NP-MRD: Showing NP-Card for Effusanin B (NP0077946)

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Record Information

Version

2.0

Created at

2022-04-28 23:05:43 UTC

Updated at

2022-04-28 23:05:43 UTC

NP-MRD ID

NP0077946

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Effusanin B

Description

Effusanin B belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Effusanin B is found in Isodon adenolomus, Isodon effusus, Isodon longitubus, Isodon parvifolius, Isodon rugosus and Isodon trichocarpus. Effusanin B was first documented in 2003 (PMID: 12567293). Based on a literature review a small amount of articles have been published on Effusanin B (PMID: 16643043).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201052D          

 28 32  0  0  1  0            999 V2000
    7.3349   -0.7720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6004    0.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9763    0.5828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341    0.4235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8274   -0.4538    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5193   -0.9618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3535   -1.7700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9705   -2.3176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8047   -3.1258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7533   -2.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9206   -0.6791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3622    0.1026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7341    0.9050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6118    1.1973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8774    1.9784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4550    0.6284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1273   -0.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845    1.5203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5366    0.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4488    1.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0491    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0821   -0.8796    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5820   -1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4244   -1.3877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8131   -0.5412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5371    1.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    1.3912    0.0000 C   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  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 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
  4 14  1  0  0  0  0
 14 15  1  1  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  6  0  0  0
 13 18  1  6  0  0  0
 12 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  1  6  0  0  0
 23 26  1  6  0  0  0
 12 26  1  6  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    5.1631    0.3077    1.1275 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9730    0.1016    0.6008 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8084   -0.6036    1.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7683   -1.0676    2.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8147   -0.6292    0.0540 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6751   -0.4942   -1.2102 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997    0.6214   -0.7639 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7942    1.8563   -0.6208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3154    1.6998   -0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8107    0.4908    0.1651 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5430   -0.0107   -0.2859 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4197   -0.8544   -1.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4845   -1.8685   -1.3767 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0789   -1.9145   -0.1102 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9549   -2.9837   -0.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0112   -2.1364    0.8815 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4673   -2.3372    2.1861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0054   -0.9810    0.8182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4003   -1.4103    0.7813 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5863   -2.9367    0.6349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9929   -1.1735    2.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3184   -0.8031   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8397    0.3763   -0.9468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5827    1.0307   -0.3727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3540    2.1043   -1.2480 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5168    3.4216   -0.8629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2810    4.5705   -1.7703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8822    3.6694    0.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9385    0.8489    0.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3836   -0.0898    2.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2064   -1.4448   -1.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1005   -0.1736   -2.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4902    0.7141   -1.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0129    2.4983   -1.5261 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2164    2.4841    0.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9953    2.5819    0.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9087    1.7298   -1.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7229    0.6841    1.2783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2640   -0.2515   -2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4154   -1.3666   -1.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3423   -3.0895    0.7956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4832   -3.1125    0.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0432   -1.8396    2.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7760   -0.3831    1.7566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7154   -3.0472    0.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2682   -3.2997   -0.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2585   -3.4789    1.5163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5211   -1.9168    2.8688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -0.1437    2.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0592   -1.4093    2.1313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6892   -1.5439   -0.9840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2954   -0.5134    0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5967    1.2197   -0.9530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6319    0.2119   -2.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8568    1.4052    0.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5100    5.2209   -1.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2030    5.2073   -1.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9363    4.2517   -2.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 28  2  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 19  1  0
 19 20  1  6
 19 21  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  1  6
 14 13  1  0
 13 12  1  0
 11 12  1  6
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  1
  3  4  2  0
  3  2  1  0
  2  1  2  3
 11 24  1  0
  5 10  1  0
 11 18  1  0
  2  7  1  0
  5 14  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 24 55  1  1
 23 53  1  0
 23 54  1  0
 22 51  1  0
 22 52  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
 21 50  1  0
 18 44  1  1
 16 42  1  6
 17 43  1  0
 15 41  1  0
 12 39  1  0
 12 40  1  0
 10 38  1  1
  9 36  1  0
  9 37  1  0
  8 34  1  0
  8 35  1  0
  7 33  1  6
  6 31  1  0
  6 32  1  0
  1 29  1  0
  1 30  1  0
M  END


  Mrv1652304292201052D          

 28 32  0  0  1  0            999 V2000
    7.3349   -0.7720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6004    0.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9763    0.5828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341    0.4235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8274   -0.4538    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5193   -0.9618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3535   -1.7700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9705   -2.3176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8047   -3.1258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7533   -2.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9206   -0.6791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3622    0.1026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7341    0.9050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6118    1.1973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8774    1.9784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4550    0.6284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1273   -0.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845    1.5203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5366    0.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4488    1.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0491    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0821   -0.8796    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5820   -1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4244   -1.3877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8131   -0.5412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5371    1.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    1.3912    0.0000 C   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  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 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
  4 14  1  0  0  0  0
 14 15  1  1  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  6  0  0  0
 13 18  1  6  0  0  0
 12 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  1  6  0  0  0
 23 26  1  6  0  0  0
 12 26  1  6  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077946

