NP-MRD: Showing NP-Card for (3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one (NP0143905)

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Record Information

Version

2.0

Created at

2022-09-01 22:45:39 UTC

Updated at

2022-09-01 22:45:40 UTC

NP-MRD ID

NP0143905

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one

Description

[(1R)-1-Methyl-3-[[(3R)-2-oxo-3alpha,7beta-dimethyl-3,3aalpha,4,7,8,8aalpha-hexahydro-2H-cyclohepta[b]furan]-6-yl]propyl]beta-D-glucopyranoside belongs to the class of organic compounds known as xanthanolides. These are sesquiterpenoids with a structure based on the xanthanolide skeleton consistsing of a cycloheptane ring usually attached to a four-carbon chain (at carbon 1 ) and a methyl group (at carbon 10), and fused to a five-member lactone ring (sharing carbons 7 and 8). The lactone ring can be conjugated with a methyl or methylene group at position 11. (3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one is found in Arnica amplexicaulis. Based on a literature review very few articles have been published on [(1R)-1-Methyl-3-[[(3R)-2-oxo-3alpha,7beta-dimethyl-3,3aalpha,4,7,8,8aalpha-hexahydro-2H-cyclohepta[b]furan]-6-yl]propyl]beta-D-glucopyranoside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022200452D          

 29 31  0  0  1  0            999 V2000
    0.7919   -2.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -1.3176    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1194   -1.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4209   -0.3064    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2278   -0.1349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3141    0.6856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0285    1.0981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5604    1.0211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3889    1.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0084    0.4080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8074    0.5310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4122   -0.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3505   -0.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650   -1.2654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7795   -0.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4940   -1.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4940   -2.0904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2084   -0.8529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9229   -1.2654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6374   -0.8529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518   -1.2654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0663   -0.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0663   -0.0279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518   -2.0904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0663   -2.5029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6374   -2.5029    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6374   -3.3279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9229   -2.0904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2084   -2.5029    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  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
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   -3.3570   -1.4055    0.8799 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0781   -0.5955    1.9368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0754    0.3520    1.3255 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3178    1.4816    2.1404 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8893    2.4268    1.3035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5322    3.4277    1.6995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6407    2.0989   -0.1223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8561    1.5258   -0.8069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6186    0.9632    0.0424 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2720    1.6334    0.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1556    0.6514    0.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1873   -0.6393    0.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9318   -1.3837    0.2770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2224   -0.5426   -0.2028 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4435   -1.4692   -0.2890 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0863   -2.5565   -1.2710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4635   -0.7172   -0.8516 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5537   -0.5626    0.0140 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7007    0.7806    0.2564 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8868    1.1451    0.8345 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9014    2.6790    0.8970 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0708    3.1473    1.4709 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1085    0.7302    0.0752 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0108    0.0157    0.8775 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7102   -0.1709   -1.0695 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1090    0.5919   -2.0770 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7923   -1.2256   -0.5279 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4706   -1.9150    0.4656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4591   -2.5882    2.4835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4182   -3.3844    0.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9310   -3.2519    1.7427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0793   -1.6468    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6401   -1.3303    2.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3462   -0.0716    2.5882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0074   -0.1878    1.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1820    2.9178   -0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5631    1.0531   -0.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3805    2.3359   -1.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1631    2.2956   -0.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2534    2.2594    1.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2260    1.0883   -0.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6781   -1.8225    1.2620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1067   -2.2331   -0.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4728    0.2537    0.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0736   -0.1368   -1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6389   -1.8201    0.7216 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3996   -2.1230   -2.0270 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9692   -2.9840   -1.7872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5392   -3.4002   -0.8050 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2791   -1.1153    0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9853    0.7935    1.9033 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9942    3.0330    1.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8180    3.0049   -0.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6639    3.4897    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6650    1.5898   -0.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6131   -0.5299    0.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6465   -0.6105   -1.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6630    0.0414   -2.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5775   -1.9366   -1.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0370   -1.8174    1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
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 28 62  1  6
 29 63  1  0
M  END


  Mrv1652309022200452D          

 29 31  0  0  1  0            999 V2000
    0.7919   -2.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6689   -1.3176    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1194   -1.0744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4209   -0.3064    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2278   -0.1349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3141    0.6856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0285    1.0981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5604    1.0211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3889    1.8281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0084    0.4080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8074    0.5310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4122   -0.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3505   -0.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650   -1.2654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7795   -0.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4940   -1.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4940   -2.0904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2084   -0.8529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9229   -1.2654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6374   -0.8529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518   -1.2654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0663   -0.8529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0663   -0.0279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3518   -2.0904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0663   -2.5029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6374   -2.5029    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6374   -3.3279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9229   -2.0904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2084   -2.5029    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  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
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 26 28  1  0  0  0  0
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 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0143905

