NP-MRD: Showing NP-Card for Derricin (NP0054750)

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Record Information

Version

2.0

Created at

2022-04-28 01:00:11 UTC

Updated at

2022-04-28 01:00:11 UTC

NP-MRD ID

NP0054750

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Derricin

Description

Derricin belongs to the class of organic compounds known as 3-prenylated chalcones. These are chalcones featuring a C5-isoprenoid unit at the 3-position. Thus, derricin is considered to be a flavonoid. Derricin is found in Derris sericea, Erythroxylum barbatum, Lonchocarpus neuroscapha, Lonchocarpus nitidus and Lonchocarpus sericeus. Derricin was first documented in 2003 (PMID: 12601679). Based on a literature review a small amount of articles have been published on Derricin (PMID: 25775405) (PMID: 33424286) (PMID: 19921586).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -2.5836   -4.5812    0.0675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9741   -3.2048    0.0719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9614   -2.2205    0.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6429   -2.6076    0.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3458   -1.6435   -0.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0401   -0.2712   -0.0761 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268    0.6979   -0.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8508    1.9207   -0.0859 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5487    0.2832   -0.0739 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4695    1.2083   -0.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8801    0.9203   -0.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8336    1.9563   -0.0697 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1724    1.6544   -0.0451 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5954    0.3396   -0.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6876   -0.6856    0.0171 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3404   -0.3623   -0.0078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2849    0.0755   -0.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7265    1.3510   -0.0987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3007   -0.8978   -0.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7237   -0.4941   -0.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0226    0.7555    0.7031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5988    1.7431    0.0367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9107    1.5398   -1.4118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9246    3.0148    0.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9800   -4.7244    0.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9548   -4.7960   -0.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4947   -5.1919    0.0587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4258   -3.6713    0.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3411   -1.9973   -0.0499 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7778   -0.7422   -0.0842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2044    2.2801   -0.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4553    2.9515   -0.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9128    2.4414   -0.0591 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6693    0.1342    0.0131 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9839   -1.7253    0.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6307   -1.1949    0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2326    2.1797   -0.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1662   -0.5222   -1.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3103   -1.3116    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7681    0.8630    1.7579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2827    2.4699   -1.8765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9620    1.2940   -1.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6616    0.7578   -1.5976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6521    2.8220    1.5011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9968    3.4435    1.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3241    3.7480   -0.0555 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  2  3
 22 23  1  0
 22 24  1  0
 19 17  1  0
 17 18  1  0
 17  6  2  0
  6  5  1  0
  5  4  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  4  3  1  0
 16 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 20 38  1  0
 20 39  1  0
 21 40  1  0
 23 41  1  0
 23 42  1  0
 23 43  1  0
 24 44  1  0
 24 45  1  0
 24 46  1  0
 18 37  1  0
  5 29  1  0
  4 28  1  0
  9 30  1  0
 10 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
M  END


  Mrv1652304282203002D          

 24 25  0  0  0  0            999 V2000
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    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
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  3 17  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
  1 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054750

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC=C(C)C)C(O)=C(C=C1)C(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O3/c1-15(2)9-11-18-20(24-3)14-12-17(21(18)23)19(22)13-10-16-7-5-4-6-8-16/h4-10,12-14,23H,11H2,1-3H3/b13-10+

> <INCHI_KEY>
HMGRVRIPKPTWTO-JLHYYAGUSA-N

> <FORMULA>
C21H22O3

> <MOLECULAR_WEIGHT>
322.404

> <EXACT_MASS>
322.156894568

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
36.828499877251986

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-1-[2-hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-3-phenylprop-2-en-1-one

> <ALOGPS_LOGP>
4.64

> <JCHEM_LOGP>
5.8076557210000015

> <ALOGPS_LOGS>
-4.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.41365468463931

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.918877071932921

> <JCHEM_PKA_STRONGEST_BASIC>
-4.858037616343821

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
99.5639

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.37e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
derricin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2    6   23                                                  
CONECT    2    1    3   18                                                  
CONECT    3    2    4   17                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    3                                                            
CONECT   18    2   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23    1   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂O₃

