NP-MRD: Showing NP-Card for n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid (NP0210046)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 07:42:04 UTC

Updated at

2022-09-05 07:42:05 UTC

NP-MRD ID

NP0210046

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid

Description

(+)-Brevisamide belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond. n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid is found in Karenia brevis. Based on a literature review very few articles have been published on (+)-Brevisamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 52  0  0  0  0  0  0  0  0999 V2000
    7.2459   -0.7208    0.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9031   -1.0937    0.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2229   -2.1260    0.9348 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4038   -0.4560   -0.6736 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1267   -0.7198   -1.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9870   -0.4575   -0.2648 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7714   -0.7315   -0.8901 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7626   -0.0852   -0.1829 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5488   -0.8002   -0.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5050   -0.0644    0.6897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8451   -0.7026    0.7203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9635   -0.0915    0.3550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7582    1.3133   -0.0967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2830   -0.7396    0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4919   -2.1402    0.8337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3625   -0.0815    0.0187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7020   -0.6392    0.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9261   -1.8070    0.3866 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7303    1.3374   -0.6238 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0883    1.4813   -1.9850 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1421    1.8726   -0.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0978    0.9869    0.1578 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9521    1.1447    1.5441 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.6610    0.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7433    0.0110    0.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1926   -0.3358    1.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1978   -2.2417    1.9433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9870   -0.0512   -2.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1206   -1.7824   -1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1210   -1.1713    0.5570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0965   -0.1188    0.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9746   -0.9291   -1.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3769   -1.8319    0.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6004    1.0021    0.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0426   -0.0573    1.7204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8745   -1.7118    1.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3707    1.9518    0.7268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6261    1.8225   -0.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0311    1.2769   -0.9665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9141   -2.7581    0.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1341   -2.1122    1.7443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5276   -2.6232    1.0841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2918    0.9474   -0.3177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5246    0.0035   -0.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1569    1.9601    0.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8853    0.9592   -1.9846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7447    1.1743   -2.8037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1683    2.5766   -2.0834 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1937    2.8863   -0.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5074    1.8566   -1.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1255    1.3863   -0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2488    0.3528    2.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 22  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  0
  2  1  1  0
  2  3  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
  8 19  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 19 45  1  1
 21 49  1  0
 21 50  1  0
 22 51  1  6
 23 52  1  0
  6 30  1  1
  5 28  1  0
  5 29  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  8 31  1  1
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
M  END


  Mrv1652309052209422D          

 23 23  0  0  1  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   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
  2  4  2  0  0  0  0
  4  5  1  4  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  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
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0210046

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H](O)[C@H](CN=C(C)O)O[C@@H]1CC\C=C(/C)\C(\C)=C\C=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H29NO4/c1-12(13(2)8-9-20)6-5-7-17-14(3)10-16(22)18(23-17)11-19-15(4)21/h6,8-9,14,16-18,22H,5,7,10-11H2,1-4H3,(H,19,21)/b12-6+,13-8+/t14-,16-,17-,18+/m1/s1

> <INCHI_KEY>
SFLJQCLAPBTFNR-CSVGCSNTSA-N

> <FORMULA>
C18H29NO4

> <MOLECULAR_WEIGHT>
323.433

> <EXACT_MASS>
323.209658418

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.09321006416865

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-{[(2S,3R,5R,6R)-6-[(3E,5E)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid

> <JCHEM_LOGP>
1.9719258809999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.166038082153019

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.368677552782037

> <JCHEM_PKA_STRONGEST_BASIC>
4.141145246782673

> <JCHEM_POLAR_SURFACE_AREA>
79.12

> <JCHEM_REFRACTIVITY>
92.03479999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-{[(2S,3R,5R,6R)-6-[(3E,5E)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       0.000   4.620   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19    8   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    6   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₉NO₄

Average Mass

323.4330 Da

Monoisotopic Mass

323.20966 Da

IUPAC Name

N-{[(2S,3R,5R,6R)-6-[(3E,5E)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid

Traditional Name

N-{[(2S,3R,5R,6R)-6-[(3E,5E)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H](O)[C@H](CN=C(C)O)O[C@@H]1CC\C=C(/C)\C(\C)=C\C=O

InChI Identifier

InChI=1S/C18H29NO4/c1-12(13(2)8-9-20)6-5-7-17-14(3)10-16(22)18(23-17)11-19-15(4)21/h6,8-9,14,16-18,22H,5,7,10-11H2,1-4H3,(H,19,21)/b12-6+,13-8+/t14-,16-,17-,18+/m1/s1

InChI Key

SFLJQCLAPBTFNR-CSVGCSNTSA-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
Karenia brevis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

C-glycosyl compound
Oxane
Alpha,beta-unsaturated aldehyde
Acetamide
Enal
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Dialkyl ether
Ether
Alcohol
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organopnictogen compound
Organic nitrogen compound
Aldehyde
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	1.97	ChemAxon
pKa (Strongest Acidic)	6.37	ChemAxon
pKa (Strongest Basic)	4.14	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.12 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	92.03 m³·mol⁻¹	ChemAxon
Polarizability	37.09 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

75566223

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53392810

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid (NP0210046)

MOL for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

3D MOL for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

3D SDF for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

3D-SDF for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

PDB for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

3D PDB for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

SMILES for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

INCHI for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

Structure for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)

3D Structure for NP0210046 (n-{[(2s,3r,5r,6r)-6-[(3e,5e)-4,5-dimethyl-7-oxohepta-3,5-dien-1-yl]-3-hydroxy-5-methyloxan-2-yl]methyl}ethanimidic acid)