NP-MRD: Showing NP-Card for (+)-2'-Hydroxy taxine II (NP0077463)

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Record Information

Version

2.0

Created at

2022-04-28 22:36:45 UTC

Updated at

2022-04-28 22:36:45 UTC

NP-MRD ID

NP0077463

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-2'-Hydroxy taxine II

Description

2'-Hydroxytaxine II belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system. (+)-2'-Hydroxy taxine II is found in Taxus cuspidata . Based on a literature review very few articles have been published on 2'-Hydroxytaxine II.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200362D          

 48 51  0  0  1  0            999 V2000
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   -2.6735   -3.8553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 48 97  1  0
  1 49  1  0
  1 50  1  0
 11 55  1  0
 12 56  1  0
 13 57  1  0
 14 58  1  0
 15 59  1  0
M  END


  Mrv1652304292200362D          

 48 51  0  0  1  0            999 V2000
   -2.2610   -4.5697    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6735   -3.8553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2610   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6735   -2.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4360   -3.1408    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0235   -3.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4360   -4.5697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0235   -2.4263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1985   -2.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2140   -3.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2140   -1.7119    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0390   -1.7119    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4515   -2.4263    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2765   -2.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -3.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515   -0.9974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390   -0.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4515    0.4316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2765    0.4316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6890   -0.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2765   -0.9974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1985   -0.9974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5145   -3.6441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2934   -4.0386    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1490   -4.1744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5148   -4.9365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3346   -5.0289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9886   -5.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1242   -5.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2770   -5.7512    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5089   -5.3738    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8814   -5.9094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038   -5.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9537   -4.8226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4763   -6.1694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1895   -6.5715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8562   -7.0575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7687   -7.8778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6104   -6.7231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1425   -4.7818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3485   -5.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4182   -4.3868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3219   -6.3528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6062   -2.8242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3621   -2.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0263   -2.9831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4538   -1.6738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7710   -5.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  6  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  5  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  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
 16 21  1  0  0  0  0
 11 22  1  6  0  0  0
  2 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
  1 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 30 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 29 40  1  0  0  0  0
 24 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 28 43  1  0  0  0  0
 23 44  1  1  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
  1 48  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0077463

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN(C)[C@H]([C@@H](O)C(=O)O[C@H]1CC[C@]2(C)[C@H]([C@H](OC(C)=O)[C@@H]3CC(=O)C(C)=C([C@@H](OC(C)=O)[C@@H]2OC(C)=O)C3(C)C)C1=C)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C37H49NO10/c1-19-26(42)18-25-32(45-21(3)39)29-20(2)27(48-35(44)31(43)30(38(9)10)24-14-12-11-13-15-24)16-17-37(29,8)34(47-23(5)41)33(46-22(4)40)28(19)36(25,6)7/h11-15,25,27,29-34,43H,2,16-18H2,1,3-10H3/t25-,27-,29-,30-,31+,32+,33+,34-,37+/m0/s1

> <INCHI_KEY>
VOMHMJTXSVWBOE-MYSYOJMRSA-N

> <FORMULA>
C37H49NO10

> <MOLECULAR_WEIGHT>
667.796

> <EXACT_MASS>
667.335646782

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
69.92014004559758

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,5S,8R,9R,10R)-2,9,10-tris(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
3.458530190333333

