NP-MRD: Showing NP-Card for (1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate (NP0257013)

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Record Information

Version

2.0

Created at

2022-09-07 22:01:12 UTC

Updated at

2022-09-07 22:01:12 UTC

NP-MRD ID

NP0257013

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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

ISOLUSHININ D 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,8s,9s,11r,16s,18r)-18-hydroxy-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 rubescens. Based on a literature review very few articles have been published on ISOLUSHININ D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082200012D          

 29 33  0  0  1  0            999 V2000
    8.0455    0.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1606    0.7090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5098    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5726   -0.7429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7125    0.5225    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3718   -0.3283    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4614   -0.5384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9937    0.2493    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2149   -0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3820   -0.4227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1174   -1.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6733    0.5475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8368    1.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087    1.6961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2614    1.1436    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9121    0.7386    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6471    1.1407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4960    0.6802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7130    0.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1851    1.3189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5685    2.0914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2438    2.9527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3604    3.7989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7089    4.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1245    4.1100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4063    2.1789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9876    1.5520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2731    1.1479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0525    1.8913    0.0000 O   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
  6 19  1  1  0  0  0
 15 20  1  0  0  0  0
 20  5  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27  2  1  1  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END

     RDKit          2D

 61 65  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
    0.7500   -1.2990    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
    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
    3.7500    1.2990    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
    1.5000    2.5981    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
    0.3828    0.5621    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
   -0.2954   -0.6125    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
   -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
   -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
   -2.7395   -1.4772    0.0000 O   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
   -1.5000   -2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895   -2.7762    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
    1.9134   -1.4419    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
    5.0906    0.8235    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
    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
    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
    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
    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
    2.3816   -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
   -0.0000    2.5981    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
   -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
   -1.9533    6.3260    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -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
 18 17  1  0
 17 16  1  0
 16 19  1  0
 19  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 15 14  1  1
 15 20  1  0
 20 21  1  0
 21 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28  5  1  0
  5  3  1  6
  3  4  2  0
  3  2  1  0
  2  1  2  3
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 15 16  1  0
  5 20  1  0
  5  6  1  0
 15  8  1  0
  2 27  1  0
 18 49  1  0
 18 50  1  0
 18 51  1  0
 16 48  1  6
  6 32  1  6
  7 33  1  0
  7 34  1  0
  8 35  1  6
 10 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 20 52  1  6
 21 53  1  1
 26 57  1  0
 26 58  1  0
 27 59  1  1
 28 60  1  1
 29 61  1  0
  1 30  1  0
  1 31  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
M  END


  Mrv1652309082200012D          

 29 33  0  0  1  0            999 V2000
    8.0455    0.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1606    0.7090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5098    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5726   -0.7429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7125    0.5225    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3718   -0.3283    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4614   -0.5384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9937    0.2493    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2149   -0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3820   -0.4227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1174   -1.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6733    0.5475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8368    1.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087    1.6961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2614    1.1436    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9121    0.7386    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6471    1.1407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4960    0.6802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7130    0.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1851    1.3189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5685    2.0914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2438    2.9527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3604    3.7989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7089    4.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1245    4.1100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4063    2.1789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9876    1.5520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2731    1.1479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0525    1.8913    0.0000 O   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
  6 19  1  1  0  0  0
 15 20  1  0  0  0  0
 20  5  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27  2  1  1  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0257013

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1O[C@H]2C[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/C23H32O6/c1-11-13-9-14(28-12(2)24)17-22-8-6-7-21(3,4)15(22)10-16(29-20(22)27-5)23(17,18(11)25)19(13)26/h13-17,19-20,26H,1,6-10H2,2-5H3/t13-,14-,15+,16-,17-,19+,20-,22-,23+/m0/s1

> <INCHI_KEY>
GZJPAFQOCRUACX-TVUWESQNSA-N

> <FORMULA>
C23H32O6

> <MOLECULAR_WEIGHT>
404.503

> <EXACT_MASS>
404.21988875

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
38.57275391908601

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3S,5S,8S,9S,11R,16S,18R)-18-hydroxy-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>
2.369316355000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.118836129392669

> <JCHEM_PKA_STRONGEST_BASIC>
-3.184221077003645

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
104.13510000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,5S,8S,9S,11R,16S,18R)-18-hydroxy-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                                 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      15.018   1.232   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.366   1.324   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.152   0.300   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.269  -1.387   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.663   0.975   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.027  -0.613   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.328  -1.005   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.455   0.465   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.001  -0.179   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.446  -0.789   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.819  -1.900   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.990   1.022   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.295   2.557   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.736   3.166   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.955   2.135   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.169   1.379   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.541   2.129   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.126   1.270   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.798   0.044   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.679   2.462   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.394   3.904   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.788   5.512   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.006   7.091   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.790   8.036   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.432   7.672   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.958   4.067   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.043   2.897   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.710   2.143   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.298   3.530   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   20   28                                             
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    8   16   20                                             
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16    6                                                       
CONECT   20   15    5   21                                                  
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   27                                                       
CONECT   27   26    2   28                                                  
CONECT   28   27    5   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₆

Average Mass

404.5030 Da

Monoisotopic Mass

404.21989 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@H]1O[C@H]2C[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/C23H32O6/c1-11-13-9-14(28-12(2)24)17-22-8-6-7-21(3,4)15(22)10-16(29-20(22)27-5)23(17,18(11)25)19(13)26/h13-17,19-20,26H,1,6-10H2,2-5H3/t13-,14-,15+,16-,17-,19+,20-,22-,23+/m0/s1

InChI Key

GZJPAFQOCRUACX-TVUWESQNSA-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 rubescens	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
Ketone
Secondary alcohol
Acetal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

25032704

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46906438

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,8s,9s,11r,16s,18r)-18-hydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate (NP0257013)

MOL for NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-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 NP0257013 ((1s,2s,3s,5s,8s,9s,11r,16s,18r)-18-hydroxy-16-methoxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-3-yl acetate)