NP-MRD: Showing NP-Card for carthamoside A2 (NP0030045)

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Record Information

Version

2.0

Created at

2021-06-19 21:30:40 UTC

Updated at

2021-06-29 23:57:47 UTC

NP-MRD ID

NP0030045

Secondary Accession Numbers

None

Natural Product Identification

Common Name

carthamoside A2

Provided By

JEOL Database JEOL Logo

Description

(2R,3R,4S,5S,6R)-2-(deca-4,6-diyn-1-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. carthamoside A2 is found in Carthamus tinctorius. carthamoside A2 was first documented in 2006 (Zhou, Y.-Z., et al.). Based on a literature review very few articles have been published on (2R,3R,4S,5S,6R)-2-(deca-4,6-diyn-1-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123303D          

 46 46  0  0  0  0            999 V2000
   -4.8549    4.1945   -0.8725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6624    3.2651   -0.7128 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7034    3.3743   -1.8970 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5599    2.4669   -1.7344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316    1.7216   -1.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385    0.7531   -1.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4240   -0.0217   -1.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4712   -0.9877   -0.7431 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0092   -2.4383   -0.9079 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7795   -2.7900   -0.0728 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0373   -2.4976    1.2994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1693   -2.4531    2.0719 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9588   -1.3312    1.6867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799   -1.2210    2.4398 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9402   -0.0075    1.8885 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1155    1.1582    1.9169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8958   -1.0777    3.9435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1146   -1.1235    4.6932 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9929   -2.2189    4.4183 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6248   -1.9927    5.7886 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2521   -2.3253    3.5450 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0241   -3.4599    3.9712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5326    5.2386   -0.9382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4229    3.9521   -1.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5268    4.0999   -0.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0210    2.2331   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1380    3.5096    0.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3427    4.4053   -1.9897 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3499   -0.8227   -1.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956   -0.8123    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8395   -3.0898   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0925   -2.2377   -0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7953   -2.1118    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2147   -0.1778    0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8535    0.1948    2.4554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3061    0.9186    1.4240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4112   -0.1178    4.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8343   -1.1279    5.6312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5453   -3.1672    4.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0856   -2.6406    5.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885   -1.4436    3.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7452   -3.5370    3.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 14 17  1  0  0  0  0
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  7  6  3  0  0  0  0
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  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  2 26  1  0  0  0  0
  2 27  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
M  END

     RDKit          3D

 46 46  0  0  0  0  0  0  0  0999 V2000
   -4.8549    4.1945   -0.8725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6624    3.2651   -0.7128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7034    3.3743   -1.8970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    2.4669   -1.7344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316    1.7216   -1.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385    0.7531   -1.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4240   -0.0217   -1.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4712   -0.9877   -0.7431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0092   -2.4383   -0.9079 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7795   -2.7900   -0.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0373   -2.4976    1.2994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1693   -2.4531    2.0719 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.1799   -1.2210    2.4398 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9402   -0.0075    1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1155    1.1582    1.9169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8958   -1.0777    3.9435 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.9929   -2.2189    4.4183 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.2521   -2.3253    3.5450 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0241   -3.4599    3.9712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5326    5.2386   -0.9382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4229    3.9521   -1.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5268    4.0999   -0.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0210    2.2331   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1380    3.5096    0.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3427    4.4053   -1.9897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2318    3.1336   -2.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499   -0.8227   -1.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956   -0.8123    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7956   -2.6478   -1.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8395   -3.0898   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632   -3.8601   -0.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925   -2.2377   -0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7215   -3.3882    1.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7953   -2.1118    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
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  8  7  1  0
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M  END


  Mrv1652306192123303D          

 46 46  0  0  0  0            999 V2000
   -4.8549    4.1945   -0.8725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6624    3.2651   -0.7128 C   0  0  2  0  0  0  0  0  0  0  0  0
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 21 45  1  6  0  0  0
 22 46  1  0  0  0  0
  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  2 26  1  0  0  0  0
  2 27  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030045

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]1([H])O[C@@]([H])(OC([H])([H])C([H])([H])C([H])([H])C#CC#CC([H])([H])C([H])([H])C([H])([H])[H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]1([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H24O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-3,8-11H2,1H3/t12-,13-,14+,15-,16-/m1/s1

> <INCHI_KEY>
RYBYAHGLHFUNIV-IBEHDNSVSA-N

> <FORMULA>
C16H24O6

> <MOLECULAR_WEIGHT>
312.362

> <EXACT_MASS>
312.157288493

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
33.435676300299235

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,4S,5S,6R)-2-(deca-4,6-diyn-1-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
1.15

> <JCHEM_LOGP>
0.871311619666667

> <ALOGPS_LOGS>
-3.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200256474083652

