NP-MRD: Showing NP-Card for n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide (NP0233218)

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Record Information

Version

2.0

Created at

2022-09-06 14:44:25 UTC

Updated at

2022-09-06 14:44:25 UTC

NP-MRD ID

NP0233218

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide

Description

N-{1-[(2R,4R,5S,6S)-5-{[(2S,3R,4S,5R,6S)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxy-1,4-dihydropyrimidin-4-ylidene}-4-(methylamino)benzamide belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars. n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide is found in Streptomyces amakusaensis. Based on a literature review very few articles have been published on N-{1-[(2R,4R,5S,6S)-5-{[(2S,3R,4S,5R,6S)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxy-1,4-dihydropyrimidin-4-ylidene}-4-(methylamino)benzamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062216442D          

 39 42  0  0  1  0            999 V2000
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  6 38  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309062216442D          

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   -1.4289  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -15.2625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -14.8500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -12.3750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  7  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  1  0  0  0
 18 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 14 34  1  0  0  0  0
 13 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 10 37  1  0  0  0  0
  6 38  1  0  0  0  0
 38 39  2  0  0  0  0
  3 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0233218

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC1=CC=C(C=C1)C(=O)N=C1C=CN([C@H]2C[C@@H](O)[C@H](O[C@@H]3O[C@@H](C)[C@@H]([C@H](O)[C@H]3O)N(C)C)[C@H](C)O2)C(O)=N1

> <INCHI_IDENTIFIER>
InChI=1S/C26H37N5O8/c1-13-20(30(4)5)21(33)22(34)25(38-13)39-23-14(2)37-19(12-17(23)32)31-11-10-18(29-26(31)36)28-24(35)15-6-8-16(27-3)9-7-15/h6-11,13-14,17,19-23,25,27,32-34H,12H2,1-5H3,(H,28,29,35,36)/t13-,14-,17+,19+,20-,21-,22+,23+,25-/m0/s1

> <INCHI_KEY>
UFIWZSNSJFCLAC-YGVMSPMASA-N

> <FORMULA>
C26H37N5O8

> <MOLECULAR_WEIGHT>
547.609

> <EXACT_MASS>
547.264213171

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
58.517537152521356

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-{1-[(2R,4R,5S,6S)-5-{[(2S,3R,4S,5R,6S)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxy-1,4-dihydropyrimidin-4-ylidene}-4-(methylamino)benzamide

> <JCHEM_LOGP>
-2.0398247670592493

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.351675254845702

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.654569741244476

> <JCHEM_PKA_STRONGEST_BASIC>
8.229120546520413

> <JCHEM_POLAR_SURFACE_AREA>
168.91000000000003

> <JCHEM_REFRACTIVITY>
141.2771

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-{1-[(2R,4R,5S,6S)-5-{[(2S,3R,4S,5R,6S)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0     -12.003  -6.930   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0     -10.669  -7.700   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0     -12.003 -14.630   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      -9.336 -14.630   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.002 -18.480   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -9.336 -19.250   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -9.336 -20.790   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.669 -21.560   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.669 -23.100   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -12.003 -23.870   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -9.336 -23.870   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -9.336 -25.410   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -8.002 -26.180   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.668 -25.410   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -5.335 -26.180   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001 -25.410   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.335 -27.720   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      -4.001 -28.490   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      -2.667 -27.720   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.001 -30.030   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.668 -28.490   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.668 -30.030   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -8.002 -27.720   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -9.336 -28.490   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -8.002 -23.100   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.668 -23.870   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -8.002 -21.560   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0     -10.669 -18.480   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -12.003 -19.250   0.000  0.00  0.00           O+0
HETATM   37  N   UNK     0     -10.669 -16.940   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0     -12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   39                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   38                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   37                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   35                                                  
CONECT   14   13   15   34                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   32                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   20   31                                                  
CONECT   31   30                                                            
CONECT   32   18   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   14                                                       
CONECT   35   13   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   10                                                       
CONECT   38    6   39                                                       
CONECT   39   38    3                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₇N₅O₈

Average Mass

547.6090 Da

Monoisotopic Mass

547.26421 Da

IUPAC Name

N-{1-[(2R,4R,5S,6S)-5-{[(2S,3R,4S,5R,6S)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxy-1,4-dihydropyrimidin-4-ylidene}-4-(methylamino)benzamide

Traditional Name

N-{1-[(2R,4R,5S,6S)-5-{[(2S,3R,4S,5R,6S)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide

CAS Registry Number

Not Available

SMILES

CNC1=CC=C(C=C1)C(=O)N=C1C=CN([C@H]2C[C@@H](O)[C@H](O[C@@H]3O[C@@H](C)[C@@H]([C@H](O)[C@H]3O)N(C)C)[C@H](C)O2)C(O)=N1

InChI Identifier

InChI=1S/C26H37N5O8/c1-13-20(30(4)5)21(33)22(34)25(38-13)39-23-14(2)37-19(12-17(23)32)31-11-10-18(29-26(31)36)28-24(35)15-6-8-16(27-3)9-7-15/h6-11,13-14,17,19-23,25,27,32-34H,12H2,1-5H3,(H,28,29,35,36)/t13-,14-,17+,19+,20-,21-,22+,23+,25-/m0/s1

InChI Key

UFIWZSNSJFCLAC-YGVMSPMASA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Streptomyces aMAKUSAENSIS	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminoglycosides

Alternative Parents

Substituents

Aminoglycoside core
Aminobenzoic acid or derivatives
Benzoic acid or derivatives
Phenylalkylamine
Aniline or substituted anilines
Benzoyl
Secondary aliphatic/aromatic amine
Pyrimidone
Benzenoid
Pyrimidine
Oxane
Monosaccharide
Hydropyrimidine
Monocyclic benzene moiety
Heteroaromatic compound
Urea
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Amino acid or derivatives
1,2-aminoalcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Amine
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	-2	ChemAxon
pKa (Strongest Acidic)	5.65	ChemAxon
pKa (Strongest Basic)	8.23	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	168.91 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	141.28 m³·mol⁻¹	ChemAxon
Polarizability	58.52 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

163046387

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide (NP0233218)

MOL for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

3D MOL for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

3D SDF for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

3D-SDF for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

PDB for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

3D PDB for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

SMILES for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

INCHI for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

Structure for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)

3D Structure for NP0233218 (n-{1-[(2r,4r,5s,6s)-5-{[(2s,3r,4s,5r,6s)-5-(dimethylamino)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]-2-hydroxypyrimidin-4-ylidene}-4-(methylamino)benzamide)