NP-MRD: Showing NP-Card for (2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol (NP0153604)

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Record Information

Version

2.0

Created at

2022-09-02 10:17:32 UTC

Updated at

2022-09-02 10:17:32 UTC

NP-MRD ID

NP0153604

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol

Description

Plumerinine belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom. (2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol is found in Plumeria rubra. (2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol was first documented in 2003 (PMID: 14620842). Based on a literature review a small amount of articles have been published on Plumerinine (PMID: 35050207) (PMID: 17268613).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
    3.6588    0.2582    0.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192    0.7539   -0.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4892    0.8835   -1.5607 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2158   -0.1909    0.3225 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4492   -1.5906   -0.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4062   -2.4911    0.3877 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4758   -3.7277   -0.2426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0071   -1.9782    0.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1127   -0.5138    0.6051 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4852   -0.0103    0.3560 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4939   -1.1204    0.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5339    0.8774   -0.8401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5927    2.0586   -0.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    1.6705   -0.0782 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1568    2.3667    1.2542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0937    0.2847    0.0446 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3864    1.0744    0.5743 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798   -0.4760   -0.2453 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4803   -0.2823    1.4212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1822    1.7559    0.3594 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3489    0.2555   -1.9171 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6432    1.9518   -1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6260    0.5322   -2.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2990   -0.2715    1.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4331   -1.9167    0.2142 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5051   -1.6354   -1.2950 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6306   -2.6305    1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5211   -3.5530   -1.2216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3564   -2.1961   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6360   -2.5605    0.9342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9495   -0.5058    1.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8233    0.6054    1.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3298   -1.6808   -0.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5357   -1.8236    1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5133   -0.6736    0.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5838    1.2081   -0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2561    0.2866   -1.7411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    2.8020   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4673    2.5372   -1.7221 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5063    2.0937   -0.7321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023    1.6903    2.0198 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5133    3.2593    1.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1701    2.6229    1.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16  4  1  0
 16  9  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  1
  5 25  1  0
  5 26  1  0
  6 27  1  1
  7 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  1
 10 32  1  1
 11 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  6
 15 41  1  0
 15 42  1  0
 15 43  1  0
M  END


  Mrv1652309022212172D          

 16 17  0  0  1  0            999 V2000
    0.7145   -2.8875    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
    1.4289   -1.6500    0.0000 C   0  0  2  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
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   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 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 N   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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  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  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
  4 16  1  0  0  0  0
  9 16  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0153604

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1C[C@H](O)C[C@@H]2[C@H](C)CC[C@@H](C)N12

> <INCHI_IDENTIFIER>
InChI=1S/C14H27NO/c1-9(2)13-7-12(16)8-14-10(3)5-6-11(4)15(13)14/h9-14,16H,5-8H2,1-4H3/t10-,11-,12+,13+,14-/m1/s1

> <INCHI_KEY>
WPYIYVXSMXASQL-PEBLQZBPSA-N

> <FORMULA>
C14H27NO

> <MOLECULAR_WEIGHT>
225.376

> <EXACT_MASS>
225.209264493

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
27.551960820260234

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4S,6R,9R,9aR)-6,9-dimethyl-4-(propan-2-yl)-octahydro-1H-quinolizin-2-ol

> <ALOGPS_LOGP>
2.85

> <JCHEM_LOGP>
2.5039803569999988

> <ALOGPS_LOGS>
-1.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.159817445914829

> <JCHEM_PKA_STRONGEST_BASIC>
10.897409018031079

> <JCHEM_POLAR_SURFACE_AREA>
23.47

> <JCHEM_REFRACTIVITY>
67.82939999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.43e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4S,6R,9R,9aR)-4-isopropyl-6,9-dimethyl-octahydro-1H-quinolizin-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       4.001  -2.310   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    4    9                                                  
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₇NO

Average Mass

225.3760 Da

Monoisotopic Mass

225.20926 Da

IUPAC Name

(2S,4S,6R,9R,9aR)-6,9-dimethyl-4-(propan-2-yl)-octahydro-1H-quinolizin-2-ol

Traditional Name

(2S,4S,6R,9R,9aR)-4-isopropyl-6,9-dimethyl-octahydro-1H-quinolizin-2-ol

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1C[C@H](O)C[C@@H]2[C@H](C)CC[C@@H](C)N12

InChI Identifier

InChI=1S/C14H27NO/c1-9(2)13-7-12(16)8-14-10(3)5-6-11(4)15(13)14/h9-14,16H,5-8H2,1-4H3/t10-,11-,12+,13+,14-/m1/s1

InChI Key

WPYIYVXSMXASQL-PEBLQZBPSA-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
Plumeria rubra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizines

Sub Class

Not Available

Direct Parent

Quinolizines

Alternative Parents

Substituents

Quinolizine
Quinolizidine
Piperidine
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Azacycle
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.85	ALOGPS
logP	2.5	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	15.16	ChemAxon
pKa (Strongest Basic)	10.9	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	23.47 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	67.83 m³·mol⁻¹	ChemAxon
Polarizability	27.55 Å³	ChemAxon
Number of Rings	2	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

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

14583329

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yusoff YM, Abbott G, Young L, Edrada-Ebel R: Metabolomic Profiling of Malaysian and New Zealand Honey Using Concatenated NMR and HRMS Datasets. Metabolites. 2022 Jan 17;12(1):85. doi: 10.3390/metabo12010085. [PubMed:35050207 ]
Michael JP: Indolizidine and quinolizidine alkaloids. Nat Prod Rep. 2007 Feb;24(1):191-222. doi: 10.1039/b509525p. Epub 2007 Jan 3. [PubMed:17268613 ]
Michael JP: Indolizidine and quinolizidine alkaloids. Nat Prod Rep. 2003 Oct;20(5):458-75. doi: 10.1039/b208137g. [PubMed:14620842 ]
LOTUS database [Link]

Showing NP-Card for (2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol (NP0153604)

MOL for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

3D MOL for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

3D SDF for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

3D-SDF for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

PDB for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

3D PDB for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

SMILES for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

INCHI for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

Structure for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)

3D Structure for NP0153604 ((2s,4s,6r,9r,9ar)-4-isopropyl-6,9-dimethyl-octahydro-1h-quinolizin-2-ol)