NP-MRD: Showing NP-Card for ajugarin-iv (NP0146539)

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Record Information

Version

2.0

Created at

2022-09-02 01:57:15 UTC

Updated at

2022-09-02 01:57:16 UTC

NP-MRD ID

NP0146539

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ajugarin-iv

Description

Ajugarin IV belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. ajugarin-iv is found in Ajuga ciliata and Cornutia pyramidata. ajugarin-iv was first documented in 2007 (PMID: 17943556). Based on a literature review very few articles have been published on Ajugarin IV.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022203572D          

 29 31  0  0  1  0            999 V2000
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3276    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1060    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6363    2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4367    2.8397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1364    3.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1939    4.0999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7684    2.7466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593    1.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    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
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 23 28  1  0  0  0  0
  5 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
   -5.0731   -0.2038    2.2387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6966   -0.3875    1.9092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2784   -0.9993    0.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1931   -1.3920   -0.0255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8854   -1.2076    0.3702 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1092   -2.0342    1.3294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2357   -1.3485    2.3097 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6210   -0.2384    1.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3066   -0.2455    0.2327 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3736    0.4153   -0.5829 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9737    1.5248    0.2093 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3053   -0.5775   -1.2152 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0856   -1.5192   -0.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1835   -1.1940    0.4105 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8109   -0.1046    0.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8810   -0.3503    1.6905 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6537    0.5013    2.1710 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8606   -1.6884    1.9650 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8642   -2.2915    1.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8080    1.0981   -1.8419 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7457    2.1954   -2.3347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5298    1.7263   -1.6249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4551    0.5344   -1.3619 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7583    1.0646   -1.4285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6875    0.7016   -2.3972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0645    1.2936   -2.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3238   -0.1478   -3.2504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1108    0.0833    0.0401 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6852    1.1274    0.9648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5441    0.5901    1.6575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6195   -1.1724    2.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1154   -0.0536    3.3402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8321   -1.7717   -0.6188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8866   -2.5864    1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5378   -2.8721    0.8589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7693   -1.0180    3.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4499   -2.1512    2.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4519    0.7338    2.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6917   -0.4871    1.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4429   -1.3499   -0.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7209    2.1208   -0.3632 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1313    2.2497    0.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3786    1.2762    1.1869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6216   -1.1863   -1.9047 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9745   -0.0575   -1.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5655   -2.1953   -1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4210   -2.3487    0.0210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6090    0.8957    0.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2238   -3.0818    0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0902   -2.6963    1.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6963    0.3890   -2.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5777    3.1330   -1.7672 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202    2.4092   -3.3845 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7860    1.8783   -2.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8014    2.2145   -2.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4582    2.4308   -0.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2467   -0.2235   -2.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1087    2.2116   -1.8316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2336    1.6127   -3.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8405    0.5495   -2.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1685    2.0771    1.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7334    0.7793    2.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7440    1.3651    0.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 10 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 23 28  1  0
 28 29  1  1
 28  5  1  0
 28  9  1  0
 19 14  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  6
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  6
 11 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 15 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  6
 21 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  6
 26 58  1  0
 26 59  1  0
 26 60  1  0
 29 61  1  0
 29 62  1  0
 29 63  1  0
M  END


  Mrv1652309022203572D          

 29 31  0  0  1  0            999 V2000
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3276    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1060    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6363    2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4367    2.8397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1364    3.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1939    4.0999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7684    2.7466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593    1.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    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
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 23 28  1  0  0  0  0
  5 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0146539

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1CCC[C@@H]2[C@@](C)(CCC3=CC(=O)OC3)[C@H](C)C[C@H](OC(C)=O)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O6/c1-14-11-19(29-15(2)24)23(4)17(21(26)27-5)7-6-8-18(23)22(14,3)10-9-16-12-20(25)28-13-16/h12,14,17-19H,6-11,13H2,1-5H3/t14-,17+,18-,19+,22+,23+/m1/s1

> <INCHI_KEY>
IPBJLEBCIOWRHJ-IKZNSBIOSA-N

> <FORMULA>
C23H34O6

> <MOLECULAR_WEIGHT>
406.519

> <EXACT_MASS>
406.235538815

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
44.8876155421126

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,4aR,5S,6R,8S,8aR)-8-(acetyloxy)-5,6,8a-trimethyl-5-[2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-decahydronaphthalene-1-carboxylate

> <ALOGPS_LOGP>
4.33

> <JCHEM_LOGP>
3.736197913

> <ALOGPS_LOGS>
-5.20

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.471545113435094

> <JCHEM_PKA_STRONGEST_BASIC>
-6.475366184344085

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
107.55359999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.55e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,4aR,5S,6R,8S,8aR)-8-(acetyloxy)-5,6,8a-trimethyl-5-[2-(5-oxo-2H-furan-3-yl)ethyl]-octahydronaphthalene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.345   1.180   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.325   1.180   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.798   2.627   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.788   3.807   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.415   5.301   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.721   6.117   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.829   7.653   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       8.901   5.127   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.324   3.699   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   28                                                  
CONECT   10    9   11   12   20                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   14                                                       
CONECT   20   10   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   23    5    9   29                                             
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₆

Average Mass

406.5190 Da

Monoisotopic Mass

406.23554 Da

IUPAC Name

methyl (1R,4aR,5S,6R,8S,8aR)-8-(acetyloxy)-5,6,8a-trimethyl-5-[2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-decahydronaphthalene-1-carboxylate

Traditional Name

methyl (1R,4aR,5S,6R,8S,8aR)-8-(acetyloxy)-5,6,8a-trimethyl-5-[2-(5-oxo-2H-furan-3-yl)ethyl]-octahydronaphthalene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1CCC[C@@H]2[C@@](C)(CCC3=CC(=O)OC3)[C@H](C)C[C@H](OC(C)=O)[C@@]12C

InChI Identifier

InChI=1S/C23H34O6/c1-14-11-19(29-15(2)24)23(4)17(21(26)27-5)7-6-8-18(23)22(14,3)10-9-16-12-20(25)28-13-16/h12,14,17-19H,6-11,13H2,1-5H3/t14-,17+,18-,19+,22+,23+/m1/s1

InChI Key

IPBJLEBCIOWRHJ-IKZNSBIOSA-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
Ajuga ciliata	LOTUS Database	35616633
Cornutia pyramidata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Tricarboxylic acid or derivatives
2-furanone
Dihydrofuran
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	4.33	ALOGPS
logP	3.74	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	7.47	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	107.55 m³·mol⁻¹	ChemAxon
Polarizability	44.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9080847

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10905588

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Manguro LO, Ogur JA, Okora DM, Wagai SO, Lemmen P: Further flavonol and iridoid glycosides from Ajuga remota aerial parts. J Asian Nat Prod Res. 2007 Sep-Dec;9(6-8):617-29. doi: 10.1080/10286020600979480. [PubMed:17943556 ]
LOTUS database [Link]

Showing NP-Card for ajugarin-iv (NP0146539)

MOL for NP0146539 (ajugarin-iv)

3D MOL for NP0146539 (ajugarin-iv)

3D SDF for NP0146539 (ajugarin-iv)

3D-SDF for NP0146539 (ajugarin-iv)

PDB for NP0146539 (ajugarin-iv)

3D PDB for NP0146539 (ajugarin-iv)

SMILES for NP0146539 (ajugarin-iv)

INCHI for NP0146539 (ajugarin-iv)

Structure for NP0146539 (ajugarin-iv)

3D Structure for NP0146539 (ajugarin-iv)