NP-MRD: Showing NP-Card for (1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate (NP0225347)

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Record Information

Version

2.0

Created at

2022-09-06 04:02:35 UTC

Updated at

2022-09-06 04:02:35 UTC

NP-MRD ID

NP0225347

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate

Description

CHEMBL399080 belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. (1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate is found in Isodon xerophilus. Based on a literature review very few articles have been published on CHEMBL399080.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062206022D          

 31 35  0  0  1  0            999 V2000
    7.9812    0.6995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0976    0.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4364    0.1404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6795   -0.7143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431    0.5023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1349    1.3161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5023    2.0925    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1632    2.9369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2900    3.7815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6447    4.2955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0578    4.0833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3525    2.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9517    1.5171    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2374    1.1121    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9649    1.8472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2098    1.1472    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5253    1.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611    1.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6183    0.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1785   -1.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4874   -0.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    0.2496    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4058   -0.5525    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8994   -1.3083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082   -0.3537    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4953   -1.2038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633   -0.0011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8469    0.7367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6336    1.1480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4627    0.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13  2  1  1  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  6  0  0  0
  6 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 23 20  1  6  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          2D

 63 67  0  0  0  0  0  0  0  0999 V2000
   -5.2841   -0.8638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9138   -0.2537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -1.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4579   -2.4955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7605    4.0753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1700    4.5883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4305    6.0655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4280    3.7714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7395   -1.4772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4095   -0.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7395   -1.4772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895   -2.7762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000   -2.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491    0.9642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0586    0.4512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4976    0.0179    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4409   -2.3556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6910    7.5427    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9077    5.8051    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4616    2.9355    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1047    4.0944    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2500    1.2990    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2435   -0.8389    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8886   -2.4414    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2565    3.4369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    4.0753    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7395    4.0753    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4095    3.1111    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7730    2.3961    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0982    0.6416    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8191   -1.0261    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0722   -1.9746    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0906    0.8235    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4791   -2.9544    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1740   -1.9158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3130   -1.9409    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9134   -1.4419    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8820   -2.2832    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6386   -3.7404    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -3.8971    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3816   -1.2136    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3951   -0.2299    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7396    1.7876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7212   -1.0104    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
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 24 25  1  0
 24 23  1  0
 23 20  1  0
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 20 22  1  0
 20 19  1  0
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 18 17  1  0
 16 17  1  6
 16  6  1  0
  6  7  1  0
  7 12  1  0
 12 13  1  0
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  5  3  1  6
  3  4  2  0
  3  2  1  0
  2  1  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 16 29  1  0
  5  6  1  0
  5 26  1  0
 16 23  1  0
  2 13  1  0
 31 61  1  0
 31 62  1  0
 31 63  1  0
 29 60  1  6
 27 59  1  0
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 25 58  1  0
 23 56  1  6
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 21 51  1  0
 21 52  1  0
 22 53  1  0
 22 54  1  0
 22 55  1  0
 19 48  1  0
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 18 46  1  0
 18 47  1  0
 17 44  1  0
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  6 34  1  6
  7 35  1  1
 12 39  1  0
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 13 41  1  1
 14 42  1  1
 15 43  1  0
  1 32  1  0
  1 33  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
M  END


  Mrv1652309062206022D          

 31 35  0  0  1  0            999 V2000
    7.9812    0.6995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0976    0.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4364    0.1404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6795   -0.7143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431    0.5023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1349    1.3161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5023    2.0925    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1632    2.9369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2900    3.7815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6447    4.2955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0578    4.0833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3525    2.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9517    1.5171    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2374    1.1121    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9649    1.8472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2098    1.1472    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5253    1.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611    1.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6183    0.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1785   -1.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4874   -0.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    0.2496    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4058   -0.5525    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8994   -1.3083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082   -0.3537    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4953   -1.2038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633   -0.0011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8469    0.7367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6336    1.1480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4627    0.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13  2  1  1  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  6  0  0  0
  6 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
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 23 20  1  6  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
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  5 26  1  0  0  0  0
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 26 28  1  0  0  0  0
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 16 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0225347

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1O[C@@]2(O)[C@@H](O)[C@@H]3C(C)(C)CCC[C@]13[C@@H]1[C@H](C[C@@H]3[C@@H](O)[C@]21C(=O)C3=C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O8/c1-10-12-9-13(30-11(2)24)14-21-8-6-7-20(3,4)15(21)18(27)23(28,31-19(21)29-5)22(14,16(10)25)17(12)26/h12-15,17-19,26-28H,1,6-9H2,2-5H3/t12-,13-,14-,15+,17+,18-,19-,21+,22-,23-/m0/s1

> <INCHI_KEY>
CWUBYYIFICODJA-DJZGZRMASA-N

> <FORMULA>
C23H32O8

> <MOLECULAR_WEIGHT>
436.501

> <EXACT_MASS>
436.20971799

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
37.6579802064993

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3S,5S,8R,9R,10S,11R,16S,18R)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-3-yl acetate

> <JCHEM_LOGP>
1.1826824363333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.62317528382351

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.455662391086058

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2237044212199697

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000002

> <JCHEM_REFRACTIVITY>
106.8869

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,5S,8R,9R,10S,11R,16S,18R)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      14.898   1.306   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.249   1.252   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.015   0.262   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.468  -1.333   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.534   0.938   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.585   2.457   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.271   3.906   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.638   5.482   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.875   7.059   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.670   8.018   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.308   7.622   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.858   3.982   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.977   2.832   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.643   2.076   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.134   3.448   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.858   2.141   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.581   3.117   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.154   2.462   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.888   0.911   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.929  -0.266   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.933  -1.963   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.643  -1.308   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.350   0.466   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.224  -1.031   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.279  -2.442   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.909  -0.660   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.258  -2.247   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       8.705  -0.002   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.047   1.375   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.516   2.143   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.064   1.212   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   14   26                                             
CONECT    6    5    7   16                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12    2   14                                                  
CONECT   14   13    5   15                                                  
CONECT   15   14                                                            
CONECT   16    6   17   23   29                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   16   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    5   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   16   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₈

Average Mass

436.5010 Da

Monoisotopic Mass

436.20972 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@H]1O[C@@]2(O)[C@@H](O)[C@@H]3C(C)(C)CCC[C@]13[C@@H]1[C@H](C[C@@H]3[C@@H](O)[C@]21C(=O)C3=C)OC(C)=O

InChI Identifier

InChI=1S/C23H32O8/c1-10-12-9-13(30-11(2)24)14-21-8-6-7-20(3,4)15(21)18(27)23(28,31-19(21)29-5)22(14,16(10)25)17(12)26/h12-15,17-19,26-28H,1,6-9H2,2-5H3/t12-,13-,14-,15+,17+,18-,19-,21+,22-,23-/m0/s1

InChI Key

CWUBYYIFICODJA-DJZGZRMASA-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
Isodon xerophilus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Oxane
Cyclic alcohol
Carboxylic acid ester
Hemiacetal
Ketone
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Alcohol
Organic oxygen compound
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

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

23311636

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44445751

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate (NP0225347)

MOL for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

3D MOL for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

3D SDF for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

3D-SDF for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

PDB for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

3D PDB for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

SMILES for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

INCHI for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

Structure for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)

3D Structure for NP0225347 ((1s,2s,3s,5s,8r,9r,10s,11r,16s,18r)-9,10,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)