NP-MRD: Showing NP-Card for (2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid (NP0183982)

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Record Information

Version

2.0

Created at

2022-09-03 22:59:49 UTC

Updated at

2022-09-03 22:59:50 UTC

NP-MRD ID

NP0183982

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid

Description

N-Coronafacoyl-L-serine belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. (2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid is found in Pseudomonas syringae. Based on a literature review very few articles have been published on N-Coronafacoyl-L-serine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
   -2.1643   -3.1148   -1.0506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3403   -2.7543    0.3864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0302   -1.3337    0.7140 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6220   -0.9882    0.3754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2445    0.2896    0.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0929    0.6572    0.2755 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5602    1.9323    0.4609 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9155   -0.1956   -0.1952 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2657   -0.0041   -0.5584 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2715   -0.4613    0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1413    0.1904    1.6805 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6440   -0.5940   -1.8543 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7826   -1.1985   -2.5177 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9219   -0.4934   -2.3474 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2661    1.1706    1.1268 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0547    2.6366    1.0521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5413    3.0570   -0.3343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5741    2.0280   -0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2483    2.0447   -1.6740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5974    1.0301    0.3917 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9038   -0.3585   -0.0449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4808   -2.3448   -1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7637   -4.0528   -1.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1107   -3.4037   -1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4151   -2.9303    0.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7510   -3.4118    1.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2319   -1.1761    1.7895 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1038   -1.6571   -0.0170 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2358    2.2244    1.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4263    1.1111   -0.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1923   -1.5490    0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3068   -0.2900    0.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5958   -0.3343    2.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1172   -0.0151   -3.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4681    0.8401    2.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8376    3.0916    1.7511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1160    3.0485    1.3561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9672    4.0736   -0.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270    2.9590   -1.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3867    1.3412    1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9663   -0.6451    0.1617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7645   -0.4194   -1.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 21  1  0
 21 20  1  0
 20 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 15  5  1  0
  5  4  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  1  0
 12 14  1  0
 12 13  2  0
  4  3  1  0
 18 20  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  1
 21 41  1  0
 21 42  1  0
 20 40  1  1
 15 35  1  1
 16 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
  4 28  1  0
  7 29  1  0
  9 30  1  6
 10 31  1  0
 10 32  1  0
 11 33  1  0
 14 34  1  0
M  END


  Mrv1652309042200592D          

 21 22  0  0  1  0            999 V2000
    4.0668    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.5396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.3646    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2089   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089   -2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  4  0  0  0
  6  8  2  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 18  1  1  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0183982

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1C[C@H]2[C@H](CCC2=O)C(=C1)C(O)=N[C@@H](CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H21NO5/c1-2-8-5-10-9(3-4-13(10)18)11(6-8)14(19)16-12(7-17)15(20)21/h6,8-10,12,17H,2-5,7H2,1H3,(H,16,19)(H,20,21)/t8-,9+,10+,12+/m1/s1

> <INCHI_KEY>
TUNPWIUIRCNHPM-WDCWCFNPSA-N

> <FORMULA>
C15H21NO5

> <MOLECULAR_WEIGHT>
295.335

> <EXACT_MASS>
295.14197278

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
30.283999295652666

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-({[(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid

> <JCHEM_LOGP>
1.3399375399999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
6.167492003418808

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9153730842723125

> <JCHEM_PKA_STRONGEST_BASIC>
0.889408716097347

> <JCHEM_POLAR_SURFACE_AREA>
107.19000000000003

> <JCHEM_REFRACTIVITY>
75.7975

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-({[(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic 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       7.591   5.923   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924  -0.237   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.258  -1.007   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       3.590  -1.007   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       3.590  -2.547   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.257  -3.317   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.257  -4.857   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.924  -3.317   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.924  -4.857   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       6.258  -2.547   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.650   5.553   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    5   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   15   21                                                  
CONECT   21   20    3                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₁NO₅

Average Mass

295.3350 Da

Monoisotopic Mass

295.14197 Da

IUPAC Name

(2S)-2-({[(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydro-1H-inden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid

Traditional Name

(2S)-2-({[(3aS,6R,7aS)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid

CAS Registry Number

Not Available

SMILES

CC[C@@H]1C[C@H]2[C@H](CCC2=O)C(=C1)C(O)=N[C@@H](CO)C(O)=O

InChI Identifier

InChI=1S/C15H21NO5/c1-2-8-5-10-9(3-4-13(10)18)11(6-8)14(19)16-12(7-17)15(20)21/h6,8-10,12,17H,2-5,7H2,1H3,(H,16,19)(H,20,21)/t8-,9+,10+,12+/m1/s1

InChI Key

TUNPWIUIRCNHPM-WDCWCFNPSA-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
Pseudomonas syringae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids

Alternative Parents

Substituents

N-acyl-alpha-amino acid
Serine or derivatives
Beta-hydroxy acid
Hydroxy acid
Ketone
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Alcohol
Organonitrogen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	1.34	ChemAxon
pKa (Strongest Acidic)	3.92	ChemAxon
pKa (Strongest Basic)	0.89	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	107.19 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	75.8 m³·mol⁻¹	ChemAxon
Polarizability	30.28 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

100929350

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid (NP0183982)

MOL for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

3D MOL for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

3D SDF for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

3D-SDF for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

PDB for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

3D PDB for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

SMILES for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

INCHI for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

Structure for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)

3D Structure for NP0183982 ((2s)-2-({[(3as,6r,7as)-6-ethyl-1-oxo-2,3,3a,6,7,7a-hexahydroinden-4-yl](hydroxy)methylidene}amino)-3-hydroxypropanoic acid)