]12C

InChI Identifier

InChI=1S/C29H46O6/c1-17(2)7-6-8-18(3)21-9-10-22-23-13-24(34-19(4)31)28(33)14-20(32)11-12-27(28,16-30)29(23)25(35-29)15-26(21,22)5/h13,17-18,20-22,24-25,30,32-33H,6-12,14-16H2,1-5H3/t18-,20+,21-,22+,24-,25-,26-,27-,28+,29+/m1/s1

InChI Key

HDUDIWVTPSZRBL-PLIUQPHZSA-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
Dysidea arenaria	LOTUS Database	35616633

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
Steroid ester
Oxepane
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxygen compound
Alcohol
Organooxygen compound
Organic oxide
Primary alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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
logP	3.21	ChemAxon
pKa (Strongest Acidic)	13.11	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.52 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	133.46 m³·mol⁻¹	ChemAxon
Polarizability	56.64 Å³	ChemAxon
Number of Rings	5	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

10368084

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23253173

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate (NP0280837)

MOL for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

3D MOL for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

3D SDF for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

3D-SDF for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

PDB for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

3D PDB for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

SMILES for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

INCHI for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

Structure for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)

3D Structure for NP0280837 ((1r,2r,5s,7r,8r,11r,14r,15r,17r)-5,7-dihydroxy-2-(hydroxymethyl)-15-methyl-14-[(2r)-6-methylheptan-2-yl]-18-oxapentacyclo[8.8.0.0¹,¹⁷.0²,⁷.0¹¹,¹⁵]octadec-9-en-8-yl acetate)