NP-MRD: Showing NP-Card for (1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate (NP0191978)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 09:05:06 UTC

Updated at

2022-09-04 09:05:06 UTC

NP-MRD ID

NP0191978

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate

Description

Punctaliatrin 5'-acetate belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety. (1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate is found in Liatris ohlingerae. Based on a literature review very few articles have been published on Punctaliatrin 5'-acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042211052D          

 30 32  0  0  1  0            999 V2000
    0.6529   -2.8609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6793   -2.0363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0278   -1.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.7600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3077   -0.7542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -0.7806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4122   -0.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0948    0.4588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    1.2511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4364    1.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9194    0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5709   -0.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8006   -0.8660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3328   -1.4965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5207   -1.6421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8320   -2.4061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8381   -2.1054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0135   -2.0790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7336   -2.8551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2657   -3.4855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0778   -3.3399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9858   -4.2616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1738   -4.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6416   -3.7768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180   -4.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3300   -4.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8621   -5.3769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6742   -5.2312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5822   -6.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619   -1.5730    0.0000 C   0  0  1  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 18 30  1  0  0  0  0
 30  2  1  1  0  0  0
  6 30  1  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
    0.8854    0.1591    2.4739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1977    0.7131    1.9693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8702    1.9641    2.3073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2296    2.9778    2.7537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1989    1.7829    2.0513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3977    0.7905    1.0011 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3925   -0.1940    1.5023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3638   -0.8292    0.9223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1668   -1.7522    1.8424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1408   -3.0646    1.4529 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8656   -0.8372   -0.4304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1969   -0.7996   -1.5532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7232   -0.7389   -1.4560 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0327   -0.6836   -2.7425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2506    0.4490   -2.0072 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2543    1.4114   -2.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0459    1.1349   -1.4710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3642    0.2732   -0.4409 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9801    0.5830   -0.2599 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9843   -0.2740   -0.6433 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6454   -1.3476   -1.1634 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4121    0.0121   -0.4715 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3202   -0.8553   -0.8620 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9496   -2.1597   -1.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7479    1.3247    0.1618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1025    1.5468    0.3162 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9640    0.8483    1.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4066    1.1473    1.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5009   -0.1030    1.8395 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0527    0.1572    0.8646 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2260   -0.7850    2.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4694    0.5920    3.2708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7360    1.4427    0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1915   -0.3727    2.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2539   -1.4374    1.7822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8065   -1.7018    2.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1909   -3.6552    2.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9686   -0.8803   -0.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6706   -0.8100   -2.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2783   -1.5169   -0.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7239    2.2829   -3.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9570    1.7087   -1.8412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8447    0.8523   -3.3792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2383    2.1654   -1.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3216    1.2455   -2.3160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3895   -0.7578   -0.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896   -0.6176   -0.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9076   -2.7280   -1.6972 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4250   -2.0333   -2.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3799   -2.8190   -0.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2078    1.3509    1.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3202    2.1020   -0.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    0.3086    1.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7719    1.3085    0.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5337    2.0462    1.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1627   -0.9272    1.1856 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  2  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 22 20  1  0
 20 21  2  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  1  6
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  2  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 30  1  0
 30 18  1  0
 13 15  1  0
 30  6  1  0
 24 48  1  0
 24 49  1  0
 24 50  1  0
 23 47  1  0
 25 51  1  0
 25 52  1  0
 28 53  1  0
 28 54  1  0
 28 55  1  0
 18 46  1  6
 17 44  1  0
 17 45  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 13 40  1  1
 12 39  1  0
 11 38  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
  7 34  1  0
  6 33  1  6
  1 31  1  0
  1 32  1  0
 30 56  1  1
M  END


  Mrv1652309042211052D          

 30 32  0  0  1  0            999 V2000
    0.6529   -2.8609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6793   -2.0363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0278   -1.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7646   -1.7600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3077   -0.7542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -0.7806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4122   -0.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0948    0.4588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    1.2511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4364    1.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9194    0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5709   -0.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8006   -0.8660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3328   -1.4965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5207   -1.6421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8320   -2.4061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8381   -2.1054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0135   -2.0790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7336   -2.8551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2657   -3.4855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0778   -3.3399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9858   -4.2616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1738   -4.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6416   -3.7768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180   -4.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3300   -4.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8621   -5.3769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6742   -5.2312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5822   -6.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3619   -1.5730    0.0000 C   0  0  1  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 18 30  1  0  0  0  0
 30  2  1  1  0  0  0
  6 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0191978

