NP-MRD: Showing NP-Card for 3-Methyl-sargaquinoic acid (NP0074984)

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Record Information

Version

2.0

Created at

2022-04-28 20:17:23 UTC

Updated at

2022-04-28 20:17:24 UTC

NP-MRD ID

NP0074984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-Methyl-sargaquinoic acid

Description

3-Methylsargaquinoic acid belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 3-Methyl-sargaquinoic acid is found in Iryanthera juruensis . Based on a literature review very few articles have been published on 3-Methylsargaquinoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222172D          

 32 32  0  0  0  0            999 V2000
    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  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 O   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
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   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
   -0.7145   -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
   -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 C   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   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    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
   -2.1434   -1.2375    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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  9  1  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  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 15 29  1  0  0  0  0
 11 30  1  0  0  0  0
  2 31  1  0  0  0  0
  1 32  1  0  0  0  0
M  END

     RDKit          3D

 70 70  0  0  0  0  0  0  0  0999 V2000
   -6.8767    3.3182    0.4764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2269    2.1815    1.1826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4327    1.9974    2.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4428    1.3041    0.5199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7980    0.1770    1.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1011   -1.1692    0.6956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5652   -1.4627   -0.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8079   -0.6172   -1.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2574   -0.8156   -2.6528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7339   -0.8192   -2.6630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1434   -1.8838   -1.8198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4063   -3.3218   -2.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3473   -1.5796   -0.7997 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2651   -2.6217    0.0706 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7931   -2.5156   -0.0001 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2513   -1.1936    0.4544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9627   -0.6999    1.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9366   -0.4255   -0.3905 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4209    0.9234    0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8926    1.0181   -0.0557 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6696    0.0309   -0.4515 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1133    0.2385   -0.4949 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8383   -0.7390   -0.8833 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6773    1.5086   -0.1090 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1418    1.7233   -0.1515 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9036    2.4959    0.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5248    3.7807    0.6730 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4767    2.3179    0.3387 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7476    3.2687    0.7183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9300   -2.7309   -1.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6182   -3.2082   -2.3713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7648   -3.6054   -0.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0980    4.0658    0.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4023    2.9611   -0.4339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5984    3.8035    1.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0341    2.8543    3.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9565    1.0293    2.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4513    1.9995    3.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3391    1.4733   -0.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6934    0.3904    1.2472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1803    0.1932    2.2853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8257   -1.9933    1.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2214   -1.2533    0.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5089    0.3225   -0.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4905    0.1843   -3.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7046   -1.5409   -3.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3110    0.1791   -2.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4517   -1.0134   -3.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9624   -3.4431   -3.0420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9957   -3.7592   -1.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4719   -3.9136   -2.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1504   -0.5330   -0.6121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0791   -3.6261   -0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0022   -2.4156    1.1231 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2619   -3.2735    0.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1038   -2.6627   -1.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2552    0.1394    1.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9080   -0.3753    2.3392 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5796   -1.5606    2.4146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1360   -0.7969   -1.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.6445   -0.6838 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0206    1.1769    1.0221 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2105   -0.9050   -0.7324 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4142    2.7961   -0.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5631    1.2576    0.7748 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.3160    3.6276    1.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0075    4.2717   -0.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3635   -3.8863    0.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
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 28 29  2  0
  7 30  1  0
 30 32  1  0
 30 31  2  0
 28 20  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  3 37  1  0
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  4 39  1  0
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 27 68  1  0
 27 69  1  0
 32 70  1  0
M  END


  Mrv1652304282222172D          

 32 32  0  0  0  0            999 V2000
    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  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 O   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
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -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
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   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
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 15 29  1  0  0  0  0
 11 30  1  0  0  0  0
  2 31  1  0  0  0  0
  1 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(=C\CC\C(C)=C\CC\C(C)=C\CC1=CC(=O)C(C)=C(C)C1=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H38O4/c1-19(2)10-7-14-24(28(31)32)15-9-13-20(3)11-8-12-21(4)16-17-25-18-26(29)22(5)23(6)27(25)30/h10-11,15-16,18H,7-9,12-14,17H2,1-6H3,(H,31,32)/b20-11+,21-16+,24-15-