> <ALOGPS_LOGS>
-5.15

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
18.484453235830657

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.022864669072918

> <JCHEM_PKA_STRONGEST_BASIC>
8.22733182238211

> <JCHEM_POLAR_SURFACE_AREA>
145.74

> <JCHEM_REFRACTIVITY>
174.96050000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.68e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,5S,8R,9R,10R)-2,9,10-tris(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -4.220  -8.530   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.990  -7.196   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.220  -5.863   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.990  -4.529   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.680  -5.863   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.910  -7.196   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.680  -8.530   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.910  -4.529   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.370  -4.529   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.400  -5.863   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.400  -3.195   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.940  -3.195   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       2.710  -4.529   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       4.250  -4.529   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.940  -5.863   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.710  -1.862   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.940  -0.528   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.710   0.806   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.250   0.806   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.020  -0.528   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.250  -1.862   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.370  -1.862   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -6.560  -6.802   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.014  -7.539   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -9.612  -7.792   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -10.294  -9.215   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -11.825  -9.387   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -9.312 -10.450   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.698 -10.341   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.117 -10.736   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.683 -10.031   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -3.512 -11.031   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -2.060 -10.516   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -1.780  -9.002   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -0.889 -11.516   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -5.954 -12.267   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -7.198 -13.174   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -7.035 -14.705   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -8.606 -12.550   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -7.733  -8.926   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -6.250  -9.344   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -6.381  -8.189   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -9.934 -11.859   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -6.732  -5.272   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -8.143  -4.655   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -9.382  -5.568   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -8.314  -3.124   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -3.306  -9.769   0.000  0.00  0.00           C+0
CONECT    1    2    7   31   48                                             
CONECT    2    1    3   23                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    1                                                       
CONECT    8    5    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   22                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   11                                                            
CONECT   23    2   24   44                                                  
CONECT   24   23   25   40                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   43                                                  
CONECT   29   28   30   40                                                  
CONECT   30   29   31   36                                                  
CONECT   31   30    1   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   30   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   29   24   41   42                                             
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   28                                                            
CONECT   44   23   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48    1                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₉NO₁₀

Average Mass

667.7960 Da

Monoisotopic Mass

667.33565 Da

IUPAC Name

(1R,2R,3R,5S,8R,9R,10R)-2,9,10-tris(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate

Traditional Name

(1R,2R,3R,5S,8R,9R,10R)-2,9,10-tris(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxotricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate

CAS Registry Number

Not Available

SMILES

CN(C)[C@H]([C@@H](O)C(=O)O[C@H]1CC[C@]2(C)[C@H]([C@H](OC(C)=O)[C@@H]3CC(=O)C(C)=C([C@@H](OC(C)=O)[C@@H]2OC(C)=O)C3(C)C)C1=C)C1=CC=CC=C1

InChI Identifier

InChI=1S/C37H49NO10/c1-19-26(42)18-25-32(45-21(3)39)29-20(2)27(48-35(44)31(43)30(38(9)10)24-14-12-11-13-15-24)16-17-37(29,8)34(47-23(5)41)33(46-22(4)40)28(19)36(25,6)7/h11-15,25,27,29-34,43H,2,16-18H2,1,3-10H3/t25-,27-,29-,30-,31+,32+,33+,34-,37+/m0/s1

InChI Key

VOMHMJTXSVWBOE-MYSYOJMRSA-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, 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
Taxus cuspidata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Taxanes and derivatives

Alternative Parents

Substituents

Taxane diterpenoid
Tetracarboxylic acid or derivatives
Cyclohexenone
Aralkylamine
Fatty acid ester
Fatty acyl
Benzenoid
Monosaccharide
Monocyclic benzene moiety
Cyclic ketone
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Ketone
Carboxylic acid ester
Amino acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	2.95	ALOGPS
logP	3.46	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	12.02	ChemAxon
pKa (Strongest Basic)	8.23	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	145.74 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	174.96 m³·mol⁻¹	ChemAxon
Polarizability	69.92 Å³	ChemAxon
Number of Rings	4	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

8803571

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10628208

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (+)-2'-Hydroxy taxine II (NP0077463)

MOL for NP0077463 ((+)-2'-Hydroxy taxine II)

3D MOL for NP0077463 ((+)-2'-Hydroxy taxine II)

3D SDF for NP0077463 ((+)-2'-Hydroxy taxine II)

3D-SDF for NP0077463 ((+)-2'-Hydroxy taxine II)

PDB for NP0077463 ((+)-2'-Hydroxy taxine II)

3D PDB for NP0077463 ((+)-2'-Hydroxy taxine II)

SMILES for NP0077463 ((+)-2'-Hydroxy taxine II)

INCHI for NP0077463 ((+)-2'-Hydroxy taxine II)

Structure for NP0077463 ((+)-2'-Hydroxy taxine II)

3D Structure for NP0077463 ((+)-2'-Hydroxy taxine II)