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CCC(C)(C)[C@H]2[C@H](O)[C@@]3(O)OC[C@@]12[C@@H]1CC[C@@H]2C[C@]31C(=O)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O6/c1-11-13-5-6-14-20-10-27-22(26,21(14,9-13)17(11)24)18(25)16(20)19(3,4)8-7-15(20)28-12(2)23/h13-16,18,25-26H,1,5-10H2,2-4H3/t13-,14+,15+,16-,18+,20-,21+,22-/m1/s1

> <INCHI_KEY>
TZECSBJPAFKEQJ-FHEFCECDSA-N

> <FORMULA>
C22H30O6

> <MOLECULAR_WEIGHT>
390.476

> <EXACT_MASS>
390.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.95693188821987

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,5R,8S,9S,10S,11R,15S)-9,10-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-15-yl acetate

> <ALOGPS_LOGP>
1.11

> <JCHEM_LOGP>
2.1345909413333333

> <ALOGPS_LOGS>
-2.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.796180958836153

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.59327652326725

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6829736673847773

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
99.5903

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.89e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5R,8S,9S,10S,11R,15S)-9,10-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-15-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      13.692  -1.441   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.187   0.037   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.022   1.088   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.450   0.790   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.878  -0.847   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.169  -1.795   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.860  -3.304   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.012  -4.326   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.702  -5.835   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      14.473  -3.840   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.185  -1.268   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.143   0.192   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.837   1.689   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.475   2.235   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.971   3.693   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      10.183   1.173   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.571  -0.145   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.811   2.838   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.602   0.741   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.438   2.272   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.268  -0.087   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.825   0.451   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.753  -1.642   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.686  -2.929   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.259  -2.590   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.118  -1.010   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.069   2.217   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.716   2.597   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   27   28                                             
CONECT    4    3    5   14                                                  
CONECT    5    4    6   11   17                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    5   12   25                                                  
CONECT   12   11   13   19   26                                             
CONECT   13   12   14   16   18                                             
CONECT   14   13    4   15                                                  
CONECT   15   14                                                            
CONECT   16   13   17                                                       
CONECT   17   16    5                                                       
CONECT   18   13                                                            
CONECT   19   12   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24   11                                                       
CONECT   26   23   12                                                       
CONECT   27    3                                                            
CONECT   28    3                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₆

Average Mass

390.4760 Da

Monoisotopic Mass

390.20424 Da

IUPAC Name

(1S,2S,5R,8S,9S,10S,11R,15S)-9,10-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-15-yl acetate

Traditional Name

(1S,2S,5R,8S,9S,10S,11R,15S)-9,10-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-15-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1CCC(C)(C)[C@H]2[C@H](O)[C@@]3(O)OC[C@@]12[C@@H]1CC[C@@H]2C[C@]31C(=O)C2=C

InChI Identifier

InChI=1S/C22H30O6/c1-11-13-5-6-14-20-10-27-22(26,21(14,9-13)17(11)24)18(25)16(20)19(3,4)8-7-15(20)28-12(2)23/h13-16,18,25-26H,1,5-10H2,2-4H3/t13-,14+,15+,16-,18+,20-,21+,22-/m1/s1

InChI Key

TZECSBJPAFKEQJ-FHEFCECDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Isodon adenolomus	LOTUS Database	35616633
Isodon effusus	LOTUS Database	35616633
Isodon longitubus	LOTUS Database	35616633
Isodon parvifolius	Plant	KNApSAcK
Isodon rugosus	LOTUS Database	35616633
Isodon trichocarpus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Oxane
Cyclic alcohol
Carboxylic acid ester
Hemiacetal
Ketone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
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	1.11	ALOGPS
logP	2.13	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	10.59	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.59 m³·mol⁻¹	ChemAxon
Polarizability	40.96 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

C00041514

Chemspider ID

29367502

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

34174831

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li LM, Li GY, Huang SX, Li SH, Zhou Y, Xiao WL, Lou LG, Ding LS, Sun HD: 7alpha,20-epoxy-ent-kauranoids from Isodon parvifolius. J Nat Prod. 2006 Apr;69(4):645-9. doi: 10.1021/np0600200. [PubMed:16643043 ]
Abbaskhan A, Choudhary MI, Tsuda Y, Parvez M, Atta-ur-Rahman, Shaheen F, Parween Z, Tareen RB, Zaidi MA: A new diepoxy-ent-kauranoid, rugosinin, from Isodon rugosus. Planta Med. 2003 Jan;69(1):94-6. doi: 10.1055/s-2003-37031. [PubMed:12567293 ]

Showing NP-Card for Effusanin B (NP0077946)

MOL for NP0077946 (Effusanin B)

3D MOL for NP0077946 (Effusanin B)

3D SDF for NP0077946 (Effusanin B)

3D-SDF for NP0077946 (Effusanin B)

PDB for NP0077946 (Effusanin B)

3D PDB for NP0077946 (Effusanin B)

SMILES for NP0077946 (Effusanin B)

INCHI for NP0077946 (Effusanin B)

Structure for NP0077946 (Effusanin B)

3D Structure for NP0077946 (Effusanin B)