NP-MRD: Showing NP-Card for (1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate (NP0151040)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 07:17:42 UTC

Updated at

2022-09-02 07:17:42 UTC

NP-MRD ID

NP0151040

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate

Description

(1S,2S,5R,7R,8R,11R,12R)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]Tetradec-3-en-2-yl (2Z)-2-methylbut-2-enoate belongs to the class of organic compounds known as cedrane and isocedrane sesquiterpenoids. These are sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position. (1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate is found in Perezia multiflora. Based on a literature review very few articles have been published on (1S,2S,5R,7R,8R,11R,12R)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]Tetradec-3-en-2-yl (2Z)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022209172D          

 27 30  0  0  1  0            999 V2000
    0.0265    3.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7968    3.8552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1635    3.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9868    3.0641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7068    2.4291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0734    1.6900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1166    2.4811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5733    1.7940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4088    1.8211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7849    1.0313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5949    1.1853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8894    1.9560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7041    2.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0894    0.5388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7730   -0.2365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3102   -0.8626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1210   -0.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9380   -0.4362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4578   -1.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6365   -1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5667   -0.2332    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1349    0.2922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5863   -0.3983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8528    0.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2266    1.0376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8991    0.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3929    0.2062    0.0000 C   0  0  1  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  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  1  1  0  0  0
 27 26  1  6  0  0  0
 10 27  1  0  0  0  0
 18 27  1  0  0  0  0
 21 27  1  0  0  0  0
M  END

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    6.0626    1.3313    1.9126 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0500    0.6817    0.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9299    0.2953    0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9623   -0.3581   -1.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6326    0.4746    0.6349 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5346    1.0109    1.7586 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529    0.0683    0.0344 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1986    0.2369    0.6329 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3415    1.2025   -0.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9509    1.0135   -0.2514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9179    2.0319   -0.6698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3293    3.2587   -0.9435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6133    3.7057   -2.2308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8691    2.1316    0.3387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5537    0.9797    0.6503 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8681    1.1878    0.1511 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7832    1.2550    1.1987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9808   -0.2016    0.0148 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3474   -1.5580    0.4590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2879   -2.4303   -0.2435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2247   -1.4495   -0.7686 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1754   -1.8672   -0.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1006   -1.5708   -1.4780 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2431   -3.3616   -0.0685 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5102   -1.0646    0.9066 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9096   -0.7357    1.4070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4867   -0.2860    0.0951 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1150    1.5293    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4810    2.2734    1.8426 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6335    0.6630    2.6842 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9882    0.5214    0.0594 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2939    0.2153   -2.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9975   -0.2930   -1.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5980   -1.3957   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3621    0.7292    1.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8435    2.0361   -0.6105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4953    1.6885   -1.5765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2545    3.0066   -2.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6936    3.9106   -2.3575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0799    4.6673   -2.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6373    0.9293    1.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7776    1.4172    0.7347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8317    0.2286    1.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5373    2.0149    1.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2042   -0.1596   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3661   -1.7348    1.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3621   -1.8088    0.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8643   -3.1165    0.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7446   -3.0056   -1.0588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3003   -1.2978   -1.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1272   -1.9167   -1.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7398   -2.1934   -2.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0432   -0.5231   -1.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0760   -3.6268    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4474   -3.8491   -0.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2693   -3.7384   -0.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0807   -1.6046    1.6592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3486   -1.6410    1.8209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7758    0.0924    2.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 11  1  0
 11 12  1  0
 12 13  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  8 25  1  0
 25 26  1  0
 26 27  1  0
 27 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 18 15  1  0
 27 10  1  6
 21 27  1  0
 22 25  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
 15 41  1  1
 11 37  1  6
 13 38  1  0
 13 39  1  0
 13 40  1  0
  9 36  1  0
  8 35  1  1
  4 32  1  0
  4 33  1  0
  4 34  1  0
  2 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 25 57  1  1
 26 58  1  0
 26 59  1  0
 18 45  1  6
 19 46  1  0
 19 47  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  6
 23 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
M  END


