NP-MRD: Showing NP-Card for Dubiusamine A (NP0086428)

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Record Information

Version

2.0

Created at

2022-04-29 06:44:00 UTC

Updated at

2022-04-29 06:44:00 UTC

NP-MRD ID

NP0086428

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dubiusamine A

Description

Dubiusamine A belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. Dubiusamine A is found in Pandanus dubius. Dubiusamine A was first documented in 2013 (PMID: 23530716). Based on a literature review very few articles have been published on Dubiusamine A (PMID: 29043822).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
   -7.9129    1.3176    0.2019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4678    0.9618   -0.1462 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0461   -0.1966    0.6849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7658    0.2094    1.3468 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6003   -0.6493    0.7937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4864   -0.4199   -0.6702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4547   -1.2223   -1.3275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0289   -1.1258   -1.0375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192   -1.3876    0.2658 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9420   -1.5805    0.0822 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6482   -0.3034   -0.2999 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1290   -0.7349   -0.4769 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071    0.4734   -0.8423 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3512    0.1500   -1.0983 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9895   -0.4311    0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4858    0.8179    0.8504 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6922    0.4814    1.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8340    1.7078   -0.2720 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6771    2.6457   -0.2736 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0781    1.3616   -1.3716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5606    1.5482    0.9960 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5886    2.0652    0.2490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7951    3.2848   -0.0782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2843    1.9832   -0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4631    0.3392    0.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9095    1.7619    1.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4008    0.7710   -1.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9318   -1.1398    0.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8454   -0.4344    1.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7956    0.0353    2.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8814   -1.6976    1.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7297   -0.4018    1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4905   -0.6217   -1.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3276    0.6801   -0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5403   -1.0654   -2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7222   -2.3388   -1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6633   -0.0873   -1.3286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4978   -1.8458   -1.7346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5972   -0.5372    0.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1232   -2.3839   -0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3351   -1.8825    1.0671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3563    0.0966   -1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5737    0.4149    0.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1692   -1.5385   -1.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4757   -1.2013    0.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8070    1.2135   -0.0043 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4299    0.9911   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4667   -0.5186   -1.9927 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9073   -0.9816   -0.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3619   -1.0470    0.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7058    1.2330    1.4906 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5826    0.2284    1.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8614    1.3642    2.3694 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4167   -0.3627    2.3423 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 18 20  1  0
  4 21  1  0
 21 22  1  0
 22 23  2  0
 22  2  1  0
 20 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  6
  3 28  1  0
  3 29  1  0
  4 30  1  1
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 14 48  1  6
 15 49  1  0
 15 50  1  0
 16 51  1  1
 17 52  1  0
 17 53  1  0
 17 54  1  0
M  END


  Mrv1652304292208442D          

 23 24  0  0  1  0            999 V2000
    3.3440   -7.0223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6795   -6.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670   -5.5542    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4465   -5.4680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8191   -4.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5727   -5.2767    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2872   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0017   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7161   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4306   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1451   -4.8642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8596   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5740   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2885   -5.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0030   -4.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7174   -5.2767    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.4711   -4.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0232   -5.5542    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.8436   -5.4680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6107   -6.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8037   -6.0971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9462   -7.0223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4865   -6.0971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 20 22  2  0  0  0  0
  6 23  1  0  0  0  0
  2 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086428

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H](CCCCNCCCC[C@@H]2C[C@@H](C)C(=O)O2)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H31NO4/c1-13-11-15(22-17(13)20)7-3-5-9-19-10-6-4-8-16-12-14(2)18(21)23-16/h13-16,19H,3-12H2,1-2H3/t13-,14-,15-,16-/m1/s1

> <INCHI_KEY>
LVGJWKBTZDPIMK-KLHDSHLOSA-N

> <FORMULA>
C18H31NO4

> <MOLECULAR_WEIGHT>
325.449

> <EXACT_MASS>
325.225308482

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.61949901048414

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,5R)-3-methyl-5-[4-({4-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]butyl}amino)butyl]oxolan-2-one

