NP-MRD: Showing NP-Card for (1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate (NP0147465)

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Record Information

Version

2.0

Created at

2022-09-02 03:04:42 UTC

Updated at

2022-09-02 03:04:42 UTC

NP-MRD ID

NP0147465

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate

Description

CHEMBL3608604 belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate is found in Leonurus macranthus. Based on a literature review very few articles have been published on CHEMBL3608604.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022205042D          

 28 30  0  0  1  0            999 V2000
   -1.5674    1.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1942    0.5638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6448   -0.1272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3704    0.5192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0028   -0.2166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8266   -0.2613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7275    0.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -0.0215    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8030    0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5924    1.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7795    1.8253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1948    0.4581    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9841    0.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0077   -0.3455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8178   -0.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2165   -0.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6528   -1.5141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2266   -2.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -2.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2087   -2.8305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8667   -3.3282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9057   -1.1641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2183   -0.5852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6170   -1.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313   -1.3887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2419   -1.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6396   -1.0648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1498   -1.3045    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
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 14 22  1  1  0  0  0
 14 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
    4.9865    2.6469    1.0215 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9420    1.5939   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8430    1.4319   -0.8789 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8791    0.7495   -0.0560 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6420   -0.2858   -0.9279 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281   -1.0399   -0.6805 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3467   -2.0487   -1.8642 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1266   -0.1916   -0.7822 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3250    1.2405   -1.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0107    1.7020   -1.6862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0875    2.6834   -2.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2418    0.9372   -1.3399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6660    0.0193   -2.4485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1895    0.3453    0.0365 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4988    1.5155    1.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227    1.4650    0.9945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2297   -0.0299    0.9446 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9731   -0.4702    2.4111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6178   -0.4721    0.6825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2933   -0.0732   -0.5669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7369   -0.5073   -1.7445 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2360   -0.5520    0.1826 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1698   -0.2099    0.3978 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7501    0.5341    1.5821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0154   -1.6715    0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2923   -2.2546    1.2759 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5267   -1.8568    0.5403 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1525   -3.0846    0.1816 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0077    2.8157    1.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580    3.6155    0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3488    2.3498    1.8797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6445    0.0892   -1.9865 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4678   -1.0131   -0.8708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6248   -2.8590   -1.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3736   -2.5158   -1.8067 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2700   -1.5303   -2.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4959   -0.6437   -1.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0225    1.3892   -1.9987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5318    1.9246   -0.3046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0485    1.7357   -1.2956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9646   -0.9817   -2.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9220   -0.0365   -3.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5808    0.4173   -2.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2035    2.4769    0.5737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2049    1.3198    2.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4183    2.0278    0.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4063    1.9111    1.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3563   -1.5314    2.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7152    0.1132    3.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9522   -0.3729    2.7215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7141   -1.6062    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3233   -0.1626    1.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3195   -0.5588   -0.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5584    1.0214   -0.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0226    0.1157   -2.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8492    0.3670    1.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6693    1.6371    1.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3330    0.1100    2.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1543   -2.1819   -0.2618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7933   -1.9312    1.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356   -3.3480    1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3848   -1.8788    2.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3054   -1.4258    1.2415 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1132   -2.9755    0.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  6
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6 27  1  0
 27 28  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  1  1
 23 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 17 22  1  0
 14 12  1  0
 14 22  1  6
 23  8  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 12 40  1  1
  9 38  1  0
  9 39  1  0
  8 37  1  6
  7 34  1  0
  7 35  1  0
  7 36  1  0
  5 32  1  0
  5 33  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 27 63  1  1
 28 64  1  0
 26 61  1  0
 26 62  1  0
 25 59  1  0
 25 60  1  0
 24 56  1  0
 24 57  1  0
 24 58  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
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 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
M  END


  Mrv1652309022205042D          

 28 30  0  0  1  0            999 V2000
   -1.5674    1.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1942    0.5638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6448   -0.1272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3704    0.5192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0028   -0.2166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8266   -0.2613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7275    0.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -0.0215    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8030    0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5924    1.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7795    1.8253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1948    0.4581    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9841    0.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0077   -0.3455    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8178   -0.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2165   -0.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6528   -1.5141    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2266   -2.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -2.0118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2087   -2.8305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8667   -3.3282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9057   -1.1641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2183   -0.5852    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6170   -1.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313   -1.3887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2419   -1.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6396   -1.0648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1498   -1.3045    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
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 14 22  1  1  0  0  0
 14 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0147465

