NP-MRD: Showing NP-Card for Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside (NP0141287)

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Record Information

Version

2.0

Created at

2022-06-29 22:43:04 UTC

Updated at

2022-06-29 22:43:04 UTC

NP-MRD ID

NP0141287

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside

Description

2-({[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]Heptan-2-yl}oxy)oxane-3,4,5-triol belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside is found in Centella erecta and Gynochthodes officinalis. 2-({[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]Heptan-2-yl}oxy)oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201504022D          

 31 34  0  0  0  0            999 V2000
    0.2085   -0.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9988    0.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050    0.9543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050   -0.6957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050   -1.5207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6340   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484    0.5418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629    0.9543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    3.0168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1099    3.5017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3649    4.2863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1899    4.2863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1036    5.1068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9969    4.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2518    5.2425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4448    3.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2294    3.2468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4919    0.9543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4919   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629   -0.6957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629   -1.5207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  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
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 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  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 20 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 67 70  0  0  0  0  0  0  0  0999 V2000
   -5.2564   -0.8687   -1.2027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0041   -0.6159    0.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2080   -0.1055    0.9464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4031   -1.8474    0.9375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1169   -1.2871    2.2960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6020    0.1178    1.9579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7708    0.2792    0.4674 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9536    1.6575   -0.0026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7719   -0.5436   -0.3106 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4765   -0.1784   -0.1333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9077    0.1645   -1.3550 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1205   -0.6643   -1.7270 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3531   -0.3759   -1.1910 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4161   -0.6196    0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6411   -0.3487    0.8350 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7049   -1.0738    0.3851 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3380   -1.7989    1.4045 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4616   -2.3106    0.7165 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0875   -1.0088    0.2258 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9078   -1.2027   -0.8704 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8786   -0.3445    1.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1083   -0.1232    2.4585 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8379   -0.2123   -0.1265 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8634    1.0458    0.4738 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8437    1.0088   -1.5276 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7480    0.9693   -2.6158 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7771    1.9628   -1.9157 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1088    3.2604   -1.4604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5578    1.6283   -1.3457 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6538    2.1831   -0.0486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0815   -1.9480    0.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3469   -1.0912   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7260   -1.7825   -1.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0471    0.0262   -1.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8627   -0.9962    1.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0285    0.4913    1.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7992    0.5041    0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0233   -2.7171    0.8907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0376   -1.2250    2.9285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3663   -1.8580    2.8706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1404    0.8996    2.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5382    0.1510    2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6080    1.7522   -1.0599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0188    1.9957    0.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3647    2.3533    0.6156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1144   -0.4970   -1.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6996    0.0337   -2.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0794   -1.0801   -1.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6332   -0.0610    0.8591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2229   -1.7178    0.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4853   -1.8257   -0.3991 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1722   -2.8767   -0.1808 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1451   -2.8461    1.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6684   -0.5701   -0.9033 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6827   -1.0513    1.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3369    0.5647    0.9245 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6181    0.4563    3.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8295   -0.1150   -1.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0538    1.0759    1.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4025    1.4335   -0.6705 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9696    0.0413   -2.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6896    2.0600   -3.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6607    3.7061   -2.1503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3061    2.2323   -1.9436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6346    3.1675   -0.1559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2961   -2.1832    0.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1234   -2.6726   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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  5  6  1  0
  6  7  1  0
  7  8  1  1
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  9 31  1  0
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 10 11  1  0
 11 12  1  0
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 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
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 23 24  1  0
 13 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
  7  2  1  0
 29 11  1  0
 31  4  1  0
 23 16  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  1
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  6
 31 66  1  0
 31 67  1  0
 11 47  1  6
 13 48  1  6
 14 49  1  0
 14 50  1  0
 16 51  1  6
 18 52  1  0
 18 53  1  0
 20 54  1  0
 21 55  1  0
 21 56  1  0
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 23 58  1  6
 24 59  1  0
 25 60  1  1
 26 61  1  0
 27 62  1  6
 28 63  1  0
 29 64  1  6
 30 65  1  0
M  END