> <ALOGPS_LOGP>
3.18

> <JCHEM_LOGP>
3.0124630996666664

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.749490018296527

> <JCHEM_POLAR_SURFACE_AREA>
64.63

> <JCHEM_REFRACTIVITY>
88.08299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.16e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,5R)-3-methyl-5-[4-({4-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]butyl}amino)butyl]oxolan-2-one

> <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  O   UNK     0       6.242 -13.108   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.868 -11.702   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.098 -10.368   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.567 -10.207   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.129  -9.223   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.536  -9.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.869  -9.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.203  -9.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.537  -9.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.870  -9.850   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      15.204  -9.080   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      16.538  -9.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.872  -9.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      19.205  -9.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.539  -9.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.873  -9.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      23.279  -9.223   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      24.310 -10.368   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      25.841 -10.207   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      23.540 -11.702   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      22.034 -11.381   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      24.166 -13.108   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       8.375 -11.381   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20   16                                                       
CONECT   22   20                                                            
CONECT   23    6    2                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₃₁NO₄

Average Mass

325.4490 Da

Monoisotopic Mass

325.22531 Da

IUPAC Name

(3R,5R)-3-methyl-5-[4-({4-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]butyl}amino)butyl]oxolan-2-one

Traditional Name

(3R,5R)-3-methyl-5-[4-({4-[(2R,4R)-4-methyl-5-oxooxolan-2-yl]butyl}amino)butyl]oxolan-2-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H](CCCCNCCCC[C@@H]2C[C@@H](C)C(=O)O2)OC1=O

InChI Identifier

InChI=1S/C18H31NO4/c1-13-11-15(22-17(13)20)7-3-5-9-19-10-6-4-8-16-12-14(2)18(21)23-16/h13-16,19H,3-12H2,1-2H3/t13-,14-,15-,16-/m1/s1

InChI Key

LVGJWKBTZDPIMK-KLHDSHLOSA-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
Pandanus dubius	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Gamma butyrolactones

Direct Parent

Gamma butyrolactones

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Gamma butyrolactone
Oxolane
Amino acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Secondary aliphatic amine
Oxacycle
Secondary amine
Hydrocarbon derivative
Organic oxide
Amine
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	3.18	ALOGPS
logP	3.01	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	10.75	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.63 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	88.08 m³·mol⁻¹	ChemAxon
Polarizability	38.62 Å³	ChemAxon
Number of Rings	2	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

C00056687

Chemspider ID

28287637

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71665429

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Jiang YJ, Zhang GP, Huang JQ, Chen D, Ding CH, Hou XL: Palladium-Catalyzed Asymmetric Allylic Alkylation of Alkyl-Substituted Allyl Reagents with Acyclic Amides. Org Lett. 2017 Nov 3;19(21):5932-5935. doi: 10.1021/acs.orglett.7b02927. [PubMed:29043822 ]
Kawasumi M, Iwabuchi Y: Concise entry to chiral 5-(4-hydroxybutyl)-2(5H)-furanone via HTIB-mediated novel oxidative fragmentation: formal total synthesis of (+)-dubiusamine A. Org Lett. 2013 Apr 5;15(7):1788-90. doi: 10.1021/ol4005239. Epub 2013 Mar 26. [PubMed:23530716 ]

Showing NP-Card for Dubiusamine A (NP0086428)

MOL for NP0086428 (Dubiusamine A)

3D MOL for NP0086428 (Dubiusamine A)

3D SDF for NP0086428 (Dubiusamine A)

3D-SDF for NP0086428 (Dubiusamine A)

PDB for NP0086428 (Dubiusamine A)

3D PDB for NP0086428 (Dubiusamine A)

SMILES for NP0086428 (Dubiusamine A)

INCHI for NP0086428 (Dubiusamine A)

Structure for NP0086428 (Dubiusamine A)

3D Structure for NP0086428 (Dubiusamine A)