NP-MRD: Showing NP-Card for [(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate (NP0187318)

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Record Information

Version

2.0

Created at

2022-09-04 03:27:11 UTC

Updated at

2022-09-04 03:27:11 UTC

NP-MRD ID

NP0187318

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate

Description

CHEMBL3814004 belongs to the class of organic compounds known as tigliane and ingenane diterpenoids. These are diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane. [(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate is found in Euphorbia segetalis. Based on a literature review very few articles have been published on CHEMBL3814004.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042205272D          

 28 31  0  0  1  0            999 V2000
    3.8096    5.8935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1702    5.3722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3991    5.6653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020    4.5578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6626    4.0365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7943    3.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5944    2.9669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9458    2.1818    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3226    1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237    1.0416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7141    1.2397    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1689    0.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3684    0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7218    0.2816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3378    1.6185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6589    2.0873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1187    1.8817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4493    2.3639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    2.7316    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3863    3.1067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1861    0.4807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6950   -0.1822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0111    0.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6593    0.7958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6109    1.6194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3484    1.2495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9952    1.7616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0508    0.8169    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 11  9  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 11 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 24 23  1  6  0  0  0
 25 24  1  6  0  0  0
  8 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    5.7329   -1.2329    0.9077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4811   -1.4129    0.1066 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6345   -2.2137    0.5464 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2780   -0.7159   -1.0731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0842   -0.9175   -1.7939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8707   -0.5694   -1.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0221   -1.5782   -0.8250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3269   -1.4054   -0.3859 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2056   -0.4020    0.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059   -0.8182    1.7991 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6005    0.9927    0.5322 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4088    1.9213    1.6162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1972    3.0043    1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5793    4.2059    1.9397 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4633    2.8821   -0.3133 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3323    3.6709   -1.1035 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3289    1.4019   -0.6230 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2351    1.1627   -1.8504 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7240    0.8309   -0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6855    1.6550   -1.0426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0415    0.8167    0.0929 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8474    2.0621    0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7614   -0.3752    0.5700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3035   -1.6788    0.8790 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1908   -2.3981    0.2087 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5495   -2.7565   -0.2290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1367   -4.0796    0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1405   -2.2759   -1.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5223   -0.9085    0.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5924   -0.4741    1.6898 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9906   -2.2112    1.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1124   -0.1693   -2.6396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9836   -1.9119   -2.2156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4054   -2.5425   -1.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9095   -0.9904   -1.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6900    1.7983    2.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2189    4.4788    2.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4888    4.0084    2.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7100    5.0800    1.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5174    3.2392   -0.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1306    3.8153   -1.9669 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1712    1.8148   -2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9341    0.7943    0.6098 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3706    1.9507   -0.3962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9732    0.8007   -1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4136    2.3694   -0.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2263    2.9175    0.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6422    1.8235    1.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3543    0.0038    1.4766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6412   -0.4596   -0.1611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5208   -2.1020    1.9146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6590   -3.1956    0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9506   -4.1964    1.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7141   -4.9271   -0.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2426   -3.9887    0.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8337   -1.2850   -1.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8904   -3.0255   -2.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2559   -2.2835   -1.3971 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25  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
  6 19  1  0
 19 20  1  0
 19 17  1  0
 17 18  1  6
 17 15  1  0
 15 16  1  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
 11 12  1  1
 11  9  1  0
  9 10  2  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 11 21  1  0
 26 24  1  0
  9  8  1  0
 11 17  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
 21 45  1  6
 23 49  1  0
 23 50  1  0
 24 51  1  1
 25 52  1  1
  8 35  1  6
  7 34  1  0
  5 32  1  0
  5 33  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 19 43  1  1
 20 44  1  0
 18 42  1  0
 15 40  1  1
 16 41  1  0
 14 37  1  0
 14 38  1  0
 14 39  1  0
 12 36  1  0
 27 53  1  0
 27 54  1  0
 27 55  1  0
 28 56  1  0
 28 57  1  0
 28 58  1  0
M  END


