NP-MRD: Showing NP-Card for 7,9,10-Trideacetylbaccatin VI (NP0077490)

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Record Information

Version

2.0

Created at

2022-04-28 22:37:59 UTC

Updated at

2022-04-28 22:37:59 UTC

NP-MRD ID

NP0077490

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,9,10-Trideacetylbaccatin VI

Description

9-Dihydrobaccatin III 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. 7,9,10-Trideacetylbaccatin VI is found in Taxus canadensis. 7,9,10-Trideacetylbaccatin VI was first documented in 2002 (PMID: 12467445). Based on a literature review a small amount of articles have been published on 9-Dihydrobaccatin III (PMID: 23007175) (PMID: 24130020).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200382D          

 42 46  0  0  1  0            999 V2000
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  1  2  1  0  0  0  0
  2  3  1  6  0  0  0
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  1 42  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292200382D          

 42 46  0  0  1  0            999 V2000
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    2.2816   -1.6071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4567   -1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0382   -2.3112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0501   -0.8823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5824    0.3981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0868   -0.2547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3995    0.2839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6993   -0.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6745    1.5056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1675    1.8668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1794    1.6509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7692    2.3667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9442    2.3694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1839    3.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7737    3.7957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1885    4.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0135    4.5062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4237    3.7904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0089    3.0772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2180   -1.3774    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  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  6  0  0  0
  4  8  1  6  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  3 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  1  0  0  0
 20 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 19 27  1  0  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 18 30  1  0  0  0  0
 17 31  1  1  0  0  0
 15 32  1  6  0  0  0
 14 33  1  1  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 36 41  1  0  0  0  0
  1 42  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0077490

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1[C@H](O)[C@]2(C)[C@@H](O)C[C@H]3OC[C@@]3(OC(C)=O)[C@H]2[C@H](OC(=O)C2=CC=CC=C2)[C@]2(O)C[C@H](O)C(C)=C1C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O11/c1-15-19(34)13-31(38)26(41-27(37)18-10-8-7-9-11-18)24-29(6,20(35)12-21-30(24,14-39-21)42-17(3)33)25(36)23(40-16(2)32)22(15)28(31,4)5/h7-11,19-21,23-26,34-36,38H,12-14H2,1-6H3/t19-,20-,21+,23+,24-,25-,26-,29+,30-,31+/m0/s1

> <INCHI_KEY>
NEAUUILPXJLPHE-UFJLMRSISA-N

> <FORMULA>
C31H40O11

> <MOLECULAR_WEIGHT>
588.65

> <EXACT_MASS>
588.257062108

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
60.085782981658284

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3R,4S,7R,9S,10S,11R,12R,15S)-4,12-bis(acetyloxy)-1,9,11,15-tetrahydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.0^{3,10}.0^{4,7}]heptadec-13-en-2-yl benzoate

> <ALOGPS_LOGP>
1.31

> <JCHEM_LOGP>
0.27536355599999923

> <ALOGPS_LOGS>
-3.13

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.659333140833763

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.063207462963053

> <JCHEM_PKA_STRONGEST_BASIC>
-3.008862033760437

> <JCHEM_POLAR_SURFACE_AREA>
169.04999999999998

> <JCHEM_REFRACTIVITY>
146.04019999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.40e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,4S,7R,9S,10S,11R,12R,15S)-4,12-bis(acetyloxy)-1,9,11,15-tetrahydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.0^{3,10}.0^{4,7}]heptadec-13-en-2-yl benzoate

> <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       7.877  -1.031   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.053   0.499   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.466   1.111   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.703   0.194   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.527  -1.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.114  -1.949   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.938  -3.479   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      11.621   1.431   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.384   2.348   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.509   2.317   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.075   3.750   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.118   4.956   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.598   3.976   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.027   1.751   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.421   2.025   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.987   2.773   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.591   2.037   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.644   0.460   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.005  -0.414   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.040  -1.673   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.611  -1.961   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.957  -3.462   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.259  -3.000   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.719  -2.987   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.938  -4.314   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.960  -1.647   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.820   0.743   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.762  -0.475   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.346   0.530   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.305  -0.301   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.259   2.810   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       5.913   3.485   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       7.801   3.082   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       7.036   4.418   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.496   4.423   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       7.810   5.749   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.044   7.085   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.819   8.416   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.359   8.412   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.124   7.075   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.350   5.744   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.874  -2.571   0.000  0.00  0.00           C+0
CONECT    1    2    6   21   42                                             
CONECT    2    1    3   14                                                  
CONECT    3    2    4    9   10                                             
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    4    9                                                       
CONECT    9    8    3                                                       
CONECT   10    3   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    2   15   33                                                  
CONECT   15   14   16   27   32                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   31                                                  
CONECT   18   17   19   30                                                  
CONECT   19   18   20   27                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20    1   22                                                  
CONECT   22   21                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   19   15   28   29                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   18                                                            
CONECT   31   17                                                            
CONECT   32   15                                                            
CONECT   33   14   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   36                                                       
CONECT   42    1                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Value	Source
9-Dihydro-baccatin III	MeSH