Average Mass

322.4040 Da

Monoisotopic Mass

322.15689 Da

IUPAC Name

(2E)-1-[2-hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]-3-phenylprop-2-en-1-one

Traditional Name

derricin

CAS Registry Number

Not Available

SMILES

COC1=C(CC=C(C)C)C(O)=C(C=C1)C(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C21H22O3/c1-15(2)9-11-18-20(24-3)14-12-17(21(18)23)19(22)13-10-16-7-5-4-6-8-16/h4-10,12-14,23H,11H2,1-3H3/b13-10+

InChI Key

HMGRVRIPKPTWTO-JLHYYAGUSA-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
Derris sericea	Plant	KNApSAcK
Erythroxylum barbatum	LOTUS Database	35616633
Lonchocarpus neuroscapha	Plant	KNApSAcK
Lonchocarpus nitidus	Plant	KNApSAcK
Lonchocarpus sericeus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-prenylated chalcones. These are chalcones featuring a C5-isoprenoid unit at the 3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

3-prenylated chalcones

Alternative Parents

Substituents

3-prenylated chalcone
2'-hydroxychalcone
Cinnamylphenol
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Benzoyl
Aryl ketone
Styrene
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Acryloyl-group
Vinylogous acid
Enone
Alpha,beta-unsaturated ketone
Ketone
Ether
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120009 )

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	4.64	ALOGPS
logP	5.81	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	6.92	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	99.56 m³·mol⁻¹	ChemAxon
Polarizability	36.83 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00007052

Chemspider ID

4791596

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6052009

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fonseca BF, Predes D, Cerqueira DM, Reis AH, Amado NG, Cayres MC, Kuster RM, Oliveira FL, Mendes FA, Abreu JG: Derricin and derricidin inhibit Wnt/beta-catenin signaling and suppress colon cancer cell growth in vitro. PLoS One. 2015 Mar 16;10(3):e0120919. doi: 10.1371/journal.pone.0120919. eCollection 2015. [PubMed:25775405 ]
Bortoluzzi AAM, Staffen IV, Banhuk FW, Griebler A, Matos PK, Ayala TS, da Silva EAA, Sarragiotto MH, Schuquel ITA, Jorge TCM, Menolli RA: Determination of chemical structure and anti-Trypanosoma cruzi activity of extracts from the roots of Lonchocarpus cultratus (Vell.) A.M.G. Azevedo & H.C. Lima. Saudi J Biol Sci. 2021 Jan;28(1):99-108. doi: 10.1016/j.sjbs.2020.08.036. Epub 2020 Sep 1. [PubMed:33424286 ]
Fontenele JB, Leal LK, Felix FH, Silveira ER, Viana GS: Studies on the anti-oedematogenic properties of a fraction rich in lonchocarpin and derricin isolated from Lonchocarpus sericeus. Nat Prod Res. 2009;23(18):1677-88. doi: 10.1080/14786410802181745. [PubMed:19921586 ]
Cunha GM, Fontenele JB, Nobre Junior HV, De Sousa FC, Silveira ER, Nogueira NA, De Moraes MO, Viana GS, Costa-Lotufo LV: Cytotoxic activity of chalcones isolated from lonchocarpus sericeus (pocr.) kunth. Phytother Res. 2003 Feb;17(2):155-9. doi: 10.1002/ptr.1096. [PubMed:12601679 ]

Showing NP-Card for Derricin (NP0054750)

MOL for NP0054750 (Derricin)

3D MOL for NP0054750 (Derricin)

3D SDF for NP0054750 (Derricin)

3D-SDF for NP0054750 (Derricin)

PDB for NP0054750 (Derricin)

3D PDB for NP0054750 (Derricin)

SMILES for NP0054750 (Derricin)

INCHI for NP0054750 (Derricin)

Structure for NP0054750 (Derricin)

3D Structure for NP0054750 (Derricin)