NP-MRD: Showing NP-Card for 11alpha-Hydroxyhomodeoxyharringtonine (NP0067773)

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Record Information

Version

2.0

Created at

2022-04-28 12:37:23 UTC

Updated at

2022-04-28 12:37:23 UTC

NP-MRD ID

NP0067773

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11alpha-Hydroxyhomodeoxyharringtonine

Description

(2S,3S,6S,12R)-12-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]Icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioate belongs to the class of organic compounds known as cephalotaxus alkaloids. These are alkaloids with a structure based on the cephalotaxine skeleton, a tetracyclic 1,3-benzodioxole-containing compound which arises from the skeletal rearrangement of the hydroaromatic component of the Erythrina group. 11alpha-Hydroxyhomodeoxyharringtonine is found in Cephalotaxus hainanensis and Cephalotaxus harringtonia var.drupacea. Based on a literature review very few articles have been published on (2S,3S,6S,12R)-12-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0²,⁶.0⁶,¹⁰.0¹⁵,¹⁹]Icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214372D          

 39 43  0  0  1  0            999 V2000
    3.8711    2.3100    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4357    1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2020    2.0143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8499    1.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7317    0.6871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9655    0.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3175    0.8919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6054    0.4753    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8357    0.7723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5880    1.5592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0488    2.2436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7630    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5009    0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0940    0.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3154    0.1321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7636   -0.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
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 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
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 16 34  1  0  0  0  0
 34 35  1  0  0  0  0
  5 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
  4 38  1  0  0  0  0
  1 39  1  6  0  0  0
M  END

     RDKit          3D

 78 82  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304282214372D          

 39 43  0  0  1  0            999 V2000
    3.8711    2.3100    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4357    1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6054    0.4753    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.5880    1.5592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5608   -0.3485    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2011   -0.8687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0458   -1.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3401   -2.4646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5661   -1.0536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3807   -1.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1906   -2.8439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4666   -1.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -1.4580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4717    0.3224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0472    0.9134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6630    1.6435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1681    3.0796    0.0000 O   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  2  0  0  0  0
  2  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
  1 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 21 19  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 21 33  1  1  0  0  0
 16 34  1  0  0  0  0
 34 35  1  0  0  0  0
  5 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
  4 38  1  0  0  0  0
  1 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0067773

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@](O)(CCCC(C)C)C(=O)O[C@H]1[C@H]2C3=CC4=C(OCO4)C=C3[C@@H](O)CN3CCC[C@@]23C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C29H39NO9/c1-17(2)7-5-9-29(34,14-24(32)36-4)27(33)39-26-23(35-3)13-28-8-6-10-30(28)15-20(31)18-11-21-22(38-16-37-21)12-19(18)25(26)28/h11-13,17,20,25-26,31,34H,5-10,14-16H2,1-4H3/t20-,25+,26+,28+,29+/m0/s1

> <INCHI_KEY>
UGSCGWGSJMKYHV-USFAGMLDSA-N

> <FORMULA>
C29H39NO9

> <MOLECULAR_WEIGHT>
545.629

> <EXACT_MASS>
545.26248184

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
58.05020981417421

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,6S,12R)-12-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioate

