NP-MRD: Showing NP-Card for Baccatin I (NP0077532)

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Record Information

Version

2.0

Created at

2022-04-28 22:40:07 UTC

Updated at

2022-04-28 22:40:07 UTC

NP-MRD ID

NP0077532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Baccatin I

Description

(1'R,2R,2'R,3'S,5'R,7'R,8'R,9'R,10'R,13'R)-2',5',7',9',10'-pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]Pentadecan]-11'-en-13'-yl acetate 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. Baccatin I is found in Taxus baccata . Based on a literature review very few articles have been published on (1'R,2R,2'R,3'S,5'R,7'R,8'R,9'R,10'R,13'R)-2',5',7',9',10'-pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0³,⁸]Pentadecan]-11'-en-13'-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200402D          

 45 48  0  0  1  0            999 V2000
    4.0463   -0.8120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304292200402D          

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    4.4436   -2.1846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0385   -2.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410   -3.5572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8310   -2.5268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4237   -0.1238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213    0.6772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0264    1.2488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4137    0.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069    1.0108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6079    0.8133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7837    0.7239    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9487    0.9791    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2376    1.4740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4459    1.1779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3670    0.3362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305   -0.2208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4951   -0.9600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3105   -1.2200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3919   -2.0410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7216   -2.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8029   -3.3430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9699   -2.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9898   -1.6122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1724   -1.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6671   -2.1528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603   -0.7370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5426    0.3386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9601   -0.3730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3386    0.1217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6038    0.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7907    1.6792    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8973    2.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2421    2.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6590    2.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2856    1.3787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9695    2.1407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1515    2.2480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4714    2.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9397   -1.6301    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  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  4 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  3 15  1  6  0  0  0
 15 16  1  0  0  0  0
  3 16  1  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 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
 23 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 22 33  1  0  0  0  0
 18 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 21 36  1  0  0  0  0
 20 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 17 41  1  1  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
  1 45  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0077532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@H]2[C@@H](OC(C)=O)[C@H]3[C@@]4(CO4)[C@@H](C[C@@H](OC(C)=O)[C@]3(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C(=C1C)C2(C)C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H44O13/c1-14-22(40-15(2)33)11-21-26(43-18(5)36)28-31(10,23(41-16(3)34)12-24(42-17(4)35)32(28)13-39-32)29(45-20(7)38)27(44-19(6)37)25(14)30(21,8)9/h21-24,26-29H,11-13H2,1-10H3/t21-,22+,23+,24+,26+,27+,28+,29-,31-,32+/m0/s1

> <INCHI_KEY>
NHMSEMKTDAYSGW-QOZDAIMOSA-N

> <FORMULA>
C32H44O13

> <MOLECULAR_WEIGHT>
636.691

> <EXACT_MASS>
636.278191477

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
64.51713112187954

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'R,2R,2'R,3'S,5'R,7'R,8'R,9'R,10'R,13'R)-2',7',9',10',13'-pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-5'-yl acetate

> <ALOGPS_LOGP>
2.72

> <JCHEM_LOGP>
0.5427979296666661

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.220397613449229

> <JCHEM_POLAR_SURFACE_AREA>
170.33

> <JCHEM_REFRACTIVITY>
151.57070000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.40e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2R,2'R,3'S,5'R,7'R,8'R,9'R,10'R,13'R)-2',7',9',10',13'-pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-5'-yl acetate

> <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       7.553  -1.516   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.922  -0.021   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.401   0.408   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.512  -0.659   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.143  -2.155   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.664  -2.583   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.295  -4.078   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.405  -5.145   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.037  -6.640   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.885  -4.717   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.991  -0.231   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      12.360   1.264   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.249   2.331   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      13.839   1.692   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.973   1.887   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.468   1.518   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.063   1.351   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.504   1.828   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.177   2.751   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.699   2.199   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.552   0.628   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.790  -0.412   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.658  -1.792   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.180  -2.277   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.331  -3.810   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.080  -4.708   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.232  -6.240   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.677  -4.073   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.714  -3.009   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.188  -2.801   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.245  -4.019   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       1.606  -1.376   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.746   0.632   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.525  -0.696   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.232   0.227   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.127   0.043   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       1.476   3.135   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.675   4.662   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       0.452   5.597   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.097   5.253   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       8.000   2.574   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       7.410   3.996   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.883   4.196   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       8.347   5.218   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       7.354  -3.043   0.000  0.00  0.00           C+0
CONECT    1    2    6   24   45                                             
CONECT    2    1    3   17                                                  
CONECT    3    2    4   15   16                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    4   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    3   16                                                       
CONECT   16   15    3                                                       
CONECT   17    2   18   41                                                  
CONECT   18   17   19   33                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   37                                                  
CONECT   21   20   22   36                                                  
CONECT   22   21   23   33                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23    1   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   23   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   22   18   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   21                                                            
CONECT   37   20   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   17   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45    1                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   96    0
END

View in JSmol

Synonyms

Value	Source
(1'r,2R,2'r,3's,5'r,7'r,8'r,9'r,10'r,13'r)-2',5',7',9',10'-Pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0,]pentadecan]-11'-en-13'-yl acetic acid	Generator

Chemical Formula

C₃₂H₄₄O₁₃

Average Mass

636.6910 Da

Monoisotopic Mass

636.27819 Da

IUPAC Name

(1'R,2R,2'R,3'S,5'R,7'R,8'R,9'R,10'R,13'R)-2',7',9',10',13'-pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-5'-yl acetate

Traditional Name

(1'R,2R,2'R,3'S,5'R,7'R,8'R,9'R,10'R,13'R)-2',7',9',10',13'-pentakis(acetyloxy)-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.0^{3,8}]pentadecan]-11'-en-5'-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@H]2[C@@H](OC(C)=O)[C@H]3[C@@]4(CO4)[C@@H](C[C@@H](OC(C)=O)[C@]3(C)[C@@H](OC(C)=O)[C@H](OC(C)=O)C(=C1C)C2(C)C)OC(C)=O

InChI Identifier

InChI=1S/C32H44O13/c1-14-22(40-15(2)33)11-21-26(43-18(5)36)28-31(10,23(41-16(3)34)12-24(42-17(4)35)32(28)13-39-32)29(45-20(7)38)27(44-19(6)37)25(14)30(21,8)9/h21-24,26-29H,11-13H2,1-10H3/t21-,22+,23+,24+,26+,27+,28+,29-,31-,32+/m0/s1

InChI Key

NHMSEMKTDAYSGW-QOZDAIMOSA-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 baccata	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
Hexacarboxylic acid or derivatives
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	2.72	ALOGPS
logP	0.54	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	170.33 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	151.57 m³·mol⁻¹	ChemAxon
Polarizability	64.52 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

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

154496226

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Baccatin I (NP0077532)

MOL for NP0077532 (Baccatin I)

3D MOL for NP0077532 (Baccatin I)

3D SDF for NP0077532 (Baccatin I)

3D-SDF for NP0077532 (Baccatin I)

PDB for NP0077532 (Baccatin I)

3D PDB for NP0077532 (Baccatin I)

SMILES for NP0077532 (Baccatin I)

INCHI for NP0077532 (Baccatin I)

Structure for NP0077532 (Baccatin I)

3D Structure for NP0077532 (Baccatin I)