NP-MRD: Showing NP-Card for Cephalostatin 18 (NP0083039)

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Record Information

Version

1.0

Created at

2022-04-29 04:05:21 UTC

Updated at

2022-04-29 04:05:21 UTC

NP-MRD ID

NP0083039

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cephalostatin 18

Description

Cephalostatin 19 belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. Cephalostatin 18 is found in Cephalodiscus gilchristi. It was first documented in 2004 (PMID: 15079895). Based on a literature review very few articles have been published on Cephalostatin 19.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292206052D          

 68 80  0  0  1  0            999 V2000
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    9.6458   -0.8471    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
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  4  5  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304292206052D          

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M  END
> <DATABASE_ID>
NP0083039

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1C2=NC3=C(C[C@@]4(C)[C@@H](CC[C@@H]5[C@@H]4C[C@@H](O)[C@@]4(C)C5=C[C@@H]5O[C@]6(O[C@](C)(CO)C[C@H]6O)[C@@H](C)[C@]45O)C3)N=C2C[C@@H]2CC[C@@H]3[C@H](CC(=O)[C@]45CO[C@@]6(OC(C)(C)C[C@H]6O)[C@@H](C)[C@H]4CC=C35)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C55H76N2O11/c1-26-32-14-15-33-30-13-11-29-17-38-45(46(64-9)50(29,7)35(30)19-41(60)52(32,33)25-65-54(26)42(61)22-47(3,4)67-54)57-37-16-28-10-12-31-34(49(28,6)21-39(37)56-38)18-40(59)51(8)36(31)20-44-53(51,63)27(2)55(66-44)43(62)23-48(5,24-58)68-55/h15,20,26-32,34-35,40,42-44,46,58-59,61-63H,10-14,16-19,21-25H2,1-9H3/t26-,27-,28-,29-,30-,31+,32+,34-,35-,40+,42+,43+,44-,46-,48-,49-,50-,51+,52+,53+,54+,55-/m0/s1

> <INCHI_KEY>
HJTADJIVGZRTHF-FVNBPLPQSA-N

> <FORMULA>
C55H76N2O11

> <MOLECULAR_WEIGHT>
941.216

> <EXACT_MASS>
940.544911275

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
144

> <JCHEM_AVERAGE_POLARIZABILITY>
109.44817771518174

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,3''R,5S,5'S,6'S,8'R,9'R,10'S,11'S,14'S,17'R,20'S,25'R,26'S,27'S,30'R,33'R,34'S,35'R,39'R,42'S)-3,3'',8',10'-tetrahydroxy-5-(hydroxymethyl)-25'-methoxy-5,5',5'',5'',9',11',26',34'-octamethyldispiro[oxolane-2,12'-[13,32]dioxa-[2,23]diazundecacyclo[22.19.0.0^{3,22}.0^{5,20}.0^{6,17}.0^{9,16}.0^{10,14}.0^{26,42}.0^{27,39}.0^{30,35}.0^{30,38}]tritetracontane-33',2''-oxolane]-1',3'(22'),15',23',37'-pentaen-29'-one

> <ALOGPS_LOGP>
5.22

> <JCHEM_LOGP>
3.67103063633333

> <ALOGPS_LOGS>
-5.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
13

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.051805014492558

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.569124954922657

> <JCHEM_PKA_STRONGEST_BASIC>
1.0445463817100464

> <JCHEM_POLAR_SURFACE_AREA>
190.14999999999998

> <JCHEM_REFRACTIVITY>
250.18430000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.62e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,3''R,5S,5'S,6'S,8'R,9'R,10'S,11'S,14'S,17'R,20'S,25'R,26'S,27'S,30'R,33'R,34'S,35'R,39'R,42'S)-3,3'',8',10'-tetrahydroxy-5-(hydroxymethyl)-25'-methoxy-5,5',5'',5'',9',11',26',34'-octamethyldispiro[oxolane-2,12'-[13,32]dioxa-[2,23]diazundecacyclo[22.19.0.0^{3,22}.0^{5,20}.0^{6,17}.0^{9,16}.0^{10,14}.0^{26,42}.0^{27,39}.0^{30,35}.0^{30,38}]tritetracontane-33',2''-oxolane]-1',3'(22'),15',23',37'-pentaen-29'-one

