NP-MRD: Showing NP-Card for (1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one (NP0330972)

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Record Information

Version

2.0

Created at

2022-09-12 16:50:34 UTC

Updated at

2022-09-12 16:50:34 UTC

NP-MRD ID

NP0330972

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Description

(1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one is found in Dendrobium moniliforme. Based on a literature review very few articles have been published on (1'S,2R,2'R,4'S,6'R,7'R,8'S,11'R)-7'-hydroxy-6'-methyl-11'-(propan-2-yl)-4'-{[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]Undecane]-10'-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122218502D          

 31 35  0  0  1  0            999 V2000
    1.1787    1.9467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6550    2.7719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0342    3.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2521    2.4463    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3973    1.5020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0870    1.9546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1631    2.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9494    3.1401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683    3.3478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7505    3.2392    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2094    3.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4499    3.5397    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4024    3.9549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2427    4.7895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8669    5.3290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7119    6.1393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3361    6.6787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1154    6.4078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0674    6.4101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2224    7.2204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6916    5.8707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4709    6.1416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5366    5.0604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1608    4.5210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5217    2.7178    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2530    1.9378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2882    2.5605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3255    2.5321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5781    1.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6134    1.7590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4124    0.8792    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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  7  1  6  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  1  0  0  0
 12 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 27  1  6  0  0  0
 25 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
  5 30  1  0  0  0  0
 30 31  1  6  0  0  0
M  END

     RDKit          3D

 63 67  0  0  0  0  0  0  0  0999 V2000
   -3.7256    1.1323    2.1129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4949    0.0742    1.4600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9067    0.6369    1.1898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0714   -0.5973    0.2638 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8330    0.1049   -1.0068 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6381   -1.0609   -1.8515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9268   -2.0059   -1.0945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4614   -3.0639   -1.5450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8523   -1.4930    0.3031 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5740   -0.7580    0.4482 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4382   -1.7419    0.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4830   -1.1871   -0.7857 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4729   -0.4745   -0.1447 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7457   -0.9444   -0.3287 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4532    0.0546   -0.9774 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0895    0.9358   -0.1373 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6766    2.1204   -0.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7167    2.8702   -1.5375 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1136    0.3623    0.7773 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3820    0.6118    0.2476 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8994   -1.1045    0.9227 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4501   -1.5332    2.1267 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3839   -1.3323    0.9843 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8895   -0.5219    1.9753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4253   -0.3477   -1.6188 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1051    0.3037   -2.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8761   -0.7373   -2.8473 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3385    0.2873   -0.6085 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5493    1.4031    0.0515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5792    0.8791   -1.1751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3712    0.9246   -2.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0107    0.8143    2.8925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2815    1.8182    1.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4465    1.7903    2.6905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7005   -0.7187    2.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5537   -0.1378    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8156    1.4418    0.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3779    0.9848    2.1081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9035   -1.3437    0.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6714    0.7009   -1.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9147   -2.2792    1.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4695   -0.3336    1.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7756   -2.7614    0.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1417   -1.8673    1.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8555   -2.0478   -1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7406   -1.8389   -0.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728    1.3648    0.5196 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1819    2.8050   -0.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4405    1.8249   -1.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3474    3.5270   -0.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0273    0.8129    1.7895 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9059   -0.2310    0.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2878   -1.7057    0.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6749   -2.4944    2.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2597   -2.4141    1.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9566   -0.8829    2.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1459    1.2802   -3.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0808   -0.0893   -3.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2933    1.7484   -0.6132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0563    1.0601    0.9822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1729    2.2989    0.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7206    1.9662   -0.9293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2488    1.1099   -3.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 12 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 29  1  1
 28 30  1  0
 30 31  1  0
  9  4  1  0
 28 10  1  0
 30  5  1  0
 23 14  1  0
 25 27  1  6
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  6
  5 40  1  6
  9 41  1  1
 10 42  1  1
 11 43  1  0
 11 44  1  0
 12 45  1  6
 14 46  1  6
 16 47  1  1
 17 48  1  0
 17 49  1  0
 18 50  1  0
 19 51  1  1
 20 52  1  0
 21 53  1  6
 22 54  1  0
 23 55  1  1
 24 56  1  0
 26 57  1  0
 26 58  1  0
 29 59  1  0
 29 60  1  0
 29 61  1  0
 30 62  1  1
 31 63  1  0
M  END


