NP-MRD: Showing NP-Card for butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate (NP0317755)

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Record Information

Version

2.0

Created at

2022-09-11 17:49:01 UTC

Updated at

2022-09-11 17:49:02 UTC

NP-MRD ID

NP0317755

Secondary Accession Numbers

None

Natural Product Identification

Common Name

butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate

Description

Butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate belongs to the class of organic compounds known as quinic acids and derivatives. Quinic acids and derivatives are compounds containing a quinic acid moiety (or a derivative thereof), which is a cyclitol made up of a cyclohexane ring that bears four hydroxyl groups at positions 1,3.4, And 5, as well as a carboxylic acid at position 1. butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate is found in Sinoadina racemosa, Spondias mombin and Urceola rosea. Based on a literature review very few articles have been published on butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112219492D          

 29 30  0  0  1  0            999 V2000
    4.6148   -7.9748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3293   -7.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0438   -7.9748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7583   -7.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4727   -7.9748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -7.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -6.7373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9017   -7.9748    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3714   -8.6067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1838   -7.1995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9963   -7.0563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.2785   -6.2810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5266   -7.6882    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3391   -7.5450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2444   -8.4635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7747   -9.0955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5872   -8.9522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8694   -8.1770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1175   -9.5842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9300   -9.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4603  -10.0729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2727   -9.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8030  -10.5617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5209  -11.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0512  -11.9689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7084  -11.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4262  -12.2554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1781  -10.8482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4320   -8.6067    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  6  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 17  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 21 28  1  0  0  0  0
 15 29  1  0  0  0  0
  8 29  1  0  0  0  0
M  END

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
   -7.2960    2.3836   -1.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0148    2.8201   -1.9736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8183    2.0418   -1.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0424    0.5838   -1.7824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9909   -0.2395   -1.3583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5661   -0.3699   -0.0524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1867    0.3124    0.7997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4406   -1.2703    0.2940 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9264   -1.9105   -0.8322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8287   -2.3253    1.2870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6365   -3.2431    1.4775 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3174   -3.7611    0.2294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4292   -2.4641    1.9925 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6093   -3.3640    2.1214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1086   -1.4234    0.9554 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1019   -0.7706    1.1512 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1566   -0.7956    0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9940   -1.4516   -0.7890 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4195   -0.0862    0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3715   -0.1479   -0.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6395    0.5299   -0.1710 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6124    0.4202   -1.1515 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8177    1.0363   -1.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0928    1.7868    0.1075 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3251    2.4025    0.2193 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1619    1.9288    1.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4406    2.6811    2.2371 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9376    1.2825    0.9389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2942   -0.4717    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0004    3.2423   -1.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0993    2.1512   -0.2612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7921    1.5497   -1.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8868    3.9061   -1.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1175    2.7108   -3.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9472    2.3824   -2.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7157    2.2510   -0.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0633    0.5078   -2.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0286    0.2603   -1.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9977   -1.2735   -1.5777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6255   -2.9484    0.8208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1912   -1.9129    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8808   -4.0927    2.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5764   -4.4251    0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7486   -2.0258    2.9609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3392   -4.2421    2.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0627   -1.9504   -0.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5388    0.4676    1.4095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2220   -0.7204   -1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4052   -0.1632   -2.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5467    0.9241   -1.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6126    2.9622    0.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7267    2.7542    2.9433 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2175    1.4117    1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5843   -0.2790    1.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0747    0.4369    0.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 29  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  2  0
 29  8  1  0
 28 21  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  1
 12 43  1  0
 13 44  1  1
 14 45  1  0
 15 46  1  6
 29 54  1  0
 29 55  1  0
 19 47  1  0
 20 48  1  0
 22 49  1  0
 23 50  1  0
 25 51  1  0
 27 52  1  0
 28 53  1  0
M  END


  Mrv1652309112219492D          

 29 30  0  0  1  0            999 V2000
    4.6148   -7.9748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3293   -7.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0438   -7.9748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7583   -7.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4727   -7.9748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -7.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1872   -6.7373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9017   -7.9748    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3714   -8.6067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1838   -7.1995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9963   -7.0563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.2785   -6.2810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5266   -7.6882    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3391   -7.5450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2444   -8.4635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7747   -9.0955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5872   -8.9522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8694   -8.1770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1175   -9.5842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9300   -9.4409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4603  -10.0729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2727   -9.9297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8030  -10.5617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5209  -11.3369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0512  -11.9689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7084  -11.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4262  -12.2554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1781  -10.8482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4320   -8.6067    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  6  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 17  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 21 28  1  0  0  0  0
 15 29  1  0  0  0  0
  8 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0317755

