NP-MRD: Showing NP-Card for (-)-Isopteleflorine (NP0083383)

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Record Information

Version

2.0

Created at

2022-04-29 04:27:03 UTC

Updated at

2022-04-29 04:27:03 UTC

NP-MRD ID

NP0083383

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Isopteleflorine

Description

Isopteleflorine belongs to the class of organic compounds known as dihydrofuranoquinolines. These are organic heterocyclic compounds with a structure based on the dihydrofuranoquinoline skeleton. (-)-Isopteleflorine is found in Orixa japonica . (-)-Isopteleflorine was first documented in 2001 (PMID: 11330697). Based on a literature review very few articles have been published on Isopteleflorine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
    0.4783   -3.5566   -0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6505   -2.3118   -1.2143 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7751   -1.1187   -0.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3566   -0.3556   -0.2019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2660    0.8302    0.4813 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9907    1.2277    0.8318 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0844    0.5102    0.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3573    0.9488    0.9077 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4783    0.2084    0.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4101   -0.9862   -0.0882 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1584   -1.4265   -0.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0282   -0.6840   -0.1524 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5495    0.9381    1.1188 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1372    2.2684    1.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7357    2.0913    1.5948 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5163    1.4083    0.6861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4830    0.3843    0.4111 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6586    1.0689   -0.2277 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1793    1.8372   -1.4398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7598    0.1092   -0.5524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1297    2.0132    0.7114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7917   -0.5940   -0.4798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3512   -4.2283   -0.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4375   -4.0729   -0.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4477   -3.3356    0.5777 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3075   -1.5434   -0.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0463   -2.3595   -1.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3440    2.9592    0.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5758    2.5650    2.3403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8021   -0.1106    1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2457    2.9399   -1.2767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1326    1.6285   -1.7022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8046    1.6221   -2.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5880   -0.8221    0.0295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7682    0.5385   -0.3637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6851   -0.1308   -1.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2932    1.5870    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9481   -0.3987   -1.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0603   -1.6493   -0.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 12  2  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
  8 15  1  0
 15 14  1  0
 14 13  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4 22  1  0
 22 17  1  0
 17 16  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  1
  4  3  1  0
  7 12  1  0
 16  5  1  0
 13  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 11 27  1  0
 10 26  1  0
 14 28  1  0
 14 29  1  0
 22 38  1  0
 22 39  1  0
 17 30  1  1
 19 31  1  0
 19 32  1  0
 19 33  1  0
 20 34  1  0
 20 35  1  0
 20 36  1  0
 21 37  1  0
M  END


  Mrv1652304292206272D          

 22 25  0  0  1  0            999 V2000
    1.9605    0.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7684    0.0341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0278   -0.7491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8358   -0.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3843   -0.2998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1922   -0.4667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4516   -1.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9031   -1.8661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3197   -2.5782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1257   -2.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2072   -1.5811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0952   -1.6992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5467   -2.3154    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7387   -2.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4793   -1.3653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6543   -1.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4039   -2.1561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6207   -2.4155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1624   -2.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3613   -1.6324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8801   -3.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0741   -2.6372    0.0000 O   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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
  8 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 17 22  1  0  0  0  0
 14 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0083383

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C=CC3=C(OCO3)C2=NC2=C1C[C@@H](O2)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C16H17NO5/c1-16(2,18)11-6-9-13(19-3)8-4-5-10-14(21-7-20-10)12(8)17-15(9)22-11/h4-5,11,18H,6-7H2,1-3H3/t11-/m1/s1

> <INCHI_KEY>
LKRBBZYDDUUFNV-LLVKDONJSA-N

> <FORMULA>
C16H17NO5

> <MOLECULAR_WEIGHT>
303.314

> <EXACT_MASS>
303.110672651

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.55139397593277

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(13R)-10-methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.0^{2,6}.0^{11,15}]hexadeca-1(16),2(6),7,9,11(15)-pentaen-13-yl]propan-2-ol

