NP-MRD: Showing NP-Card for (3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione (NP0282181)

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Record Information

Version

2.0

Created at

2022-09-09 08:55:20 UTC

Updated at

2022-09-09 08:55:20 UTC

NP-MRD ID

NP0282181

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

Description

(3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione is found in Cichorium endivia.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241221292D          

 34 37  0  0  1  0            999 V2000
    8.3029   -3.7923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4812   -3.8663    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0581   -4.5745    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4160   -5.3178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0581   -6.0611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2537   -6.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0702   -7.0490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087   -5.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087   -4.9053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2537   -4.3909    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1798   -3.5692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9384   -3.2450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1220   -2.4407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8241   -4.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5692   -3.8657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3392   -5.3178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8241   -5.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5692   -6.7698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4373   -5.1952    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8831   -4.5745    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2410   -5.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3952   -4.1084    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5072   -1.5747    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7226   -1.8297    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7226   -2.6546    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5073   -2.9096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9922   -2.2422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -0.7901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5692   -0.6186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0552   -1.3448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0552   -3.1395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -3.6942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9239   -3.4929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1374   -4.2898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 32  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 19  1  6  0  0  0
  3 20  1  1  0  0  0
  4 21  1  1  0  0  0
  9 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  1  0  0  0  0
 23 28  1  1  0  0  0
 28 29  1  0  0  0  0
 24 30  1  6  0  0  0
 25 31  1  1  0  0  0
 26 32  1  0  0  0  0
 26 33  1  6  0  0  0
 33 34  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
   -3.8971   -3.8085   -0.3205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5908   -2.3622   -0.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3002   -2.0767   -0.3835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2258   -3.0184   -0.6042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3934   -4.2680   -0.7212 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0014   -2.2526   -0.6566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2411   -0.9665   -0.4927 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8001    0.1357   -0.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0628   -0.3928   -0.6812 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0822    0.4951   -0.6956 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9884    1.4399   -1.8926 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0394    0.6273   -3.0275 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2672   -0.2514   -0.9060 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3108    0.5611   -0.5599 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5127   -0.3118   -0.2415 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1366   -1.1379    0.8210 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8787    1.2419    0.6974 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3512    2.5492    0.7933 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3596    1.2146    0.5785 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8532    0.6389    1.7072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6817   -0.7373   -0.3466 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0819   -0.0298    0.9300 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2985    1.1091    1.1339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0623    2.0453    1.7866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6572    2.9623    2.5565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4894    1.8045    1.4351 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9170    2.9360    0.5011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833    0.5455    0.6370 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5076   -0.4477    1.0507 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7173    0.1908    1.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7674   -1.4906   -0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3781   -4.3808    0.5003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9793   -4.0114   -0.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6495   -4.2302   -1.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0141   -2.6594   -0.8107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4969    0.9049   -1.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8566    0.6436    0.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8542    2.1194   -1.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0575    2.0432   -1.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791   -0.1046   -2.9034 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6132    1.2645   -1.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8405   -0.8968   -1.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3053    0.3598    0.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8848   -1.3023    1.4243 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2069    0.6227    1.5624 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7796    3.0148    1.4621 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0209    2.2601    0.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4040   -0.0392    2.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0753   -0.1107   -1.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1204   -0.7323    1.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1329    1.7643    2.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2695    2.8550   -0.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9632    2.7352    0.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8049    3.9193    0.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6015    0.7346   -0.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1830   -0.9883    1.9748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1463    0.3769    0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1118   -0.9934   -0.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6302   -2.1142    0.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 23  1  0
 23 24  1  0
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 29 30  1  0
 29 31  1  0
 31  2  1  0
  2  1  1  0
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  4  6  1  0
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 10  9  1  1
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 13 14  1  0
 14 15  1  0
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 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  7 21  1  0
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 21  3  1  0
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 31 58  1  0
 31 59  1  0
  1 32  1  0
  1 33  1  0
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  6 35  1  0
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 15 43  1  0
 16 44  1  0
 17 45  1  1
 18 46  1  0
 19 47  1  6
 20 48  1  0
 21 49  1  6
M  END


  Mrv0541 02241221292D          

 34 37  0  0  1  0            999 V2000
    8.3029   -3.7923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4812   -3.8663    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0581   -4.5745    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4160   -5.3178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0581   -6.0611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2537   -6.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0702   -7.0490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087   -5.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087   -4.9053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2537   -4.3909    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1798   -3.5692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8241   -5.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5692   -6.7698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5072   -1.5747    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.9922   -2.2422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7622   -0.7901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5692   -0.6186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0552   -1.3448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7622   -3.6942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9239   -3.4929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1374   -4.2898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 15 32  1  0  0  0  0
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 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 19  1  6  0  0  0
  3 20  1  1  0  0  0
  4 21  1  1  0  0  0
  9 22  1  1  0  0  0
 23 24  1  0  0  0  0
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 25 26  1  0  0  0  0
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 23 28  1  1  0  0  0
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 24 30  1  6  0  0  0
 25 31  1  1  0  0  0
 26 32  1  0  0  0  0
 26 33  1  6  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0282181

