NP-MRD: Showing NP-Card for (1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate (NP0201389)

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Record Information

Version

2.0

Created at

2022-09-04 20:25:27 UTC

Updated at

2022-09-04 20:25:27 UTC

NP-MRD ID

NP0201389

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

Description

CHEMBL1836958 belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate is found in Ferula communis. Based on a literature review very few articles have been published on CHEMBL1836958.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042222252D          

 32 34  0  0  1  0            999 V2000
    0.8580    5.2293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6464    4.9861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8299    4.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6183    3.9387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8019    3.1343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1971    2.5732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3807    1.7689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7759    1.2077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1690    1.5257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526    0.7214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1569    0.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5149   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -0.9488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526   -1.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1690   -1.9367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076   -0.6180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5603   -1.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230   -0.8729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6680   -1.6576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8611   -1.8291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6061   -2.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3090   -1.2160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4380   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230    0.4619    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585    1.2156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085    0.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085    1.6994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4940    0.4619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.2070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4087    2.8164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2252    3.6207    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
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  1  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 30 25  1  6  0  0  0
 10 30  1  0  0  0  0
 17 30  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  2  0  0  0  0
  3 32  1  0  0  0  0
M  END

     RDKit          3D

 66 68  0  0  0  0  0  0  0  0999 V2000
    8.4130   -1.5925   -0.2018 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2739   -1.8724   -0.9805 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0950   -1.2010   -0.7178 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9869   -1.4770   -1.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7920   -0.7955   -1.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7023    0.1331   -0.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7502    2.0881   -1.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0318    1.9523   -3.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7870    2.0461   -1.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8684    2.1497    0.4657 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4981    3.4359    0.8771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8919    1.1890    1.1002 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0522    1.8269    2.1559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6999    0.0779    1.7364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7627   -0.2310    0.8593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0999   -0.1273    1.1942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0970   -0.4908    0.1561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4005    0.2617    2.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6814   -1.0272    1.8342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6975   -0.8024    0.7084 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5581   -0.7261    1.2759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7067   -2.0078   -0.1980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0431   -2.2867   -0.8123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2984   -3.1974    0.6255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0622    0.4696    0.0356 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8258    0.3923    0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0315   -0.2760    0.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1939   -1.7038    0.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7515   -0.5315   -0.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2624   -2.2487   -0.4276 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0816   -2.2152   -2.2613 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9540   -1.0432   -1.8314 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2982    2.0259    0.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    2.0960   -2.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863    3.3294   -1.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2801    0.9005   -3.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9202    2.5596   -3.6161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1902    2.3133   -3.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7626    1.9118   -1.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9002    1.9852    0.7783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3014    4.0096    0.8090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6491    1.7977    3.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1610    1.2256    2.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8539    2.9014    1.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0670    0.4137    2.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0610   -1.5665   -0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7861    0.0410   -0.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1162   -0.1373    0.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2014   -0.9334    2.8416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798   -1.9941    1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1266   -1.5107    1.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0479   -1.8119   -0.9893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4351   -1.5063   -1.4605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7567   -2.6277   -0.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
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 32  3  1  0
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 31 65  1  0
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 22 51  1  0
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 22 53  1  0
M  END


  Mrv1652309042222252D          

 32 34  0  0  1  0            999 V2000
    0.8580    5.2293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6464    4.9861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8299    4.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6183    3.9387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8019    3.1343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1971    2.5732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3807    1.7689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7759    1.2077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1690    1.5257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526    0.7214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1569    0.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5149   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3526   -1.1324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1690   -1.9367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076   -0.6180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5603   -1.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230   -0.8729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6680   -1.6576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8611   -1.8291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6061   -2.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3090   -1.2160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4380   -0.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230    0.4619    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585    1.2156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085    0.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2085    1.6994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4940    0.4619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.2070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4087    2.8164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2252    3.6207    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
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
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  3 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201389

