NP-MRD: Showing NP-Card for Ad-I (NP0070839)

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Record Information

Version

2.0

Created at

2022-04-28 16:15:44 UTC

Updated at

2022-04-28 16:15:44 UTC

NP-MRD ID

NP0070839

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ad-I

Description

(3S,4R)-2,2-dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoate 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. Ad-I is found in Peucedanum decursivum MAXIM. Based on a literature review very few articles have been published on (3S,4R)-2,2-dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218152D          

 31 33  0  0  1  0            999 V2000
   -0.7145   -1.2375    0.0000 C   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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
    0.0000    0.8250    0.0000 O   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    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   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 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   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
    3.5724    2.0625    0.0000 C   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
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3272    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   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
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   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
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  1  0  0  0
  9 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  1 31  1  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
    6.1653    0.2430    0.8348 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7779    0.0975    0.2893 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3546   -0.9824   -0.3227 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2676   -2.1262   -0.4972 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9966   -1.0444   -0.8220 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5852   -2.0787   -1.4103 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1350    0.0031   -0.6710 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7832    0.0130   -1.1373 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1490    0.1142   -0.0026 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0217   -1.0228    0.0655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0584   -1.8716    1.1528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2591   -1.5818    2.1080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9549   -3.0510    1.2382 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6364   -4.1126    0.2299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4129   -2.6569    1.1447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2981   -3.8558    1.4096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9853    1.3242    0.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6235    1.6853    1.2056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4196    2.8296    1.2571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0663    3.2025    2.4280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8375    4.3458    2.4073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9588    5.0948    1.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6672    6.1548    1.2102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3227    4.6895    0.1757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5766    3.6137    0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9440    3.2686   -1.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1775    2.1464   -1.0590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5259    1.7609   -2.2189 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6789    1.0302   -2.2038 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8078    2.0488   -2.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8041    0.4037   -3.5866 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4769    1.3092    0.7970 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2022   -0.0469    1.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8285   -0.3947    0.2224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1218    0.9509    0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5166   -2.4990    0.5261 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1908   -1.8561   -1.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7339   -2.9295   -1.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6472   -0.9998   -1.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4259    0.1109    0.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8224   -3.5079    2.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9287   -5.0886    0.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2077   -3.8639   -0.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5374   -4.0537    0.0062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6883   -1.8668    1.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5929   -2.3513    0.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0704   -3.6499    2.1827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8231   -4.1976    0.4914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6933   -4.7378    1.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502    1.1235    2.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9652    2.6145    3.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3722    4.6964    3.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0584    3.8758   -1.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4432    3.0878   -2.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5901    1.8761   -2.8699 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3037    2.0060   -1.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1632   -0.5221   -3.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3639    1.0402   -4.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    0.1893   -3.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  8 29  1  0
 29 30  1  1
 29 31  1  0
 29 28  1  0
 28 27  1  0
 27 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
 17  9  1  0
 25 19  1  0
 26 27  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 15 45  1  0
 15 46  1  0
 13 41  1  1
 14 42  1  0
 14 43  1  0
 14 44  1  0
  9 40  1  1
  8 39  1  6
  4 36  1  0
  4 37  1  0
  4 38  1  0
  2 35  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 30 54  1  0
 30 55  1  0
 30 56  1  0
 31 57  1  0
 31 58  1  0
 31 59  1  0
 18 50  1  0
 20 51  1  0
 21 52  1  0
 26 53  1  0
M  END


  Mrv1652304282218152D          

 31 33  0  0  1  0            999 V2000
   -0.7145   -1.2375    0.0000 C   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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
    0.0000    0.8250    0.0000 O   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    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   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 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   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
    3.5724    2.0625    0.0000 C   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
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3272    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   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
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   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
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  1  0  0  0
  9 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  1 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0070839

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O7/c1-7-13(3)22(26)29-20-16-11-15-9-10-19(25)28-17(15)12-18(16)31-24(5,6)21(20)30-23(27)14(4)8-2/h8-13,20-21H,7H2,1-6H3/b14-8+/t13-,20-,21+/m1/s1

> <INCHI_KEY>
IUKIVKHFEGKFJN-GNUYHPAUSA-N

> <FORMULA>
C24H28O7

> <MOLECULAR_WEIGHT>
428.481

> <EXACT_MASS>
428.183503242

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.196898274470705

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R)-2,2-dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoate

> <ALOGPS_LOGP>
4.83

> <JCHEM_LOGP>
5.155550895333333

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.900577829283043

> <JCHEM_POLAR_SURFACE_AREA>
88.13000000000001

> <JCHEM_REFRACTIVITY>
114.33209999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.35e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R)-2,2-dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-3H,4H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.611   3.670   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.057   3.670   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    6   31                                                  
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   25   26                                             
CONECT    9    8   10   18                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14                                                            
CONECT   18    9   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21                                                            
CONECT   25    8                                                            
CONECT   26    8                                                            
CONECT   27    2   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    1                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
(3S,4R)-2,2-Dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₄H₂₈O₇

Average Mass

428.4810 Da

Monoisotopic Mass

428.18350 Da

IUPAC Name

(3S,4R)-2,2-dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoate

Traditional Name

(3S,4R)-2,2-dimethyl-4-{[(2R)-2-methylbutanoyl]oxy}-8-oxo-3H,4H-pyrano[3,2-g]chromen-3-yl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C24H28O7/c1-7-13(3)22(26)29-20-16-11-15-9-10-19(25)28-17(15)12-18(16)31-24(5,6)21(20)30-23(27)14(4)8-2/h8-13,20-21H,7H2,1-6H3/b14-8+/t13-,20-,21+/m1/s1

InChI Key

IUKIVKHFEGKFJN-GNUYHPAUSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Peucedanum decursivum MAXIM	Plant	KNApSAcK

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
1-benzopyran
Benzopyran
Chromane
Pyranone
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Benzenoid
Pyran
Dicarboxylic acid or derivatives
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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
logP	4.83	ALOGPS
logP	5.16	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	88.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	114.33 m³·mol⁻¹	ChemAxon
Polarizability	45.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

163104477

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Ad-I (NP0070839)

MOL for NP0070839 (Ad-I)

3D MOL for NP0070839 (Ad-I)

3D SDF for NP0070839 (Ad-I)

3D-SDF for NP0070839 (Ad-I)

PDB for NP0070839 (Ad-I)

3D PDB for NP0070839 (Ad-I)

SMILES for NP0070839 (Ad-I)

INCHI for NP0070839 (Ad-I)

Structure for NP0070839 (Ad-I)

3D Structure for NP0070839 (Ad-I)