NP-MRD: Showing NP-Card for (2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid (NP0240616)

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Record Information

Version

2.0

Created at

2022-09-07 00:29:08 UTC

Updated at

2022-09-07 00:29:09 UTC

NP-MRD ID

NP0240616

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid

Description

[1-O-[(S)-2-Amino-3-sulfopropyl]-5-deoxy-beta-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. (2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid is found in Sargassum lacerifolium and Sphaerotrichia divaricata. Based on a literature review very few articles have been published on [1-O-[(S)-2-Amino-3-sulfopropyl]-5-deoxy-beta-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 43  0  0  0  0  0  0  0  0999 V2000
   -5.2864    2.1436   -0.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1646    0.9259    0.4172 As  0  0  0  0  0  5  0  0  0  0  0  0
   -4.8589   -0.8921    0.2716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3362    1.3951    2.0048 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3058    1.0965   -0.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6506   -0.1975   -0.4728 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3572    0.0522   -0.7889 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5055   -0.4967    0.1453 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1713    0.5259    0.7241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5143    0.6352    0.6335 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1158    0.8191   -0.7144 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8298   -0.3250   -1.5436 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5807    1.1407   -0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6258   -0.0487   -0.0028 S   0  0  0  0  0  6  0  0  0  0  0  0
    7.0444    0.4731   -0.0729 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5350   -1.3473   -0.7762 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2453   -0.2584    1.6074 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3235   -1.2338    1.1723 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1769   -2.5097    1.4078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7006   -1.2350    0.6130 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9629   -2.5150    0.1108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2992    2.1940   -0.1966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3833    1.8188   -1.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8672    3.1800   -0.5928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7835   -1.4539    1.2243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3939   -1.4262   -0.5810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9687   -0.8046    0.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6821    1.5329    0.7492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2178    1.7826   -0.9533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1567   -0.6408   -1.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0814   -1.2630   -0.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0409   -0.2059    1.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8053    1.5434    1.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6461    1.7528   -1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9858   -0.1430   -2.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2931   -1.1963   -1.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6742    2.1473   -0.2356 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.3260   -1.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4863   -1.1831    1.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2743   -0.6900    2.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3654   -3.0033    0.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4346   -0.9697    1.3856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1844   -2.4460   -0.8504 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
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 17  1  0
 14 15  2  0
 14 16  2  0
  8 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  6
  8 31  1  6
 10 32  1  0
 10 33  1  0
 11 34  1  6
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 17 39  1  0
 18 40  1  1
 19 41  1  0
 20 42  1  1
 21 43  1  0
M  END


  Mrv1652309072202292D          

 21 21  0  0  1  0            999 V2000
   -0.8612    2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 As  0  0  0  0  0  0  0  0  0  0  0  0
   -0.5592    1.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2658    3.0663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1296   -1.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6145   -2.2438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4350   -2.1576    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790   -2.9975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639   -3.6649    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.2488   -4.3324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0965   -4.1498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4313   -3.1800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    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
  2  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  2  0  0  0  0
 14 17  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0240616

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[As](C)(=O)C[C@H]1O[C@@H](OC[C@H](N)CS(O)(=O)=O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H22AsNO8S/c1-11(2,15)3-7-8(13)9(14)10(20-7)19-4-6(12)5-21(16,17)18/h6-10,13-14H,3-5,12H2,1-2H3,(H,16,17,18)/t6-,7+,8+,9+,10+/m0/s1

> <INCHI_KEY>
NNPLCCFMFSSSQS-VAPHQMJDSA-N

> <FORMULA>
C10H22AsNO8S

> <MOLECULAR_WEIGHT>
391.27

> <EXACT_MASS>
391.028208

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.92408462246553

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-3-{[(2R,3R,4S,5S)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid

