NP-MRD: Showing NP-Card for Miaosporone D (NP0044720)

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Record Information

Version

2.0

Created at

2022-02-24 21:13:30 UTC

Updated at

2022-02-24 21:13:31 UTC

NP-MRD ID

NP0044720

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Miaosporone D

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
   -5.6019    0.2964    0.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1114    0.1936    0.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3006    1.1767    0.7760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9020    1.1351    0.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2645    2.1942    1.2925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3248    0.0465    0.0957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1096   -0.9601   -0.4280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4870   -0.8755   -0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5360   -2.2207   -1.0350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1618   -2.4708   -0.4098 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6942   -1.2933   -0.5525 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9566   -1.1112   -1.9396 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0196   -1.4078    0.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4900   -2.4521    0.5489 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7860   -0.1251    0.0776 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0820   -0.1226    0.5420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6365   -1.3019    0.9868 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8279    1.0332    0.5685 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2433    2.2056    0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9527    2.2277   -0.3531 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2227    1.0625   -0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7956    1.0419   -0.8777 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2230    2.2556   -0.9994 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1122    0.0021   -0.0293 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6621    0.1766    1.2752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8923    1.3822    0.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0866   -0.1912   -0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9759   -0.0585    1.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7746    2.0270    1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3450    2.4367    1.4600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1053   -1.6764   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1998   -3.0403   -0.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5217   -2.0960   -2.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3301   -2.7688    0.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2604   -3.3407   -0.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5751   -1.8518   -2.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889   -1.3372    1.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8597    1.0369    0.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7905    3.1448    0.1148 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4665    3.1422   -0.7182 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9388    0.6786   -1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4266    2.2653   -1.7404 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2730   -0.4591    1.9047 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  8  2  0
  8  7  1  0
  7  6  2  0
  6  4  1  0
  4  5  1  0
  4  3  2  0
  6 24  1  0
 24 25  1  1
 24 22  1  0
 22 23  1  0
 22 21  1  0
 21 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 15 13  1  0
 13 14  2  0
 13 11  1  0
 11 12  1  6
 11 10  1  0
 10  9  1  0
  3  2  1  0
 11 24  1  0
  9  7  1  0
 20 21  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  8 31  1  0
  5 30  1  0
  3 29  1  0
 25 43  1  0
 22 41  1  6
 23 42  1  0
 17 37  1  0
 18 38  1  0
 19 39  1  0
 20 40  1  0
 12 36  1  0
 10 34  1  0
 10 35  1  0
  9 32  1  0
  9 33  1  0
M  END


  Mrv1652302242222132D          

 25 28  0  0  1  0            999 V2000
   -1.6203   -3.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802   -4.5473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6203   -2.9882    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3502   -3.7677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604   -3.6118    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8903   -4.3914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -3.4559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405   -2.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507   -2.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207   -1.7409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5908   -3.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207   -3.9236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106   -4.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7004   -2.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -1.2732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903   -2.2086    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1604   -1.4291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502   -1.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -1.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  2  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 13 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  4 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0044720

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC2=C(C(O)=C1)[C@]1(O)[C@@H](O)C3=C(C(O)=CC=C3)C(=O)[C@@]1(O)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O6/c1-9-7-10-5-6-18(24)17(23)14-11(3-2-4-12(14)20)16(22)19(18,25)15(10)13(21)8-9/h2-4,7-8,16,20-22,24-25H,5-6H2,1H3/t16-,18-,19-/m0/s1

> <INCHI_KEY>
WOMSNJDIGBBGDA-WDSOQIARSA-N

> <FORMULA>
C19H18O6

> <MOLECULAR_WEIGHT>
342.347

> <EXACT_MASS>
342.1103383

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
34.77918568559195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6aR,12S,12aS)-1,6a,8,12,12a-pentahydroxy-3-methyl-5,6,6a,7,12,12a-hexahydrotetraphen-7-one

> <ALOGPS_LOGP>
1.08

> <JCHEM_LOGP>
2.181106673333333

> <ALOGPS_LOGS>
-2.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.855870578536665

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.429909422320629

> <JCHEM_PKA_STRONGEST_BASIC>
-3.749805730177589

> <JCHEM_POLAR_SURFACE_AREA>
118.22000000000001

> <JCHEM_REFRACTIVITY>
89.76839999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6aR,12S,12aS)-1,6a,8,12,12a-pentahydroxy-3-methyl-6,12-dihydro-5H-tetraphen-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-22         0                                  
HETATM    1  C   UNK     0      -3.024  -6.742   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.512  -6.451   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.008  -4.996   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.504  -4.705   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.512  -5.869   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.008  -7.324   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.016  -8.488   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.504  -7.615   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.024  -5.578   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.520  -7.033   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.033  -6.742   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.529  -8.197   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.545  -6.451   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.049  -4.996   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.561  -4.705   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.065  -3.250   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.569  -5.869   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.065  -7.324   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.553  -7.615   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.041  -3.832   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.545  -2.377   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.529  -4.123   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.033  -2.668   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.520  -2.959   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.008  -3.250   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    2                                                       
CONECT    9    5   10   11   22                                             
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   19                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   13                                                       
CONECT   20   14   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    9   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24    4                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₈O₆

Average Mass

342.3470 Da

Monoisotopic Mass

342.11034 Da

IUPAC Name

(6aR,12S,12aS)-1,6a,8,12,12a-pentahydroxy-3-methyl-5,6,6a,7,12,12a-hexahydrotetraphen-7-one

Traditional Name

(6aR,12S,12aS)-1,6a,8,12,12a-pentahydroxy-3-methyl-6,12-dihydro-5H-tetraphen-7-one

CAS Registry Number

Not Available

SMILES

CC1=CC2=C(C(O)=C1)[C@]1(O)[C@@H](O)C3=C(C(O)=CC=C3)C(=O)[C@@]1(O)CC2

InChI Identifier

InChI=1S/C19H18O6/c1-9-7-10-5-6-18(24)17(23)14-11(3-2-4-12(14)20)16(22)19(18,25)15(10)13(21)8-9/h2-4,7-8,16,20-22,24-25H,5-6H2,1H3/t16-,18-,19-/m0/s1

InChI Key

WOMSNJDIGBBGDA-WDSOQIARSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Dimethylsulfoxide-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Actinomadura	Linington's dataset npmrd_submissions_20220207	34748348

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	1.08	ALOGPS
logP	2.18	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	8.43	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	118.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	89.77 m³·mol⁻¹	ChemAxon
Polarizability	34.78 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Showing NP-Card for Miaosporone D (NP0044720)

MOL for NP0044720 (Miaosporone D)

3D MOL for NP0044720 (Miaosporone D)

3D SDF for NP0044720 (Miaosporone D)

3D-SDF for NP0044720 (Miaosporone D)

PDB for NP0044720 (Miaosporone D)

3D PDB for NP0044720 (Miaosporone D)

SMILES for NP0044720 (Miaosporone D)

INCHI for NP0044720 (Miaosporone D)

Structure for NP0044720 (Miaosporone D)

3D Structure for NP0044720 (Miaosporone D)