NP-MRD: Showing NP-Card for (24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside (NP0335061)

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Record Information

Version

2.0

Created at

2024-09-10 23:43:22 UTC

Updated at

2024-09-10 23:43:23 UTC

NP-MRD ID

NP0335061

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside

Description

Based on a literature review very few articles have been published on (24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262302152D          

 42 47  0  0  0  0            999 V2000
    0.2312   -0.9659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3607   -0.7610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7102    0.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7590   -0.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3912   -0.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0278   -0.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0278   -1.1942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3912   -1.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7479   -1.1942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0906   -1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6378   -1.3224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5961   -0.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2074   -0.0702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9331   -0.2570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3007    0.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8411    0.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0641   -0.1566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0906    0.5773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4971    0.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726    0.6636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726    1.4992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4567    2.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2562    1.6289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4442    1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8536    1.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0404    1.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498    2.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6559    1.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8481    1.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6489    0.2319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7451   -1.6079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4693   -1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4832   -0.3544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2144    0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9331   -0.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9331   -1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2144   -1.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2214   -2.4338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6559   -1.6106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6545    0.0676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2173    0.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4943    1.3071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 12  1  0  0  0  0
  2  9  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  9  1  0  0  0  0
  4 17  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
  7 31  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 13 20  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 20  1  0  0  0  0
 16 26  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 29  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 37  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 41  1  0  0  0  0
 35 36  1  0  0  0  0
 35 40  1  0  0  0  0
 36 37  1  0  0  0  0
 36 39  1  0  0  0  0
 37 38  1  0  0  0  0
 41 42  1  0  0  0  0
M  END


  Mrv2104 05262302152D          

 42 47  0  0  0  0            999 V2000
    0.2312   -0.9659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3607   -0.7610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7102    0.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7590   -0.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3912   -0.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0278   -0.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0278   -1.1942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3912   -1.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7479   -1.1942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0906   -1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6378   -1.3224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5961   -0.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2074   -0.0702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9331   -0.2570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3007    0.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8411    0.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0641   -0.1566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0906    0.5773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4971    0.9882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726    0.6636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726    1.4992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4567    2.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2562    1.6289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4442    1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8536    1.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0404    1.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498    2.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6559    1.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8481    1.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6489    0.2319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7451   -1.6079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4693   -1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4832   -0.3544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2144    0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9331   -0.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9331   -1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2144   -1.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2214   -2.4338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6559   -1.6106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6545    0.0676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2173    0.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4943    1.3071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 12  1  0  0  0  0
  2  9  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  9  1  0  0  0  0
  4 17  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
  7 31  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 13 20  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 20  1  0  0  0  0
 16 26  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 29  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 37  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 41  1  0  0  0  0
 35 36  1  0  0  0  0
 35 40  1  0  0  0  0
 36 37  1  0  0  0  0
 36 39  1  0  0  0  0
 37 38  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0335061

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(C)\C=C\C(C)C1CCC2C1(C)CCC1C3(C)CCC(CC33OOC21C=C3)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1/C34H54O8/c1-19(2)20(3)7-8-21(4)23-9-10-25-31(23,5)13-12-26-32(6)14-11-22(17-33(32)15-16-34(25,26)42-41-33)39-30-29(38)28(37)27(36)24(18-35)40-30/h7-8,15-16,19-30,35-38H,9-14,17-18H2,1-6H3/b8-7+

> <INCHI_KEY>
CKJZKFPVVUQBMB-BQYQJAHWNA-N

> <FORMULA>
C34H54O8

> <MOLECULAR_WEIGHT>
590.798

> <EXACT_MASS>
590.381868699

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
96

> <JCHEM_AVERAGE_POLARIZABILITY>
67.9768080083712

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({5-[(3E)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadec-18-en-13-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
4.577103202

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200094961551097

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210573995231531

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835415693235

> <JCHEM_POLAR_SURFACE_AREA>
117.84000000000002

> <JCHEM_REFRACTIVITY>
159.2374

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-({5-[(3E)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadec-18-en-13-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  O   UNK     0       0.432  -1.803   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      -0.673  -1.421   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.326   0.709   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.417  -0.851   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.597  -0.170   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.785  -0.851   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.785  -2.229   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.597  -2.918   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.396  -2.229   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.169  -3.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.191  -2.468   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.113  -0.898   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.254  -0.131   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.608  -0.480   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.295   0.709   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.437   1.751   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.120  -0.292   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.169   1.078   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.928   1.845   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.189   1.239   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.189   2.799   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.319   4.543   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.945   3.041   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.429   2.596   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.327   3.698   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.809   3.256   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.706   4.358   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.558   2.372   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.050   1.936   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.678   0.433   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -5.124  -3.001   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -6.476  -2.222   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -6.502  -0.662   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -7.867   0.095   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -9.208  -0.662   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -9.208  -2.222   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -7.867  -2.983   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -7.880  -4.543   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0     -10.558  -3.006   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0     -10.555   0.126   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -7.872   1.655   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -6.523   2.440   0.000  0.00  0.00           O+0
CONECT    1    2   12                                                       
CONECT    2    1    9                                                       
CONECT    3    4                                                            
CONECT    4    3    5    9   17                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   31                                                  
CONECT    8    7    9                                                       
CONECT    9    2    4    8   10                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12    1   11   13   17                                             
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   20   26                                                  
CONECT   17    4   12   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   13   16   19   21                                             
CONECT   21   20                                                            
CONECT   22   23                                                            
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   16   25   27                                                  
CONECT   27   26                                                            
CONECT   28   29                                                            
CONECT   29   23   28   30                                                  
CONECT   30   29                                                            
CONECT   31    7   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   41                                                  
CONECT   35   34   36   40                                                  
CONECT   36   35   37   39                                                  
CONECT   37   32   36   38                                                  
CONECT   38   37                                                            
CONECT   39   36                                                            
CONECT   40   35                                                            
CONECT   41   34   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₅₄O₈

Average Mass

590.7980 Da

Monoisotopic Mass

590.38187 Da

IUPAC Name

2-({5-[(3E)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadec-18-en-13-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

2-({5-[(3E)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadec-18-en-13-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC(C)C(C)\C=C\C(C)C1CCC2C1(C)CCC1C3(C)CCC(CC33OOC21C=C3)OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1/C34H54O8/c1-19(2)20(3)7-8-21(4)23-9-10-25-31(23,5)13-12-26-32(6)14-11-22(17-33(32)15-16-34(25,26)42-41-33)39-30-29(38)28(37)27(36)24(18-35)40-30/h7-8,15-16,19-30,35-38H,9-14,17-18H2,1-6H3/b8-7+

InChI Key

CKJZKFPVVUQBMB-BQYQJAHWNA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Classification

Not classified

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	4.58	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	117.84 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	159.24 m³·mol⁻¹	ChemAxon
Polarizability	67.98 Å³	ChemAxon
Number of Rings	6	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside (NP0335061)

MOL for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

3D MOL for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

3D SDF for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

3D-SDF for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

PDB for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

3D PDB for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

SMILES for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

INCHI for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

Structure for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)

3D Structure for NP0335061 ((24R)-5b,8b-Epidioxyergosta-6,22E-dien-3b-ol 3-glucoside)