NP-MRD: Showing NP-Card for 7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one (NP0188058)

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Record Information

Version

2.0

Created at

2022-09-04 04:19:18 UTC

Updated at

2022-09-04 04:19:18 UTC

NP-MRD ID

NP0188058

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one

Description

7-Amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-5,6,7,8-tetrahydro-2H-1,3-oxazocin-8-one belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids. 7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one is found in Pseudobaeospora pyrifera. 7-Amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-5,6,7,8-tetrahydro-2H-1,3-oxazocin-8-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
    1.4671   -1.6905    1.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6310   -0.4953    0.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1714    0.6557    1.4631 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1425    1.4693    0.6766 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4630    0.9016   -0.6912 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1580    1.7907   -1.4784 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4230    1.3380   -1.8317 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200    0.4893   -1.4043 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9379    0.7754   -2.7233 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2916   -0.2170   -0.7212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0554   -0.6319   -1.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1008   -0.3276   -2.5464 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0699   -1.3529   -0.6998 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0651   -2.8488   -1.0109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3147   -0.8660   -1.3280 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6415   -0.8057   -0.8559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4462   -0.6251   -1.8327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3579   -0.8938    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2106    0.3802    1.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7865    0.9219    1.1576 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6035    2.0384    2.0378 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8870   -0.2069    1.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7692   -0.3589    2.7138 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1807   -1.0894    0.6853 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7365   -1.8160    2.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1096   -2.5398    0.6528 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6918    0.2308    2.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3454    1.2690    1.8782 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0552    1.6237    1.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6925    2.4911    0.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1051    0.0131   -0.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3712    0.3798   -2.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8725    2.0784   -2.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1074    1.2475   -0.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5861    1.7177   -2.9249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3272   -3.4503   -0.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7511   -3.0368   -1.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0411   -3.0781   -1.3963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1658   -0.5098   -2.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4202   -1.1007    0.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9744   -1.7343    1.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4060    0.2039    2.3236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9382    1.1079    0.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6540    1.2778    0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9989    2.7806    1.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5236    2.4938    2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 10  1  0
 10 11  1  0
 11 12  2  0
 13 11  1  6
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 22 24  1  0
 10  8  2  0
  8  9  1  0
  8  5  1  0
 24 13  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
  5 31  1  1
  4 29  1  0
  4 30  1  0
  3 27  1  0
  3 28  1  0
  1 25  1  0
  1 26  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 18 40  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  6
 21 45  1  0
 21 46  1  0
  9 35  1  0
M  END


  Mrv1533004261504292D          

 24 25  0  0  0  0            999 V2000
   -0.8456   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1311   -0.9959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1311   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8456   -2.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8456   -3.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1311   -3.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1311   -4.2959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834   -3.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834   -2.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2978   -1.8209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2978   -3.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0123   -3.0584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2978   -4.2959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5009   -4.0823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0947   -4.0823    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8092   -4.4948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4637   -3.9926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0227   -5.2917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6102   -6.0062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8133   -6.2197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7056   -7.0377    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0989   -5.8072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4443   -6.3095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8853   -5.0103    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 13 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188058

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CCC(=C)C(C(=O)C2(C)NC(=O)CCC(N)C(=O)O2)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H22N2O6/c1-8-4-6-10(23-3)13(20)12(8)14(21)16(2)18-11(19)7-5-9(17)15(22)24-16/h9-10,20H,1,4-7,17H2,2-3H3,(H,18,19)

> <INCHI_KEY>
GEWKQRPLHHMQHV-UHFFFAOYSA-N

> <FORMULA>
C16H22N2O6

> <MOLECULAR_WEIGHT>
338.36

> <EXACT_MASS>
338.147786436

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
32.95897561127172

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-amino-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-1,3-oxazocane-4,8-dione

> <ALOGPS_LOGP>
-0.80

> <JCHEM_LOGP>
-0.21009965133333344

> <ALOGPS_LOGS>
-1.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
10.393455052503235

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.108057160278221

> <JCHEM_PKA_STRONGEST_BASIC>
6.9758293129426745

> <JCHEM_POLAR_SURFACE_AREA>
127.95

> <JCHEM_REFRACTIVITY>
84.9152

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.25e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-amino-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-1,3-oxazocane-4,8-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      -1.578  -1.089   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.245  -1.859   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.245  -3.399   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.578  -4.169   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.578  -5.709   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.245  -6.479   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.245  -8.019   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.089  -5.709   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.089  -4.169   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.423  -3.399   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.423  -6.479   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.756  -5.709   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.423  -8.019   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.935  -7.620   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       3.910  -7.620   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.244  -8.390   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.466  -7.453   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.642  -9.878   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.872 -11.212   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.385 -11.610   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       3.184 -13.137   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       2.051 -10.840   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.829 -11.778   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.653  -9.353   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   11                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   24                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   13                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₂N₂O₆

Average Mass

338.3600 Da

Monoisotopic Mass

338.14779 Da

IUPAC Name

7-amino-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-1,3-oxazocane-4,8-dione

Traditional Name

7-amino-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-1,3-oxazocane-4,8-dione

CAS Registry Number

Not Available

SMILES

COC1CCC(=C)C(C(=O)C2(C)NC(=O)CCC(N)C(=O)O2)=C1O

InChI Identifier

InChI=1S/C16H22N2O6/c1-8-4-6-10(23-3)13(20)12(8)14(21)16(2)18-11(19)7-5-9(17)15(22)24-16/h9-10,20H,1,4-7,17H2,2-3H3,(H,18,19)

InChI Key

GEWKQRPLHHMQHV-UHFFFAOYSA-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
Pseudobaeospora pyrifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acid esters

Alternative Parents

Substituents

Alpha-amino acid ester
Alpha-acyloxy ketone
Vinylogous acid
Carboxamide group
Carboxylic acid ester
Ketone
Lactam
Lactone
Secondary carboxylic acid amide
Dialkyl ether
Enol
Ether
Oxacycle
Monocarboxylic acid or derivatives
Azacycle
Organoheterocyclic compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Amine
Organic nitrogen compound
Primary aliphatic amine
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Primary amine
Organopnictogen compound
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	-0.8	ALOGPS
logP	-0.21	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	9.11	ChemAxon
pKa (Strongest Basic)	6.98	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	127.95 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	84.92 m³·mol⁻¹	ChemAxon
Polarizability	32.96 Å³	ChemAxon
Number of Rings	2	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one (NP0188058)

MOL for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

3D MOL for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

3D SDF for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

3D-SDF for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

PDB for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

3D PDB for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

SMILES for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

INCHI for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

Structure for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)

3D Structure for NP0188058 (7-amino-4-hydroxy-2-(2-hydroxy-3-methoxy-6-methylidenecyclohex-1-ene-1-carbonyl)-2-methyl-6,7-dihydro-5h-1,3-oxazocin-8-one)