NP-MRD: Showing NP-Card for (+)-Roxiamine A (NP0083407)

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Record Information

Version

2.0

Created at

2022-04-29 04:28:00 UTC

Updated at

2022-04-29 04:28:00 UTC

NP-MRD ID

NP0083407

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Roxiamine A

Description

Roxiamine A belongs to the class of organic compounds known as furanoquinolines. Furanoquinolines are compounds containing a furan ring fused to a quinoline. (+)-Roxiamine A is found in Euodia roxburghiana and Melicope lunu-ankenda. Based on a literature review very few articles have been published on Roxiamine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
    7.9390   -0.4455   -0.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5790   -0.7346   -0.3926 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5776    0.2013   -0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9008    1.4125   -0.1571 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1586   -0.1541   -0.1119 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8815   -1.0658    1.0686 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2568    1.0575   -0.0080 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    0.5295    0.0971 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8897    1.5439    0.2001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4442    1.1916    0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3841    2.1944    0.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7323    1.8486    0.5083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0922    0.5269    0.5071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4248    0.1795    0.6096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3821    1.2030    0.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8990    1.6713   -0.5336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8305   -1.1198    0.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0910   -1.7078    0.7036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272   -3.0668    0.6497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5373   -3.2699    0.5377 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8886   -2.1183    0.5109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5952   -1.7708    0.4116 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1664   -0.5001    0.4059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8465   -0.1307    0.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3710   -0.2874    0.5185 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4586   -1.3619   -0.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1849    0.3754   -1.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8292   -0.6874   -1.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7810   -1.6801    1.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207   -1.7044    0.7851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6229   -0.4186    1.9431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4744    1.5351    0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3901    1.7548   -0.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6268   -0.0382   -0.8486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7478   -0.1228    0.9736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1434    3.2488    0.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4770    2.6329    0.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2920    0.7561   -1.0635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0427    2.0174   -1.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7015    2.4023   -0.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0067   -1.1734    0.7923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6307   -3.8080    0.6990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0962   -0.9166    0.2240 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  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 23  1  0
 23 24  2  0
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 14  2  0
 14 15  1  0
 15 16  1  0
 24 10  1  0
 17 21  1  0
 14 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  5 28  1  6
  6 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 11 36  1  0
 12 37  1  0
 24 43  1  0
 19 42  1  0
 18 41  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
M  END


  Mrv1652304292206282D          

 24 26  0  0  1  0            999 V2000
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  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   -2.0625    0.0000 O   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
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136   -3.5549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136   -2.2201    0.0000 O   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
   -0.7145   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
  9 19  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  6 20  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0083407

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](C)CCOC1=CC=C2C(=C1)N=C1OC=CC1=C2OC

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO5/c1-11(18(20)22-3)6-8-23-12-4-5-13-15(10-12)19-17-14(7-9-24-17)16(13)21-2/h4-5,7,9-11H,6,8H2,1-3H3/t11-/m0/s1

> <INCHI_KEY>
WOPDGNHIWBYEOT-NSHDSACASA-N

> <FORMULA>
C18H19NO5

> <MOLECULAR_WEIGHT>
329.352

> <EXACT_MASS>
329.126322716

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
34.76869117103415

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2S)-4-({4-methoxyfuro[2,3-b]quinolin-7-yl}oxy)-2-methylbutanoate

> <ALOGPS_LOGP>
3.66

> <JCHEM_LOGP>
3.0346809796666663

> <ALOGPS_LOGS>
-3.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.117043147879389

> <JCHEM_POLAR_SURFACE_AREA>
70.78999999999999

> <JCHEM_REFRACTIVITY>
86.58200000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S)-4-({4-methoxyfuro[2,3-b]quinolin-7-yl}oxy)-2-methylbutanoate

> <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       8.002  -6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.001  -3.850   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.334  -8.470   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.132  -6.636   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.037  -5.390   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.132  -4.144   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      -1.334  -3.850   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.003  -3.850   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.336  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   19                                                       
CONECT   19    9   18   20                                                  
CONECT   20   19    6                                                       
CONECT   21    2   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₉NO₅

Average Mass

329.3520 Da

Monoisotopic Mass

329.12632 Da

IUPAC Name

methyl (2S)-4-({4-methoxyfuro[2,3-b]quinolin-7-yl}oxy)-2-methylbutanoate

Traditional Name

methyl (2S)-4-({4-methoxyfuro[2,3-b]quinolin-7-yl}oxy)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](C)CCOC1=CC=C2C(=C1)N=C1OC=CC1=C2OC

InChI Identifier

InChI=1S/C18H19NO5/c1-11(18(20)22-3)6-8-23-12-4-5-13-15(10-12)19-17-14(7-9-24-17)16(13)21-2/h4-5,7,9-11H,6,8H2,1-3H3/t11-/m0/s1

InChI Key

WOPDGNHIWBYEOT-NSHDSACASA-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
Euodia roxburghiana	Plant	KNApSAcK
Melicope lunu-ankenda	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoquinolines. Furanoquinolines are compounds containing a furan ring fused to a quinoline.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Furanoquinolines

Direct Parent

Furanoquinolines

Alternative Parents

Substituents

Furanoquinoline
Furopyridine
Alkyl aryl ether
Fatty acid ester
Pyridine
Benzenoid
Fatty acyl
Heteroaromatic compound
Furan
Methyl ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Azacycle
Ether
Carboxylic acid derivative
Oxacycle
Carbonyl group
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic oxide
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	3.66	ALOGPS
logP	3.03	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Basic)	3.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	70.79 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	86.58 m³·mol⁻¹	ChemAxon
Polarizability	34.77 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

C00052088

Chemspider ID

2272382

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3000862

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (+)-Roxiamine A (NP0083407)

MOL for NP0083407 ((+)-Roxiamine A)

3D MOL for NP0083407 ((+)-Roxiamine A)

3D SDF for NP0083407 ((+)-Roxiamine A)

3D-SDF for NP0083407 ((+)-Roxiamine A)

PDB for NP0083407 ((+)-Roxiamine A)

3D PDB for NP0083407 ((+)-Roxiamine A)

SMILES for NP0083407 ((+)-Roxiamine A)

INCHI for NP0083407 ((+)-Roxiamine A)

Structure for NP0083407 ((+)-Roxiamine A)

3D Structure for NP0083407 ((+)-Roxiamine A)