> <JCHEM_LOGP>
-4.4910819439248515

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.294095709945323

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.5881472897435236

> <JCHEM_PKA_STRONGEST_BASIC>
8.76448710612873

> <JCHEM_POLAR_SURFACE_AREA>
156.38

> <JCHEM_REFRACTIVITY>
67.6229

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-3-{[(2R,3R,4S,5S)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.608   5.160   0.000  0.00  0.00           C+0
HETATM    2 As   UNK     0      -0.274   4.390   0.000  0.00  0.00          As+0
HETATM    3  C   UNK     0      -1.044   3.056   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.496   5.724   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.735  -1.536   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.109  -2.943   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.014  -4.188   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       4.545  -4.027   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       2.387  -5.595   0.000  0.00  0.00           C+0
HETATM   14  S   UNK     0       3.293  -6.841   0.000  0.00  0.00           S+0
HETATM   15  O   UNK     0       4.198  -8.087   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       2.047  -7.746   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.539  -5.936   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.615  -1.536   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.651   1.651   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14                                                            
CONECT   18    8   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    6   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
[1-O-[(S)-2-Amino-3-sulfopropyl]-5-deoxy-b-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt	Generator
[1-O-[(S)-2-Amino-3-sulfopropyl]-5-deoxy-β-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt	Generator
[1-O-[(S)-2-Amino-3-sulphopropyl]-5-deoxy-b-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt	Generator
[1-O-[(S)-2-Amino-3-sulphopropyl]-5-deoxy-beta-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt	Generator
[1-O-[(S)-2-Amino-3-sulphopropyl]-5-deoxy-β-D-ribofuranos-5-yl]dimethyloxoarsenic(V) salt	Generator

Chemical Formula

C₁₀H₂₂AsNO₈S

Average Mass

391.2700 Da

Monoisotopic Mass

391.02821 Da

IUPAC Name

(2S)-2-amino-3-{[(2R,3R,4S,5S)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid

Traditional Name

(2S)-2-amino-3-{[(2R,3R,4S,5S)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid

CAS Registry Number

Not Available

SMILES

C[As](C)(=O)C[C@H]1O[C@@H](OC[C@H](N)CS(O)(=O)=O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C10H22AsNO8S/c1-11(2,15)3-7-8(13)9(14)10(20-7)19-4-6(12)5-21(16,17)18/h6-10,13-14H,3-5,12H2,1-2H3,(H,16,17,18)/t6-,7+,8+,9+,10+/m0/s1

InChI Key

NNPLCCFMFSSSQS-VAPHQMJDSA-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
Sargassum lacerifolium	LOTUS Database	35616633
Sphaerotrichia divaricata	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Pentose monosaccharide
Monosaccharide
Pentaorganoarsane
Organic sulfonic acid or derivatives
Organosulfonic acid or derivatives
Organosulfonic acid
Trialkylarsane oxide
Sulfonyl
Tetrahydrofuran
Alkanesulfonic acid
1,2-diol
Secondary alcohol
Organoheterocyclic compound
Organic metalloid salt
Oxacycle
Sulfur-containing organoarsenic compound
Oxygen-containing organoarsenic compound
Acetal
Alkylarsine oxide
Organic nitrogen compound
Primary amine
Organic salt
Organosulfur compound
Organonitrogen compound
Organoarsenic compound
Hydrocarbon derivative
Organic oxide
Primary aliphatic amine
Amine
Alcohol
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	-4.5	ChemAxon
pKa (Strongest Acidic)	-1.6	ChemAxon
pKa (Strongest Basic)	8.76	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	156.38 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	67.62 m³·mol⁻¹	ChemAxon
Polarizability	32.92 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

14252080

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-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid (NP0240616)

MOL for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

3D MOL for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

3D SDF for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

3D-SDF for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

PDB for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

3D PDB for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

SMILES for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

INCHI for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

Structure for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)

3D Structure for NP0240616 ((2s)-2-amino-3-{[(2r,3r,4s,5s)-5-[(dimethylarsoryl)methyl]-3,4-dihydroxyoxolan-2-yl]oxy}propane-1-sulfonic acid)