> <INCHI_KEY>
LFQUGWZUSHDCOE-XKACVPJNSA-N

> <FORMULA>
C28H38O4

> <MOLECULAR_WEIGHT>
438.608

> <EXACT_MASS>
438.277009704

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
52.425084322762544

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z,6E,10E)-12-(4,5-dimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-trienoic acid

> <ALOGPS_LOGP>
5.94

> <JCHEM_LOGP>
7.596746313333336

> <ALOGPS_LOGS>
-5.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.178833464864114

> <JCHEM_PKA_STRONGEST_BASIC>
-7.788388230815102

> <JCHEM_POLAR_SURFACE_AREA>
71.44

> <JCHEM_REFRACTIVITY>
136.4267

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.07e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,6E,10E)-12-(4,5-dimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-trienoic acid

> <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       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -10.669 -16.940   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -10.669 -18.480   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -12.003 -16.170   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -10.669 -12.320   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
CONECT    1    2    7   32                                                  
CONECT    2    1    3   31                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    1    8                                                  
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   29                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   19   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   15                                                            
CONECT   30   11                                                            
CONECT   31    2                                                            
CONECT   32    1                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

View in JSmol

Synonyms

Value	Source
3-Methylsargaquinoate	Generator

Chemical Formula

C₂₈H₃₈O₄

Average Mass

438.6080 Da

Monoisotopic Mass

438.27701 Da

IUPAC Name

(2Z,6E,10E)-12-(4,5-dimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-trienoic acid

Traditional Name

(2Z,6E,10E)-12-(4,5-dimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-6,10-dimethyl-2-(4-methylpent-3-en-1-yl)dodeca-2,6,10-trienoic acid

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(=C\CC\C(C)=C\CC\C(C)=C\CC1=CC(=O)C(C)=C(C)C1=O)C(O)=O

InChI Identifier

InChI=1S/C28H38O4/c1-19(2)10-7-14-24(28(31)32)15-9-13-20(3)11-8-12-21(4)16-17-25-18-26(29)22(5)23(6)27(25)30/h10-11,15-16,18H,7-9,12-14,17H2,1-6H3,(H,31,32)/b20-11+,21-16+,24-15-

InChI Key

LFQUGWZUSHDCOE-XKACVPJNSA-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
Iryanthera juruensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Long-chain fatty acid
Prenylbenzoquinone
P-benzoquinone
Quinone
Methyl-branched fatty acid
Branched fatty acid
Unsaturated fatty acid
Fatty acid
Fatty acyl
Cyclic ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	5.94	ALOGPS
logP	7.6	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	5.18	ChemAxon
pKa (Strongest Basic)	-7.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71.44 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	136.43 m³·mol⁻¹	ChemAxon
Polarizability	52.43 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00036557

Chemspider ID

8782027

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10606660

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3-Methyl-sargaquinoic acid (NP0074984)

MOL for NP0074984 (3-Methyl-sargaquinoic acid)

3D MOL for NP0074984 (3-Methyl-sargaquinoic acid)

3D SDF for NP0074984 (3-Methyl-sargaquinoic acid)

3D-SDF for NP0074984 (3-Methyl-sargaquinoic acid)

PDB for NP0074984 (3-Methyl-sargaquinoic acid)

3D PDB for NP0074984 (3-Methyl-sargaquinoic acid)

SMILES for NP0074984 (3-Methyl-sargaquinoic acid)

INCHI for NP0074984 (3-Methyl-sargaquinoic acid)

Structure for NP0074984 (3-Methyl-sargaquinoic acid)

3D Structure for NP0074984 (3-Methyl-sargaquinoic acid)