NP-MRD: Showing NP-Card for (1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate (NP0271069)

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Record Information

Version

2.0

Created at

2022-09-08 17:14:02 UTC

Updated at

2022-09-08 17:14:02 UTC

NP-MRD ID

NP0271069

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate

Description

(1S,6S,7R,7aS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoate belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open. (1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate is found in Valeriana sorbifolia. Based on a literature review very few articles have been published on (1S,6S,7R,7aS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082219142D          

 31 33  0  0  1  0            999 V2000
    1.4045   -4.4656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1190   -4.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -4.4656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8334   -3.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5479   -4.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2624   -4.4656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2624   -3.6406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769   -4.8781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6913   -4.4656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7776   -3.6451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5845   -3.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970   -2.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5845   -2.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970   -1.3301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5845   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7595   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970    0.0988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8220   -2.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2345   -3.4736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8220   -4.1880    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2345   -4.9025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0595   -4.9025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4720   -5.6170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4720   -4.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2970   -4.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7095   -3.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7095   -4.9025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970   -4.1880    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4450   -4.8011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9970   -5.4142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1901   -5.5857    0.0000 O   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  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 12 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 20 28  1  0  0  0  0
 28 11  1  6  0  0  0
 28 29  1  0  0  0  0
  9 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 31  1  6  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
   -5.3229   -2.5056    1.4481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8153   -1.0825    1.3446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0932   -0.4135    0.1759 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3593   -1.1164   -1.1172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6404   -0.3380    0.5377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8508    0.3058   -0.5529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4249    0.6963   -1.5933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4943    0.4784   -0.4334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6693    1.0747   -1.4099 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0390    2.2707   -0.8870 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2721    1.9866   -0.5382 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190    2.8547    0.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9985    4.1522    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1359    4.0024    1.7636 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7669    5.1584    2.4343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1309    5.1443    3.6213 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1963    6.2788    2.0418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5599    2.4180   -0.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8553    1.2150   -0.6589 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9488    0.2826   -1.1683 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3537   -1.0575   -0.8402 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7830   -1.9707   -1.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8177   -1.5958   -2.9772 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1886   -3.3255   -1.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1886   -3.8125   -0.2445 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7569   -2.9687    0.8914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6127   -5.2007    0.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5138    0.5525   -0.7956 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4957    0.1823   -1.7880 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4168   -0.7915   -2.7625 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9026    0.4630   -3.1839 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7501   -2.8246    0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1838   -3.1862    1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6036   -2.6225    2.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9056   -1.0003    1.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5158   -0.5425    2.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5317    0.6237    0.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6530   -0.4133   -1.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2477   -1.8008   -0.9841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5179   -1.7227   -1.4833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5644    0.3312    1.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2829   -1.3563    0.7631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2831    1.3733   -2.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4381    3.2525   -0.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9275    4.6063    1.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5488    4.8512   -0.0772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4660    4.8564    4.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5965    6.1421    3.7581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0004    4.4431    3.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3458    3.0509    0.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0338    0.3465   -2.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5104   -3.9687   -2.2664 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7106   -2.6185    0.7859 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4734   -2.1065    0.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8063   -3.5151    1.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4249   -5.8291   -0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6907   -5.2837    0.2606 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0098   -5.6404    0.8608 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2990   -0.0536    0.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5949   -1.0742   -3.1773 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018   -1.6565   -2.8259 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 28  1  0
 28 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  3
 25 26  1  0
 25 27  1  0
 20 19  1  0
 19 18  1  0
 18 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 29  9  1  0
 29 31  1  6
 12 11  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  6
  4 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  9 43  1  6
 10 44  1  0
 28 59  1  1
 20 51  1  6
 24 52  1  0
 26 53  1  0
 26 54  1  0
 26 55  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 18 50  1  0
 13 45  1  0
 13 46  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 30 60  1  0
 30 61  1  0
M  END