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C(=O)O[C@H]1CC(C)=C[C@H](O)[C@@]2(C)[C@H](C[C@@](O)(C(C)C)[C@H]12)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O7/c1-14(2)25(29)13-21(31-16(4)26)24(5)20(27)12-15(3)11-19(22(24)25)32-23(28)17-7-9-18(30-6)10-8-17/h7-10,12,14,19-22,27,29H,11,13H2,1-6H3/t19-,20-,21-,22+,24-,25+/m0/s1

> <INCHI_KEY>
QUWQRANGMXSSTD-IJPOMDLSSA-N

> <FORMULA>
C25H34O7

> <MOLECULAR_WEIGHT>
446.54

> <EXACT_MASS>
446.230453435

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
48.36665670291872

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,3aS,4S,8S,8aS)-1-(acetyloxy)-3,8-dihydroxy-6,8a-dimethyl-3-(propan-2-yl)-1,2,3,3a,4,5,8,8a-octahydroazulen-4-yl 4-methoxybenzoate

> <JCHEM_LOGP>
2.7627389509999993

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.511423254405756

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.901221618516619

> <JCHEM_PKA_STRONGEST_BASIC>
-3.13468331510024

> <JCHEM_POLAR_SURFACE_AREA>
102.29

> <JCHEM_REFRACTIVITY>
119.04380000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,3aS,4S,8S,8aS)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.602   9.761   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.073   9.307   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.416   7.806   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.887   7.352   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.230   5.851   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.101   4.803   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.444   3.302   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.315   2.254   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       5.916   2.848   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.258   1.347   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.760   1.004   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.428  -0.384   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.968  -0.384   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.760  -1.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.258  -2.114   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.916  -3.615   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.054  -1.154   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.779  -2.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.590  -1.629   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.114  -3.094   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.607  -3.414   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.131  -4.879   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.577  -2.270   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.684  -0.384   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.590   0.862   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.216   2.269   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.256   1.632   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.256   3.172   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.922   0.862   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.054   0.386   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.630   5.257   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.287   6.759   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   31                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   30                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   30                                             
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25                                                       
CONECT   25   24   26   27   30                                             
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   10   17                                                  
CONECT   31    6   32                                                       
CONECT   32   31    3                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄O₇

Average Mass

446.5400 Da

Monoisotopic Mass

446.23045 Da

IUPAC Name

(1S,3R,3aS,4S,8S,8aS)-1-(acetyloxy)-3,8-dihydroxy-6,8a-dimethyl-3-(propan-2-yl)-1,2,3,3a,4,5,8,8a-octahydroazulen-4-yl 4-methoxybenzoate

Traditional Name

(1S,3R,3aS,4S,8S,8aS)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C(=O)O[C@H]1CC(C)=C[C@H](O)[C@@]2(C)[C@H](C[C@@](O)(C(C)C)[C@H]12)OC(C)=O

InChI Identifier

InChI=1S/C25H34O7/c1-14(2)25(29)13-21(31-16(4)26)24(5)20(27)12-15(3)11-19(22(24)25)32-23(28)17-7-9-18(30-6)10-8-17/h7-10,12,14,19-22,27,29H,11,13H2,1-6H3/t19-,20-,21-,22+,24-,25+/m0/s1

InChI Key

QUWQRANGMXSSTD-IJPOMDLSSA-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
Ferula communis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Daucane sesquiterpenoid
P-methoxybenzoic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Anisole
Methoxybenzene
Benzoyl
Phenoxy compound
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Ether
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	2.76	ChemAxon
pKa (Strongest Acidic)	13.9	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	119.04 m³·mol⁻¹	ChemAxon
Polarizability	48.37 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

26616815

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54597863

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate (NP0201389)

MOL for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

3D MOL for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

3D SDF for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

3D-SDF for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

PDB for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

3D PDB for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

SMILES for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

INCHI for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

Structure for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)

3D Structure for NP0201389 ((1s,3r,3as,4s,8s,8as)-1-(acetyloxy)-3,8-dihydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-methoxybenzoate)