NP-MRD: Showing NP-Card for (3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol (NP0300453)

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Record Information

Version

1.0

Created at

2022-09-10 12:51:25 UTC

Updated at

2022-09-10 12:51:25 UTC

NP-MRD ID

NP0300453

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol

Description

Lepistamide C belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. (3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol is found in Lepista sordida. It was first documented in 2022 (PMID: 36116040). Based on a literature review a significant number of articles have been published on Lepistamide C (PMID: 36116039) (PMID: 36116037) (PMID: 36116005) (PMID: 36115991).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
    1.1826    3.1042   -0.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8020    2.0402    0.3120 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9610    0.8993    0.2883 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5769   -0.2278    1.0738 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7882   -0.7834    0.4833 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6953   -1.8358   -0.4102 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8224   -2.4029   -1.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0550   -1.8783   -0.6688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299   -0.8274    0.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0196   -0.2629    0.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7208    0.6163   -1.0807 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4368    0.3849   -1.5396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6685    0.1046   -2.8981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6132    0.3991   -0.6542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0226   -1.0431   -0.4605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3031   -1.1865    0.3188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5905   -2.6705    0.4361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2306   -0.6020    1.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6375    1.0808   -1.3640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2812    2.4134   -1.5465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4149    1.0899    0.5722 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2605    1.3387    1.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0995    2.0169    2.2419 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9535    2.8502   -1.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8639    3.9722   -0.2417 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2727    3.3746    0.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8061   -1.0101    1.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8331    0.1780    2.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7491   -2.2792   -0.7013 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7619   -3.2206   -1.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9531   -2.2956   -1.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1173   -0.4312    0.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1291    0.5703    1.5176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5189    0.4632   -3.3074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2174   -1.5705    0.0600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1993   -1.4965   -1.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693   -0.7331   -0.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5867   -2.8590    0.8869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8195   -3.1014    1.1024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5109   -3.0880   -0.5871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2607   -0.7330    2.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5428    0.4629    1.7345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9821   -1.1513    2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1323    2.9196   -0.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0862    2.9397   -2.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3500    2.5409   -2.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7415    1.9303    2.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 14 19  1  6
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 14 21  1  0
 21 22  2  0
 22 23  1  0
 22  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  3  2  1  6
  2  1  1  0
  3 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 10  5  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 15 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
 17 39  1  0
 17 40  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 23 47  1  0
  4 27  1  0
  4 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 13 34  1  0
M  END


  Mrv1652309102214512D          

 23 24  0  0  1  0            999 V2000
    3.0539   -1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2414   -0.9683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -1.6002    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1808   -0.9683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4630   -0.1930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9327    0.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2148    1.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0273    1.3575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5576    0.7255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256   -2.0127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256   -2.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -3.2502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -3.2502    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2414   -3.8822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -4.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4895   -5.2895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -4.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808   -3.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3683   -3.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9966   -2.8377    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9966   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2822   -1.6002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  3 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  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 14 19  1  6  0  0  0
 19 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  2  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300453

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@]1(CC(C)C)N=C(O)[C@](CC2=CC=CC=C2)(OC)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C17H24N2O4/c1-12(2)10-16(22-3)14(20)19-17(23-4,15(21)18-16)11-13-8-6-5-7-9-13/h5-9,12H,10-11H2,1-4H3,(H,18,21)(H,19,20)/t16-,17-/m0/s1

> <INCHI_KEY>
BMACKMSINBGRRE-IRXDYDNUSA-N

> <FORMULA>
C17H24N2O4

> <MOLECULAR_WEIGHT>
320.389

> <EXACT_MASS>
320.173607261

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.121435081587954

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,6S)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)-3,6-dihydropyrazine-2,5-diol

> <JCHEM_LOGP>
4.230467210666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
2.6398241724632108

