NP-MRD: Showing NP-Card for [(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate (NP0274556)

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Record Information

Version

2.0

Created at

2022-09-08 21:59:24 UTC

Updated at

2022-09-08 21:59:24 UTC

NP-MRD ID

NP0274556

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate

Description

Anisodorin 5 belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton. Based on a literature review very few articles have been published on Anisodorin 5.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082223592D          

 29 31  0  0  1  0            999 V2000
   -0.0296    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6021    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5206    0.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3045   -1.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3045   -0.4377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6048   -0.8749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1236   -0.4876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8233   -0.9247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1524    0.3369    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
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 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
 11 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END

     RDKit          3D

 69 71  0  0  0  0  0  0  0  0999 V2000
    4.2099    4.1122    1.3674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2873    3.7224    0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0290    4.5963   -0.5976 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7139    2.4755    0.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8571    2.1725   -0.8241 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2741    0.8142   -0.8463 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1330    0.5764    0.1204 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5039    0.6577    1.5511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8406    1.7416   -0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2031    1.4362    0.4927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6987    0.1971   -0.2138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1737    0.0154   -0.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7922    1.3214   -0.6531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7089   -0.1786    1.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6168   -1.0645   -1.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4286   -1.7256   -1.6837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4128   -2.1627   -0.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8639   -0.9865    0.1468 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9080   -1.3555    1.6007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4700   -0.7361   -0.3301 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5081   -1.8203   -0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6209   -1.6274   -1.1553 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2551   -0.2961   -0.9289 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0510   -0.0364   -2.0750 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2175   -0.4115    0.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0806   -1.5075   -0.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1060   -1.9217    0.6641 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605   -3.0603    0.2328 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2887   -1.3266    1.7418 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0196    5.1695    1.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2506    4.0947    0.9683 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0981    3.5085    2.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591    2.2709   -1.7785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1031    2.9796   -0.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7412    0.7619   -1.8527 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5858   -0.2798    2.1023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2247    1.2821    2.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4803    1.1993    1.7323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0113    1.9176   -1.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3980    2.6197    0.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8448    2.3000    0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1753    1.3577    1.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4916    0.3902   -1.3118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1666    1.7719   -1.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7679    1.0641   -1.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9866    2.0140    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0097   -1.2639    1.3443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0761    0.1649    2.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6920    0.3675    1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2643   -0.7014   -1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2097   -1.8600   -0.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7967   -2.6953   -2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9684   -1.1804   -2.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6695   -2.7536   -1.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9759   -2.8658    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0194   -2.0329    1.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7926   -0.5275    2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7872   -2.0197    1.8296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5752   -0.6217   -1.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1484   -2.8466   -0.2614 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0326   -1.8203    0.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1213   -1.6387   -2.1348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3674   -2.4309   -1.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4244   -0.8976   -2.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8708    0.4514    0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7425   -0.7537    1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6946   -2.7756   -0.5438 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3191   -3.8487   -0.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4652   -3.4930    1.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6 23  1  0
 23 24  1  6
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
  7  6  1  0
 18 11  1  0
 18 20  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  6
 24 64  1  0
 25 65  1  0
 25 66  1  0
 28 67  1  0
 28 68  1  0
 28 69  1  0
 22 62  1  0
 22 63  1  0
 21 60  1  0
 21 61  1  0
 20 59  1  6
  8 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  6
 13 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 14 49  1  0
 15 50  1  0
 15 51  1  0
 16 52  1  0
 16 53  1  0
 17 54  1  0
 17 55  1  0
 19 56  1  0
 19 57  1  0
 19 58  1  0
M  END


  Mrv1652309082223592D          

 29 31  0  0  1  0            999 V2000
   -0.0296    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6021    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5206    0.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3045   -1.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3045   -0.4377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6048   -0.8749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1236   -0.4876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8233   -0.9247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1524    0.3369    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
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 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
 11 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0274556

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@H]1[C@@](O)(COC(C)=O)CC[C@@H]2[C@]1(C)CC[C@@H]1C(C)(C)CCC[C@@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C24H40O5/c1-16(25)28-14-20-23(6)12-8-18-21(3,4)10-7-11-22(18,5)19(23)9-13-24(20,27)15-29-17(2)26/h18-20,27H,7-15H2,1-6H3/t18-,19+,20-,22-,23+,24+/m1/s1

> <INCHI_KEY>
QJBPQDKOQUZRJS-JQBUYCCYSA-N

> <FORMULA>
C24H40O5

> <MOLECULAR_WEIGHT>
408.579

> <EXACT_MASS>
408.287574388

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
47.35864456354827

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,2R,4aS,4bR,8aR,10aS)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-tetradecahydrophenanthren-2-yl]methyl acetate

> <JCHEM_LOGP>
3.552521618333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.679970715552777

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3761808090172147

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
111.02979999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2R,4aS,4bR,8aR,10aS)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.055   2.461   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.485   2.461   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.255   3.795   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.255   1.127   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.795   1.127   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   1.127   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.457   1.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.172   0.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.645  -2.874   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.435  -2.263   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.435  -0.817   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.129  -1.633   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.231  -0.910   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.537  -1.726   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -0.285   0.629   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                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8    9   20                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   11   19   20                                             
CONECT   19   18                                                            
CONECT   20   18    7   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    6   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₄₀O₅

Average Mass

408.5790 Da

Monoisotopic Mass

408.28757 Da

IUPAC Name

[(1S,2R,4aS,4bR,8aR,10aS)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-tetradecahydrophenanthren-2-yl]methyl acetate

Traditional Name

[(1S,2R,4aS,4bR,8aR,10aS)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@H]1[C@@](O)(COC(C)=O)CC[C@@H]2[C@]1(C)CC[C@@H]1C(C)(C)CCC[C@@]21C

InChI Identifier

InChI=1S/C24H40O5/c1-16(25)28-14-20-23(6)12-8-18-21(3,4)10-7-11-22(18,5)19(23)9-13-24(20,27)15-29-17(2)26/h18-20,27H,7-15H2,1-6H3/t18-,19+,20-,22-,23+,24+/m1/s1

InChI Key

QJBPQDKOQUZRJS-JQBUYCCYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Isocopalane and spongiane diterpenoids

Alternative Parents

Substituents

Isocopalane diterpenoid
13-hydroxysteroid
Hydroxysteroid
Steroid
Phenanthrene
Hydrophenanthrene
Dicarboxylic acid or derivatives
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.55	ChemAxon
pKa (Strongest Acidic)	13.68	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	111.03 m³·mol⁻¹	ChemAxon
Polarizability	47.36 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	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00049357

Chemspider ID

9010608

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10835309

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate (NP0274556)

MOL for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

3D MOL for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

3D SDF for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

3D-SDF for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

PDB for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

3D PDB for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

SMILES for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

INCHI for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

Structure for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)

3D Structure for NP0274556 ([(1s,2r,4as,4br,8ar,10as)-1-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-2-yl]methyl acetate)