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCOC(=O)[C@]1(O)C[C@@H](O)[C@@H](O)[C@@H](C1)OC(=O)C=CC1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O9/c1-2-3-8-28-19(26)20(27)10-15(23)18(25)16(11-20)29-17(24)7-5-12-4-6-13(21)14(22)9-12/h4-7,9,15-16,18,21-23,25,27H,2-3,8,10-11H2,1H3/t15-,16-,18-,20+/m1/s1

> <INCHI_KEY>
VNLREARKISTOAD-CIWUYKSXSA-N

> <FORMULA>
C20H26O9

> <MOLECULAR_WEIGHT>
410.419

> <EXACT_MASS>
410.157682417

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.68700613466544

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate

> <JCHEM_LOGP>
1.2012633126666672

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.015382798822111

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.208106199600504

> <JCHEM_PKA_STRONGEST_BASIC>
-3.231828504111257

> <JCHEM_POLAR_SURFACE_AREA>
153.75

> <JCHEM_REFRACTIVITY>
101.8774

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       8.614 -14.886   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.948 -14.116   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.282 -14.886   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.615 -14.116   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.949 -14.886   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      15.283 -14.116   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      15.283 -12.576   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      16.616 -14.886   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      15.627 -16.066   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      17.143 -13.439   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.660 -13.172   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      19.186 -11.725   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      19.650 -14.351   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      21.166 -14.084   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      19.123 -15.799   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      20.113 -16.978   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      21.629 -16.711   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      22.156 -15.264   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      22.619 -17.891   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      24.136 -17.623   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      25.126 -18.803   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      26.642 -18.535   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      27.632 -19.715   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      27.106 -21.162   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      28.096 -22.342   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      25.589 -21.430   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      25.062 -22.877   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      24.599 -20.250   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      17.606 -16.066   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   29                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   29                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   28                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   21                                                       
CONECT   29   15    8                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
Butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	Generator

Chemical Formula

C₂₀H₂₆O₉

Average Mass

410.4190 Da

Monoisotopic Mass

410.15768 Da

IUPAC Name

butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate

Traditional Name

butyl (1S,3R,4R,5R)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate

CAS Registry Number

Not Available

SMILES

CCCCOC(=O)[C@]1(O)C[C@@H](O)[C@@H](O)[C@@H](C1)OC(=O)C=CC1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C20H26O9/c1-2-3-8-28-19(26)20(27)10-15(23)18(25)16(11-20)29-17(24)7-5-12-4-6-13(21)14(22)9-12/h4-7,9,15-16,18,21-23,25,27H,2-3,8,10-11H2,1H3/t15-,16-,18-,20+/m1/s1

InChI Key

VNLREARKISTOAD-CIWUYKSXSA-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
Sinoadina racemosa	LOTUS Database	35616633
Spondias mombin	LOTUS Database	35616633
Urceola rosea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinic acids and derivatives. Quinic acids and derivatives are compounds containing a quinic acid moiety (or a derivative thereof), which is a cyclitol made up of a cyclohexane ring that bears four hydroxyl groups at positions 1,3.4, And 5, as well as a carboxylic acid at position 1.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Quinic acids and derivatives

Alternative Parents

Substituents

Quinic acid
Cinnamic acid or derivatives
Coumaric acid or derivatives
Cinnamic acid ester
Hydroxycinnamic acid or derivatives
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Cyclohexanol
Fatty acid ester
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Polyol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.2	ChemAxon
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.75 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	101.88 m³·mol⁻¹	ChemAxon
Polarizability	41.69 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

4982319

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6481825

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate (NP0317755)

MOL for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

3D MOL for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

3D SDF for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

3D-SDF for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

PDB for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

3D PDB for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

SMILES for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

INCHI for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

Structure for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)

3D Structure for NP0317755 (butyl (1s,3r,4r,5r)-3-{[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylate)