NP-MRD: Showing NP-Card for (1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate (NP0252128)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 15:32:46 UTC

Updated at

2022-09-07 15:32:46 UTC

NP-MRD ID

NP0252128

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate

Description

(1S,2Z,4S,8R,9R,11S,12R)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]Tetradec-2-en-9-yl (2R)-2-methylbutanoate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate is found in Aldama bracteata. Based on a literature review very few articles have been published on (1S,2Z,4S,8R,9R,11S,12R)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]Tetradec-2-en-9-yl (2R)-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072217322D          

 29 31  0  0  1  0            999 V2000
   -0.5639    4.3908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    4.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9840    4.7713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8978    5.5918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985    4.3588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5270    3.5518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2414    3.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5770    2.3856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3975    2.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8824    1.8044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4055    1.5787    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1199    1.1662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7924    1.0266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9719    0.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8004    0.1334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157   -0.1215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2574    1.3529    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6443    0.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9219    2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0934    2.9136    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3789    3.3261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3356    2.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3356    2.0886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0500    3.3261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0500    4.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7645    2.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4790    3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    3.4656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3032    1.7343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  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  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 28  1  0  0  0  0
 28  2  1  6  0  0  0
  6 28  1  0  0  0  0
 17 29  1  0  0  0  0
 11 29  1  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
    1.8444    3.5174   -0.3165 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6211    3.1494   -0.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0609    3.4450   -1.8915 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4653    3.9993   -2.9039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3898    2.9915   -1.7415 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2052    1.7916   -0.9406 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5573    0.8566   -1.8364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798   -0.3844   -1.9503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0159   -1.0812   -3.2999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2068   -2.2142   -3.2718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4159   -1.0942   -0.7258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1274   -2.4647   -1.0068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8533   -1.0415   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8893   -0.7131    1.0651 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5609   -1.6156    1.8310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6485   -1.0968    2.5182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498   -0.5106    1.4516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0658   -1.4202    2.6269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1293    0.8983    1.8675 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0965    1.4740    1.1859 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9650    0.5142    0.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2482    0.2832    1.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6684    1.0109    2.0821 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1150   -0.7889    0.5378 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4720   -0.6771    1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3024   -0.4939   -0.9471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2418   -1.4526   -1.5979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3573    2.3968    0.1449 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6676   -0.8345    0.3925 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3077    3.2803    0.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4462    4.0878   -1.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1787    1.5449   -0.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    1.1516   -2.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0810   -1.3518   -3.4537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7105   -0.4294   -4.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7345   -2.9392   -3.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9444   -2.9000   -1.3996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3757   -2.0443   -0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4828   -0.3849   -1.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3923    0.2789    1.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4194   -0.6671    1.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3565   -0.3860    3.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1284   -1.9606    3.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625   -2.4265    2.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1893   -1.0130    3.1719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8943   -1.4806    3.3637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0519    0.9648    2.9841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0296    1.5117    1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6073    2.0662    1.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6650   -1.7828    0.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2305   -1.3201    0.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7596    0.4014    1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3341   -0.9347    2.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475   -0.3799   -1.4778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7963    0.5198   -0.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3102   -1.1951   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1566   -1.3189   -2.6969 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0365   -2.5030   -1.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0306    3.1660    0.6333 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  1
 17 29  1  0
 29 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 11  8  1  0
  8  9  1  0
  9 10  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 28  1  0
 28 20  1  0
 14 17  1  0
 28  6  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 26 54  1  0
 26 55  1  0
 24 50  1  6
 25 51  1  0
 25 52  1  0
 25 53  1  0
 20 49  1  1
 19 47  1  0
 19 48  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  6
 16 41  1  0
 16 42  1  0
 16 43  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
  7 33  1  0
  6 32  1  1
  1 30  1  0
  1 31  1  0
 28 59  1  1
M  END


  Mrv1652309072217322D          

 29 31  0  0  1  0            999 V2000
   -0.5639    4.3908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    4.2193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9840    4.7713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8978    5.5918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985    4.3588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5270    3.5518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2414    3.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5770    2.3856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3975    2.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8824    1.8044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4055    1.5787    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1199    1.1662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7924    1.0266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9719    0.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8004    0.1334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157   -0.1215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2574    1.3529    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6443    0.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9219    2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0934    2.9136    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3789    3.3261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3356    2.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3356    2.0886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0500    3.3261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0500    4.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7645    2.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4790    3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    3.4656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3032    1.7343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  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  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 28  1  0  0  0  0
 28  2  1  6  0  0  0
  6 28  1  0  0  0  0
 17 29  1  0  0  0  0
 11 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252128

