NP-MRD: Showing NP-Card for (2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid (NP0226461)

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Record Information

Version

2.0

Created at

2022-09-06 05:30:28 UTC

Updated at

2022-09-06 05:30:28 UTC

NP-MRD ID

NP0226461

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid

Description

(2Z)-3-[(2S,3R)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoic acid belongs to the class of organic compounds known as 4'-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C4' atom of the flavonoid backbone. (2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid is found in Mallotus apelta. Based on a literature review very few articles have been published on (2Z)-3-[(2S,3R)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062207302D          

 30 32  0  0  1  0            999 V2000
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 O   0  0  0  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
   -2.1434   -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   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    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
    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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   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
    1.4289   -2.4750    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  1  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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    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
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  6  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -3.1209   -2.3968   -2.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0956   -1.7483   -2.1514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6213   -0.8216   -1.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2886   -0.5160   -1.0882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8364    0.4254   -0.1524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3949    0.7073   -0.0366 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3596   -0.4976    0.0343 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7237   -0.4182    0.2743 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2433    0.6614    0.9960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5904    0.7137    1.2143 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4948   -0.2597    0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8770   -0.1917    1.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9459   -0.2713    0.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9892   -0.4299   -0.9763 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1560   -0.5704   -1.5080 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9283   -0.4488   -1.8260 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9338   -1.2993    0.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7122   -2.3181   -0.4207 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5694   -1.3931   -0.1920 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0275   -2.5541   -0.9656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381    1.7156    1.5047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0870    1.5727    1.1257 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5586    2.8613    0.8181 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7781    1.0433    0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1420    0.7484    0.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0402    1.4020    1.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6121    2.3481    2.2524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5435   -0.1830   -0.4353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8794   -0.4667   -0.5575 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6614    0.2867   -1.4650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6095   -3.1069   -3.6771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3650   -2.9130   -2.3359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5763   -1.5839   -3.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5572   -1.0146   -1.7135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0799    1.1718   -1.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0211    1.5392    1.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0208   -0.0457    2.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9007   -0.2049    1.0341 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4563    0.4012   -2.1045 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3174   -3.0856   -0.9330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5317   -2.5520   -1.9606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9409   -2.5500   -1.0123 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3800   -3.4649   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4126    1.6837    2.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7472    2.7402    1.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6607    1.1534    2.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4568    2.9947   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4907    1.7674    1.3610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2270    3.2624    1.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8042    1.9759    2.9208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4764    2.6536    2.9029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0337    0.8277   -2.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2689    1.0623   -0.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3520   -0.4132   -1.9773 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  2  0
 28 29  1  0
 29 30  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 21  1  0
 21 22  1  0
 22 23  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 16  1  0
 14 15  2  0
 11 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 28  3  1  0
 22  6  1  0
 19  8  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
 24 48  1  0
 27 49  1  0
 27 50  1  0
 27 51  1  0
 30 52  1  0
 30 53  1  0
 30 54  1  0
  6 35  1  6
 21 44  1  0
 21 45  1  0
 22 46  1  1
 23 47  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 16 39  1  0
 18 40  1  0
 20 41  1  0
 20 42  1  0
 20 43  1  0
M  END


  Mrv1652309062207302D          

 30 32  0  0  1  0            999 V2000
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 O   0  0  0  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
   -2.1434   -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   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    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
    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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   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
    1.4289   -2.4750    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  1  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
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    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
   -3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  6  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226461

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1OC)[C@@H]1OC2=C(C[C@H]1O)C=C(\C=C/C(O)=O)C(O)=C2C

> <INCHI_IDENTIFIER>
InChI=1S/C22H24O8/c1-11-19(26)12(5-6-18(24)25)7-13-8-15(23)21(30-20(11)13)14-9-16(27-2)22(29-4)17(10-14)28-3/h5-7,9-10,15,21,23,26H,8H2,1-4H3,(H,24,25)/b6-5-/t15-,21+/m1/s1

> <INCHI_KEY>
WYFGKJLNVXNNMM-AUVXLDHESA-N

> <FORMULA>
C22H24O8

> <MOLECULAR_WEIGHT>
416.426

> <EXACT_MASS>
416.147117733

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.99412014476776

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-3-[(2S,3R)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoic acid

> <JCHEM_LOGP>
2.909051016666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.919836354508172

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.787016138253837

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2740552118218895

> <JCHEM_POLAR_SURFACE_AREA>
114.68000000000002

> <JCHEM_REFRACTIVITY>
109.4897

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-3-[(2S,3R)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.668  -2.310   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000  -3.080   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       1.334  -0.770   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  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   21                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    8   20                                                  
CONECT   20   19                                                            
CONECT   21    9   22                                                       
CONECT   22   21    6   23                                                  
CONECT   23   22                                                            
CONECT   24    5   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25    3   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
(2Z)-3-[(2S,3R)-3,7-Dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoate	Generator

Chemical Formula

C₂₂H₂₄O₈

Average Mass

416.4260 Da

Monoisotopic Mass

416.14712 Da

IUPAC Name

(2Z)-3-[(2S,3R)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoic acid

Traditional Name

(2Z)-3-[(2S,3R)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-6-yl]prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1OC)[C@@H]1OC2=C(C[C@H]1O)C=C(\C=C/C(O)=O)C(O)=C2C

InChI Identifier

InChI=1S/C22H24O8/c1-11-19(26)12(5-6-18(24)25)7-13-8-15(23)21(30-20(11)13)14-9-16(27-2)22(29-4)17(10-14)28-3/h5-7,9-10,15,21,23,26H,8H2,1-4H3,(H,24,25)/b6-5-/t15-,21+/m1/s1

InChI Key

WYFGKJLNVXNNMM-AUVXLDHESA-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
Mallotus apelta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 4'-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C4' atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

4'-O-methylated flavonoids

Alternative Parents

Substituents

3p-methoxyflavonoid-skeleton
4p-methoxyflavonoid-skeleton
3-hydroxyflavonoid
7-hydroxyflavonoid
Flavan-3-ol
Hydroxyflavonoid
Flavan
1-benzopyran
Chromane
Benzopyran
Phenoxy compound
Methoxybenzene
Anisole
Styrene
Phenol ether
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
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	2.91	ChemAxon
pKa (Strongest Acidic)	3.79	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	114.68 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	109.49 m³·mol⁻¹	ChemAxon
Polarizability	42.99 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

163189541

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid (NP0226461)

MOL for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

3D MOL for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

3D SDF for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

3D-SDF for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

PDB for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

3D PDB for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

SMILES for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

INCHI for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

Structure for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)

3D Structure for NP0226461 ((2z)-3-[(2s,3r)-3,7-dihydroxy-8-methyl-2-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2h-1-benzopyran-6-yl]prop-2-enoic acid)