> <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      22.637   1.066   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      23.401  -0.270   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      22.625  -1.601   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.085  -1.594   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.321  -0.257   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.097   1.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      18.781  -0.251   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.005  -1.581   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.770  -2.918   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.310  -2.925   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      17.994  -4.249   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      16.454  -4.242   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.690  -2.905   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      16.465  -1.575   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      14.150  -2.899   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.374  -4.229   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.139  -5.566   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.679  -5.573   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.363  -6.896   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.823  -6.890   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.059  -5.553   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.834  -4.223   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.070  -2.886   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.747  -2.869   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.766  -1.542   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.754  -4.210   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.519  -5.546   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.483  -6.687   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.079  -6.054   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.247  -4.523   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.221  -3.375   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.703  -1.912   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.211  -1.598   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       9.236  -2.747   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.171  -2.066   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.550  -0.657   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.699   0.369   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.030  -0.407   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       4.812   1.628   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.317   1.779   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.395  -3.397   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       4.884  -4.139   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      12.610  -2.892   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      13.385  -1.562   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      14.161  -0.231   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      21.850  -2.931   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      23.390  -2.938   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      24.930  -2.944   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      25.705  -1.614   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      24.941  -0.277   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      25.976   0.863   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      27.381   0.231   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      27.213  -1.300   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      28.617  -1.932   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      29.653  -0.792   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      28.888   0.545   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      30.688   0.348   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      32.092  -0.285   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      31.925  -1.815   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      30.417  -2.129   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      29.785  -3.533   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      33.632  -0.275   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      34.410  -1.604   0.000  0.00  0.00           O+0
HETATM   64  C   UNK     0      32.882   1.038   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0      28.931  -3.440   0.000  0.00  0.00           C+0
HETATM   66  O   UNK     0      27.046  -2.831   0.000  0.00  0.00           O+0
HETATM   67  C   UNK     0      26.175  -3.081   0.000  0.00  0.00           C+0
HETATM   68  O   UNK     0      25.694  -4.281   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   50                                                  
CONECT    3    2    4   47                                                  
CONECT    4    3    5   10   46                                             
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    8                                                       
CONECT   15   13   16   44                                                  
CONECT   16   15   17   22   43                                             
CONECT   17   16   18   19                                                  
CONECT   18   17   12                                                       
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   16   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   30   34                                             
CONECT   27   26   21   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   26   31                                                  
CONECT   31   30   32   42                                                  
CONECT   32   31   33   35   38                                             
CONECT   33   32   34                                                       
CONECT   34   33   26                                                       
CONECT   35   32   36   41                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39   40                                             
CONECT   38   37   32                                                       
CONECT   39   37                                                            
CONECT   40   37                                                            
CONECT   41   35                                                            
CONECT   42   31                                                            
CONECT   43   16                                                            
CONECT   44   15   45                                                       
CONECT   45   44                                                            
CONECT   46    4                                                            
CONECT   47    3   48                                                       
CONECT   48   47   49   68                                                  
CONECT   49   48   50   53   67                                             
CONECT   50   49    2   51                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53   56                                                  
CONECT   53   52   49   54   66                                             
CONECT   54   53   55   65                                                  
CONECT   55   54   56   57   60                                             
CONECT   56   55   52                                                       
CONECT   57   55   58                                                       
CONECT   58   57   59   62   64                                             
CONECT   59   58   60                                                       
CONECT   60   59   55   61                                                  
CONECT   61   60                                                            
CONECT   62   58   63                                                       
CONECT   63   62                                                            
CONECT   64   58                                                            
CONECT   65   54                                                            
CONECT   66   53                                                            
CONECT   67   49                                                            
CONECT   68   48                                                            
MASTER        0    0    0    0    0    0    0    0   68    0  160    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₅H₇₆N₂O₁₁