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)C(=O)O[C@@H]1C[C@]2(C)O[C@@](O)(C[C@H]2OC)\C(CO)=C/[C@@H]2OC(=O)C(=C)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O8/c1-6-11(2)18(23)28-15-8-20(4)16(26-5)9-21(25,29-20)13(10-22)7-14-17(15)12(3)19(24)27-14/h7,11,14-17,22,25H,3,6,8-10H2,1-2,4-5H3/b13-7-/t11-,14+,15-,16-,17+,20+,21+/m1/s1

> <INCHI_KEY>
OEKVPPIIFHRGBC-UUXZUGTBSA-N

> <FORMULA>
C21H30O8

> <MOLECULAR_WEIGHT>
410.463

> <EXACT_MASS>
410.194067926

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.811912719845715

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2Z,4S,8R,9R,11S,12R)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-2-en-9-yl (2R)-2-methylbutanoate

> <JCHEM_LOGP>
1.706055147333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.091701103419428

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.32661871258586

> <JCHEM_PKA_STRONGEST_BASIC>
-2.800026966363445

> <JCHEM_POLAR_SURFACE_AREA>
111.52000000000002

> <JCHEM_REFRACTIVITY>
102.2394

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2Z,4S,8R,9R,11S,12R)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-2-en-9-yl (2R)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.053   8.196   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.559   7.876   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.703   8.906   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.543  10.438   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -5.037   8.136   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.717   6.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.051   5.860   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.677   4.453   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.209   4.614   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -9.114   3.368   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -6.357   2.947   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -7.691   2.177   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -5.212   1.916   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.681   1.755   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.361   0.249   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.896  -0.227   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.347   2.525   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.203   1.495   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.721   3.932   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.041   5.439   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.707   6.209   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.626   5.439   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.626   3.899   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.960   6.209   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.960   7.749   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.294   5.439   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.627   6.209   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.185   6.469   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.299   3.237   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13   29                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19   29                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   20    2    6                                                  
CONECT   29   17   11                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
(1S,2Z,4S,8R,9R,11S,12R)-1-Hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0,]tetradec-2-en-9-yl (2R)-2-methylbutanoic acid	Generator

Chemical Formula

C₂₁H₃₀O₈

Average Mass

410.4630 Da

Monoisotopic Mass

410.19407 Da

IUPAC Name

(1S,2Z,4S,8R,9R,11S,12R)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-2-en-9-yl (2R)-2-methylbutanoate

Traditional Name

(1S,2Z,4S,8R,9R,11S,12R)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0^{4,8}]tetradec-2-en-9-yl (2R)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)O[C@@H]1C[C@]2(C)O[C@@](O)(C[C@H]2OC)\C(CO)=C/[C@@H]2OC(=O)C(=C)[C@H]12

InChI Identifier

InChI=1S/C21H30O8/c1-6-11(2)18(23)28-15-8-20(4)16(26-5)9-21(25,29-20)13(10-22)7-14-17(15)12(3)19(24)27-14/h7,11,14-17,22,25H,3,6,8-10H2,1-2,4-5H3/b13-7-/t11-,14+,15-,16-,17+,20+,21+/m1/s1

InChI Key

OEKVPPIIFHRGBC-UUXZUGTBSA-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
Aldama bracteata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Monosaccharide
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Lactone
Hemiacetal
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
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	1.71	ChemAxon
pKa (Strongest Acidic)	11.33	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	111.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	102.24 m³·mol⁻¹	ChemAxon
Polarizability	41.81 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

163077383

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate (NP0252128)

MOL for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

3D MOL for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

3D SDF for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

3D-SDF for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

PDB for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

3D PDB for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

SMILES for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

INCHI for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

Structure for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)

3D Structure for NP0252128 ((1s,2z,4s,8r,9r,11s,12r)-1-hydroxy-2-(hydroxymethyl)-12-methoxy-11-methyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradec-2-en-9-yl (2r)-2-methylbutanoate)