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O8/c1-5-15(11-27-13(3)24)21(26)29-17-9-22(4)18(30-22)7-6-14(10-23)8-16-19(17)12(2)20(25)28-16/h5-8,16-19,23H,2,9-11H2,1,3-4H3/b7-6-,14-8+,15-5-/t16-,17-,18-,19+,22-/m1/s1

> <INCHI_KEY>
DFBYEUMOPVSHIP-BMJPBUAUSA-N

> <FORMULA>
C22H26O8

> <MOLECULAR_WEIGHT>
418.442

> <EXACT_MASS>
418.162767797

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.21893552654397

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,4R,6R,7Z,9E,11R)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0^{4,6}]tetradeca-7,9-dien-2-yl (2Z)-2-[(acetyloxy)methyl]but-2-enoate

> <JCHEM_LOGP>
1.3839354673333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.119632305139461

> <JCHEM_PKA_STRONGEST_BASIC>
-2.746472829731978

> <JCHEM_POLAR_SURFACE_AREA>
111.66000000000003

> <JCHEM_REFRACTIVITY>
107.7273

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4R,6R,7Z,9E,11R)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0^{4,6}]tetradeca-7,9-dien-2-yl (2Z)-2-[(acetyloxy)methyl]but-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.219  -5.340   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.268  -3.801   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.052  -2.857   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.427  -3.285   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       0.574  -1.408   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.114  -1.457   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.636  -0.008   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.910   0.856   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.481   2.335   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.548   3.446   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.449   0.807   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.666  -0.138   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.095  -1.617   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.088  -2.793   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.572  -3.065   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.153  -4.491   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.298  -3.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.759  -3.881   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.236  -5.329   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.229  -6.506   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.745  -6.235   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.707  -7.955   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.191  -8.227   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.198  -7.050   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.700  -9.132   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.216  -8.860   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.209 -10.037   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.725  -9.765   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.687 -11.485   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.542  -2.936   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13   15                                                       
CONECT   15   14   13   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   30                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   18    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
Punctaliatrin 5'-acetic acid	Generator

Chemical Formula

C₂₂H₂₆O₈

Average Mass

418.4420 Da

Monoisotopic Mass

418.16277 Da

IUPAC Name

(1R,2R,4R,6R,7Z,9E,11R)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0^{4,6}]tetradeca-7,9-dien-2-yl (2Z)-2-[(acetyloxy)methyl]but-2-enoate

Traditional Name

(1R,2R,4R,6R,7Z,9E,11R)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0^{4,6}]tetradeca-7,9-dien-2-yl (2Z)-2-[(acetyloxy)methyl]but-2-enoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H26O8/c1-5-15(11-27-13(3)24)21(26)29-17-9-22(4)18(30-22)7-6-14(10-23)8-16-19(17)12(2)20(25)28-16/h5-8,16-19,23H,2,9-11H2,1,3-4H3/b7-6-,14-8+,15-5-/t16-,17-,18-,19+,22-/m1/s1

InChI Key

DFBYEUMOPVSHIP-BMJPBUAUSA-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
Liatris ohlingerae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Germacranolides and derivatives

Alternative Parents

Substituents

Germacranolide
Sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	1.38	ChemAxon
pKa (Strongest Acidic)	15.12	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	111.66 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	107.73 m³·mol⁻¹	ChemAxon
Polarizability	42.22 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

101677682

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate (NP0191978)

MOL for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

3D MOL for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

3D SDF for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

3D-SDF for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

PDB for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

3D PDB for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

SMILES for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

INCHI for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

Structure for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)

3D Structure for NP0191978 ((1r,2r,4r,6r,7z,9e,11r)-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradeca-7,9-dien-2-yl (2z)-2-[(acetyloxy)methyl]but-2-enoate)