Average Mass

941.2160 Da

Monoisotopic Mass

940.54491 Da

IUPAC Name

(2S,3R,3''R,5S,5'S,6'S,8'R,9'R,10'S,11'S,14'S,17'R,20'S,25'R,26'S,27'S,30'R,33'R,34'S,35'R,39'R,42'S)-3,3'',8',10'-tetrahydroxy-5-(hydroxymethyl)-25'-methoxy-5,5',5'',5'',9',11',26',34'-octamethyldispiro[oxolane-2,12'-[13,32]dioxa-[2,23]diazundecacyclo[22.19.0.0^{3,22}.0^{5,20}.0^{6,17}.0^{9,16}.0^{10,14}.0^{26,42}.0^{27,39}.0^{30,35}.0^{30,38}]tritetracontane-33',2''-oxolane]-1',3'(22'),15',23',37'-pentaen-29'-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@H]1C2=NC3=C(C[C@@]4(C)[C@@H](CC[C@@H]5[C@@H]4C[C@@H](O)[C@@]4(C)C5=C[C@@H]5O[C@]6(O[C@](C)(CO)C[C@H]6O)[C@@H](C)[C@]45O)C3)N=C2C[C@@H]2CC[C@@H]3[C@H](CC(=O)[C@]45CO[C@@]6(OC(C)(C)C[C@H]6O)[C@@H](C)[C@H]4CC=C35)[C@@]12C

InChI Identifier

InChI=1S/C55H76N2O11/c1-26-32-14-15-33-30-13-11-29-17-38-45(46(64-9)50(29,7)35(30)19-41(60)52(32,33)25-65-54(26)42(61)22-47(3,4)67-54)57-37-16-28-10-12-31-34(49(28,6)21-39(37)56-38)18-40(59)51(8)36(31)20-44-53(51,63)27(2)55(66-44)43(62)23-48(5,24-58)68-55/h15,20,26-32,34-35,40,42-44,46,58-59,61-63H,10-14,16-19,21-25H2,1-9H3/t26-,27-,28-,29-,30-,31+,32+,34-,35-,40+,42+,43+,44-,46-,48-,49-,50-,51+,52+,53+,54+,55-/m0/s1

InChI Key

HJTADJIVGZRTHF-FVNBPLPQSA-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
Cephalodiscus gilchristi	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

23-hydroxysteroid
12-hydroxysteroid
Hydroxysteroid
12-oxosteroid
Oxosteroid
17-hydroxysteroid
Phenazine
Ketal
Monosaccharide
Oxane
Pyrazine
Heteroaromatic compound
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Ketone
Secondary alcohol
Acetal
Polyol
Azacycle
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Primary alcohol
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
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	5.22	ALOGPS
logP	3.67	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	12.57	ChemAxon
pKa (Strongest Basic)	1.04	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	190.15 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	250.18 m³·mol⁻¹	ChemAxon
Polarizability	109.45 Å³	ChemAxon
Number of Rings	13	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00050036

Chemspider ID

8923732

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10748407

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Flessner T, Jautelat R, Scholz U, Winterfeldt E: Cephalostatin analogues--synthesis and biological activity. Fortschr Chem Org Naturst. 2004;87:1-80. doi: 10.1007/978-3-7091-0581-8_1. [PubMed:15079895 ]

Showing NP-Card for Cephalostatin 18 (NP0083039)

MOL for NP0083039 (Cephalostatin 18)

3D MOL for NP0083039 (Cephalostatin 18)

3D SDF for NP0083039 (Cephalostatin 18)

3D-SDF for NP0083039 (Cephalostatin 18)

PDB for NP0083039 (Cephalostatin 18)

3D PDB for NP0083039 (Cephalostatin 18)

SMILES for NP0083039 (Cephalostatin 18)

INCHI for NP0083039 (Cephalostatin 18)

Structure for NP0083039 (Cephalostatin 18)

3D Structure for NP0083039 (Cephalostatin 18)