> <ALOGPS_LOGP>
2.50

> <JCHEM_LOGP>
2.4367892173333323

> <ALOGPS_LOGS>
-3.50

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.00345899211743

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.084615953494996

> <JCHEM_PKA_STRONGEST_BASIC>
8.925883432686057

> <JCHEM_POLAR_SURFACE_AREA>
123.99000000000002

> <JCHEM_REFRACTIVITY>
141.4463

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,6S,12R)-12-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       7.226   4.312   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.280   3.189   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.710   3.760   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.920   2.807   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.699   1.283   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.269   0.712   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.059   1.665   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.730   0.887   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.293   1.442   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       4.831   2.911   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       5.691   4.188   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.291   2.925   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.802   1.465   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.909   0.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.322   0.246   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.159  -1.046   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.647  -0.650   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.842  -1.622   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.599  -3.142   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.160  -3.692   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.794  -4.113   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.989  -5.085   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.745  -6.605   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.940  -7.577   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.697  -9.097   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.892 -10.068   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.258  -9.647   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.765  -2.918   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.285  -3.162   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.835  -4.601   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      12.257  -1.967   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      13.777  -2.210   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.822  -5.309   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       4.604  -2.483   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.083  -2.722   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      12.080   0.602   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      13.155   1.705   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.438   3.068   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       7.780   5.749   0.000  0.00  0.00           O+0
CONECT    1    2   11   39                                                  
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   38                                                  
CONECT    5    4    6   36                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9   17                                                  
CONECT    9    8   10   14   15                                             
CONECT   10    9   11   12                                                  
CONECT   11   10    1                                                       
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    9   16                                                       
CONECT   16   15   17   34                                                  
CONECT   17   16    8   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   28   33                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   21   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31                                                            
CONECT   33   21                                                            
CONECT   34   16   35                                                       
CONECT   35   34                                                            
CONECT   36    5   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37    4                                                       
CONECT   39    1                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
(2S,3S,6S,12R)-12-Hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0,.0,.0,]icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioic acid	Generator

Chemical Formula

C₂₉H₃₉NO₉

Average Mass

545.6290 Da

Monoisotopic Mass

545.26248 Da

IUPAC Name

(2S,3S,6S,12R)-12-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioate

Traditional Name

(2S,3S,6S,12R)-12-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(20),4,13,15(19)-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-methylpentyl)butanedioate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@](O)(CCCC(C)C)C(=O)O[C@H]1[C@H]2C3=CC4=C(OCO4)C=C3[C@@H](O)CN3CCC[C@@]23C=C1OC

InChI Identifier

InChI=1S/C29H39NO9/c1-17(2)7-5-9-29(34,14-24(32)36-4)27(33)39-26-23(35-3)13-28-8-6-10-30(28)15-20(31)18-11-21-22(38-16-37-21)12-19(18)25(26)28/h11-13,17,20,25-26,31,34H,5-10,14-16H2,1-4H3/t20-,25+,26+,28+,29+/m0/s1

InChI Key

UGSCGWGSJMKYHV-USFAGMLDSA-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
Cephalotaxus hainanensis	Plant	KNApSAcK
Cephalotaxus harringtonia var.drupacea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cephalotaxus alkaloids. These are alkaloids with a structure based on the cephalotaxine skeleton, a tetracyclic 1,3-benzodioxole-containing compound which arises from the skeletal rearrangement of the hydroaromatic component of the Erythrina group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cephalotaxus alkaloids

Sub Class

Not Available

Direct Parent

Cephalotaxus alkaloids

Alternative Parents

Substituents

Cephalotaxine
Cephalotaxus alkaloid skeleton
Benzazepine
Benzodioxole
Aralkylamine
Fatty acid methyl ester
Fatty acid ester
Azepine
Fatty acyl
Benzenoid
N-alkylpyrrolidine
Dicarboxylic acid or derivatives
Methyl ester
Tertiary alcohol
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Carboxylic acid ester
Amino acid or derivatives
1,2-aminoalcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	2.5	ALOGPS
logP	2.44	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	12.08	ChemAxon
pKa (Strongest Basic)	8.93	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	123.99 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	141.45 m³·mol⁻¹	ChemAxon
Polarizability	58.05 Å³	ChemAxon
Number of Rings	5	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

163106163

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 11alpha-Hydroxyhomodeoxyharringtonine (NP0067773)

MOL for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

3D MOL for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

3D SDF for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

3D-SDF for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

PDB for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

3D PDB for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

SMILES for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

INCHI for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

Structure for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)

3D Structure for NP0067773 (11alpha-Hydroxyhomodeoxyharringtonine)