Chemical Formula

C₃₁H₄₀O₁₁

Average Mass

588.6500 Da

Monoisotopic Mass

588.25706 Da

IUPAC Name

(1S,2S,3R,4S,7R,9S,10S,11R,12R,15S)-4,12-bis(acetyloxy)-1,9,11,15-tetrahydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.0^{3,10}.0^{4,7}]heptadec-13-en-2-yl benzoate

Traditional Name

(1S,2S,3R,4S,7R,9S,10S,11R,12R,15S)-4,12-bis(acetyloxy)-1,9,11,15-tetrahydroxy-10,14,17,17-tetramethyl-6-oxatetracyclo[11.3.1.0^{3,10}.0^{4,7}]heptadec-13-en-2-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1[C@H](O)[C@]2(C)[C@@H](O)C[C@H]3OC[C@@]3(OC(C)=O)[C@H]2[C@H](OC(=O)C2=CC=CC=C2)[C@]2(O)C[C@H](O)C(C)=C1C2(C)C

InChI Identifier

InChI=1S/C31H40O11/c1-15-19(34)13-31(38)26(41-27(37)18-10-8-7-9-11-18)24-29(6,20(35)12-21-30(24,14-39-21)42-17(3)33)25(36)23(40-16(2)32)22(15)28(31,4)5/h7-11,19-21,23-26,34-36,38H,12-14H2,1-6H3/t19-,20-,21+,23+,24-,25-,26-,29+,30-,31+/m0/s1

InChI Key

NEAUUILPXJLPHE-UFJLMRSISA-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 canadensis	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
Benzoate ester
Tricarboxylic acid or derivatives
Benzoic acid or derivatives
Benzoyl
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Oxetane
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	1.31	ALOGPS
logP	0.28	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	13.06	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	169.05 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	146.04 m³·mol⁻¹	ChemAxon
Polarizability	60.09 Å³	ChemAxon
Number of Rings	5	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

8135723

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9960116

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chao Z, Tan M, Paudel MK, Sakamoto S, Ma L, Sasaki-Tabata K, Tanaka H, Shoyama Y, Xuan L, Morimoto S: Development of an indirect competitive enzyme-linked immunosorbent assay (icELISA) using highly specific monoclonal antibody against paclitaxel. J Nat Med. 2013 Jul;67(3):512-8. doi: 10.1007/s11418-012-0708-1. Epub 2012 Sep 25. [PubMed:23007175 ]
Li Y, Qin F, Wang SM, Guo RX, Zhang YF, Gu YC, Shi QW: Chemical studies on Taxus canadensis. Chem Biodivers. 2013 Oct;10(10):1729-53. doi: 10.1002/cbdv.201200032. [PubMed:24130020 ]
Brincat MC, Gibson DM, Shuler ML: Alterations in Taxol production in plant cell culture via manipulation of the phenylalanine ammonia lyase pathway. Biotechnol Prog. 2002 Nov-Dec;18(6):1149-56. doi: 10.1021/bp0256115. [PubMed:12467445 ]

Showing NP-Card for 7,9,10-Trideacetylbaccatin VI (NP0077490)

MOL for NP0077490 (7,9,10-Trideacetylbaccatin VI)

3D MOL for NP0077490 (7,9,10-Trideacetylbaccatin VI)

3D SDF for NP0077490 (7,9,10-Trideacetylbaccatin VI)

3D-SDF for NP0077490 (7,9,10-Trideacetylbaccatin VI)

PDB for NP0077490 (7,9,10-Trideacetylbaccatin VI)

3D PDB for NP0077490 (7,9,10-Trideacetylbaccatin VI)

SMILES for NP0077490 (7,9,10-Trideacetylbaccatin VI)

INCHI for NP0077490 (7,9,10-Trideacetylbaccatin VI)

Structure for NP0077490 (7,9,10-Trideacetylbaccatin VI)

3D Structure for NP0077490 (7,9,10-Trideacetylbaccatin VI)