NP-MRD: Showing NP-Card for Musellarin B (NP0138668)

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Record Information

Version

2.0

Created at

2022-06-29 17:40:09 UTC

Updated at

2022-06-29 17:40:09 UTC

NP-MRD ID

NP0138668

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Musellarin B

Description

Based on a literature review very few articles have been published on Musellarin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292219402D          

 26 29  0  0  1  0            999 V2000
    7.3145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    0.4125    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  9  7  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
  9 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 12 22  1  0  0  0  0
 17 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 25  1  0  0  0  0
  4 26  1  0  0  0  0
M  END

     RDKit          3D

 48 51  0  0  0  0  0  0  0  0999 V2000
    5.2099    0.3597    1.8190 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4563   -0.5273    0.7550 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4334   -0.7895   -0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2005   -0.1874   -0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1273   -0.3774   -0.8392 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8024    0.2316   -0.7195 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7607    1.4666    0.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3690    2.2064    0.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4720    1.7280   -0.7797 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3740    0.8050   -0.0725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3874    0.6254    1.2902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2951   -0.2711    1.8679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3421   -0.4827    3.2404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4445    0.2310    4.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1901   -0.9913    1.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0953   -1.8827    1.6615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1718   -0.8060   -0.2706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2824    0.0716   -0.8328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2806    0.2389   -2.3184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8204    0.1400   -2.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9233    1.1178   -2.0242 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3459    0.6024   -1.9614 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3488   -1.2577   -1.9079 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5720   -1.8690   -2.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6122   -1.6460   -1.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8402   -2.2700   -1.3903 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8673    1.3504    1.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4702   -0.0139    2.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1401    0.5700    2.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0713    0.4875    0.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1199   -0.5477   -0.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5787    1.7507    0.7226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4527    3.0838    0.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0830    2.6396   -1.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6959    1.1778    1.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4398   -0.1889    5.1005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7730    1.2890    4.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4116    0.1445    3.6492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754   -1.9895    2.6748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8842   -1.3823   -0.8535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7425    1.1888   -2.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8140   -0.6303   -2.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6891    0.2426   -3.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5003   -0.8814   -2.3609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8266    1.9993   -2.7583 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5377   -1.4407   -2.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7298   -2.5522   -2.9099 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6115   -2.1269   -0.7810 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 25  2  0
 25 26  1  0
 25 24  1  0
 24 23  2  0
 23  5  1  0
  5  4  2  0
  5  6  1  0
  6 22  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  2  0
 17 15  1  0
 15 16  1  0
 15 12  2  0
 12 13  1  0
 13 14  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  4  3  1  0
  7  6  1  0
  9 21  1  0
 10 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 26 48  1  0
 24 47  1  0
 23 46  1  0
  4 30  1  0
  6 31  1  1
 21 45  1  6
 20 43  1  0
 20 44  1  0
 19 41  1  0
 19 42  1  0
 17 40  1  0
 16 39  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 11 35  1  0
  9 34  1  6
  8 33  1  0
  7 32  1  0
M  END


  Mrv1652306292219402D          

 26 29  0  0  1  0            999 V2000
    7.3145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    0.4125    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  9  7  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
  9 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 12 22  1  0  0  0  0
 17 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 25  1  0  0  0  0
  4 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138668

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=CC(=C1)[C@@H]1O[C@H]2CCC3=CC(O)=C(OC)C=C3[C@H]2C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O5/c1-24-20-10-13(3-6-16(20)22)18-8-5-14-15-11-21(25-2)17(23)9-12(15)4-7-19(14)26-18/h3,5-6,8-11,14,18-19,22-23H,4,7H2,1-2H3/t14-,18-,19+/m1/s1

> <INCHI_KEY>
HCKMOHZJLHPQOV-ZMYBRWDISA-N

> <FORMULA>
C21H22O5

> <MOLECULAR_WEIGHT>
354.402

> <EXACT_MASS>
354.146723808

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
38.2527914489235

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4aS,10bR)-3-(4-hydroxy-3-methoxyphenyl)-9-methoxy-3H,4aH,5H,6H,10bH-benzo[f]chromen-8-ol

> <ALOGPS_LOGP>
3.11

> <JCHEM_LOGP>
3.6736694229999998

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.26019469223927

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.652419696289945

> <JCHEM_PKA_STRONGEST_BASIC>
-4.073708874792066

> <JCHEM_POLAR_SURFACE_AREA>
68.15

> <JCHEM_REFRACTIVITY>
99.43549999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.02e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4aS,10bR)-3-(4-hydroxy-3-methoxyphenyl)-9-methoxy-3H,4aH,5H,6H,10bH-benzo[f]chromen-8-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      13.654   3.437   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      12.114   3.437   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.724  -0.564   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.746   3.437   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   26                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7    3                                                       
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    9                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21   12   17                                                  
CONECT   23   20   24                                                       
CONECT   24   23                                                            
CONECT   25   19                                                            
CONECT   26    4                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂O₅

Average Mass

354.4020 Da

Monoisotopic Mass

354.14672 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

1392476-32-2

SMILES

COC1=C(O)C=CC(=C1)[C@@H]1O[C@H]2CCC3=CC(O)=C(OC)C=C3[C@H]2C=C1

InChI Identifier

InChI=1S/C21H22O5/c1-24-20-10-13(3-6-16(20)22)18-8-5-14-15-11-21(25-2)17(23)9-12(15)4-7-19(14)26-18/h3,5-6,8-11,14,18-19,22-23H,4,7H2,1-2H3/t14-,18-,19+/m1/s1

InChI Key

HCKMOHZJLHPQOV-ZMYBRWDISA-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

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

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

62773998

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122384907

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Musellarin B (NP0138668)

MOL for NP0138668 (Musellarin B)

3D MOL for NP0138668 (Musellarin B)

3D SDF for NP0138668 (Musellarin B)

3D-SDF for NP0138668 (Musellarin B)

PDB for NP0138668 (Musellarin B)

3D PDB for NP0138668 (Musellarin B)

SMILES for NP0138668 (Musellarin B)

INCHI for NP0138668 (Musellarin B)

Structure for NP0138668 (Musellarin B)

3D Structure for NP0138668 (Musellarin B)