NP-MRD: Showing NP-Card for (1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate (NP0146668)

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Record Information

Version

2.0

Created at

2022-09-02 02:06:31 UTC

Updated at

2022-09-02 02:06:32 UTC

NP-MRD ID

NP0146668

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate

Description

3-(Hydroxymethyl)-5alpha-acetoxy-6beta-isopropyl-2-cyclohexene-1beta,4alpha-diol 1,4-bis[(E)-2-methyl-2-butenoate] belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. (1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate is found in Sphaeranthus suaveolens. Based on a literature review very few articles have been published on 3-(Hydroxymethyl)-5alpha-acetoxy-6beta-isopropyl-2-cyclohexene-1beta,4alpha-diol 1,4-bis[(E)-2-methyl-2-butenoate].

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204062D          

 29 29  0  0  1  0            999 V2000
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  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
    2.8579    2.4750    0.0000 C   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
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    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  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
   -5.0869   -3.2369   -1.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1895   -2.1891   -0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6530   -1.2454    0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0971   -1.2590    0.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8085   -0.2094    0.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2813    0.6694    1.6523 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4398   -0.1285    0.6311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6084    0.8768    1.1666 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6828    0.1842    2.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4814   -0.3096    1.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3719   -0.9849    2.6853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7962   -0.9929    3.9373 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8603   -0.1654    0.3144 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2687   -0.3262    0.1248 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7885   -1.3464   -0.6573 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0333   -2.1717   -1.2312 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2400   -1.4999   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8285   -2.5619   -1.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0706   -0.6423   -0.2495 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5516   -0.7641   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5268    1.2265   -0.1392 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5088    2.0843    0.4236 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4547    2.7427   -0.3382 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850    3.6414    0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295    2.5622   -1.5835 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8662    1.6767    0.1448 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6037    1.8886   -1.1459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9750    0.6710   -1.8847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8260    2.7434   -0.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6657   -3.6065   -1.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1000   -2.8108   -1.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1511   -4.1198   -0.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1405   -2.2145   -0.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7125   -1.0278   -0.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3779   -0.5217    1.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3739   -2.2683    1.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2563    1.5267    1.7906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9587    0.0756    3.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506   -0.4639    2.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5519   -2.0470    2.3481 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8498   -0.0860    4.3204 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3716   -0.9619   -0.2516 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5601   -2.1408   -2.4004 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1109   -3.1554   -2.2259 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4166   -3.2625   -1.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7147    0.1601    0.3629 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0604   -0.5390    0.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8427    0.0064   -1.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8378   -1.7874   -0.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7178    1.2358   -1.2527 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609    4.6699    0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6534    3.4167    1.3301 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4185    3.6646   -0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7670    2.7162    0.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9073    2.5175   -1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8204    0.8634   -2.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0934    0.5241   -1.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253   -0.2391   -1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7548    2.1461   -0.7858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9113    3.5223   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6789    3.2734    0.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 13 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 26  8  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  4 34  1  0
  4 35  1  0
  4 36  1  0
  8 37  1  1
  9 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  6
 18 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  6
 24 51  1  0
 24 52  1  0
 24 53  1  0
 26 54  1  1
 27 55  1  0
 28 56  1  0
 28 57  1  0
 28 58  1  0
 29 59  1  0
 29 60  1  0
 29 61  1  0
M  END


  Mrv1652309022204062D          

 29 29  0  0  1  0            999 V2000
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  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
    2.8579    2.4750    0.0000 C   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
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    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  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146668

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@H]1C=C(CO)[C@H](OC(=O)C(\C)=C\C)[C@H](OC(C)=O)[C@H]1C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O7/c1-8-13(5)21(25)28-17-10-16(11-23)19(29-22(26)14(6)9-2)20(27-15(7)24)18(17)12(3)4/h8-10,12,17-20,23H,11H2,1-7H3/b13-8+,14-9+/t17-,18-,19-,20+/m0/s1

> <INCHI_KEY>
CUSTUSNKTKJKCL-VBCAGKPSSA-N

> <FORMULA>
C22H32O7

> <MOLECULAR_WEIGHT>
408.491

> <EXACT_MASS>
408.21480337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
44.136813687778016

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,5S,6R)-6-(acetyloxy)-2-(hydroxymethyl)-4-{[(2E)-2-methylbut-2-enoyl]oxy}-5-(propan-2-yl)cyclohex-2-en-1-yl (2E)-2-methylbut-2-enoate

> <ALOGPS_LOGP>
3.49

> <JCHEM_LOGP>
3.736671901666667

> <ALOGPS_LOGS>
-3.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.070019392119445

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7681735178869546

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000002

> <JCHEM_REFRACTIVITY>
109.50529999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.97e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,5S,6R)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2E)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2E)-2-methylbut-2-enoate

> <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       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.667   1.540   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   13   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21    8   27                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Value	Source
3-(Hydroxymethyl)-5a-acetoxy-6b-isopropyl-2-cyclohexene-1b,4a-diol 1,4-bis[(e)-2-methyl-2-butenoate]	Generator
3-(Hydroxymethyl)-5a-acetoxy-6b-isopropyl-2-cyclohexene-1b,4a-diol 1,4-bis[(e)-2-methyl-2-butenoic acid]	Generator
3-(Hydroxymethyl)-5alpha-acetoxy-6beta-isopropyl-2-cyclohexene-1beta,4alpha-diol 1,4-bis[(e)-2-methyl-2-butenoic acid]	Generator
3-(Hydroxymethyl)-5α-acetoxy-6β-isopropyl-2-cyclohexene-1β,4α-diol 1,4-bis[(e)-2-methyl-2-butenoate]	Generator
3-(Hydroxymethyl)-5α-acetoxy-6β-isopropyl-2-cyclohexene-1β,4α-diol 1,4-bis[(e)-2-methyl-2-butenoic acid]	Generator

Chemical Formula

C₂₂H₃₂O₇

Average Mass

408.4910 Da

Monoisotopic Mass

408.21480 Da

IUPAC Name

(1S,4S,5S,6R)-6-(acetyloxy)-2-(hydroxymethyl)-4-{[(2E)-2-methylbut-2-enoyl]oxy}-5-(propan-2-yl)cyclohex-2-en-1-yl (2E)-2-methylbut-2-enoate

Traditional Name

(1S,4S,5S,6R)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2E)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@H]1C=C(CO)[C@H](OC(=O)C(\C)=C\C)[C@H](OC(C)=O)[C@H]1C(C)C

InChI Identifier

InChI=1S/C22H32O7/c1-8-13(5)21(25)28-17-10-16(11-23)19(29-22(26)14(6)9-2)20(27-15(7)24)18(17)12(3)4/h8-10,12,17-20,23H,11H2,1-7H3/b13-8+,14-9+/t17-,18-,19-,20+/m0/s1

InChI Key

CUSTUSNKTKJKCL-VBCAGKPSSA-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
Sphaeranthus suaveolens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Monocyclic monoterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Cyclitol or derivatives
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Carboxylic acid derivative
Primary alcohol
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	3.49	ALOGPS
logP	3.74	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	15.07	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	109.51 m³·mol⁻¹	ChemAxon
Polarizability	44.14 Å³	ChemAxon
Number of Rings	1	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101705718

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate (NP0146668)

MOL for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

PDB for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

Structure for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0146668 ((1s,4s,5s,6r)-6-(acetyloxy)-2-(hydroxymethyl)-5-isopropyl-4-{[(2e)-2-methylbut-2-enoyl]oxy}cyclohex-2-en-1-yl (2e)-2-methylbut-2-enoate)