  Mrv1652309042205272D          

 28 31  0  0  1  0            999 V2000
    3.8096    5.8935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1702    5.3722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3991    5.6653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020    4.5578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6626    4.0365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7943    3.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5944    2.9669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9458    2.1818    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3226    1.6970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237    1.0416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7141    1.2397    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1689    0.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3684    0.7939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7218    0.2816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3378    1.6185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6589    2.0873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1187    1.8817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4493    2.3639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    2.7316    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3863    3.1067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1861    0.4807    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6950   -0.1822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0111    0.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6593    0.7958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6109    1.6194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3484    1.2495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9952    1.7616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0508    0.8169    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 11  9  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  6  0  0  0
 11 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 24 23  1  6  0  0  0
 25 24  1  6  0  0  0
  8 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0187318

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H]2[C@H]([C@@H]3C=C(COC(C)=O)[C@@H](O)[C@]4(O)[C@@H](O)C(C)=C[C@@]14C3=O)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O6/c1-10-8-21-11(2)6-15-16(20(15,4)5)14(19(21)26)7-13(9-28-12(3)23)18(25)22(21,27)17(10)24/h7-8,11,14-18,24-25,27H,6,9H2,1-5H3/t11-,14+,15-,16+,17+,18-,21+,22-/m1/s1

> <INCHI_KEY>
UYVVZRYSWYDKCS-BSKUVLGKSA-N

> <FORMULA>
C22H30O6

> <MOLECULAR_WEIGHT>
390.476

> <EXACT_MASS>
390.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.90745458725869

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,4S,5R,6R,9S,10R,12R,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0^{1,5}.0^{10,12}]pentadeca-2,7-dien-7-yl]methyl acetate

> <JCHEM_LOGP>
0.7337934366666661

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.446577675642182

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.109538817587135

> <JCHEM_PKA_STRONGEST_BASIC>
-3.533330303135969

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
103.17839999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,4S,5R,6R,9S,10R,12R,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0^{1,5}.0^{10,12}]pentadeca-2,7-dien-7-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       7.111  11.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.918  10.028   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.478  10.575   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.164   8.508   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.970   7.535   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.216   6.015   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.710   5.538   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.365   4.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.202   3.168   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.138   1.944   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.066   2.314   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.049   1.072   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.554   1.482   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.347   0.526   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.497   3.021   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.230   3.896   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.955   3.513   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.705   4.413   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.959   5.099   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.588   5.799   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.947   0.897   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.031  -0.340   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.487   0.486   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.697   1.485   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.607   3.023   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.984   2.332   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.191   3.288   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.295   1.525   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17   21                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18   19                                             
CONECT   18   17                                                            
CONECT   19   17    6   20                                                  
CONECT   20   19                                                            
CONECT   21   11   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24    8   26                                                  
CONECT   26   25   24   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₆

Average Mass

390.4760 Da

Monoisotopic Mass

390.20424 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H]2[C@H]([C@@H]3C=C(COC(C)=O)[C@@H](O)[C@]4(O)[C@@H](O)C(C)=C[C@@]14C3=O)C2(C)C

InChI Identifier

InChI=1S/C22H30O6/c1-10-8-21-11(2)6-15-16(20(15,4)5)14(19(21)26)7-13(9-28-12(3)23)18(25)22(21,27)17(10)24/h7-8,11,14-18,24-25,27H,6,9H2,1-5H3/t11-,14+,15-,16+,17+,18-,21+,22-/m1/s1

InChI Key

UYVVZRYSWYDKCS-BSKUVLGKSA-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
Euphorbia segetalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tigliane and ingenane diterpenoids. These are diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Tigliane and ingenane diterpenoids

Alternative Parents

Substituents

Ingenane diterpenoid
Tertiary alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

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

58925870

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

86765207

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate (NP0187318)

MOL for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

3D MOL for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

3D SDF for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

3D-SDF for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

PDB for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

3D PDB for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

SMILES for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

INCHI for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

Structure for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)

3D Structure for NP0187318 ([(1s,4s,5r,6r,9s,10r,12r,14r)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl]methyl acetate)