NP-MRD: Showing NP-Card for Cuminoside A (NP0075236)

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Record Information

Version

2.0

Created at

2022-04-28 20:32:42 UTC

Updated at

2022-04-28 20:32:42 UTC

NP-MRD ID

NP0075236

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cuminoside A

Description

Cuminoside A belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. Cuminoside A is found in Cuminum cymimum L and Cuminum cyminum . Based on a literature review very few articles have been published on Cuminoside A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222322D          

 29 32  0  0  1  0            999 V2000
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5607    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6412   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6763    1.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1689   -2.4374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6488   -3.1085    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4700   -3.0284    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9499   -3.6994    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6087   -4.4506    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7876   -4.5307    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3077   -3.8596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4464   -5.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9263   -5.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0886   -5.1216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7710   -3.6193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8111   -2.2773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7019   -1.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  1  6  1  6  0  0  0
  3  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  1 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  1  0  0  0
 13 16  1  0  0  0  0
 10 17  1  6  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 21 26  1  6  0  0  0
 20 27  1  1  0  0  0
 19 28  1  6  0  0  0
 10 29  1  1  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
   -4.8348   -1.8862    1.5862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945   -0.9433    1.8309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5278   -0.1911    2.8837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2908    0.6005    2.7682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5376   -0.1898    1.7180 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5833   -0.7388    0.8676 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1143    0.0247   -0.2778 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5832   -0.7866   -1.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0445   -0.3347   -2.4922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2113   -0.7836   -3.6714 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2009    0.8053   -2.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3976    1.6359   -3.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2522    1.0004   -0.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4793    2.1003   -0.2410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2324    1.4790    0.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2880    0.3692    1.2166 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4189    0.9086    2.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630   -0.7396    0.7383 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6868   -0.4450    0.2462 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7812   -0.8422   -1.1146 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9383   -0.3195   -1.6564 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9254   -0.5883   -3.1541 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8212    0.0101   -3.7548 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1920   -0.8720   -1.0302 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2886   -0.2689   -1.6003 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0928   -0.6162    0.4622 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1967   -1.0498    1.1568 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8096   -1.2574    0.9098 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6631   -1.3570    2.2614 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4042   -2.8357    1.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3207   -2.1239    2.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5354   -1.5100    0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1990   -0.1418    3.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7825    0.5303    3.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4149    1.6539    2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1929   -1.0993    2.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3298   -1.7714    0.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0405    0.5972    0.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6503    1.2776   -4.1816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7213    2.6873   -3.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3276    1.5674   -2.9347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0791    2.6825    0.4529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1506    2.8434   -1.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055    1.1131   -0.6645 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4332    2.3463    0.5718 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3388    1.4449    2.2108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2823    1.6811    2.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5235    0.1407    3.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0141    0.5951    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9207    0.7775   -1.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779   -0.1479   -3.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8995   -1.6836   -3.3115 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9793    0.9879   -3.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2030   -1.9643   -1.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8818    0.1578   -0.9331 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9395    0.4981    0.5629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0908   -1.9670    1.5082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8039   -2.2931    0.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2148   -0.7684    2.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  6
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
  6  2  1  0
 13  7  1  0
 28 19  1  0
 16  5  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  1
  6 37  1  6
  7 38  1  1
 12 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  6
 21 50  1  6
 22 51  1  0
 22 52  1  0
 23 53  1  0
 24 54  1  1
 25 55  1  0
 26 56  1  6
 27 57  1  0
 28 58  1  6
 29 59  1  0
M  END


  Mrv1652304282222322D          

 29 32  0  0  1  0            999 V2000
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5607    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6412   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6763    1.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1689   -2.4374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6488   -3.1085    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4700   -3.0284    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9499   -3.6994    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6087   -4.4506    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7876   -4.5307    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3077   -3.8596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4464   -5.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9263   -5.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0886   -5.1216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7710   -3.6193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8111   -2.2773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7019   -1.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  1  6  1  6  0  0  0
  3  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  1 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  1  0  0  0
 13 16  1  0  0  0  0
 10 17  1  6  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 21 26  1  6  0  0  0
 20 27  1  1  0  0  0
 19 28  1  6  0  0  0
 10 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0075236

