NP-MRD: Showing NP-Card for (2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate (NP0329125)

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Record Information

Version

1.0

Created at

2022-09-12 13:13:13 UTC

Updated at

2022-09-12 13:13:14 UTC

NP-MRD ID

NP0329125

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate

Description

(2S)-2-[(1R,2R,3R,6R,8S,9S,12S,14S)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]Tetradecan-3-yl]propyl acetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate is found in Fossombronia alaskana. Based on a literature review very few articles have been published on (2S)-2-[(1R,2R,3R,6R,8S,9S,12S,14S)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]Tetradecan-3-yl]propyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122215132D          

 30 33  0  0  1  0            999 V2000
    4.1722   -4.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2641   -4.0144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0200   -3.6840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6000   -3.5248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6919   -2.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0278   -2.2155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2719   -2.5458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1197   -1.3956    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9255   -1.5727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2948   -1.3899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0452   -0.6035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7160   -0.1232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0044    0.2942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8079    0.6966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5639    1.0270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6558    1.8468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4118    2.1772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5037    2.9970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0759    1.6877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2280    0.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3199    1.3573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9840    0.8678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6480    0.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4040    0.7086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5561   -0.4416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3760   -0.5335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4642   -1.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8001   -0.7719    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1361   -0.2824    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3801   -0.6128    0.0000 C   0  0  1  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  1  6  0  0  0
  8  6  1  1  0  0  0
  8  9  1  6  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  1  0  0  0
 12 14  1  0  0  0  0
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 15 16  1  6  0  0  0
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 15 20  1  0  0  0  0
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 28 27  1  1  0  0  0
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 29 28  1  6  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 12  1  1  0  0  0
  8 30  1  0  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
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    0.8326    1.1938   -2.1957 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7694    1.8266    0.5235 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7740    2.4596   -0.2755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2482   -0.3247   -0.5147 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8925   -0.7036    0.8146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9434   -1.1451   -1.5754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6742   -2.5685   -1.2765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2815   -3.3999   -1.9414 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7440   -3.0543   -0.2542 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2875   -4.1249    0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3044   -3.3016   -0.5970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7354   -2.0725    0.2288 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7685   -0.7655   -0.4755 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0101    0.3481    0.0673 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.1644   -0.3639   -1.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3848    2.0441    1.2637 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669    1.4631   -0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2785    3.1919   -0.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2515    2.8828    0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3879    1.8515   -3.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537    0.1798   -2.6344 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9003    1.5101   -2.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3941    2.9734   -1.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4633    1.8940   -2.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3290    1.2814   -1.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9044    4.1350    1.6081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5167    3.5521    2.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0983    2.6439    2.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1447   -0.8527    1.6177 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4730   -0.8897   -2.5520 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3198   -4.3959    0.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
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 30  8  1  0
 30 12  1  0
 29 20  1  0
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 27 63  1  0
 28 64  1  1
 29 65  1  6
 30 66  1  1
M  END


  Mrv1652309122215132D          

 30 33  0  0  1  0            999 V2000
    4.1722   -4.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2641   -4.0144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0200   -3.6840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6000   -3.5248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6919   -2.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0452   -0.6035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6558    1.8468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4118    2.1772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0759    1.6877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2280    0.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3199    1.3573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9840    0.8678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6480    0.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4040    0.7086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3760   -0.5335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4642   -1.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8001   -0.7719    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1361   -0.2824    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3801   -0.6128    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  8 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0329125

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](COC(C)=O)[C@@]1(O)CC[C@]2(C)C[C@H](OC(C)=O)[C@@]3(C)CC(=O)[C@@]4(C)C[C@H]4[C@@H]3[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C24H36O6/c1-13(12-29-14(2)25)24(28)8-7-21(4)11-18(30-15(3)26)23(6)10-17(27)22(5)9-16(22)19(23)20(21)24/h13,16,18-20,28H,7-12H2,1-6H3/t13-,16-,18-,19+,20+,21+,22-,23+,24-/m0/s1

> <INCHI_KEY>
FWLYMJIZCBOQPY-ZMWYUHEZSA-N

> <FORMULA>
C24H36O6

> <MOLECULAR_WEIGHT>
420.546

> <EXACT_MASS>
420.251188879

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.29567890013312

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-[(1R,2R,3R,6R,8S,9S,12S,14S)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0^{2,6}.0^{12,14}]tetradecan-3-yl]propyl acetate

> <JCHEM_LOGP>
2.2359691453333324

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.645434728278577

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.260352116815813

> <JCHEM_PKA_STRONGEST_BASIC>
-3.122313392185454

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
109.68619999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(1R,2R,3R,6R,8S,9S,12S,14S)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0^{2,6}.0^{12,14}]tetradecan-3-yl]propyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       7.788  -9.024   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.960  -7.493   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.371  -6.877   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.720  -6.580   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.892  -5.049   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.652  -4.136   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.241  -4.752   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.824  -2.605   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.328  -2.936   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.284  -2.594   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.818  -1.127   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.070  -0.230   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.742   0.549   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.241   1.300   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.653   1.917   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.824   3.447   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.235   4.064   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.407   5.594   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.475   3.150   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.892   1.003   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.064   2.534   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.303   1.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.543   0.706   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.954   1.323   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.371  -0.824   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.902  -0.996   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.200  -2.355   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.960  -1.441   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.721  -0.527   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.310  -1.144   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    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   30                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   30                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21   22   29                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   25   29                                                  
CONECT   29   28   20   30                                                  
CONECT   30   29   12    8                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
(2S)-2-[(1R,2R,3R,6R,8S,9S,12S,14S)-8-(Acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0,.0,]tetradecan-3-yl]propyl acetic acid	Generator

Chemical Formula

C₂₄H₃₆O₆

Average Mass

420.5460 Da

Monoisotopic Mass

420.25119 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H](COC(C)=O)[C@@]1(O)CC[C@]2(C)C[C@H](OC(C)=O)[C@@]3(C)CC(=O)[C@@]4(C)C[C@H]4[C@@H]3[C@@H]12

InChI Identifier

InChI=1S/C24H36O6/c1-13(12-29-14(2)25)24(28)8-7-21(4)11-18(30-15(3)26)23(6)10-17(27)22(5)9-16(22)19(23)20(21)24/h13,16,18-20,28H,7-12H2,1-6H3/t13-,16-,18-,19+,20+,21+,22-,23+,24-/m0/s1

InChI Key

FWLYMJIZCBOQPY-ZMWYUHEZSA-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
Fossombronia alaskana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Verrucosane, neoverrucosane, homoverrucosane, or homoneoverrucosane diterpenoid
Diterpenoid
Dicarboxylic acid or derivatives
Tertiary alcohol
Cyclic alcohol
Ketone
Carboxylic acid ester
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

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

163047642

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate (NP0329125)

MOL for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

3D MOL for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

3D SDF for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

3D-SDF for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

PDB for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

3D PDB for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

SMILES for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

INCHI for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

Structure for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)

3D Structure for NP0329125 ((2s)-2-[(1r,2r,3r,6r,8s,9s,12s,14s)-8-(acetyloxy)-3-hydroxy-6,9,12-trimethyl-11-oxotetracyclo[7.5.0.0²,⁶.0¹²,¹⁴]tetradecan-3-yl]propyl acetate)