  Mrv1652309022209172D          

 27 30  0  0  1  0            999 V2000
    0.0265    3.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7968    3.8552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1635    3.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9868    3.0641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7068    2.4291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0734    1.6900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1166    2.4811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5733    1.7940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4088    1.8211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7849    1.0313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5949    1.1853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8894    1.9560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7041    2.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0894    0.5388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7730   -0.2365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3102   -0.8626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1210   -0.7105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9380   -0.4362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4578   -1.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6365   -1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5667   -0.2332    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1349    0.2922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5863   -0.3983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8528    0.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2266    1.0376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8991    0.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3929    0.2062    0.0000 C   0  0  1  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  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  1  1  0  0  0
 27 26  1  6  0  0  0
 10 27  1  0  0  0  0
 18 27  1  0  0  0  0
 21 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0151040

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1O[C@@H](OC)C2=C[C@H](OC(=O)C(\C)=C/C)[C@H]3C[C@@]22[C@H]1CC[C@@H]2C3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O5/c1-7-12(2)18(23)26-16-10-14-20(25-6)27-19(24-5)13-8-9-17-21(3,4)15(16)11-22(13,14)17/h7,10,13,15-17,19-20H,8-9,11H2,1-6H3/b12-7-/t13-,15+,16-,17+,19+,20+,22+/m0/s1

> <INCHI_KEY>
BJUQFXHEOFGDTN-PEJXRLDSSA-N

> <FORMULA>
C22H32O5

> <MOLECULAR_WEIGHT>
376.493

> <EXACT_MASS>
376.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.4663024092701

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,5R,7R,8R,11R,12R)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradec-3-en-2-yl (2Z)-2-methylbut-2-enoate

> <ALOGPS_LOGP>
3.72

> <JCHEM_LOGP>
4.126900003999999

> <ALOGPS_LOGS>
-4.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8967226701849618

> <JCHEM_POLAR_SURFACE_AREA>
53.99000000000001

> <JCHEM_REFRACTIVITY>
102.69640000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.98e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5R,7R,8R,11R,12R)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradec-3-en-2-yl (2Z)-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       0.050   7.293   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.487   7.196   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.172   5.817   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.709   5.720   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.319   4.534   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.004   3.155   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.218   4.631   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.070   3.349   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.630   3.399   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.332   1.925   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.844   2.213   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.394   3.651   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.914   3.894   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.767   1.006   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.176  -0.441   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.179  -1.610   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.693  -1.326   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.618  -0.814   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.721  -2.163   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.188  -1.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.058  -0.435   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.252   0.545   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.094  -0.744   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.592   1.304   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.423   1.937   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.678   1.129   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.600   0.385   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   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22    8   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   10   18   21                                             
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,5R,7R,8R,11R,12R)-5,7-Dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0,.0,]tetradec-3-en-2-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₂H₃₂O₅

Average Mass

376.4930 Da

Monoisotopic Mass

376.22497 Da

IUPAC Name

(1S,2S,5R,7R,8R,11R,12R)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradec-3-en-2-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(1S,2S,5R,7R,8R,11R,12R)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradec-3-en-2-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CO[C@@H]1O[C@@H](OC)C2=C[C@H](OC(=O)C(\C)=C/C)[C@H]3C[C@@]22[C@H]1CC[C@@H]2C3(C)C

InChI Identifier

InChI=1S/C22H32O5/c1-7-12(2)18(23)26-16-10-14-20(25-6)27-19(24-5)13-8-9-17-21(3,4)15(16)11-22(13,14)17/h7,10,13,15-17,19-20H,8-9,11H2,1-6H3/b12-7-/t13-,15+,16-,17+,19+,20+,22+/m0/s1

InChI Key

BJUQFXHEOFGDTN-PEJXRLDSSA-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
Perezia multiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cedrane and isocedrane sesquiterpenoids. These are sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Cedrane and isocedrane sesquiterpenoids

Alternative Parents

Substituents

Isocedrane sesquiterpenoid
Fatty acid ester
Oxane
Fatty acyl
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Acetal
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
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	3.72	ALOGPS
logP	4.13	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	53.99 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	102.7 m³·mol⁻¹	ChemAxon
Polarizability	42.47 Å³	ChemAxon
Number of Rings	4	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

162943761

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate (NP0151040)

MOL for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

PDB for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

Structure for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0151040 ((1s,2s,5r,7r,8r,11r,12r)-5,7-dimethoxy-14,14-dimethyl-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradec-3-en-2-yl (2z)-2-methylbut-2-enoate)