  Mrv1652309122218502D          

 31 35  0  0  1  0            999 V2000
    1.1787    1.9467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6550    2.7719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0342    3.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2521    2.4463    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3973    1.5020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0870    1.9546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1631    2.7761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9494    3.1401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683    3.3478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7505    3.2392    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2094    3.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4499    3.5397    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4024    3.9549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2427    4.7895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8669    5.3290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7119    6.1393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3361    6.6787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1154    6.4078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0674    6.4101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2224    7.2204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6916    5.8707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4709    6.1416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5366    5.0604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1608    4.5210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5217    2.7178    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2530    1.9378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2882    2.5605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3255    2.5321    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5781    1.8481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6134    1.7590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4124    0.8792    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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  7  1  6  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  1  0  0  0
 12 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 27  1  6  0  0  0
 25 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
  5 30  1  0  0  0  0
 30 31  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0330972

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@H]1[C@@H]2OC(=O)[C@H]1[C@H]1C[C@H](O[C@H]3O[C@H](CO)[C@H](O)[C@@H](O)[C@H]3O)[C@]3(CO3)[C@@]1(C)[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O10/c1-7(2)11-12-8-4-10(30-19-15(25)14(24)13(23)9(5-22)29-19)21(6-28-21)20(8,3)17(26)16(11)31-18(12)27/h7-17,19,22-26H,4-6H2,1-3H3/t8-,9-,10+,11-,12+,13+,14-,15-,16+,17+,19-,20-,21-/m1/s1

> <INCHI_KEY>
VDOXHFZQCMWZFW-NSOVWAARSA-N

> <FORMULA>
C21H32O10

> <MOLECULAR_WEIGHT>
444.477

> <EXACT_MASS>
444.19954723

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
44.15249335828662

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,2'R,4'S,6'R,7'R,8'S,11'R)-7'-hydroxy-6'-methyl-11'-(propan-2-yl)-4'-{[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0^{2,6}]undecane]-10'-one

> <JCHEM_LOGP>
-1.4807784289999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.07740555977081

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.19395232356406

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835547286016

> <JCHEM_POLAR_SURFACE_AREA>
158.44

> <JCHEM_REFRACTIVITY>
101.18510000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,2'R,4'S,6'R,7'R,8'S,11'R)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0^{2,6}]undecane]-10'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       2.200   3.634   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.089   5.174   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.930   6.277   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.204   4.566   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.475   2.804   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.762   3.649   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.905   5.182   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.372   5.861   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.794   6.249   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.268   6.047   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.257   7.209   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.840   6.607   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.751   7.382   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.453   8.940   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.618   9.947   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.329  11.460   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.494  12.467   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.949  11.961   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.126  11.966   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.415  13.478   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.291  10.959   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.746  11.464   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.002   9.446   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.167   8.439   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.974   5.073   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.472   3.617   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.538   4.780   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.474   4.727   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.079   3.450   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.012   3.283   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.637   1.641   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    9                                                  
CONECT    5    4    6   30                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    4   10                                                  
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   25                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   14   24                                                  
CONECT   24   23                                                            
CONECT   25   12   26   27   28                                             
CONECT   26   25   27                                                       
CONECT   27   26   25                                                       
CONECT   28   25   10   29   30                                             
CONECT   29   28                                                            
CONECT   30   28    5   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₂O₁₀

Average Mass

444.4770 Da

Monoisotopic Mass

444.19955 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)[C@H]1[C@@H]2OC(=O)[C@H]1[C@H]1C[C@H](O[C@H]3O[C@H](CO)[C@H](O)[C@@H](O)[C@H]3O)[C@]3(CO3)[C@@]1(C)[C@H]2O

InChI Identifier

InChI=1S/C21H32O10/c1-7(2)11-12-8-4-10(30-19-15(25)14(24)13(23)9(5-22)29-19)21(6-28-21)20(8,3)17(26)16(11)31-18(12)27/h7-17,19,22-26H,4-6H2,1-3H3/t8-,9-,10+,11-,12+,13+,14-,15-,16+,17+,19-,20-,21-/m1/s1

InChI Key

VDOXHFZQCMWZFW-NSOVWAARSA-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
Dendrobium moniliforme	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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

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

162943136

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one (NP0330972)

MOL for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

3D MOL for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

3D SDF for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

3D-SDF for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

PDB for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

3D PDB for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

SMILES for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

INCHI for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

Structure for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)

3D Structure for NP0330972 ((1's,2r,2'r,4's,6'r,7'r,8's,11'r)-7'-hydroxy-11'-isopropyl-6'-methyl-4'-{[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9'-oxaspiro[oxirane-2,5'-tricyclo[6.2.1.0²,⁶]undecan]-10'-one)