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210986866576546

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810834105647066

> <JCHEM_POLAR_SURFACE_AREA>
99.38000000000001

> <JCHEM_REFRACTIVITY>
80.87700000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.85e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S,6R)-2-(deca-4,6-diyn-1-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 46  0  0  0  0  0  0  0  0999 V2000
   -4.8549    4.1945   -0.8725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6624    3.2651   -0.7128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7034    3.3743   -1.8970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    2.4669   -1.7344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316    1.7216   -1.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385    0.7531   -1.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4240   -0.0217   -1.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4712   -0.9877   -0.7431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0092   -2.4383   -0.9079 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7795   -2.7900   -0.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0373   -2.4976    1.2994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1693   -2.4531    2.0719 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9588   -1.3312    1.6867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799   -1.2210    2.4398 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9402   -0.0075    1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1155    1.1582    1.9169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8958   -1.0777    3.9435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1146   -1.1235    4.6932 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9929   -2.2189    4.4183 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6248   -1.9927    5.7886 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2521   -2.3253    3.5450 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0241   -3.4599    3.9712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5326    5.2386   -0.9382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4229    3.9521   -1.7764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5268    4.0999   -0.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0210    2.2331   -0.6125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1380    3.5096    0.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3427    4.4053   -1.9897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2318    3.1336   -2.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499   -0.8227   -1.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956   -0.8123    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7956   -2.6478   -1.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8395   -3.0898   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632   -3.8601   -0.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925   -2.2377   -0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7215   -3.3882    1.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7953   -2.1118    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2147   -0.1778    0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8535    0.1948    2.4554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3061    0.9186    1.4240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4112   -0.1178    4.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8343   -1.1279    5.6312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5453   -3.1672    4.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0856   -2.6406    5.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885   -1.4436    3.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7452   -3.5370    3.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 14 17  1  0
 19 21  1  0
 21 12  1  0
 12 13  1  0
 13 14  1  0
 17 19  1  0
 12 11  1  0
 21 22  1  0
 17 18  1  0
  7  6  3  0
 16 15  1  0
  6  5  1  0
  5  4  3  0
 10  9  1  0
  4  3  1  0
 11 10  1  0
  3  2  1  0
  9  8  1  0
  2  1  1  0
 14 15  1  0
 19 20  1  0
 10 34  1  0
 10 35  1  0
  9 32  1  0
  9 33  1  0
  8 30  1  0
  8 31  1  0
 14 37  1  1
 15 38  1  0
 15 39  1  0
 18 42  1  0
 17 41  1  6
 16 40  1  0
 20 44  1  0
 19 43  1  1
 12 36  1  1
 21 45  1  6
 22 46  1  0
  3 28  1  0
  3 29  1  0
  2 26  1  0
  2 27  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.855   4.194  -0.873  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.662   3.265  -0.713  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.703   3.374  -1.897  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.560   2.467  -1.734  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.632   1.722  -1.581  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.539   0.753  -1.339  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.424  -0.022  -1.102  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.471  -0.988  -0.743  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.009  -2.438  -0.908  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.780  -2.790  -0.073  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.037  -2.498   1.299  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.169  -2.453   2.072  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.959  -1.331   1.687  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.180  -1.221   2.440  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.940  -0.008   1.889  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.115   1.158   1.917  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.896  -1.078   3.943  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.115  -1.123   4.693  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.993  -2.219   4.418  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.625  -1.993   5.789  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.252  -2.325   3.545  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.024  -3.460   3.971  0.00  0.00           O+0
HETATM   23  H   UNK     0      -4.533   5.239  -0.938  0.00  0.00           H+0
HETATM   24  H   UNK     0      -5.423   3.952  -1.776  0.00  0.00           H+0
HETATM   25  H   UNK     0      -5.527   4.100  -0.014  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.021   2.233  -0.613  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.138   3.510   0.219  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.343   4.405  -1.990  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.232   3.134  -2.827  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.350  -0.823  -1.378  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.796  -0.812   0.289  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.796  -2.648  -1.963  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.840  -3.090  -0.609  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.563  -3.860  -0.168  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.093  -2.238  -0.440  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.722  -3.388   1.908  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.795  -2.112   2.258  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.215  -0.178   0.842  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.853   0.195   2.455  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.306   0.919   1.424  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.411  -0.118   4.160  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.834  -1.128   5.631  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.545  -3.167   4.417  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.086  -2.641   5.972  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.889  -1.444   3.691  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.745  -3.537   3.314  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    3    1   26   27                                             
CONECT    3    4    2   28   29                                             
CONECT    4    5    3                                                       
CONECT    5    6    4                                                       
CONECT    6    7    5                                                       
CONECT    7    8    6                                                       
CONECT    8    7    9   30   31                                             
CONECT    9   10    8   32   33                                             
CONECT   10    9   11   34   35                                             
CONECT   11   12   10                                                       
CONECT   12   21   13   11   36                                             
CONECT   13   12   14                                                       
CONECT   14   17   13   15   37                                             
CONECT   15   16   14   38   39                                             
CONECT   16   15   40                                                       
CONECT   17   14   19   18   41                                             
CONECT   18   17   42                                                       
CONECT   19   21   17   20   43                                             
CONECT   20   19   44                                                       
CONECT   21   19   12   22   45                                             
CONECT   22   21   46                                                       
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    2                                                            
CONECT   27    2                                                            
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    8                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   10                                                            
CONECT   36   12                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   19                                                            
CONECT   44   20                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   92    0
END