  Mrv1652309082219142D          

 31 33  0  0  1  0            999 V2000
    1.4045   -4.4656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1190   -4.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -4.4656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8334   -3.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5479   -4.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2624   -4.4656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2624   -3.6406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769   -4.8781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6913   -4.4656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7776   -3.6451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5845   -3.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970   -2.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5845   -2.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970   -1.3301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5845   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7595   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970    0.0988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8220   -2.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2345   -3.4736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8220   -4.1880    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2345   -4.9025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0595   -4.9025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4720   -5.6170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4720   -4.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2970   -4.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7095   -3.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7095   -4.9025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9970   -4.1880    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4450   -4.8011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9970   -5.4142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1901   -5.5857    0.0000 O   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  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 12 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 20 28  1  0  0  0  0
 28 11  1  6  0  0  0
 28 29  1  0  0  0  0
  9 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 31  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0271069

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)CC(=O)O[C@H]1C=C2[C@H]([C@H](OC(=O)C=C(C)C)OC=C2COC(C)=O)[C@@]11CO1

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O8/c1-6-14(4)8-20(26)30-18-9-17-16(10-27-15(5)24)11-28-22(21(17)23(18)12-29-23)31-19(25)7-13(2)3/h7,9,11,14,18,21-22H,6,8,10,12H2,1-5H3/t14-,18-,21+,22-,23+/m0/s1

> <INCHI_KEY>
KLQIXIQHWLZXBE-CWDKFGSUSA-N

> <FORMULA>
C23H30O8

> <MOLECULAR_WEIGHT>
434.485

> <EXACT_MASS>
434.194067926

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
46.05726675372239

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,6S,7R,7aS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoate

> <JCHEM_LOGP>
2.868591117666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.22781479459414

> <JCHEM_PKA_STRONGEST_BASIC>
-4.145410078096423

> <JCHEM_POLAR_SURFACE_AREA>
100.66

> <JCHEM_REFRACTIVITY>
110.68159999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,6S,7R,7aS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       2.622  -8.336   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.955  -9.106   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.289  -8.336   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.289  -6.796   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.623  -9.106   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.956  -8.336   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.956  -6.796   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       9.290  -9.106   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.624  -8.336   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.785  -6.804   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.291  -6.484   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.061  -5.150   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.291  -3.817   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      13.061  -2.483   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.291  -1.149   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.751  -1.149   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.061   0.184   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      14.601  -5.150   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.371  -6.484   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      14.601  -7.818   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      15.371  -9.151   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      16.911  -9.151   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      17.681 -10.485   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      17.681  -7.818   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      19.221  -7.818   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      19.991  -6.484   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      19.991  -9.151   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.061  -7.818   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.031  -8.962   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.061 -10.107   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      11.555 -10.427   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   29                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   12   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   20   11   29                                                  
CONECT   29   28    9   30   31                                             
CONECT   30   29   31                                                       
CONECT   31   30   29                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
(1S,6S,7R,7AS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoic acid	Generator

Chemical Formula

C₂₃H₃₀O₈

Average Mass

434.4850 Da

Monoisotopic Mass

434.19407 Da

IUPAC Name

(1S,6S,7R,7aS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoate

Traditional Name

(1S,6S,7R,7aS)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxirane]-6-yl (3S)-3-methylpentanoate

CAS Registry Number

Not Available

SMILES

CC[C@H](C)CC(=O)O[C@H]1C=C2[C@H]([C@H](OC(=O)C=C(C)C)OC=C2COC(C)=O)[C@@]11CO1

InChI Identifier

InChI=1S/C23H30O8/c1-6-14(4)8-20(26)30-18-9-17-16(10-27-15(5)24)11-28-22(21(17)23(18)12-29-23)31-19(25)7-13(2)3/h7,9,11,14,18,21-22H,6,8,10,12H2,1-5H3/t14-,18-,21+,22-,23+/m0/s1

InChI Key

KLQIXIQHWLZXBE-CWDKFGSUSA-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
Valeriana sorbifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

Iridoid-skeleton
Bicyclic monoterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
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	2.87	ChemAxon
pKa (Strongest Acidic)	18.23	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	100.66 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	110.68 m³·mol⁻¹	ChemAxon
Polarizability	46.06 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

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

162880146

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate (NP0271069)

MOL for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

3D MOL for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

3D SDF for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

3D-SDF for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

PDB for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

3D PDB for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

SMILES for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

INCHI for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

Structure for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)

3D Structure for NP0271069 ((1s,6s,7r,7as)-4-[(acetyloxy)methyl]-1-[(3-methylbut-2-enoyl)oxy]-6,7a-dihydro-1h-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl (3s)-3-methylpentanoate)