NP-MRD: Showing NP-Card for n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid (NP0194225)

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Record Information

Version

2.0

Created at

2022-09-04 11:51:11 UTC

Updated at

2022-09-04 11:51:11 UTC

NP-MRD ID

NP0194225

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid

Description

Colchicoside belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid is found in Colchicum autumnale and Gloriosa superba. n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid was first documented in 2016 (PMID: 27765363). Based on a literature review a small amount of articles have been published on Colchicoside (PMID: 32353376) (PMID: 28211687) (PMID: 27169190) (PMID: 27093343).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042213512D          

 39 42  0  0  1  0            999 V2000
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    4.7863   -1.2943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0611   -2.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 18 39  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309042213512D          

 39 42  0  0  1  0            999 V2000
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    1.2984    1.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5096    2.0518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8827    2.5882    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1048    2.3134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5221    2.8497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0463    1.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2648    2.3839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9953    2.0006    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  1  0  0  0  0
  6  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
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  6  0  0  0
  4 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 23 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  1  0  0  0
 34 35  2  0  0  0  0
 35 36  1  4  0  0  0
 35 37  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  1  0  0  0  0
 18 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194225

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC2OC(CO)[C@@H](O)[C@H](O)[C@H]2O)C=C2CC[C@H](N=C(C)O)C3=CC(=O)C(OC)=CC=C3C2=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C27H33NO11/c1-12(30)28-16-7-5-13-9-19(38-27-24(34)23(33)22(32)20(11-29)39-27)25(36-3)26(37-4)21(13)14-6-8-18(35-2)17(31)10-15(14)16/h6,8-10,16,20,22-24,27,29,32-34H,5,7,11H2,1-4H3,(H,28,30)/t16-,20?,22+,23-,24+,27?/m0/s1

> <INCHI_KEY>
UXAFRQPVHYZDED-ABYJKEICSA-N

> <FORMULA>
C27H33NO11

> <MOLECULAR_WEIGHT>
547.557

> <EXACT_MASS>
547.205360887

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
55.61204602607798

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(10S)-3,4,14-trimethoxy-13-oxo-5-{[(3R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0^{2,7}]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid

> <JCHEM_LOGP>
-0.13236945199999967

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.20001293670043

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.557629855790773

> <JCHEM_PKA_STRONGEST_BASIC>
2.9525116994308394

> <JCHEM_POLAR_SURFACE_AREA>
176.73

> <JCHEM_REFRACTIVITY>
139.55939999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[(10S)-3,4,14-trimethoxy-13-oxo-5-{[(3R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0^{2,7}]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       6.419  -3.304   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.420  -2.134   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.908  -0.682   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.909   0.488   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.423   0.206   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.936  -1.246   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.934  -2.416   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.447  -3.868   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.446  -5.038   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.959  -6.490   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.961  -4.150   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.474  -5.602   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      11.962  -2.980   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      13.476  -3.262   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      11.450  -1.528   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      12.451  -0.358   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.396   1.940   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.882   2.222   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.881   1.052   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.394  -0.400   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.393  -1.570   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.905  -3.022   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.342   1.105   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.947  -0.384   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.538  -1.004   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.174  -0.288   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.062  -1.206   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.885  -2.736   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.117   1.224   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.605   1.619   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.885   2.395   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.424   2.341   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.818   3.830   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0       1.648   4.831   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0       0.196   4.318   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.975   5.319   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.086   2.804   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.228   4.450   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.591   3.734   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    6   16                                                  
CONECT   16   15                                                            
CONECT   17    4   18                                                       
CONECT   18   17   19   39                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19    3   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19   24   32                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   23   33                                                  
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   33   39                                                       
CONECT   39   38   18                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₃NO₁₁

Average Mass

547.5570 Da

Monoisotopic Mass

547.20536 Da

IUPAC Name

N-[(10S)-3,4,14-trimethoxy-13-oxo-5-{[(3R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0^{2,7}]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid

Traditional Name

N-[(10S)-3,4,14-trimethoxy-13-oxo-5-{[(3R,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0^{2,7}]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