RDKit          3D

46 46  0  0  0  0  0  0  0  0999 V2000
   -4.8549    4.1945   -0.8725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6624    3.2651   -0.7128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7034    3.3743   -1.8970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    2.4669   -1.7344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316    1.7216   -1.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5385    0.7531   -1.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4240   -0.0217   -1.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4712   -0.9877   -0.7431 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0092   -2.4383   -0.9079 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7795   -2.7900   -0.0728 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0373   -2.4976    1.2994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1693   -2.4531    2.0719 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9588   -1.3312    1.6867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799   -1.2210    2.4398 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9402   -0.0075    1.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3499   -0.8227   -1.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956   -0.8123    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7956   -2.6478   -1.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8395   -3.0898   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632   -3.8601   -0.1676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0925   -2.2377   -0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7215   -3.3882    1.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7953   -2.1118    2.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2147   -0.1778    0.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8535    0.1948    2.4554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3061    0.9186    1.4240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4112   -0.1178    4.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8343   -1.1279    5.6312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5453   -3.1672    4.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0856   -2.6406    5.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885   -1.4436    3.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7452   -3.5370    3.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
 14 17  1  0
 19 21  1  0
 21 12  1  0
 12 13  1  0
 13 14  1  0
 17 19  1  0
 12 11  1  0
 21 22  1  0
 17 18  1  0
  7  6  3  0
 16 15  1  0
  6  5  1  0
  5  4  3  0
 10  9  1  0
  4  3  1  0
 11 10  1  0
  3  2  1  0
  9  8  1  0
  2  1  1  0
 14 15  1  0
 19 20  1  0
 10 34  1  0
 10 35  1  0
  9 32  1  0
  9 33  1  0
  8 30  1  0
  8 31  1  0
 14 37  1  1
 15 38  1  0
 15 39  1  0
 18 42  1  0
 17 41  1  6
 16 40  1  0
 20 44  1  0
 19 43  1  1
 12 36  1  1
 21 45  1  6
 22 46  1  0
  3 28  1  0
  3 29  1  0
  2 26  1  0
  2 27  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₄O₆

Average Mass

312.3620 Da

Monoisotopic Mass

312.15729 Da

IUPAC Name

(2R,3R,4S,5S,6R)-2-(deca-4,6-diyn-1-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2R,3R,4S,5S,6R)-2-(deca-4,6-diyn-1-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@@]1([H])O[C@@]([H])(OC([H])([H])C([H])([H])C([H])([H])C#CC#CC([H])([H])C([H])([H])C([H])([H])[H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]1([H])O[H]

InChI Identifier

InChI=1S/C16H24O6/c1-2-3-4-5-6-7-8-9-10-21-16-15(20)14(19)13(18)12(11-17)22-16/h12-20H,2-3,8-11H2,1H3/t12-,13-,14+,15-,16-/m1/s1

InChI Key

RYBYAHGLHFUNIV-IBEHDNSVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Carthamus tinctorius	JEOL database	Zhou, Y.-Z., et al, Chem. Pharm. Bull. 54, 1455 (2006)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Monosaccharide
Oxane
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Alcohol
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	1.15	ALOGPS
logP	0.87	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	99.38 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	80.88 m³·mol⁻¹	ChemAxon
Polarizability	33.44 Å³	ChemAxon
Number of Rings	1	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

101412416

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhou, Y.-Z., et al. (2006). Zhou, Y.-Z., et al, Chem. Pharm. Bull. 54, 1455 (2006). Chem. Pharm. Bull..

Showing NP-Card for carthamoside A2 (NP0030045)

MOL for NP0030045 (carthamoside A2)

3D MOL for NP0030045 (carthamoside A2)

3D SDF for NP0030045 (carthamoside A2)

3D-SDF for NP0030045 (carthamoside A2)

PDB for NP0030045 (carthamoside A2)

3D PDB for NP0030045 (carthamoside A2)

SMILES for NP0030045 (carthamoside A2)

INCHI for NP0030045 (carthamoside A2)

Structure for NP0030045 (carthamoside A2)

3D Structure for NP0030045 (carthamoside A2)