  Mrv1533004201504022D          

 31 34  0  0  0  0            999 V2000
    0.2085   -0.1075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9988    0.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050    0.9543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050   -0.6957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2050   -1.5207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6340   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484    0.5418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629    0.9543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    3.0168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1099    3.5017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3649    4.2863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1899    4.2863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1036    5.1068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9969    4.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2518    5.2425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4448    3.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2294    3.2468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774    0.5418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4919    0.9543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7774   -0.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4919   -0.6957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629   -0.6957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0629   -1.5207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  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
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
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 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 14 26  1  0  0  0  0
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 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0141287

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C2CCC1(C)C(C2)OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O10/c1-19(2)10-4-5-20(19,3)12(6-10)31-17-15(25)14(24)13(23)11(30-17)7-28-18-16(26)21(27,8-22)9-29-18/h10-18,22-27H,4-9H2,1-3H3

> <INCHI_KEY>
RVQFSOHDFFWTLD-UHFFFAOYSA-N

> <FORMULA>
C21H36O10

> <MOLECULAR_WEIGHT>
448.509

> <EXACT_MASS>
448.230847359

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
46.78767510539382

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.34

> <JCHEM_LOGP>
-1.0578768213333347

> <ALOGPS_LOGS>
-1.84

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.31822053580622

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.705016769934259

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1423790163389214

> <JCHEM_POLAR_SURFACE_AREA>
158.3

> <JCHEM_REFRACTIVITY>
104.39780000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.52e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       0.389  -0.201   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.864   0.241   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.389   0.683   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.249   1.781   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.916   1.011   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.916  -0.529   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.249  -1.299   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.249  -2.839   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.583  -0.529   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.583   1.011   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.917  -1.299   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.250  -0.529   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.250   1.011   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.584   1.781   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.584   3.321   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.918   4.091   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.918   5.631   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.672   6.537   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.148   8.001   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.688   8.001   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.527   9.533   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.194   8.321   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.670   9.786   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.164   6.537   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.628   6.061   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.918   1.011   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.251   1.781   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.918  -0.529   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.251  -1.299   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.584  -1.299   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.584  -2.839   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    7                                             
CONECT    3    2                                                            
CONECT    4    2    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    2    8    9                                             
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13   30                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   24                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22                                                            
CONECT   24   20   17   25                                                  
CONECT   25   24                                                            
CONECT   26   14   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   12   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
Borneol 7-O-[b-D-apiofuranosyl-(1->6)]-b-D-glucopyranoside	Generator
Borneol 7-O-[β-D-apiofuranosyl-(1->6)]-β-D-glucopyranoside	Generator
1-Borneol-beta-apisyl-beta-glucopyranoside	MeSH
BBABGP	MeSH

Chemical Formula

C₂₁H₃₆O₁₀

Average Mass

448.5090 Da

Monoisotopic Mass

448.23085 Da

IUPAC Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

Traditional Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-({1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl}oxy)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC1(C)C2CCC1(C)C(C2)OC1OC(COC2OCC(O)(CO)C2O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C21H36O10/c1-19(2)10-4-5-20(19,3)12(6-10)31-17-15(25)14(24)13(23)11(30-17)7-28-18-16(26)21(27,8-22)9-29-18/h10-18,22-27H,4-9H2,1-3H3

InChI Key

RVQFSOHDFFWTLD-UHFFFAOYSA-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
Centella erecta	LOTUS Database	35616633
Morinda officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
Bornane monoterpenoid
Bicyclic monoterpenoid
Norbornane monoterpenoid
Monoterpenoid
Oxane
Tetrahydrofuran
Tertiary alcohol
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Primary alcohol
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	-0.34	ALOGPS
logP	-1.1	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	11.71	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	158.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	104.4 m³·mol⁻¹	ChemAxon
Polarizability	46.79 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

14526908

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside (NP0141287)

MOL for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

3D MOL for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

3D SDF for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

3D-SDF for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

PDB for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

3D PDB for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

SMILES for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

INCHI for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

Structure for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)

3D Structure for NP0141287 (Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside)