NP-MRD: Showing NP-Card for 4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one (NP0259264)

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Record Information

Version

2.0

Created at

2022-09-08 01:04:24 UTC

Updated at

2022-09-08 01:04:24 UTC

NP-MRD ID

NP0259264

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one

Description

4-[(6S)-1,5,5-trimethyl-5H,6H,7H-cyclopenta[c]pyridin-6-yl]butan-2-one belongs to the class of organic compounds known as methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group. 4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one is found in Cyperus rotundus. Based on a literature review very few articles have been published on 4-[(6S)-1,5,5-trimethyl-5H,6H,7H-cyclopenta[c]pyridin-6-yl]butan-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    5.2298    0.6882    0.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9654   -0.0703   -0.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0654   -1.0909   -0.7051 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6525    0.4141    0.4979 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6053   -0.5583    0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2213   -0.2301    0.5080 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2876    1.0829    0.0270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7469    0.8601   -0.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9933   -0.5006   -0.3505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2508   -0.9682   -0.6035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3054   -0.1038   -0.7701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0701    1.2084   -0.6784 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8244    1.6951   -0.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6667    3.1621   -0.3443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7219   -1.2173   -0.1378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9638   -2.3850    0.7643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2277   -1.6976   -1.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9879    0.4510   -0.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6304    0.3250    1.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0825    1.7745    0.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4633    1.4499    0.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7358    0.4021    1.6133 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8723   -1.5519    0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6638   -0.6630   -1.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1363   -0.2915    1.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1797    1.4639   -0.8854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181    1.8470    0.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4121   -2.0253   -0.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2901   -0.5320   -0.9704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5918    3.5575    0.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7763    3.4361    0.2576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5951    3.5822   -1.3635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0047   -2.8539    1.0671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4785   -2.0017    1.6894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6003   -3.1300    0.2792 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6268   -2.3823   -1.4177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0272   -0.8636   -2.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0658   -2.2827   -1.9326 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  9 15  1  0
 15 16  1  0
 15 17  1  0
 15  6  1  0
 13  8  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  1
  7 26  1  0
  7 27  1  0
 10 28  1  0
 11 29  1  0
 14 30  1  0
 14 31  1  0
 14 32  1  0
 16 33  1  0
 16 34  1  0
 16 35  1  0
 17 36  1  0
 17 37  1  0
 17 38  1  0
M  END


  Mrv1652309082203042D          

 17 18  0  0  1  0            999 V2000
   -3.1034   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1034   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0196    0.7782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7508    0.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  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
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259264

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)CC[C@H]1CC2=C(C=CN=C2C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H21NO/c1-10(17)5-6-12-9-13-11(2)16-8-7-14(13)15(12,3)4/h7-8,12H,5-6,9H2,1-4H3/t12-/m0/s1

> <INCHI_KEY>
RNURUJBYBMGADV-LBPRGKRZSA-N

> <FORMULA>
C15H21NO

> <MOLECULAR_WEIGHT>
231.339

> <EXACT_MASS>
231.1623143

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
27.29042037156127

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(6S)-1,5,5-trimethyl-5H,6H,7H-cyclopenta[c]pyridin-6-yl]butan-2-one

> <JCHEM_LOGP>
2.6672354993333327

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.63964347775642

> <JCHEM_PKA_STRONGEST_BASIC>
6.595719379466017

> <JCHEM_POLAR_SURFACE_AREA>
29.96

> <JCHEM_REFRACTIVITY>
69.36460000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-[(6S)-1,5,5-trimethyl-6H,7H-cyclopenta[c]pyridin-6-yl]butan-2-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.793  -3.970   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.023  -2.637   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.793  -1.303   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -3.483  -2.637   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.713  -1.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.268  -2.549   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       3.864  -2.073   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.530  -4.383   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.268  -0.057   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.037   1.453   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.401   0.985   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13                                                            
CONECT   15    9    6   16   17                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₁NO

Average Mass

231.3390 Da

Monoisotopic Mass

231.16231 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)CC[C@H]1CC2=C(C=CN=C2C)C1(C)C

InChI Identifier

InChI=1S/C15H21NO/c1-10(17)5-6-12-9-13-11(2)16-8-7-14(13)15(12,3)4/h7-8,12H,5-6,9H2,1-4H3/t12-/m0/s1

InChI Key

RNURUJBYBMGADV-LBPRGKRZSA-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
Cyperus rotundus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methylpyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a methyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

Methylpyridines

Direct Parent

Methylpyridines

Alternative Parents

Substituents

Methylpyridine
Heteroaromatic compound
Ketone
Azacycle
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	2.67	ChemAxon
pKa (Strongest Acidic)	19.64	ChemAxon
pKa (Strongest Basic)	6.6	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.96 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	69.36 m³·mol⁻¹	ChemAxon
Polarizability	27.29 Å³	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

162995585

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one (NP0259264)

MOL for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

3D MOL for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

3D SDF for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

3D-SDF for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

PDB for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

3D PDB for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

SMILES for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

INCHI for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

Structure for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)

3D Structure for NP0259264 (4-[(6s)-1,5,5-trimethyl-6h,7h-cyclopenta[c]pyridin-6-yl]butan-2-one)