NP-MRD: Showing NP-Card for methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate (NP0214947)

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Record Information

Version

2.0

Created at

2022-09-05 14:23:21 UTC

Updated at

2022-09-05 14:23:21 UTC

NP-MRD ID

NP0214947

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate

Description

methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate is found in Characella pachastrelloides.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 44  0  0  0  0  0  0  0  0999 V2000
    6.8377   -0.0514    0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5723    0.4960    0.4022 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4903   -0.3299    0.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6191   -1.5506    0.3900 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2070    0.2272   -0.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1269   -0.4910   -0.3668 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1806   -1.9561   -0.1874 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8261    0.1271   -0.7691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2258   -0.1512    0.2418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5803    0.3972    0.0202 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5789    1.9210   -0.0865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3171    0.1315    1.3235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6521   -0.4384    2.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6009    0.4453    1.3346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2835    1.0279    0.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7560    0.4557   -1.1389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4218   -0.2341   -1.0229 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8664   -0.3382   -2.3989 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8876   -1.1424    0.5908 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9780    0.0936    1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6469    0.4279    0.2067 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0962    1.3101   -0.3227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8887   -2.4396   -0.9057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4294   -2.2185    0.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1950   -2.4284   -0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0162    1.2032   -0.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5983   -0.3493   -1.7427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1522    0.3003    1.2081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3328   -1.2322    0.4781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9685    2.4243    0.8099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1573    2.2636   -0.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5313    2.3123   -0.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4354   -0.6563    3.2709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1772   -1.4213    2.3058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8796    0.2231    2.9533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1613    0.2704    2.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3558    0.7369    0.2151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2754    2.1403    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6647    1.2629   -1.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4601   -0.2924   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6258   -1.2922   -0.6803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3258    0.5398   -2.7720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7596   -0.4070   -3.1045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3551   -1.3170   -2.5965 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
 10  9  1  1
 10 11  1  0
 10 17  1  0
 17 18  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
 12 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  9 28  1  0
  9 29  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
 17 41  1  1
 18 42  1  0
 18 43  1  0
 18 44  1  0
 16 39  1  0
 16 40  1  0
 15 37  1  0
 15 38  1  0
 14 36  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
M  END


  Mrv1652309052216232D          

 18 18  0  0  0  0            999 V2000
    5.2731    3.3357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7428    2.7037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303    2.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6481    3.6222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    2.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3054    3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    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
    2.1434    1.2375    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
    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 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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 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  0  0  0  0
 16 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214947

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)\C=C(/C)CCC1(C)C(C)CCC=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O2/c1-12(11-15(17)18-5)9-10-16(4)13(2)7-6-8-14(16)3/h7,11,14H,6,8-10H2,1-5H3/b12-11+

> <INCHI_KEY>
YYMPTLYVILCRSD-VAWYXSNFSA-N

> <FORMULA>
C16H26O2

> <MOLECULAR_WEIGHT>
250.382

> <EXACT_MASS>
250.193280077

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
30.150983317777133

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2E)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate

> <JCHEM_LOGP>
4.501381963333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.794026843086566

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
76.79069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2E)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       9.843   6.227   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.853   5.047   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.337   5.314   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.810   6.761   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.347   4.135   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.830   4.402   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.303   5.849   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.840   3.222   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.324   3.490   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       0.344   3.490   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   17                                             
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   10   18                                                  
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₆O₂

Average Mass

250.3820 Da

Monoisotopic Mass

250.19328 Da

IUPAC Name

methyl (2E)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate

Traditional Name

methyl (2E)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)\C=C(/C)CCC1(C)C(C)CCC=C1C

InChI Identifier

InChI=1S/C16H26O2/c1-12(11-15(17)18-5)9-10-16(4)13(2)7-6-8-14(16)3/h7,11,14H,6,8-10H2,1-5H3/b12-11+

InChI Key

YYMPTLYVILCRSD-VAWYXSNFSA-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
Characella pachastrelloides	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.5	ChemAxon
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	76.79 m³·mol⁻¹	ChemAxon
Polarizability	30.15 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate (NP0214947)

MOL for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

3D MOL for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

3D SDF for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

3D-SDF for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

PDB for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

3D PDB for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

SMILES for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

INCHI for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

Structure for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)

3D Structure for NP0214947 (methyl (2e)-3-methyl-5-(1,2,6-trimethylcyclohex-2-en-1-yl)pent-2-enoate)