NP-MRD: Showing NP-Card for 4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate (NP0194009)

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Record Information

Version

2.0

Created at

2022-09-04 11:35:16 UTC

Updated at

2022-09-04 11:35:16 UTC

NP-MRD ID

NP0194009

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate

Description

4-[(2,3-Dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]Pentadeca-2,7-dien-12-yl octanoate 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. 4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate is found in Euphorbia esula. 4-[(2,3-Dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]Pentadeca-2,7-dien-12-yl octanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004251516112D          

 42 45  0  0  0  0            999 V2000
    1.2800   -6.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0901   -5.8788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6302   -6.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -6.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -6.9701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7906   -6.8142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3307   -7.4379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1408   -7.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809   -7.9056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4108   -6.5024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2210   -6.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0156   -5.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5661   -4.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1718   -4.1512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4434   -4.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0324   -4.0083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5336   -3.3481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3109   -2.5537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3050   -3.6517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9942   -3.1983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9461   -2.3747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6352   -1.9212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2087   -2.0046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4131   -2.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1606   -1.1810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4233   -0.8108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8498   -0.7275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2784   -4.4867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9914   -4.0718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0492   -4.8928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7188   -4.4107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1851   -5.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5981   -6.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7541   -6.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9844   -6.6593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3317   -7.1640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5134   -7.9688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6376   -7.6099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5931   -5.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7848   -5.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9719   -5.9726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1501   -6.7782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 19 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  0  0  0  0
 11 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 34 39  1  0  0  0  0
 15 39  1  0  0  0  0
 39 40  2  0  0  0  0
 32 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END


  Mrv1533004251516112D          

 42 45  0  0  0  0            999 V2000
    1.2800   -6.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0901   -5.8788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6302   -6.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -6.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -6.9701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7906   -6.8142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3307   -7.4379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1408   -7.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809   -7.9056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4108   -6.5024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2210   -6.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0156   -5.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5661   -4.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1718   -4.1512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4434   -4.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0324   -4.0083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5336   -3.3481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3109   -2.5537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3050   -3.6517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9942   -3.1983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9461   -2.3747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6352   -1.9212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2087   -2.0046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4131   -2.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1606   -1.1810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4233   -0.8108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8498   -0.7275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2784   -4.4867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9914   -4.0718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0492   -4.8928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7188   -4.4107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1851   -5.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5981   -6.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7541   -6.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9844   -6.6593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3317   -7.1640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5134   -7.9688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6376   -7.6099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5931   -5.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7848   -5.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9719   -5.9726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1501   -6.7782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 19 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  0  0  0  0
 11 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 34 39  1  0  0  0  0
 15 39  1  0  0  0  0
 39 40  2  0  0  0  0
 32 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194009

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)OC12CC(C)C34C=C(C)C(OC(=O)C(C)C(C)C)C3(O)C(O)C(CO)=CC(C1C2(C)C)C4=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H52O8/c1-9-10-11-12-13-14-25(36)42-33-17-21(5)32-16-20(4)29(41-30(39)22(6)19(2)3)34(32,40)27(37)23(18-35)15-24(28(32)38)26(33)31(33,7)8/h15-16,19,21-22,24,26-27,29,35,37,40H,9-14,17-18H2,1-8H3

> <INCHI_KEY>
HPALJQSDBYRKNK-UHFFFAOYSA-N

> <FORMULA>
C34H52O8

> <MOLECULAR_WEIGHT>
588.782

> <EXACT_MASS>
588.366218634

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
67.29783812986825

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate

> <ALOGPS_LOGP>
4.48

> <JCHEM_LOGP>
4.9920618706666655

> <ALOGPS_LOGS>
-5.21

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.530549736762438

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.005377826981741

> <JCHEM_PKA_STRONGEST_BASIC>
-2.763744837328404

> <JCHEM_POLAR_SURFACE_AREA>
130.35999999999999

> <JCHEM_REFRACTIVITY>
159.7639

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.65e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.389 -11.265   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.902 -10.974   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.910 -12.138   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.422 -11.847   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.430 -13.011   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.942 -12.720   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.951 -13.884   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.463 -13.593   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.471 -14.757   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      11.967 -12.138   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      13.479 -11.847   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.096 -10.317   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.123  -9.102   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.387  -7.749   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.761  -8.891   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.994  -7.482   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.929  -6.250   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.514  -4.767   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.369  -6.817   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      18.656  -5.970   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      18.566  -4.433   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      19.852  -3.586   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      17.190  -3.742   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      15.705  -4.149   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.100  -2.204   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.723  -1.514   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      18.386  -1.358   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.320  -8.375   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      18.651  -7.601   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      18.759  -9.133   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      20.008  -8.233   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      19.012 -10.685   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      17.916 -11.807   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      16.341 -11.729   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.904 -12.431   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.686 -13.373   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.025 -14.875   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.390 -14.205   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      16.040 -10.280   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      14.532 -10.588   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      20.481 -11.149   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      20.814 -12.653   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   35   36                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   28   39                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   19   15   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   41                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   39                                                  
CONECT   35   34   11   36                                                  
CONECT   36   35   11   37   38                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   34   15   40                                                  
CONECT   40   39                                                            
CONECT   41   32   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

View in JSmol

Synonyms

Value	Source
4-[(2,3-Dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0,.0,]pentadeca-2,7-dien-12-yl octanoic acid	Generator
4-[(2,3-Dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoic acid	Generator

Chemical Formula

C₃₄H₅₂O₈

Average Mass

588.7820 Da

Monoisotopic Mass

588.36622 Da

IUPAC Name

4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate

Traditional Name

4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)OC12CC(C)C34C=C(C)C(OC(=O)C(C)C(C)C)C3(O)C(O)C(CO)=CC(C1C2(C)C)C4=O

InChI Identifier

InChI=1S/C34H52O8/c1-9-10-11-12-13-14-25(36)42-33-17-21(5)32-16-20(4)29(41-30(39)22(6)19(2)3)34(32,40)27(37)23(18-35)15-24(28(32)38)26(33)31(33,7)8/h15-16,19,21-22,24,26-27,29,35,37,40H,9-14,17-18H2,1-8H3

InChI Key

HPALJQSDBYRKNK-UHFFFAOYSA-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 esula	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
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Tertiary alcohol
Carboxylic acid ester
Ketone
Secondary alcohol
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Primary alcohol
Carbonyl group
Hydrocarbon derivative
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	4.48	ALOGPS
logP	4.99	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	11.01	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	159.76 m³·mol⁻¹	ChemAxon
Polarizability	67.3 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74326965

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate (NP0194009)

MOL for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

3D MOL for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

3D SDF for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

3D-SDF for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

PDB for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

3D PDB for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

SMILES for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

INCHI for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

Structure for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)

3D Structure for NP0194009 (4-[(2,3-dimethylbutanoyl)oxy]-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-12-yl octanoate)