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12OC(=O)[C@@H](C)[C@]1([H])[C@@H](O)CC(C)=C1C(=O)C=C(CO[C@]3(CO)O[C@H](CO)[C@@H](O)[C@@H]3O)[C@]21[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O10/c1-8-3-11(24)15-9(2)20(28)30-18(15)16-10(4-12(25)14(8)16)6-29-21(7-23)19(27)17(26)13(5-22)31-21/h4,9,11,13,15-19,22-24,26-27H,3,5-7H2,1-2H3/t9-,11-,13+,15+,16-,17+,18-,19-,21+/m0/s1

> <INCHI_KEY>
VPJIBVRZDKWNNF-YHMCHQIZSA-N

> <FORMULA>
C21H28O10

> <MOLECULAR_WEIGHT>
440.441

> <EXACT_MASS>
440.168247116

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
44.07130248973699

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,3aR,4S,9aS,9bR)-9-({[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <ALOGPS_LOGP>
-0.77

> <JCHEM_LOGP>
-1.7556915696666666

> <ALOGPS_LOGS>
-1.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.012773465989216

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.056624306176957

> <JCHEM_PKA_STRONGEST_BASIC>
-2.900163293354602

> <JCHEM_POLAR_SURFACE_AREA>
162.98

> <JCHEM_REFRACTIVITY>
104.91239999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.18e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,3aR,4S,9aS,9bR)-9-({[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3H,3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      15.499  -7.079   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.965  -7.217   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.175  -8.539   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.843  -9.927   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.175 -11.314   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.674 -11.657   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.331 -13.158   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.470 -10.697   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.470  -9.157   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.674  -8.196   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.536  -6.663   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      12.952  -6.057   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.294  -4.556   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.005  -8.681   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.529  -7.216   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.100  -9.927   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.005 -11.172   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.529 -12.637   0.000  0.00  0.00           O+0
HETATM   19  H   UNK     0      12.016  -9.698   0.000  0.00  0.00           H+0
HETATM   20  H   UNK     0      14.715  -8.539   0.000  0.00  0.00           H+0
HETATM   21  O   UNK     0      15.383  -9.927   0.000  0.00  0.00           O+0
HETATM   22  H   UNK     0      10.071  -7.669   0.000  0.00  0.00           H+0
HETATM   23  C   UNK     0       6.547  -2.939   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.082  -3.415   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.082  -4.955   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.547  -5.431   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.452  -4.185   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.023  -1.475   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.529  -1.155   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       3.836  -2.510   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       3.836  -5.860   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       7.023  -6.896   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.458  -6.520   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.856  -8.008   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4   10   20                                             
CONECT    4    3    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   17                                                  
CONECT    9    8   10   14   22                                             
CONECT   10    9    3   11   19                                             
CONECT   11   10   12                                                       
CONECT   12   11    2   13                                                  
CONECT   13   12                                                            
CONECT   14    9   15   16                                                  
CONECT   15   14   32                                                       
CONECT   16   14   17                                                       
CONECT   17   16    8   18                                                  
CONECT   18   17                                                            
CONECT   19   10                                                            
CONECT   20    3                                                            
CONECT   21    4                                                            
CONECT   22    9                                                            
CONECT   23   24   27   28                                                  
CONECT   24   23   25   30                                                  
CONECT   25   24   26   31                                                  
CONECT   26   25   27   32   33                                             
CONECT   27   26   23                                                       
CONECT   28   23   29                                                       
CONECT   29   28                                                            
CONECT   30   24                                                            
CONECT   31   25                                                            
CONECT   32   15   26                                                       
CONECT   33   26   34                                                       
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈O₁₀

Average Mass

440.4410 Da

Monoisotopic Mass

440.16825 Da

IUPAC Name

(3S,3aR,4S,9aS,9bR)-9-({[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

Traditional Name

(3S,3aR,4S,9aS,9bR)-9-({[(2R,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3H,3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

CAS Registry Number

Not Available

SMILES

[H][C@]12OC(=O)[C@@H](C)[C@]1([H])[C@@H](O)CC(C)=C1C(=O)C=C(CO[C@]3(CO)O[C@H](CO)[C@@H](O)[C@@H]3O)[C@]21[H]

InChI Identifier

InChI=1S/C21H28O10/c1-8-3-11(24)15-9(2)20(28)30-18(15)16-10(4-12(25)14(8)16)6-29-21(7-23)19(27)17(26)13(5-22)31-21/h4,9,11,13,15-19,22-24,26-27H,3,5-7H2,1-2H3/t9-,11-,13+,15+,16-,17+,18-,19-,21+/m0/s1

InChI Key

VPJIBVRZDKWNNF-YHMCHQIZSA-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
Cichorium endivia	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

C-glycosyl compound
Pentose monosaccharide
Ketal
Gamma butyrolactone
Monosaccharide
Tetrahydrofuran
Carboxylic acid ester
Ketone
Secondary alcohol
Lactone
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organic oxide
Primary alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-0.77	ALOGPS
logP	-1.8	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	12.06	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	162.98 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	104.91 m³·mol⁻¹	ChemAxon
Polarizability	44.07 Å³	ChemAxon
Number of Rings	4	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

FDB001798

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

102476813

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione (NP0282181)

MOL for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D MOL for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D SDF for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D-SDF for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

PDB for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D PDB for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

SMILES for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

INCHI for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

Structure for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D Structure for NP0282181 ((3s,3ar,4s,9as,9br)-9-({[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}methyl)-4-hydroxy-3,6-dimethyl-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)