NP-MRD: Showing NP-Card for (3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate (NP0147456)

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Record Information

Version

2.0

Created at

2022-09-02 03:04:02 UTC

Updated at

2022-09-02 03:04:02 UTC

NP-MRD ID

NP0147456

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate

Description

(3AR,4R,9aR,9bR)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. (3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate is found in Mikania vitifolia. Based on a literature review very few articles have been published on (3aR,4R,9aR,9bR)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022205042D          

 26 28  0  0  1  0            999 V2000
    0.5751    2.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3431    3.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4660    3.9357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9881    2.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7560    2.9069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    1.7897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101    1.2753    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2534    1.6333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9967    1.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417    1.7897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4097    1.4883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1803    0.4710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527    0.1811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6412    0.6356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157   -0.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5607   -1.1574    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.1204   -0.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305   -1.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6659   -0.1740    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.1740    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3864   -0.8625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912   -0.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461   -1.1574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541    0.1811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8656    0.6356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3265    0.4710    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 17  1  6  0  0  0
 12 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
 26 24  1  6  0  0  0
  7 26  1  0  0  0  0
 20 26  1  0  0  0  0
M  END

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
    4.8359    0.4998    0.7332 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6267    0.2099    0.2887 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4821   -0.2186   -1.1159 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4965    0.3250    1.1981 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6775    0.6940    2.3821 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1927    0.0454    0.8323 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0679    0.1407    1.6661 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6364   -1.1888    1.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8772   -1.8977    0.5577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3407   -3.2698    0.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681   -3.2711    0.6136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5320   -1.4251   -0.4759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7768   -2.0675   -1.7452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4031   -3.1924   -2.1093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5734   -1.1214   -2.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1567   -1.4369   -4.1864 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.8083   -0.0140   -1.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5906    1.1720   -2.3707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1810   -0.0697   -0.5825 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0684    0.9369   -0.4171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3611    2.2172   -0.8812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4690    3.1064   -0.2514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0241    4.1814   -0.7298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1881    2.4949    1.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5171    3.0719    1.9958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8576    1.1738    1.0623 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7165    0.4353    0.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0205    0.8241    1.7620 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4138   -0.1452   -1.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743   -1.2443   -1.2919 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0475    0.4439   -1.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2982    0.4862    2.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6395   -0.9527    2.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1052   -1.7854    2.5824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6489   -3.7740    1.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7232   -3.9327   -0.2703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3507   -4.2007    0.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9366    1.7976   -1.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5084    0.8123   -2.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9937    1.7294   -3.1353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9140    0.0933    0.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1698    0.5338   -0.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6751    2.5491    2.9381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9495    4.0333    1.8823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8270    1.2005    1.5979 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  0
 12 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  3
 24 26  1  0
 19 17  1  0
 17 18  1  0
 17 15  2  0
 15 16  1  0
 15 13  1  0
 13 14  2  0
 26  7  1  0
 13 12  1  0
 26 20  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  1 27  1  0
  1 28  1  0
  7 32  1  1
  8 33  1  0
  8 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 19 41  1  1
 20 42  1  6
 25 43  1  0
 25 44  1  0
 26 45  1  1
 18 38  1  0
 18 39  1  0
 18 40  1  0
M  END


  Mrv1652309022205042D          

 26 28  0  0  1  0            999 V2000
    0.5751    2.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3431    3.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4660    3.9357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9881    2.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7560    2.9069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    1.7897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101    1.2753    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2534    1.6333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9967    1.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417    1.7897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4097    1.4883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1803    0.4710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527    0.1811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6412    0.6356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157   -0.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5607   -1.1574    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.1204   -0.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305   -1.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6659   -0.1740    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.1740    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3864   -0.8625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912   -0.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461   -1.1574    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541    0.1811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8656    0.6356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3265    0.4710    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 19 17  1  6  0  0  0
 12 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
 26 24  1  6  0  0  0
  7 26  1  0  0  0  0
 20 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147456

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C(=O)O[C@@H]1CC(CO)=C2[C@@H]([C@H]3OC(=O)C(=C)[C@H]13)C(C)=C(Cl)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H19ClO6/c1-7(2)18(23)25-11-5-10(6-21)14-13(8(3)15(20)16(14)22)17-12(11)9(4)19(24)26-17/h11-13,17,21H,1,4-6H2,2-3H3/t11-,12-,13+,17+/m1/s1

> <INCHI_KEY>
KFPWRPCTAULPMU-FJZAXULXSA-N

> <FORMULA>
C19H19ClO6

> <MOLECULAR_WEIGHT>
378.81

> <EXACT_MASS>
378.087016

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.66364386179574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4R,9aR,9bR)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate

> <ALOGPS_LOGP>
1.96

> <JCHEM_LOGP>
2.1975134370000005

> <ALOGPS_LOGS>
-3.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.08714608995329

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7606823002544214

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
94.81270000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.38e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4R,9aR,9bR)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylprop-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       1.073   5.261   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.507   5.824   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.737   7.347   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.711   4.864   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.145   5.426   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       3.482   3.341   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.686   2.381   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.073   3.049   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.461   2.381   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.665   3.341   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.098   2.778   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.803   0.879   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.245   0.338   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.530   1.186   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.176  -1.200   0.000  0.00  0.00           C+0
HETATM   16 Cl   UNK     0      10.380  -2.161   0.000  0.00  0.00          Cl+0
HETATM   17  C   UNK     0       7.691  -1.610   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.150  -3.052   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.843  -0.325   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.303  -0.325   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.455  -1.610   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.970  -1.200   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.766  -2.161   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.901   0.338   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.616   1.186   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.343   0.879   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   26                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12   20                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    7   20                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
(3AR,4R,9ar,9BR)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-2H,3H,3ah,4H,5H,7H,9ah,9BH-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoic acid	Generator

Chemical Formula

C₁₉H₁₉ClO₆

Average Mass

378.8100 Da

Monoisotopic Mass

378.08702 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=C)C(=O)O[C@@H]1CC(CO)=C2[C@@H]([C@H]3OC(=O)C(=C)[C@H]13)C(C)=C(Cl)C2=O

InChI Identifier

InChI=1S/C19H19ClO6/c1-7(2)18(23)25-11-5-10(6-21)14-13(8(3)15(20)16(14)22)17-12(11)9(4)19(24)26-17/h11-13,17,21H,1,4-6H2,2-3H3/t11-,12-,13+,17+/m1/s1

InChI Key

KFPWRPCTAULPMU-FJZAXULXSA-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
Mikania vitifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Gamma butyrolactones

Direct Parent

Gamma butyrolactones

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Gamma butyrolactone
Alpha-haloketone
Alpha-chloroketone
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Ketone
Carboxylic acid ester
Oxacycle
Chloroalkene
Haloalkene
Vinyl chloride
Vinyl halide
Carboxylic acid derivative
Organochloride
Organohalogen compound
Hydrocarbon derivative
Organooxygen compound
Primary alcohol
Carbonyl group
Organic oxygen compound
Organic oxide
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

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

162919906

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate (NP0147456)

MOL for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

3D MOL for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

3D SDF for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

3D-SDF for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

PDB for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

3D PDB for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

SMILES for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

INCHI for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

Structure for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)

3D Structure for NP0147456 ((3ar,4r,9ar,9br)-8-chloro-6-(hydroxymethyl)-9-methyl-3-methylidene-2,7-dioxo-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylprop-2-enoate)