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C(=O)C[C@H]2[C@@](C)(COC(C)=O)[C@H](O)CC[C@]2(C)[C@@]11CC[C@@](C)(CCO)O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O6/c1-14-16(25)12-17-20(4,13-27-15(2)24)18(26)6-7-21(17,5)22(14)9-8-19(3,28-22)10-11-23/h14,17-18,23,26H,6-13H2,1-5H3/t14-,17+,18-,19+,20-,21+,22-/m1/s1

> <INCHI_KEY>
CBDKPIJNECSIQI-DBPZYVDISA-N

> <FORMULA>
C22H36O6

> <MOLECULAR_WEIGHT>
396.524

> <EXACT_MASS>
396.251188879

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
43.55338291958936

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,2S,4aS,5S,5'S,6R,8aS)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-octahydro-2H-spiro[naphthalene-1,2'-oxolane]-5-yl]methyl acetate

> <ALOGPS_LOGP>
1.79

> <JCHEM_LOGP>
1.4552772283333322

> <ALOGPS_LOGS>
-3.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.903829289367266

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.605584963412308

> <JCHEM_PKA_STRONGEST_BASIC>
-2.413250423955052

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
104.26879999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.48e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4aS,5S,5'S,6R,8aS)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolane]-5-ylmethyl acetate

> <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      -2.926   2.426   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.229   1.053   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -3.070  -0.238   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.691   0.969   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.005  -0.404   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.543  -0.488   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.358   1.041   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.017  -0.040   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.366   1.460   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.839   1.907   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.188   3.407   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.964   0.855   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.437   1.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.614  -0.645   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.127  -0.354   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.871  -1.702   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.818  -2.826   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.023  -4.145   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.047  -3.755   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.856  -5.284   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.084  -6.213   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       5.424  -2.173   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.141  -1.092   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.885  -2.441   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.792  -2.592   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.318  -3.040   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.194  -1.988   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.280  -2.435   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                                                       
CONECT    6    5    7    8   27                                             
CONECT    7    6                                                            
CONECT    8    6    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   22   23                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   22                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   17   14                                                       
CONECT   23   14    8   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26    6   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₆O₆

Average Mass

396.5240 Da

Monoisotopic Mass

396.25119 Da

IUPAC Name

[(1R,2S,4aS,5S,5'S,6R,8aS)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-octahydro-2H-spiro[naphthalene-1,2'-oxolane]-5-yl]methyl acetate

Traditional Name

(1R,2S,4aS,5S,5'S,6R,8aS)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolane]-5-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C(=O)C[C@H]2[C@@](C)(COC(C)=O)[C@H](O)CC[C@]2(C)[C@@]11CC[C@@](C)(CCO)O1

InChI Identifier

InChI=1S/C22H36O6/c1-14-16(25)12-17-20(4,13-27-15(2)24)18(26)6-7-21(17,5)22(14)9-8-19(3,28-22)10-11-23/h14,17-18,23,26H,6-13H2,1-5H3/t14-,17+,18-,19+,20-,21+,22-/m1/s1

InChI Key

CBDKPIJNECSIQI-DBPZYVDISA-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
Leonurus macranthus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Grindelane diterpenoid
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Ketone
Secondary alcohol
Cyclic ketone
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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	1.79	ALOGPS
logP	1.46	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	14.61	ChemAxon
pKa (Strongest Basic)	-2.4	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	5	ChemAxon
Refractivity	104.27 m³·mol⁻¹	ChemAxon
Polarizability	43.55 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	No	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

59001137

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122187007

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate (NP0147465)

MOL for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

3D MOL for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

3D SDF for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

3D-SDF for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

PDB for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

3D PDB for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

SMILES for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

INCHI for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

Structure for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)

3D Structure for NP0147465 ((1r,2s,4as,5s,5's,6r,8as)-6-hydroxy-5'-(2-hydroxyethyl)-2,5,5',8a-tetramethyl-3-oxo-hexahydrospiro[naphthalene-1,2'-oxolan]-5-ylmethyl acetate)