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCC1=CC[C@H]2[C@@H](C[C@@H]1C)OC(=O)[C@@H]2C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O8/c1-10-8-15-14(12(3)20(26)28-15)7-6-13(10)5-4-11(2)27-21-19(25)18(24)17(23)16(9-22)29-21/h6,10-12,14-19,21-25H,4-5,7-9H2,1-3H3/t10-,11+,12+,14+,15+,16+,17+,18-,19+,21+/m0/s1

> <INCHI_KEY>
BLRVOJKFYCRLAO-CJQKKZMYSA-N

> <FORMULA>
C21H34O8

> <MOLECULAR_WEIGHT>
414.495

> <EXACT_MASS>
414.225368055

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
43.42527502711728

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,3aR,7S,8aR)-3,7-dimethyl-6-[(3R)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-2H,3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-2-one

> <ALOGPS_LOGP>
1.17

> <JCHEM_LOGP>
0.6886760609999991

> <ALOGPS_LOGS>
-2.42

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200101071569264

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210589729946511

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835402804763

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
103.6068

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,3aR,7S,8aR)-3,7-dimethyl-6-[(3R)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.478  -3.982   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.249  -2.460   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.223  -2.006   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.786  -0.572   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.292  -0.252   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.453   1.280   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.787   2.050   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.046   1.906   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.726   3.412   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.016   0.762   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.507   0.991   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.636  -0.056   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.521  -1.592   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.855  -2.362   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.188  -1.592   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.522  -2.362   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.522  -3.902   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.856  -1.592   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.189  -2.362   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.523  -1.592   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      11.857  -2.362   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.190  -1.592   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.190  -0.052   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.857  -3.902   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.190  -4.672   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.523  -4.672   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.523  -6.212   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.189  -3.902   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.856  -4.672   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    2   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   19   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
[(1R)-1-Methyl-3-[[(3R)-2-oxo-3a,7b-dimethyl-3,3aalpha,4,7,8,8aalpha-hexahydro-2H-cyclohepta[b]furan]-6-yl]propyl]b-D-glucopyranoside	Generator
[(1R)-1-Methyl-3-[[(3R)-2-oxo-3α,7β-dimethyl-3,3aalpha,4,7,8,8aalpha-hexahydro-2H-cyclohepta[b]furan]-6-yl]propyl]β-D-glucopyranoside	Generator

Chemical Formula

C₂₁H₃₄O₈

Average Mass

414.4950 Da

Monoisotopic Mass

414.22537 Da

IUPAC Name

(3R,3aR,7S,8aR)-3,7-dimethyl-6-[(3R)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-2H,3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-2-one

Traditional Name

(3R,3aR,7S,8aR)-3,7-dimethyl-6-[(3R)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3H,3aH,4H,7H,8H,8aH-cyclohepta[b]furan-2-one

CAS Registry Number

Not Available

SMILES

C[C@H](CCC1=CC[C@H]2[C@@H](C[C@@H]1C)OC(=O)[C@@H]2C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C21H34O8/c1-10-8-15-14(12(3)20(26)28-15)7-6-13(10)5-4-11(2)27-21-19(25)18(24)17(23)16(9-22)29-21/h6,10-12,14-19,21-25H,4-5,7-9H2,1-3H3/t10-,11+,12+,14+,15+,16+,17+,18-,19+,21+/m0/s1

InChI Key

BLRVOJKFYCRLAO-CJQKKZMYSA-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
Arnica amplexicaulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthanolides. These are sesquiterpenoids with a structure based on the xanthanolide skeleton consistsing of a cycloheptane ring usually attached to a four-carbon chain (at carbon 1 ) and a methyl group (at carbon 10), and fused to a five-member lactone ring (sharing carbons 7 and 8). The lactone ring can be conjugated with a methyl or methylene group at position 11.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Xanthanolides

Alternative Parents

Substituents

Xanthanolide-skeleton
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Sesquiterpenoid
Xanthane sesquiterpenoid
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acyl
Gamma butyrolactone
Oxane
Monosaccharide
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Polyol
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Primary alcohol
Carbonyl group
Organooxygen compound
Organic oxide
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	1.17	ALOGPS
logP	0.69	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	12.21	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	6	ChemAxon
Refractivity	103.61 m³·mol⁻¹	ChemAxon
Polarizability	43.43 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

100961118

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one (NP0143905)

MOL for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

3D MOL for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

3D SDF for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

3D-SDF for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

PDB for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

3D PDB for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

SMILES for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

INCHI for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

Structure for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)

3D Structure for NP0143905 ((3r,3ar,7s,8ar)-3,7-dimethyl-6-[(3r)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3h,3ah,4h,7h,8h,8ah-cyclohepta[b]furan-2-one)