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.6412442778135476

> <JCHEM_PKA_STRONGEST_BASIC>
-2.579171235109732

> <JCHEM_POLAR_SURFACE_AREA>
83.64000000000001

> <JCHEM_REFRACTIVITY>
86.73880000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       5.701  -2.075   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.184  -1.807   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.194  -2.987   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.204  -1.807   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.731  -0.360   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.741   0.819   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.268   2.267   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.784   2.534   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.774   1.354   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.247  -0.093   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       4.528  -3.757   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       4.528  -5.297   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.861  -6.067   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.194  -6.067   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.184  -7.247   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.657  -8.694   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.647  -9.874   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.141  -8.961   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.204  -7.247   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.688  -6.979   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       1.860  -5.297   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       1.860  -3.757   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.527  -2.987   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   11   22                                             
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5                                                       
CONECT   11    3   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19   21                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20                                                       
CONECT   20   19                                                            
CONECT   21   14   22                                                       
CONECT   22   21    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₄N₂O₄

Average Mass

320.3890 Da

Monoisotopic Mass

320.17361 Da

IUPAC Name

(3S,6S)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)-3,6-dihydropyrazine-2,5-diol

Traditional Name

(3S,6S)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol

CAS Registry Number

Not Available

SMILES

CO[C@]1(CC(C)C)N=C(O)[C@](CC2=CC=CC=C2)(OC)N=C1O

InChI Identifier

InChI=1S/C17H24N2O4/c1-12(2)10-16(22-3)14(20)19-17(23-4,15(21)18-16)11-13-8-6-5-7-9-13/h5-9,12H,10-11H2,1-4H3,(H,18,21)(H,19,20)/t16-,17-/m0/s1

InChI Key

BMACKMSINBGRRE-IRXDYDNUSA-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
Lepista sordida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

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 acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Dioxopiperazine
2,5-dioxopiperazine
Monocyclic benzene moiety
1,4-diazinane
Piperazine
Benzenoid
Secondary carboxylic acid amide
Lactam
Carboxamide group
Organoheterocyclic compound
Azacycle
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	4.23	ChemAxon
pKa (Strongest Acidic)	1.64	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.64 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	86.74 m³·mol⁻¹	ChemAxon
Polarizability	34.12 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

78440863

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54597488

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ranta-Aho J, Olive M, Vandroux M, Roticiani G, Dominguez C, Johari M, Torella A, Bohm J, Turon J, Nigro V, Hackman P, Laporte J, Udd B, Savarese M: Mutation update for the ACTN2 gene. Hum Mutat. 2022 Sep 18. doi: 10.1002/humu.24470. [PubMed:36116040 ]
Treimer E, Kalayci T, Schumann S, Suer I, Greco S, Schanze D, Schmeisser MJ, Kuhl SJ, Zenker M: Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome. Hum Mutat. 2022 Sep 18. doi: 10.1002/humu.24472. [PubMed:36116039 ]
Savage SA, Jones K, Teshome K, Lori A, McReynolds LJ, Niewisch MR: Next-generation sequencing errors due to genetic variation in WRAP53 encoding TCAB1 on chromosome 17. Hum Mutat. 2022 Sep 18. doi: 10.1002/humu.24469. [PubMed:36116037 ]
Alsheikh S, Alghamdi R, Alqatari A, Alfareed A, AlSaleh M: Combined Factor V and VIII Deficiency with LMAN1 Mutation: A Report of 3 Saudi Siblings. Am J Case Rep. 2022 Sep 18;23:e937312. doi: 10.12659/AJCR.937312. [PubMed:36116005 ]
Salman M, Verma A, Chaurasia S, Prasad D, Kannabiran C, Singh V, Ramappa M: Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy. Orphanet J Rare Dis. 2022 Sep 17;17(1):361. doi: 10.1186/s13023-022-02521-4. [PubMed:36115991 ]
LOTUS database [Link]

Showing NP-Card for (3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol (NP0300453)

MOL for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

3D MOL for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

3D SDF for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

3D-SDF for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

PDB for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

3D PDB for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

SMILES for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

INCHI for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

Structure for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)

3D Structure for NP0300453 ((3s,6s)-3-benzyl-3,6-dimethoxy-6-(2-methylpropyl)pyrazine-2,5-diol)