NP-MRD: Showing NP-Card for rhodojaponin i (NP0323024)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 02:10:34 UTC

Updated at

2022-09-12 02:10:34 UTC

NP-MRD ID

NP0323024

Secondary Accession Numbers

None

Natural Product Identification

Common Name

rhodojaponin i

Description

Rhodojaponin I belongs to the class of organic compounds known as grayanoids. These are diterpenoids containing a skeleton based on or derived from the ent-kaurane moiety. Grayanoids usually possess either one of the grayanane, the 2,4-seco-grayanane, the 9,10-seco-grayanane, the 1,5-seco-grayanane, the kalmane, or the leucothane skeleton. Some derivatives also include the 1,5-seco-kalmane skeleton. rhodojaponin i is found in Rhododendron catawbiense. Based on a literature review very few articles have been published on Rhodojaponin I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122204102D          

 32 36  0  0  1  0            999 V2000
    1.9713    1.8928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3049    1.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5505    1.7405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4057    0.4656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -0.2732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4317    0.1455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9248    0.8653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7765    0.7886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0934   -0.0157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5916   -0.7427    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9482   -1.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7396   -1.7795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4970   -2.6352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8615   -3.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0308   -4.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0775   -2.9474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4264   -1.3137    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7144   -2.0975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5057   -0.4926    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3111   -0.3142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1361   -0.3072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7297   -1.0251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1829   -1.6429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0459   -1.8564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156   -2.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9162    0.0851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6188    0.6375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3134    0.9080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8197   -1.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1260   -0.6743    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5371   -1.2450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6401   -0.2553    0.0000 O   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  6  0  0  0
 22 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 26  1  0  0  0  0
  9 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  1  0  0  0
 10 29  1  6  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  1  0  0  0
M  END

     RDKit          3D

 68 72  0  0  0  0  0  0  0  0999 V2000
    2.2073    3.3357    2.4325 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9706    1.9037    2.1285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5209    1.1887    3.0604 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2044    1.3141    0.9201 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9879   -0.0446    0.6014 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3010   -0.7189    0.2022 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0688   -2.1717    0.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6012   -2.4772   -0.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9064   -1.5208   -1.0914 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2104   -0.1547   -0.6941 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1440    0.8743   -0.7487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9375    0.7971    0.2990 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6512    2.0438    0.1630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7670    2.9896    1.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5281    4.2275    0.8641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2265    2.8130    2.2270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9708   -0.2306   -0.0872 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5339    0.1552   -1.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3888   -1.5828   -0.0780 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6351   -2.4655   -0.0233 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7248   -2.0794   -0.8027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7216   -1.6663    0.5055 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1099   -0.3350    0.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6550   -0.4917    2.3290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1205    0.7409    0.6932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5040   -1.9706   -1.2027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0964   -1.7513   -2.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4570   -3.3978   -1.1199 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2914    0.3803   -1.6642 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6071   -0.0562   -1.0888 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3338   -0.8936   -2.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4194    1.0643   -0.8243 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    3.3741    3.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9255    3.8200    1.7742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2842    3.9339    2.4710 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5841   -0.6535    1.4075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0918   -0.5447    0.9575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259   -2.6996    0.9326 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5938   -2.6345   -0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5193   -3.4897   -0.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0712   -2.5442    0.8489 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3773   -1.7896   -2.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6712    1.8583   -0.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2898    1.0518   -1.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5103    0.6856    1.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8053    5.0653    0.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2229    4.4853    1.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1069    4.1800   -0.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3112    1.0796   -1.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8533   -1.7510    0.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5380   -3.5155    0.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5460   -2.0454    1.1228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9168    0.2239    2.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5649   -0.3542    2.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3509   -1.5525    2.4771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8536    1.3337   -0.1848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1725    1.4351    1.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1269    0.2971    0.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7165   -0.8536   -3.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1945   -1.7967   -2.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8145   -2.5915   -3.2880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2849   -3.7747   -1.5381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2758    1.4644   -1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0933   -0.0510   -2.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9065   -0.1921   -2.7623 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6509   -1.4368   -2.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1157   -1.5397   -1.6328 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2122    1.7026   -1.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  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  1  0
 10 29  1  6
 29 30  1  0
 30 31  1  0
 30 32  1  1
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 12 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 19 26  1  0
 26 27  1  0
 26 28  1  1
 10  5  1  0
 23 17  1  0
 30  6  1  0
 22 20  1  0
 26  9  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  1
  6 37  1  1
  7 38  1  0
  7 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  6
 29 63  1  0
 29 64  1  0
 31 65  1  0
 31 66  1  0
 31 67  1  0
 32 68  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  1
 15 46  1  0
 15 47  1  0
 15 48  1  0
 18 49  1  0
 19 50  1  1
 20 51  1  1
 22 52  1  1
 24 53  1  0
 24 54  1  0
 24 55  1  0
 25 56  1  0
 25 57  1  0
 25 58  1  0
 27 59  1  0
 27 60  1  0
 27 61  1  0
 28 62  1  0
M  END


  Mrv1652309122204102D          

 32 36  0  0  1  0            999 V2000
    1.9713    1.8928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3049    1.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5505    1.7405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4057    0.4656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -0.2732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4317    0.1455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9248    0.8653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7765    0.7886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0934   -0.0157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5916   -0.7427    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9482   -1.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7396   -1.7795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4970   -2.6352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8615   -3.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0308   -4.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0775   -2.9474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4264   -1.3137    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7144   -2.0975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5057   -0.4926    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3111   -0.3142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1361   -0.3072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7297   -1.0251    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1829   -1.6429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0459   -1.8564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156   -2.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9162    0.0851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6188    0.6375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3134    0.9080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8197   -1.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1260   -0.6743    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5371   -1.2450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6401   -0.2553    0.0000 O   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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  6  0  0  0
 22 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 26  1  0  0  0  0
  9 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  1  0  0  0
 10 29  1  6  0  0  0
 29 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0323024

