NP-MRD: Showing NP-Card for n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid (NP0231985)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 13:03:47 UTC

Updated at

2022-09-06 13:03:47 UTC

NP-MRD ID

NP0231985

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid

Description

(S)-Banchromene belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. Based on a literature review very few articles have been published on (S)-Banchromene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
   -6.3691   -0.9135    2.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1484   -0.7859    1.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2735   -1.8400    1.4968 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9595    0.2781    0.9023 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8637    0.6520    0.0282 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0716   -0.0265   -1.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0865   -1.4153   -1.1871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5296    0.3189    0.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4471    0.7572   -0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7012    1.4617   -1.2919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0338    0.3813   -0.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3111   -0.3944    1.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6292   -0.7331    1.2820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6549   -0.3092    0.4272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2956    0.4749   -0.6664 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742    0.7987   -0.8641 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6462    1.5967   -1.9851 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3918    0.8804   -1.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6357    0.5399   -1.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0120   -0.2887   -0.1511 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9916    0.5088    0.7161 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7826   -1.5035   -0.6810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9599   -0.6431    0.6452 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2978   -1.7763    3.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5011    0.0330    2.9508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2850   -1.0330    1.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6530   -2.7353    1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9358    1.7391   -0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3764    0.2796   -2.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0966    0.2619   -1.7237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4491   -1.8266   -2.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4385   -0.8105    0.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3668    0.7342    1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4955   -0.7139    1.7132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9024   -1.3425    2.1334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2305    1.1506   -2.8186 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8161    2.6190   -1.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1650    1.5037   -2.4066 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4386    0.8877   -2.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5279    1.4553    1.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2015   -0.1095    1.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8934    0.7974    0.1410 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3124   -1.8405   -1.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8021   -1.1604   -0.8853 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8054   -2.2900    0.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 23  1  0
 23 20  1  0
 20 21  1  0
 20 22  1  0
 20 19  1  0
 19 18  2  0
 18 15  1  0
 15 16  2  0
 16 17  1  0
 16 11  1  0
 15 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  5 28  1  6
  6 29  1  0
  6 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
 12 34  1  0
 13 35  1  0
 21 40  1  0
 21 41  1  0
 21 42  1  0
 22 43  1  0
 22 44  1  0
 22 45  1  0
 19 39  1  0
 18 38  1  0
 17 36  1  0
 17 37  1  0
M  END


  Mrv1652309062215032D          

 23 24  0  0  1  0            999 V2000
   -4.2868   -3.3000    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
   -3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 O   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
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 N   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
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704   -3.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -4.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  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
 20 23  1  0  0  0  0
 14 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231985

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(O)=N[C@H](CO)CC(=O)C1=CC=C2OC(C)(C)C=CC2=C1N

> <INCHI_IDENTIFIER>
InChI=1S/C17H22N2O4/c1-10(21)19-11(9-20)8-14(22)12-4-5-15-13(16(12)18)6-7-17(2,3)23-15/h4-7,11,20H,8-9,18H2,1-3H3,(H,19,21)/t11-/m0/s1

> <INCHI_KEY>
JWWKBOBMBFAOAR-NSHDSACASA-N

> <FORMULA>
C17H22N2O4

> <MOLECULAR_WEIGHT>
318.373

> <EXACT_MASS>
318.157957196

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.958513959620625

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(2S)-4-(5-amino-2,2-dimethyl-2H-chromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid

> <JCHEM_LOGP>
1.5735894643333341

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.408806839407156

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.692660514052428

> <JCHEM_PKA_STRONGEST_BASIC>
3.0214551829531944

> <JCHEM_POLAR_SURFACE_AREA>
105.14

> <JCHEM_REFRACTIVITY>
89.54169999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-[(2S)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid

> <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      -8.002  -6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -6.668  -3.850   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      -5.335  -6.160   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.334  -3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       1.334  -3.850   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.851  -7.433   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.861  -9.147   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -8.470   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    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   11   17                                                  
CONECT   17   16                                                            
CONECT   18   15   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   14                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₂N₂O₄

Average Mass

318.3730 Da

Monoisotopic Mass

318.15796 Da

IUPAC Name

N-[(2S)-4-(5-amino-2,2-dimethyl-2H-chromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid

Traditional Name

N-[(2S)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

CC(O)=N[C@H](CO)CC(=O)C1=CC=C2OC(C)(C)C=CC2=C1N

InChI Identifier

InChI=1S/C17H22N2O4/c1-10(21)19-11(9-20)8-14(22)12-4-5-15-13(16(12)18)6-7-17(2,3)23-15/h4-7,11,20H,8-9,18H2,1-3H3,(H,19,21)/t11-/m0/s1

InChI Key

JWWKBOBMBFAOAR-NSHDSACASA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Butyrophenone
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Benzenoid
Acetamide
Vinylogous amide
Amino acid or derivatives
Carboxamide group
Secondary carboxylic acid amide
Ketone
Oxacycle
Carboxylic acid derivative
Ether
Alcohol
Organonitrogen compound
Organooxygen compound
Primary alcohol
Primary amine
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
Amine
Organic nitrogen 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	1.57	ChemAxon
pKa (Strongest Acidic)	5.69	ChemAxon
pKa (Strongest Basic)	3.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.14 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	89.54 m³·mol⁻¹	ChemAxon
Polarizability	33.96 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

78436384

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101878853

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)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid (NP0231985)

MOL for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

3D MOL for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

3D SDF for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

3D-SDF for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

PDB for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

3D PDB for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

SMILES for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

INCHI for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

Structure for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)

3D Structure for NP0231985 (n-[(2s)-4-(5-amino-2,2-dimethylchromen-6-yl)-1-hydroxy-4-oxobutan-2-yl]ethanimidic acid)