NP-MRD: Showing NP-Card for streptobiosamine (NP0315499)

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Record Information

Version

2.0

Created at

2022-09-11 14:09:39 UTC

Updated at

2022-09-11 14:09:39 UTC

NP-MRD ID

NP0315499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

streptobiosamine

Description

Streptobiosamine belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars. Streptobiosamine is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. streptobiosamine is found in Trypanosoma brucei. Based on a literature review very few articles have been published on streptobiosamine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 46  0  0  0  0  0  0  0  0999 V2000
   -2.1122    1.5444    2.8931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2510    0.6982    2.1222 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7846    0.2373    0.8984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9140   -0.8077    0.2689 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1817   -0.3695   -0.4207 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3740   -1.0632   -0.1275 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8485   -1.7510   -1.3697 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2645   -1.5498   -2.3980 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3902   -0.0583    0.2860 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5849    0.8221   -0.8122 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8782    0.7390    1.4511 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130    1.9199    1.3207 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7098   -0.6629    0.6099 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6759    0.4296    1.0701 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3454   -1.3482   -0.3966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7163   -1.4763   -0.7105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0780   -0.6583   -1.7395 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4840   -1.0533   -2.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4894   -2.3805   -2.6192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9908    0.8037   -1.5300 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8306    1.3654   -2.1073 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1153    1.2936   -0.1251 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4583    1.6559    0.1023 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9739    0.9949    3.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5092    1.8957    3.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    2.4710    2.3755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0280   -0.1336    2.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7415   -0.3215    1.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7123   -1.6080    1.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1614   -1.7686    0.6706 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6863   -2.4025   -1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9305    0.2914   -1.5661 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6765    0.2250    2.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6275   -1.3621    1.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2983    0.8608    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7690    1.1312    0.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6572   -0.0877    1.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3255   -1.2245   -0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4294   -0.9127   -2.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1977   -0.9846   -1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8657   -0.3977   -2.9873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9701   -2.9287   -1.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8269    1.2752   -2.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8047    2.3301   -1.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5233    2.2196   -0.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8698    2.1074   -0.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
 20 17  1  0
 17 18  1  0
 18 19  1  0
 17 16  1  0
 16  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  6  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  2  0
  9 13  1  0
 13 14  1  0
 13 15  1  0
  4  3  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  1
 22 45  1  6
 23 46  1  0
 20 43  1  6
 21 44  1  0
 17 39  1  6
 18 40  1  0
 18 41  1  0
 19 42  1  0
  4 29  1  1
  6 30  1  1
  7 31  1  0
 10 32  1  0
 11 33  1  0
 13 34  1  1
 14 35  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
M  END


  Mrv1652309112216092D          

 23 23  0  0  1  0            999 V2000
   -3.6061    0.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8196   -0.6406    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2362   -1.2239    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4394   -1.0104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2258   -0.2135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2154    0.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7988    1.3803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8456   -0.5834    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289   -1.1667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622   -1.1667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5347   -0.9532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4757    0.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5347   -0.2135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8560   -1.5938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0695   -2.3907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4862   -2.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6893   -2.7605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8664   -2.6042    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0799   -3.4011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4498   -2.0208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2467   -2.2344    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  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
 11 12  2  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  6  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0315499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H](C=O)[C@@](O)(C=O)[C@H](C)O

> <INCHI_IDENTIFIER>
InChI=1S/C13H23NO9/c1-6(18)13(21,5-17)8(4-16)23-12-9(14-2)11(20)10(19)7(3-15)22-12/h4-12,14-15,18-21H,3H2,1-2H3/t6-,7-,8-,9-,10-,11-,12-,13+/m0/s1

> <INCHI_KEY>
UNTJYOFZBHSHIU-HXYRURAXSA-N

> <FORMULA>
C13H23NO9

> <MOLECULAR_WEIGHT>
337.325

> <EXACT_MASS>
337.137281325

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.71806353896749

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-2-hydroxy-2-[(1S)-1-hydroxyethyl]butanedial

> <JCHEM_LOGP>
-3.7887384980000007

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.744896852557492

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.101700785915105

> <JCHEM_PKA_STRONGEST_BASIC>
7.915750346953748

> <JCHEM_POLAR_SURFACE_AREA>
165.78

> <JCHEM_REFRACTIVITY>
73.88380000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-2-hydroxy-2-[(1S)-1-hydroxyethyl]butanedial

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.731   0.292   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -7.130  -1.196   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -6.041  -2.285   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.553  -1.886   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -4.155  -0.399   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.269   1.488   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.358   2.576   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.578  -1.089   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.667  -2.178   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.489  -2.178   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.998  -1.779   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.489   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.888   1.488   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.998  -0.399   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -3.465  -2.975   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.863  -4.463   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.774  -5.552   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.287  -5.153   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.351  -4.861   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -5.749  -6.349   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -6.440  -3.772   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -7.927  -4.171   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11   13                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11                                                            
CONECT   13    9   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    4   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₃NO₉

Average Mass

337.3250 Da

Monoisotopic Mass

337.13728 Da

IUPAC Name

(2R,3R)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-2-hydroxy-2-[(1S)-1-hydroxyethyl]butanedial

Traditional Name

(2R,3R)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-2-hydroxy-2-[(1S)-1-hydroxyethyl]butanedial

CAS Registry Number

Not Available

SMILES

CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H](C=O)[C@@](O)(C=O)[C@H](C)O

InChI Identifier

InChI=1S/C13H23NO9/c1-6(18)13(21,5-17)8(4-16)23-12-9(14-2)11(20)10(19)7(3-15)22-12/h4-12,14-15,18-21H,3H2,1-2H3/t6-,7-,8-,9-,10-,11-,12-,13+/m0/s1

InChI Key

UNTJYOFZBHSHIU-HXYRURAXSA-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
Trypanosoma brucei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminoglycosides

Alternative Parents

Substituents

Aminoglycoside core
Glycosyl compound
O-glycosyl compound
Beta-hydroxy aldehyde
Monosaccharide
Oxane
Tertiary alcohol
Alpha-hydroxyaldehyde
Secondary alcohol
1,2-aminoalcohol
Secondary amine
Acetal
Organoheterocyclic compound
Oxacycle
Secondary aliphatic amine
Primary alcohol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organopnictogen compound
Organic nitrogen compound
Amine
Aldehyde
Alcohol
Organonitrogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

amino disaccharide (CHEBI:9283 )

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	-3.8	ChemAxon
pKa (Strongest Acidic)	11.1	ChemAxon
pKa (Strongest Basic)	7.92	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	165.78 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	73.88 m³·mol⁻¹	ChemAxon
Polarizability	31.72 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

16739596

KEGG Compound ID

C07655

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

20056682

PDB ID

Not Available

ChEBI ID

9283

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for streptobiosamine (NP0315499)

MOL for NP0315499 (streptobiosamine)

3D MOL for NP0315499 (streptobiosamine)

3D SDF for NP0315499 (streptobiosamine)

3D-SDF for NP0315499 (streptobiosamine)

PDB for NP0315499 (streptobiosamine)

3D PDB for NP0315499 (streptobiosamine)

SMILES for NP0315499 (streptobiosamine)

INCHI for NP0315499 (streptobiosamine)

Structure for NP0315499 (streptobiosamine)

3D Structure for NP0315499 (streptobiosamine)