NP-MRD: Showing NP-Card for 33-Demethoxy-myxovirescin A1 (NP0061983)

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Record Information

Version

2.0

Created at

2022-04-28 06:40:31 UTC

Updated at

2022-04-28 06:40:31 UTC

NP-MRD ID

NP0061983

Secondary Accession Numbers

None

Natural Product Identification

Common Name

33-Demethoxy-myxovirescin A1

Description

(2R,6R,8R,9R,14Z,16R,25S,27S)-16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. 33-Demethoxy-myxovirescin A1 is found in Myxococcus flavescens AJ12298. Based on a literature review very few articles have been published on (2R,6R,8R,9R,14Z,16R,25S,27S)-16-ethyl-3,6,8,9-tetrahydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-3,12,14-triene-20,28-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282208402D          

 42 42  0  0  1  0            999 V2000
    4.2868    3.4666    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


  Mrv1652304282208402D          

 42 42  0  0  1  0            999 V2000
    4.2868    3.4666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7567    4.1448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5789    4.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9312    3.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4614    2.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6392    2.7207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8138    1.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3440    1.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6963    0.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2265   -0.1954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5789   -0.9413    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1090   -1.6195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4614   -2.3654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9916   -3.0436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1694   -2.9758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3440   -3.7895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8741   -4.4677    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0519   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5821   -5.0780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6995   -3.6539    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773   -3.5861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5250   -2.8401    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9948   -2.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6424   -1.4160    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1122   -0.7379    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7599    0.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2297    0.6862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    1.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3472    2.1103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948    2.8563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4646    3.5344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0551    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9345   -0.8057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8202   -1.3482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7027   -2.7723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2265   -5.2136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7567   -5.8918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1090   -6.6377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2836   -2.4332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4011   -1.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9345    4.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1122    4.2804    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  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 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
 18 20  1  0  0  0  0
 20 21  1  0  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
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
  1 31  1  0  0  0  0
 28 32  1  0  0  0  0
 25 33  1  1  0  0  0
 24 34  1  1  0  0  0
 22 35  1  6  0  0  0
 17 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 13 39  1  6  0  0  0
 11 40  1  6  0  0  0
  1 41  1  1  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0061983

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC[C@H]1OC(=O)[C@@H](C)C[C@@H](C)CCCCC(=O)CCC[C@@H](CC)\C=C/C=C(C)/CC[C@@H](O)[C@H](O)C[C@@H](O)CNC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H59NO7/c1-6-12-32-33(40)35-23-29(37)22-31(39)30(38)20-19-24(3)14-10-15-27(7-2)16-11-18-28(36)17-9-8-13-25(4)21-26(5)34(41)42-32/h10,14-15,25-27,29-32,37-39H,6-9,11-13,16-23H2,1-5H3,(H,35,40)/b15-10-,24-14+/t25-,26-,27-,29+,30+,31+,32+/m0/s1

> <INCHI_KEY>
QTLCLULKZUFQLC-XSIQLTHFSA-N

> <FORMULA>
C34H59NO7

> <MOLECULAR_WEIGHT>
593.846

> <EXACT_MASS>
593.429153244

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
70.15259657156743

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,6R,8R,9R,12E,14Z,16R,25S,27S)-16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

> <ALOGPS_LOGP>
4.80

> <JCHEM_LOGP>
5.764070290333332

> <ALOGPS_LOGS>
-5.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.388447410777232

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.714749149673278

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8906200126869432

> <JCHEM_POLAR_SURFACE_AREA>
133.16

> <JCHEM_REFRACTIVITY>
168.52870000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.52e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,6R,8R,9R,12E,14Z,16R,25S,27S)-16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

> <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       8.002   6.471   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.879   7.737   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.414   7.610   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.072   6.218   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.195   4.952   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.660   5.079   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.852   3.560   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.975   2.294   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.633   0.901   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.756  -0.365   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.414  -1.757   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.537  -3.023   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.195  -4.415   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.318  -5.681   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.783  -5.555   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       9.975  -7.074   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.098  -8.340   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.564  -8.213   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.687  -9.479   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0       6.906  -6.821   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       5.371  -6.694   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.713  -5.302   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.590  -4.036   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.932  -2.643   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.810  -1.377   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.152   0.015   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.029   1.281   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.371   2.673   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.248   3.939   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.590   5.332   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.467   6.598   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.836   2.800   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.344  -1.504   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       3.398  -2.517   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       3.178  -5.175   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       9.756  -9.732   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.879 -10.998   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.537 -12.390   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.729  -4.542   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.949  -1.884   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.344   7.863   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.810   7.990   0.000  0.00  0.00           C+0
CONECT    1    2   31   41                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   40                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   39                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   36                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   34                                                  
CONECT   25   24   26   33                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30    1                                                       
CONECT   32   28                                                            
CONECT   33   25                                                            
CONECT   34   24                                                            
CONECT   35   22                                                            
CONECT   36   17   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37                                                            
CONECT   39   13                                                            
CONECT   40   11                                                            
CONECT   41    1   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₅₉NO₇

Average Mass

593.8460 Da

Monoisotopic Mass

593.42915 Da

IUPAC Name

(2R,6R,8R,9R,12E,14Z,16R,25S,27S)-16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

Traditional Name

(2R,6R,8R,9R,12E,14Z,16R,25S,27S)-16-ethyl-6,8,9-trihydroxy-12,25,27-trimethyl-2-propyl-1-oxa-4-azacyclooctacosa-12,14-diene-3,20,28-trione

CAS Registry Number

Not Available

SMILES

CCC[C@H]1OC(=O)[C@@H](C)C[C@@H](C)CCCCC(=O)CCC[C@@H](CC)\C=C/C=C(C)/CC[C@@H](O)[C@H](O)C[C@@H](O)CNC1=O

InChI Identifier

InChI=1S/C34H59NO7/c1-6-12-32-33(40)35-23-29(37)22-31(39)30(38)20-19-24(3)14-10-15-27(7-2)16-11-18-28(36)17-9-8-13-25(4)21-26(5)34(41)42-32/h10,14-15,25-27,29-32,37-39H,6-9,11-13,16-23H2,1-5H3,(H,35,40)/b15-10-,24-14+/t25-,26-,27-,29+,30+,31+,32+/m0/s1

InChI Key

QTLCLULKZUFQLC-XSIQLTHFSA-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
Myxococcus flavescens AJ12298	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Cyclic carboximidic acid
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	4.8	ALOGPS
logP	5.76	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	13.71	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.16 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	168.53 m³·mol⁻¹	ChemAxon
Polarizability	70.15 Å³	ChemAxon
Number of Rings	1	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

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

162946446

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 33-Demethoxy-myxovirescin A1 (NP0061983)

MOL for NP0061983 (33-Demethoxy-myxovirescin A1)

3D MOL for NP0061983 (33-Demethoxy-myxovirescin A1)

3D SDF for NP0061983 (33-Demethoxy-myxovirescin A1)

3D-SDF for NP0061983 (33-Demethoxy-myxovirescin A1)

PDB for NP0061983 (33-Demethoxy-myxovirescin A1)

3D PDB for NP0061983 (33-Demethoxy-myxovirescin A1)

SMILES for NP0061983 (33-Demethoxy-myxovirescin A1)

INCHI for NP0061983 (33-Demethoxy-myxovirescin A1)

Structure for NP0061983 (33-Demethoxy-myxovirescin A1)

3D Structure for NP0061983 (33-Demethoxy-myxovirescin A1)