NP-MRD: Showing NP-Card for (1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate (NP0315374)

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Record Information

Version

2.0

Created at

2022-09-11 13:58:33 UTC

Updated at

2022-09-11 13:58:34 UTC

NP-MRD ID

NP0315374

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate

Description

Scupolin E belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. Based on a literature review very few articles have been published on Scupolin E.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309112215582D          

 37 40  0  0  1  0            999 V2000
    1.7884   -4.4031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2329   -3.7931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4834   -3.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9279   -2.3971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2894   -2.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8449   -3.4409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399   -2.0449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9844   -1.4350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1784   -1.6110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5137   -2.0997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6230   -1.0011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1077   -0.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1187   -1.6540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8735   -0.2150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0558   -0.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    0.6093    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1094    0.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5878    0.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3544    0.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8811    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7044    0.2740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4400   -0.4761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6407   -0.2719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5372    1.0504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5037    1.8747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7731    2.2579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2009    2.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6794   -0.0390    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9299    0.7471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7359    0.9232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2914    0.3132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0409   -0.4728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8270   -0.7233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2170   -1.2788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2349   -0.6489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7904   -1.2589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5460   -1.5902    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  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
 11 13  1  6  0  0  0
 11 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 16 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 34  1  1  0  0  0
 32 35  1  0  0  0  0
  8 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
M  END


  Mrv1652309112215582D          

 37 40  0  0  1  0            999 V2000
    1.7884   -4.4031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2329   -3.7931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4834   -3.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9279   -2.3971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2894   -2.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8449   -3.4409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399   -2.0449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9844   -1.4350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1784   -1.6110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5137   -2.0997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6230   -1.0011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1077   -0.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1187   -1.6540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8735   -0.2150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0558   -0.1048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    0.6093    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1094    0.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5878    0.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3544    0.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8811    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7044    0.2740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4400   -0.4761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6407   -0.2719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5372    1.0504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5037    1.8747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7731    2.2579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2009    2.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6794   -0.0390    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9299    0.7471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7359    0.9232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2914    0.3132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0409   -0.4728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8270   -0.7233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2170   -1.2788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2349   -0.6489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7904   -1.2589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5460   -1.5902    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  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
 11 13  1  6  0  0  0
 11 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 16 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 34  1  1  0  0  0
 32 35  1  0  0  0  0
  8 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315374

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)O[C@H]1[C@H](O)[C@](C)(O)[C@](C)([C@H](CC2=CC(=O)OC2)OC(C)=O)[C@H]2CCC[C@]3(CO3)[C@]12CO

> <INCHI_IDENTIFIER>
InChI=1S/C27H40O10/c1-6-15(2)23(32)37-22-21(31)25(5,33)24(4,18-8-7-9-26(14-35-26)27(18,22)13-28)19(36-16(3)29)10-17-11-20(30)34-12-17/h11,15,18-19,21-22,28,31,33H,6-10,12-14H2,1-5H3/t15?,18-,19+,21+,22+,24+,25+,26+,27+/m1/s1

> <INCHI_KEY>
MRDDGKKTFVCTJI-LVYFPGLHSA-N

> <FORMULA>
C27H40O10

> <MOLECULAR_WEIGHT>
524.607

> <EXACT_MASS>
524.262147488

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
53.96991501984206

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4aR,5S,6R,7S,8R,8aR)-5-[(1S)-1-(acetyloxy)-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8-yl 2-methylbutanoate

> <JCHEM_LOGP>
1.1494103456666651

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.877054066868332

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.1052220590020445

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8325562129503323

> <JCHEM_POLAR_SURFACE_AREA>
152.12

> <JCHEM_REFRACTIVITY>
129.63459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4aR,5S,6R,7S,8R,8aR)-5-[(1S)-1-(acetyloxy)-2-(5-oxo-2H-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxirane]-8-yl 2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       3.338  -8.219   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.301  -7.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.769  -5.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.732  -4.475   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.274  -5.285   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.310  -6.423   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       4.741  -3.817   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.704  -2.679   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.200  -3.007   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.959  -3.920   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.163  -1.869   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.201  -1.153   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.222  -3.088   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.630  -0.401   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.104  -0.196   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.568   1.137   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.204   1.853   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.097   1.029   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.528   1.598   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.511   0.413   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -5.048   0.511   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -2.688  -0.889   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.196  -0.508   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.869   1.961   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.807   3.500   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.443   4.215   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.108   4.323   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.135  -0.073   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.603   1.395   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.107   1.723   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.144   0.585   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.676  -0.883   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.144  -1.350   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.005  -2.387   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.172  -1.211   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.209  -2.350   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       6.619  -2.968   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   35                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   16   28                                             
CONECT   15   14                                                            
CONECT   16   14   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   18                                                       
CONECT   24   16   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   14   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   35                                             
CONECT   33   32   34                                                       
CONECT   34   33   32                                                       
CONECT   35   32    8   28   36                                             
CONECT   36   35   37                                                       
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₀O₁₀

Average Mass

524.6070 Da

Monoisotopic Mass

524.26215 Da

IUPAC Name

(1R,4aR,5S,6R,7S,8R,8aR)-5-[(1S)-1-(acetyloxy)-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8-yl 2-methylbutanoate

Traditional Name

(1R,4aR,5S,6R,7S,8R,8aR)-5-[(1S)-1-(acetyloxy)-2-(5-oxo-2H-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxirane]-8-yl 2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)O[C@H]1[C@H](O)[C@](C)(O)[C@](C)([C@H](CC2=CC(=O)OC2)OC(C)=O)[C@H]2CCC[C@]3(CO3)[C@]12CO

InChI Identifier

InChI=1S/C27H40O10/c1-6-15(2)23(32)37-22-21(31)25(5,33)24(4,18-8-7-9-26(14-35-26)27(18,22)13-28)19(36-16(3)29)10-17-11-20(30)34-12-17/h11,15,18-19,21-22,28,31,33H,6-10,12-14H2,1-5H3/t15?,18-,19+,21+,22+,24+,25+,26+,27+/m1/s1

InChI Key

MRDDGKKTFVCTJI-LVYFPGLHSA-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 tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid ester
Cyclitol or derivatives
2-furanone
Fatty acyl
Cyclic alcohol
Dihydrofuran
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Carboxylic acid ester
Ether
Oxirane
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
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	1.15	ChemAxon
pKa (Strongest Acidic)	7.11	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	152.12 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	129.63 m³·mol⁻¹	ChemAxon
Polarizability	53.97 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	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

8896193

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10720855

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate (NP0315374)

MOL for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

3D MOL for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

3D SDF for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

3D-SDF for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

PDB for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

3D PDB for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

SMILES for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

INCHI for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

Structure for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)

3D Structure for NP0315374 ((1r,4ar,5s,6r,7s,8r,8ar)-5-[(1s)-1-(acetyloxy)-2-(5-oxo-2h-furan-3-yl)ethyl]-6,7-dihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-hexahydrospiro[naphthalene-1,2'-oxiran]-8-yl 2-methylbutanoate)