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1[C@H]2CC[C@@H]3[C@@]1(C[C@@]2(C)O)C[C@@H](OC(C)=O)[C@@]1(O)[C@@H]([C@@H]2O[C@@H]2C1(C)C)[C@]3(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C24H36O8/c1-11(25)30-15-9-23-10-21(5,27)13(18(23)31-12(2)26)7-8-14(23)22(6,28)17-16-19(32-16)20(3,4)24(15,17)29/h13-19,27-29H,7-10H2,1-6H3/t13-,14+,15-,16+,17+,18-,19+,21-,22-,23+,24-/m1/s1

> <INCHI_KEY>
BQXZYRJBFJGDSL-PLZLAMROSA-N

> <FORMULA>
C24H36O8

> <MOLECULAR_WEIGHT>
452.544

> <EXACT_MASS>
452.241018119

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
47.16641478802408

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,4R,6R,8S,9S,10R,11R,14R,15R,17R)-17-(acetyloxy)-4,10,15-trihydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0^{1,11}.0^{4,9}.0^{6,8}]heptadecan-3-yl acetate

> <JCHEM_LOGP>
0.01571311766666781

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.275023218098877

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.017596878113736

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9372974380097068

> <JCHEM_POLAR_SURFACE_AREA>
125.82000000000001

> <JCHEM_REFRACTIVITY>
110.74619999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4R,6R,8S,9S,10R,11R,14R,15R,17R)-17-(acetyloxy)-4,10,15-trihydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0^{1,11}.0^{4,9}.0^{6,8}]heptadecan-3-yl acetate

> <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       3.680   3.533   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.436   2.625   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.028   3.249   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.624   0.869   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.942  -0.510   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.806   0.272   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.726   1.615   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.316   1.472   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.908  -0.029   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.971  -1.386   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.637  -2.829   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.114  -3.322   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.661  -4.919   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.475  -5.982   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.791  -7.489   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.011  -5.502   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.396  -2.452   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.934  -3.915   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.544  -0.919   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.047  -0.586   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.587  -0.573   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.829  -1.914   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.808  -3.067   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.419  -3.465   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.496  -4.895   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.444   0.159   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.755   1.190   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.185   1.695   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.530  -2.239   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.235  -1.259   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.003  -2.324   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.195  -0.477   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   26                                                  
CONECT   10    9    5   11   29                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18   19   23                                             
CONECT   18   17                                                            
CONECT   19   17   20   26                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   22                                                       
CONECT   22   21   20   23                                                  
CONECT   23   22   17   24   25                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   19    9   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   10   30                                                       
CONECT   30   29    6   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₆O₈

Average Mass

452.5440 Da

Monoisotopic Mass

452.24102 Da

IUPAC Name

(1S,3R,4R,6R,8S,9S,10R,11R,14R,15R,17R)-17-(acetyloxy)-4,10,15-trihydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0^{1,11}.0^{4,9}.0^{6,8}]heptadecan-3-yl acetate

Traditional Name

(1S,3R,4R,6R,8S,9S,10R,11R,14R,15R,17R)-17-(acetyloxy)-4,10,15-trihydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.0^{1,11}.0^{4,9}.0^{6,8}]heptadecan-3-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1[C@H]2CC[C@@H]3[C@@]1(C[C@@]2(C)O)C[C@@H](OC(C)=O)[C@@]1(O)[C@@H]([C@@H]2O[C@@H]2C1(C)C)[C@]3(C)O

InChI Identifier

InChI=1S/C24H36O8/c1-11(25)30-15-9-23-10-21(5,27)13(18(23)31-12(2)26)7-8-14(23)22(6,28)17-16-19(32-16)20(3,4)24(15,17)29/h13-19,27-29H,7-10H2,1-6H3/t13-,14+,15-,16+,17+,18-,19+,21-,22-,23+,24-/m1/s1

InChI Key

BQXZYRJBFJGDSL-PLZLAMROSA-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
Rhododendron catawbiense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as grayanoids. These are diterpenoids containing a skeleton based on or derived from the ent-kaurane moiety. Grayanoids usually possess either one of the grayanane, the 2,4-seco-grayanane, the 9,10-seco-grayanane, the 1,5-seco-grayanane, the kalmane, or the leucothane skeleton. Some derivatives also include the 1,5-seco-kalmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Grayanoids

Alternative Parents

Substituents

Grayanoid
Dicarboxylic acid or derivatives
Oxane
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Polyol
Organoheterocyclic compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organooxygen compound
Organic oxygen 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	0.016	ChemAxon
pKa (Strongest Acidic)	13.02	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	125.82 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	110.75 m³·mol⁻¹	ChemAxon
Polarizability	47.17 Å³	ChemAxon
Number of Rings	5	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

C00003479

Chemspider ID

58827909

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101306700

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for rhodojaponin i (NP0323024)

MOL for NP0323024 (rhodojaponin i)

3D MOL for NP0323024 (rhodojaponin i)

3D SDF for NP0323024 (rhodojaponin i)

3D-SDF for NP0323024 (rhodojaponin i)

PDB for NP0323024 (rhodojaponin i)

3D PDB for NP0323024 (rhodojaponin i)

SMILES for NP0323024 (rhodojaponin i)

INCHI for NP0323024 (rhodojaponin i)

Structure for NP0323024 (rhodojaponin i)

3D Structure for NP0323024 (rhodojaponin i)