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC[C@H]2[C@@H]1[C@@H]1OC(=O)C(C)=C1CC[C@]2(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O8/c1-9-4-5-12-14(9)18-11(10(2)19(26)28-18)6-7-21(12,3)29-20-17(25)16(24)15(23)13(8-22)27-20/h4,12-18,20,22-25H,5-8H2,1-3H3/t12-,13+,14+,15+,16-,17+,18+,20-,21-/m0/s1

> <INCHI_KEY>
WHKZFBZPPKMCMS-OLWLSHKLSA-N

> <FORMULA>
C21H30O8

> <MOLECULAR_WEIGHT>
410.463

> <EXACT_MASS>
410.194067926

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.53095419863753

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6S,6aS,9aS,9bS)-3,6,9-trimethyl-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-2-one

> <ALOGPS_LOGP>
-0.01

> <JCHEM_LOGP>
0.25528672233333294

> <ALOGPS_LOGS>
-2.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.039908571269319

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.18751143391109

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810836734484694

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
102.09069999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.24e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6S,6aS,9aS,9bS)-3,6,9-trimethyl-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H,5H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.843  -0.442   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.803  -1.646   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.245  -1.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.176   0.433   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.380   1.393   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       7.691   0.843   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.530  -1.954   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.461  -3.148   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.073  -3.816   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.686  -3.148   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.343  -1.646   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.303  -0.442   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.455   0.843   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.970   0.433   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.901  -1.105   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.996   2.285   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.049  -4.550   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.945  -5.803   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.477  -5.653   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.373  -6.906   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.736  -8.308   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.203  -8.457   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.308  -7.205   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.567  -9.859   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.462 -11.112   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.632  -9.560   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.906  -6.756   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.114  -4.251   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.177  -3.457   0.000  0.00  0.00           C+0
CONECT    1    2    6   12                                                  
CONECT    2    1    3    8                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    1                                                       
CONECT    7    3                                                            
CONECT    8    2    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   17   29                                             
CONECT   11   10   12   15                                                  
CONECT   12   11    1   13                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14   11                                                       
CONECT   16   13                                                            
CONECT   17   10   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   28                                                  
CONECT   20   19   21   27                                                  
CONECT   21   20   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22   18                                                       
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   21                                                            
CONECT   27   20                                                            
CONECT   28   19                                                            
CONECT   29   10                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₈

Average Mass

410.4630 Da

Monoisotopic Mass

410.19407 Da

IUPAC Name

(6S,6aS,9aS,9bS)-3,6,9-trimethyl-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-2-one

Traditional Name

(6S,6aS,9aS,9bS)-3,6,9-trimethyl-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H,5H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-2-one

CAS Registry Number

Not Available

SMILES

CC1=CC[C@H]2[C@@H]1[C@@H]1OC(=O)C(C)=C1CC[C@]2(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C21H30O8/c1-9-4-5-12-14(9)18-11(10(2)19(26)28-18)6-7-21(12,3)29-20-17(25)16(24)15(23)13(8-22)27-20/h4,12-18,20,22-25H,5-8H2,1-3H3/t12-,13+,14+,15+,16-,17+,18+,20-,21-/m0/s1

InChI Key

WHKZFBZPPKMCMS-OLWLSHKLSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Cuminum cymimum L	Plant	KNApSAcK
Cuminum cyminum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Guaianolide-skeleton
Terpene glycoside
Sesquiterpenoid
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
2-furanone
Monosaccharide
Oxane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Dihydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Monocarboxylic acid or derivatives
Acetal
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Polyol
Primary alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Alcohol
Organooxygen compound
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	-0.01	ALOGPS
logP	0.26	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.68 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.09 m³·mol⁻¹	ChemAxon
Polarizability	42.53 Å³	ChemAxon
Number of Rings	4	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

C00031817

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

101252065

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cuminoside A (NP0075236)

MOL for NP0075236 (Cuminoside A)

3D MOL for NP0075236 (Cuminoside A)

3D SDF for NP0075236 (Cuminoside A)

3D-SDF for NP0075236 (Cuminoside A)

PDB for NP0075236 (Cuminoside A)

3D PDB for NP0075236 (Cuminoside A)

SMILES for NP0075236 (Cuminoside A)

INCHI for NP0075236 (Cuminoside A)

Structure for NP0075236 (Cuminoside A)

3D Structure for NP0075236 (Cuminoside A)