NP-MRD: Showing NP-Card for (6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one (NP0216182)

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Record Information

Version

2.0

Created at

2022-09-05 16:02:12 UTC

Updated at

2022-09-05 16:02:12 UTC

NP-MRD ID

NP0216182

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one

Description

(6R,7R)-8,8-dimethyl-6-(2-methylbut-2-enoyl)-7-(3-methylbutanoyl)-2H,6H,7H,8H-pyrano[3,2-g]chromen-2-one belongs to the class of organic compounds known as linear pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety. (6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one is found in Angelica decursiva. Based on a literature review very few articles have been published on (6R,7R)-8,8-dimethyl-6-(2-methylbut-2-enoyl)-7-(3-methylbutanoyl)-2H,6H,7H,8H-pyrano[3,2-g]chromen-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052218022D          

 29 31  0  0  1  0            999 V2000
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -3.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  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
  7  5  1  1  0  0  0
  7  8  1  0  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  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
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  8 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
   -2.5175    3.4815   -0.9450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7135    2.2753   -0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9438    2.3294    0.5508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9230    3.6272    1.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1459    1.2286    1.0128 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5330    1.4893    2.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0226   -0.1129    0.4113 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3114   -0.8072    0.1766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2962   -0.8489    1.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5025   -1.4914    0.9810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4708   -1.5210    1.9658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6735   -2.1825    1.7491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8227   -2.7890    0.5135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9249   -3.3958    0.3137 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8861   -2.7453   -0.4043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7412   -2.1257   -0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7573   -2.0806   -1.1872 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5439   -1.4475   -1.0476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5804   -1.4280   -2.0552 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7711   -1.3089   -1.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1301   -2.5491   -0.8648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6998   -1.1026   -2.8192 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8444   -0.0315   -0.8157 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2333    0.3686   -0.4951 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7153    1.3801   -0.9685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0837   -0.4329    0.4033 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4492    0.1919    0.6036 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3940    1.5583    1.1996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2834    0.1351   -0.6576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1315    3.8640   -0.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8356    4.3028   -1.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0947    3.1987   -1.8269 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1184   -0.3486    2.1104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2941   -1.0255    2.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4580   -2.2285    2.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9414   -2.5826   -2.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6834   -1.5739   -2.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2563   -1.5998   -3.6945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4144    0.7476   -1.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6000   -0.5063    1.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3203   -1.4457   -0.0406 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769   -0.4860    1.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4196    1.7845    1.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1604    1.6592    1.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6794    2.3346    0.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7285    0.3598   -1.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0763    0.9157   -0.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8355   -0.8414   -0.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
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  5  6  2  0
  5  7  1  0
  7 23  1  0
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 18  8  2  0
  8  9  1  0
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 13 15  1  0
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  8  7  1  0
 16 10  1  0
 17 18  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  4 34  1  0
  4 35  1  0
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  7 37  1  1
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 22 45  1  0
 22 46  1  0
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  9 38  1  0
 11 39  1  0
 12 40  1  0
 17 41  1  0
M  END


  Mrv1652309052218022D          

 29 31  0  0  1  0            999 V2000
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -3.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -2.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  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
  7  5  1  1  0  0  0
  7  8  1  0  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  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
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
  8 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0216182

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)[C@@H]1[C@@H](C(=O)CC(C)C)C(C)(C)OC2=C1C=C1C=CC(=O)OC1=C2

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O5/c1-7-14(4)23(27)21-16-11-15-8-9-20(26)28-18(15)12-19(16)29-24(5,6)22(21)17(25)10-13(2)3/h7-9,11-13,21-22H,10H2,1-6H3/b14-7+/t21-,22+/m0/s1

> <INCHI_KEY>
PLYNNHYAFLIKKZ-OTRDLXLWSA-N

> <FORMULA>
C24H28O5

> <MOLECULAR_WEIGHT>
396.483

> <EXACT_MASS>
396.193674002

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.78857016500757

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11R,12R)-13,13-dimethyl-11-[(2E)-2-methylbut-2-enoyl]-12-(3-methylbutanoyl)-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1(10),2,6,8-tetraen-5-one

> <JCHEM_LOGP>
5.038546845333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.019711478866107

> <JCHEM_PKA_STRONGEST_BASIC>
-4.470388701180108

> <JCHEM_POLAR_SURFACE_AREA>
69.67000000000002

> <JCHEM_REFRACTIVITY>
112.86219999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(11R,12R)-13,13-dimethyl-11-[(2E)-2-methylbut-2-enoyl]-12-(3-methylbutanoyl)-4,14-dioxatricyclo[8.4.0.0^{3,8}]tetradeca-1(10),2,6,8-tetraen-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.141  -6.067   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.151  -4.353   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.334  -0.770   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   23                                                  
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17    8   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20    7   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₅

Average Mass

396.4830 Da

Monoisotopic Mass

396.19367 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)[C@@H]1[C@@H](C(=O)CC(C)C)C(C)(C)OC2=C1C=C1C=CC(=O)OC1=C2

InChI Identifier

InChI=1S/C24H28O5/c1-7-14(4)23(27)21-16-11-15-8-9-20(26)28-18(15)12-19(16)29-24(5,6)22(21)17(25)10-13(2)3/h7-9,11-13,21-22H,10H2,1-6H3/b14-7+/t21-,22+/m0/s1

InChI Key

PLYNNHYAFLIKKZ-OTRDLXLWSA-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
Angelica decursiva	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Pyranocoumarins

Direct Parent

Linear pyranocoumarins

Alternative Parents

Substituents

Linear pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
1-benzopyran
Alkyl aryl ether
Pyranone
Pyran
Alpha-branched alpha,beta-unsaturated-ketone
Benzenoid
Acryloyl-group
Heteroaromatic compound
Enone
Alpha,beta-unsaturated ketone
Lactone
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

163185712

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one (NP0216182)

MOL for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

3D MOL for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

3D SDF for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

3D-SDF for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

PDB for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

3D PDB for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

SMILES for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

INCHI for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

Structure for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)

3D Structure for NP0216182 ((6r,7r)-8,8-dimethyl-6-[(2e)-2-methylbut-2-enoyl]-7-(3-methylbutanoyl)-6h,7h-pyrano[3,2-g]chromen-2-one)