NP-MRD: Showing NP-Card for (1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate (NP0151156)

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Record Information

Version

2.0

Created at

2022-09-02 07:25:32 UTC

Updated at

2022-09-02 07:25:32 UTC

NP-MRD ID

NP0151156

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate

Description

Casearin O belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. (1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate is found in Casearia sylvestris. (1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate was first documented in 2019 (PMID: 31175947). Based on a literature review a small amount of articles have been published on Casearin O.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022209252D          

 41 43  0  0  1  0            999 V2000
   -7.1004   -4.5046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4008   -4.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4296   -3.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1580   -2.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7299   -2.8057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7587   -1.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0591   -1.5440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7500   -2.3090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6111   -0.9309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4181   -1.1025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3562   -0.1463    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9082    0.4668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7152    0.2952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2672    0.9083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0742    0.7368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6262    1.3499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3862    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0808    1.6339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
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 29 28  1  1  0  0  0
  7 29  1  0  0  0  0
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 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309022209252D          

 41 43  0  0  1  0            999 V2000
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   -6.4008   -4.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4296   -3.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1580   -2.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7299   -2.8057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7587   -1.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0591   -1.5440    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7500   -2.3090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6111   -0.9309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4181   -1.1025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3562   -0.1463    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9082    0.4668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7152    0.2952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2672    0.9083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0742    0.7368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6262    1.3499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7822    0.0374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2942    0.8098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8463    1.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6533    1.2514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5913    2.2075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9972   -0.5879    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1902   -0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6382   -1.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8931   -1.8141    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3411   -2.4272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5960   -3.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7001   -1.9856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2521   -1.3725    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1039    0.4041    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3895    0.8166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6750    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9605    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2461    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4684    0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8576    0.7397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4097    0.1266    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2301    0.2128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5657    0.9665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3862    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0808    1.6339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 29 28  1  1  0  0  0
  7 29  1  0  0  0  0
 22 29  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 30 36  1  0  0  0  0
 36 37  1  0  0  0  0
 22 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0151156

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCO[C@@H]1O[C@@H](OC(C)=O)[C@@]23[C@@H](OC(C)=O)[C@H](OCCCC)[C@@H](C)[C@@](C)(C\C=C(/C)C=C)[C@@H]2C[C@@H](OC)C=C13

> <INCHI_IDENTIFIER>
InChI=1S/C33H52O8/c1-10-13-17-37-28-22(5)32(8,16-15-21(4)12-3)27-20-25(36-9)19-26-30(38-18-14-11-2)41-31(40-24(7)35)33(26,27)29(28)39-23(6)34/h12,15,19,22,25,27-31H,3,10-11,13-14,16-18,20H2,1-2,4-9H3/b21-15+/t22-,25+,27+,28-,29+,30-,31-,32-,33-/m1/s1

> <INCHI_KEY>
LANRPOQDTFNEEN-GSRCGCQASA-N

> <FORMULA>
C33H52O8

> <MOLECULAR_WEIGHT>
576.771

> <EXACT_MASS>
576.366218634

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
66.35868353209298

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,5R,6aS,7S,8S,9R,10R,10aS)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dien-1-yl]-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[1,8a-c]furan-1-yl acetate

> <ALOGPS_LOGP>
5.53

> <JCHEM_LOGP>
5.950729672

> <ALOGPS_LOGS>
-6.20

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6721339391564256

> <JCHEM_POLAR_SURFACE_AREA>
89.52000000000001

> <JCHEM_REFRACTIVITY>
158.1141

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.64e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,5R,6aS,7S,8S,9R,10R,10aS)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dien-1-yl]-1H,3H,5H,6H,6aH,8H,9H,10H-naphtho[1,8a-c]furan-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0     -13.254  -8.409   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.948  -7.592   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.002  -6.053   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -13.362  -5.330   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.696  -5.237   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -10.750  -3.698   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.444  -2.882   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.867  -4.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.474  -1.738   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.980  -2.058   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.998  -0.273   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0     -11.029   0.871   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0     -12.535   0.551   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -13.565   1.696   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -15.072   1.375   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -16.102   2.520   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.927   0.070   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -8.016   1.512   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -9.046   2.656   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -10.553   2.336   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -8.571   4.121   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -7.461  -1.097   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.955  -0.777   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.925  -1.922   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.400  -3.386   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.370  -4.531   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -4.846  -5.995   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.907  -3.706   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.937  -2.562   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.794   0.754   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -4.460   1.524   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -3.127   0.754   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.793   1.524   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.459   0.754   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.874   1.524   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -7.201   1.381   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -8.231   0.236   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -9.763   0.397   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -10.389   1.804   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -11.921   1.965   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -9.484   3.050   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   29                                             
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   11   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23   29   37                                             
CONECT   23   22   24   30                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29                                                       
CONECT   29   28    7   22                                                  
CONECT   30   23   31   36                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   30   37                                                       
CONECT   37   36   22   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₅₂O₈

Average Mass

576.7710 Da

Monoisotopic Mass

576.36622 Da

IUPAC Name

(1S,3R,5R,6aS,7S,8S,9R,10R,10aS)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dien-1-yl]-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[1,8a-c]furan-1-yl acetate

Traditional Name

(1S,3R,5R,6aS,7S,8S,9R,10R,10aS)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2E)-3-methylpenta-2,4-dien-1-yl]-1H,3H,5H,6H,6aH,8H,9H,10H-naphtho[1,8a-c]furan-1-yl acetate

CAS Registry Number

Not Available

SMILES

CCCCO[C@@H]1O[C@@H](OC(C)=O)[C@@]23[C@@H](OC(C)=O)[C@H](OCCCC)[C@@H](C)[C@@](C)(C\C=C(/C)C=C)[C@@H]2C[C@@H](OC)C=C13

InChI Identifier

InChI=1S/C33H52O8/c1-10-13-17-37-28-22(5)32(8,16-15-21(4)12-3)27-20-25(36-9)19-26-30(38-18-14-11-2)41-31(40-24(7)35)33(26,27)29(28)39-23(6)34/h12,15,19,22,25,27-31H,3,10-11,13-14,16-18,20H2,1-2,4-9H3/b21-15+/t22-,25+,27+,28-,29+,30-,31-,32-,33-/m1/s1

InChI Key

LANRPOQDTFNEEN-GSRCGCQASA-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
Casearia sylvestris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Naphthofuran
Dicarboxylic acid or derivatives
Tetrahydrofuran
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.53	ALOGPS
logP	5.95	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	89.52 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	158.11 m³·mol⁻¹	ChemAxon
Polarizability	66.36 Å³	ChemAxon
Number of Rings	3	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

101602074

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Oda FB, Crevelin EJ, Crotti AEM, Orlando AB, de Medeiros AI, Nogueira FAR, Dos Santos AG: Acidic and hepatic derivatives of bioactive clerodane diterpenes casearins J and O. Fitoterapia. 2019 Sep;137:104197. doi: 10.1016/j.fitote.2019.104197. Epub 2019 Jun 5. [PubMed:31175947 ]
LOTUS database [Link]

Showing NP-Card for (1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate (NP0151156)

MOL for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

3D MOL for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

3D SDF for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

3D-SDF for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

PDB for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

3D PDB for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

SMILES for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

INCHI for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

Structure for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)

3D Structure for NP0151156 ((1s,3r,5r,6as,7s,8s,9r,10r,10as)-10-(acetyloxy)-3,9-dibutoxy-5-methoxy-7,8-dimethyl-7-[(2e)-3-methylpenta-2,4-dien-1-yl]-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-1-yl acetate)