> <ALOGPS_LOGP>
2.44

> <JCHEM_LOGP>
2.139954195

> <ALOGPS_LOGS>
-2.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.293446565770534

> <JCHEM_PKA_STRONGEST_BASIC>
2.602926751682949

> <JCHEM_POLAR_SURFACE_AREA>
70.04

> <JCHEM_REFRACTIVITY>
77.3152

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(13R)-10-methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.0^{2,6}.0^{11,15}]hexadeca-1(16),2(6),7,9,11(15)-pentaen-13-yl]propan-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       3.660   0.375   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.168   0.064   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.652  -1.398   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.160  -1.710   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.184  -0.560   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.692  -0.871   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.176  -2.333   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.152  -3.483   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.930  -4.813   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.435  -4.484   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.587  -2.951   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.644  -3.172   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       6.620  -4.322   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       5.112  -4.011   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.628  -2.549   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.088  -2.557   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.621  -4.025   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.159  -4.509   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.303  -4.993   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.674  -3.047   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.643  -5.971   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.872  -4.923   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    7                                                       
CONECT   12    8    4   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14    3   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   17   14                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₇NO₅

Average Mass

303.3140 Da

Monoisotopic Mass

303.11067 Da

IUPAC Name

2-[(13R)-10-methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.0^{2,6}.0^{11,15}]hexadeca-1(16),2(6),7,9,11(15)-pentaen-13-yl]propan-2-ol

Traditional Name

2-[(13R)-10-methoxy-3,5,14-trioxa-16-azatetracyclo[7.7.0.0^{2,6}.0^{11,15}]hexadeca-1(16),2(6),7,9,11(15)-pentaen-13-yl]propan-2-ol

CAS Registry Number

Not Available

SMILES

COC1=C2C=CC3=C(OCO3)C2=NC2=C1C[C@@H](O2)C(C)(C)O

InChI Identifier

InChI=1S/C16H17NO5/c1-16(2,18)11-6-9-13(19-3)8-4-5-10-14(21-7-20-10)12(8)17-15(9)22-11/h4-5,11,18H,6-7H2,1-3H3/t11-/m1/s1

InChI Key

LKRBBZYDDUUFNV-LLVKDONJSA-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
Orixa japonica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydrofuranoquinolines. These are organic heterocyclic compounds with a structure based on the dihydrofuranoquinoline skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Dihydrofuranoquinolines

Direct Parent

Dihydrofuranoquinolines

Alternative Parents

Substituents

Dihydrofuranoquinoline
Benzodioxole
Alkyl aryl ether
Pyridine
Benzenoid
Tertiary alcohol
Heteroaromatic compound
Oxacycle
Azacycle
Acetal
Ether
Alcohol
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
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	2.44	ALOGPS
logP	2.14	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	14.29	ChemAxon
pKa (Strongest Basic)	2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	70.04 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	77.32 m³·mol⁻¹	ChemAxon
Polarizability	31.55 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00052060

Chemspider ID

171129

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

197708

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Noshita T, Tando M, Suzuki K, Murata K, Funayama S: New quinoline alkaloids from the leaves and stems of Orixa japonica, orijanone, isopteleflorine and 3'-O-methylorixine. Biosci Biotechnol Biochem. 2001 Mar;65(3):710-3. doi: 10.1271/bbb.65.710. [PubMed:11330697 ]

Showing NP-Card for (-)-Isopteleflorine (NP0083383)

MOL for NP0083383 ((-)-Isopteleflorine)

3D MOL for NP0083383 ((-)-Isopteleflorine)

3D SDF for NP0083383 ((-)-Isopteleflorine)

3D-SDF for NP0083383 ((-)-Isopteleflorine)

PDB for NP0083383 ((-)-Isopteleflorine)

3D PDB for NP0083383 ((-)-Isopteleflorine)

SMILES for NP0083383 ((-)-Isopteleflorine)

INCHI for NP0083383 ((-)-Isopteleflorine)

Structure for NP0083383 ((-)-Isopteleflorine)

3D Structure for NP0083383 ((-)-Isopteleflorine)