COC1=C(OC2OC(CO)[C@@H](O)[C@H](O)[C@H]2O)C=C2CC[C@H](N=C(C)O)C3=CC(=O)C(OC)=CC=C3C2=C1OC

InChI Identifier

InChI=1S/C27H33NO11/c1-12(30)28-16-7-5-13-9-19(38-27-24(34)23(33)22(32)20(11-29)39-27)25(36-3)26(37-4)21(13)14-6-8-18(35-2)17(31)10-15(14)16/h6,8-10,16,20,22-24,27,29,32-34H,5,7,11H2,1-4H3,(H,28,30)/t16-,20?,22+,23-,24+,27?/m0/s1

InChI Key

UXAFRQPVHYZDED-ABYJKEICSA-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
Colchicum autumnale	LOTUS Database	35616633
Gloriosa superba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
O-glycosyl compound
Anisole
Tropone
Alkyl aryl ether
Fatty acyl
Benzenoid
Oxane
Monosaccharide
Acetamide
Secondary alcohol
Secondary carboxylic acid amide
Cyclic ketone
Carboxamide group
Acetal
Carboxylic acid derivative
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Primary alcohol
Organonitrogen compound
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	-0.13	ChemAxon
pKa (Strongest Acidic)	5.56	ChemAxon
pKa (Strongest Basic)	2.95	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	176.73 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	139.56 m³·mol⁻¹	ChemAxon
Polarizability	55.61 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

44205568

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24721008

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Azadbakht M, Davoodi A, Hosseinimehr SJ, Keighobadi M, Fakhar M, Valadan R, Faridnia R, Emami S, Azadbakht M, Bakhtiyari A: Tropolone alkaloids from Colchicum kurdicum (Bornm.) Stef. (Colchicaceae) as the potent novel antileishmanial compounds; purification, structure elucidation, antileishmanial activities and molecular docking studies. Exp Parasitol. 2020 Jun;213:107902. doi: 10.1016/j.exppara.2020.107902. Epub 2020 Apr 27. [PubMed:32353376 ]
Zarev Y, Foubert K, Ionkova I, Apers S, Pieters L: Isolation and Structure Elucidation of Glucosylated Colchicinoids from the Seeds of Gloriosa superba by LC-DAD-SPE-NMR. J Nat Prod. 2017 Apr 28;80(4):1187-1191. doi: 10.1021/acs.jnatprod.6b01024. Epub 2017 Feb 17. [PubMed:28211687 ]
Capistrano I R, Vangestel C, Vanpachtenbeke H, Fransen E, Staelens S, Apers S, Pieters L: Coadministration of a Gloriosa superba extract improves the in vivo antitumoural activity of gemcitabine in a murine pancreatic tumour model. Phytomedicine. 2016 Nov 15;23(12):1434-1440. doi: 10.1016/j.phymed.2016.07.012. Epub 2016 Aug 1. [PubMed:27765363 ]
Gumustas M, Polat DC, Kilic CS, Akalin K, Ozkan SA, Coskun M: Comparison of Seeds of Colchicum speciosum and Gloriosa superba in respect to Colchicine and Colchicoside Contents by RP-LC. Nat Prod Commun. 2016 Mar;11(3):397-400. [PubMed:27169190 ]
Capistrano R, Vangestel C, Wouters A, Dockx Y, Pauwels P, Stroobants S, Apers S, Lardon F, Pieters L, Staelens S: Efficacy Screening of Gloriosa Superba Extracts in a Murine Pancreatic Cancer Model Using (18)F-FDG PET/CT for Monitoring Treatment Response. Cancer Biother Radiopharm. 2016 Apr;31(3):99-109. doi: 10.1089/cbr.2015.1954. [PubMed:27093343 ]
LOTUS database [Link]

Showing NP-Card for n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid (NP0194225)

MOL for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

3D MOL for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

3D SDF for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

3D-SDF for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

PDB for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

3D PDB for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

SMILES for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

INCHI for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

Structure for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)

3D Structure for NP0194225 (n-[(10s)-3,4,14-trimethoxy-13-oxo-5-{[(3r,4s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricyclo[9.5.0.0²,⁷]hexadeca-1(16),2,4,6,11,14-hexaen-10-yl]ethanimidic acid)