NP-MRD: Showing NP-Card for (1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate (NP0219886)

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Record Information

Version

2.0

Created at

2022-09-05 21:01:36 UTC

Updated at

2022-09-05 21:01:36 UTC

NP-MRD ID

NP0219886

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate

Description

(1R,2R,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]Pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoate 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. Based on a literature review very few articles have been published on (1R,2R,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]Pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052223012D          

 31 34  0  0  1  0            999 V2000
   -3.3658   -3.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7636   -2.8293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -3.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7870   -3.8724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3719   -2.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5825   -2.7447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5591   -1.7016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9569   -1.1377    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3930   -1.7399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4105   -1.5527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9743   -2.1550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -0.7633    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1674   -1.4060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862   -0.1611    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2055    0.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9181    1.0710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8528    1.8934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5323    2.3612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6875    0.7730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9342   -0.0142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5105    0.5761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7271   -0.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775    0.2656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555   -1.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4392   -1.5282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -1.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4725   -0.6980    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7172   -0.3483    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5207   -0.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0299    0.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3048   -0.7920    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
 10  9  1  0  0  0  0
 10 11  1  6  0  0  0
 12 10  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 20 19  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 27 26  1  6  0  0  0
 27 20  1  0  0  0  0
 12 27  1  0  0  0  0
 14 28  1  0  0  0  0
 28  8  1  0  0  0  0
 28 29  1  1  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END


  Mrv1652309052223012D          

 31 34  0  0  1  0            999 V2000
   -3.3658   -3.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7636   -2.8293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -3.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7870   -3.8724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3719   -2.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5825   -2.7447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5591   -1.7016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9569   -1.1377    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3930   -1.7399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4105   -1.5527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9743   -2.1550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -0.7633    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1674   -1.4060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862   -0.1611    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2055    0.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9181    1.0710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8528    1.8934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5323    2.3612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6875    0.7730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9342   -0.0142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5105    0.5761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7271   -0.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3775    0.2656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555   -1.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4392   -1.5282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -1.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4725   -0.6980    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7172   -0.3483    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5207   -0.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0299    0.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3048   -0.7920    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
 10  9  1  0  0  0  0
 10 11  1  6  0  0  0
 12 10  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 20 19  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 27 26  1  6  0  0  0
 27 20  1  0  0  0  0
 12 27  1  0  0  0  0
 14 28  1  0  0  0  0
 28  8  1  0  0  0  0
 28 29  1  1  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219886

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@@]12C[C@@H](C)[C@]3(O)[C@H]4C=C(C)C(=O)[C@@]4(O)CC(CO)=C[C@H]3[C@@H]1C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O6/c1-7-13(2)21(28)31-24-10-15(4)25(30)17(19(24)22(24,5)6)9-16(12-26)11-23(29)18(25)8-14(3)20(23)27/h7-9,15,17-19,26,29-30H,10-12H2,1-6H3/b13-7+/t15-,17+,18+,19-,23-,24+,25-/m1/s1

> <INCHI_KEY>
GFAGCYRBGVCTPP-RWXQRNLFSA-N

> <FORMULA>
C25H34O6

> <MOLECULAR_WEIGHT>
430.541

> <EXACT_MASS>
430.235538815

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.41595426788038

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.4654013703333346

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.00713904492109

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.574633341583965

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7316130087890764

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
118.34449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.283  -6.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.159  -5.281   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.685  -5.729   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.336  -7.228   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.561  -4.676   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.087  -5.123   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -2.910  -3.176   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.786  -2.124   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.734  -3.248   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.766  -2.898   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.819  -4.023   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.214  -1.425   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.179  -2.625   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.161  -0.301   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.384   1.223   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.714   1.999   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.592   3.534   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.860   4.408   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.150   1.443   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.610  -0.027   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.686   1.075   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.091  -0.452   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.305   0.496   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.144  -1.991   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.420  -2.853   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.696  -2.517   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.749  -1.303   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.339  -0.650   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.839  -1.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.789   0.212   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.302  -1.478   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   28   29                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   27                                             
CONECT   13   12                                                            
CONECT   14   12   15   28                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20                                                       
CONECT   20   19   21   22   27                                             
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   20   12                                                  
CONECT   28   14    8   29                                                  
CONECT   29   28    8   30   31                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,6R,10S,11R,13S,15R)-1,6-Dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0,.0,]pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₅H₃₄O₆

Average Mass

430.5410 Da

Monoisotopic Mass

430.23554 Da

IUPAC Name

(1R,2R,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoate

Traditional Name

(1R,2R,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0^{2,6}.0^{11,13}]pentadeca-3,8-dien-13-yl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@@]12C[C@@H](C)[C@]3(O)[C@H]4C=C(C)C(=O)[C@@]4(O)CC(CO)=C[C@H]3[C@@H]1C2(C)C

InChI Identifier

InChI=1S/C25H34O6/c1-7-13(2)21(28)31-24-10-15(4)25(30)17(19(24)22(24,5)6)9-16(12-26)11-23(29)18(25)8-14(3)20(23)27/h7-9,15,17-19,26,29-30H,10-12H2,1-6H3/b13-7+/t15-,17+,18+,19-,23-,24+,25-/m1/s1

InChI Key

GFAGCYRBGVCTPP-RWXQRNLFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

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

Tigliane diterpenoid
Fatty acid ester
Fatty acyl
Cyclic alcohol
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Primary alcohol
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	2.47	ChemAxon
pKa (Strongest Acidic)	12.57	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.34 m³·mol⁻¹	ChemAxon
Polarizability	47.42 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

14239458

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate (NP0219886)

MOL for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

PDB for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

Structure for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0219886 ((1r,2r,6r,10s,11r,13s,15r)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxotetracyclo[8.5.0.0²,⁶.0¹¹,¹³]pentadeca-3,8-dien-13-yl (2e)-2-methylbut-2-enoate)