NP-MRD: Showing NP-Card for (+)-Epiyangambin (NP0054877)

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Record Information

Version

2.0

Created at

2022-04-28 01:05:23 UTC

Updated at

2022-04-28 01:05:23 UTC

NP-MRD ID

NP0054877

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Epiyangambin

Description

Epiyangambin belongs to the class of organic compounds known as furanoid lignans. These are lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units. (+)-Epiyangambin is found in Achillea holosericea, Artemisia absinthium, Artemisia arborescens, Artemisia argentea, Hernandia nymphaeifolia , Hernandia ovigera , Leucophyllum frutescens, Ocotea duckei and Virola elongata. (+)-Epiyangambin was first documented in 2002 (PMID: 12141878). Based on a literature review a small amount of articles have been published on Epiyangambin (PMID: 32988347) (PMID: 31631708) (PMID: 22782878).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282203052D          

 32 35  0  0  1  0            999 V2000
    1.2695   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0146    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2076    1.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0473    2.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5047    2.7664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3117    2.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5666    1.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8637    3.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6707    3.0364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2498    3.5510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018    4.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543    2.3248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1092    3.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8388    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0937   -1.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9007   -1.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1556   -2.6631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6036   -3.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7966   -3.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417   -2.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2446   -3.7178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4376   -3.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655   -4.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626   -2.8347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0542   -0.6674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  6 14  1  0  0  0  0
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  3 16  1  0  0  0  0
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 19 32  1  0  0  0  0
 32  1  1  1  0  0  0
 16 32  1  0  0  0  0
M  END

     RDKit          3D

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    5.3013    0.7852   -0.5793 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6959   -0.4310   -0.3453 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3725   -1.5752   -0.7378 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8503   -2.8756   -0.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4464   -0.4888    0.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3432   -0.4956    2.2200 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3773   -1.3607    1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6372   -0.4586    1.1279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2923    0.3581   -0.5980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6467    0.6195   -0.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1564    1.8000   -1.1686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2418    2.7303   -1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5679   -0.2808   -0.1173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9441   -0.0328   -0.1379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7740   -0.4144   -1.2032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3362   -4.1890    1.8983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8125   -3.2855    2.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2235    5.1753   -0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5810    0.7897   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8846   -0.1678    0.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4939   -3.0536    0.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6698   -3.5952   -0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0846   -3.0421   -1.3222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0496   -1.4732    0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0410   -1.9282    2.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984   -2.0116    0.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6092    1.0902   -1.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7956    2.3812   -2.6253 H   0  0  0  0  0  0  0  0  0  0  0  0
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 30  3  1  0
 25  6  1  0
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 26 56  1  0
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 29 59  1  0
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  6 37  1  1
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 25 55  1  1
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M  END


  Mrv1652304282203052D          

 32 35  0  0  1  0            999 V2000
    1.2695   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0146    1.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6036   -3.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5417   -2.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8585   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6655   -4.2324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0542   -0.6674    0.0000 C   0  0  1  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  1  1  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
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M  END
> <DATABASE_ID>
NP0054877

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1OC)[C@H]1OC[C@H]2[C@@H]1CO[C@H]2C1=CC(OC)=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O8/c1-25-17-7-13(8-18(26-2)23(17)29-5)21-15-11-32-22(16(15)12-31-21)14-9-19(27-3)24(30-6)20(10-14)28-4/h7-10,15-16,21-22H,11-12H2,1-6H3/t15-,16-,21-,22+/m0/s1

> <INCHI_KEY>
HRLFUIXSXUASEX-WWLNLUSPSA-N

> <FORMULA>
C24H30O8

> <MOLECULAR_WEIGHT>
446.496

> <EXACT_MASS>
446.194067926

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
46.79047946472776

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3aR,4S,6aR)-1,4-bis(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan

> <ALOGPS_LOGP>
2.76

> <JCHEM_LOGP>
2.254205128

> <ALOGPS_LOGS>
-4.88

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6922839370300733

> <JCHEM_POLAR_SURFACE_AREA>
73.84000000000002

> <JCHEM_REFRACTIVITY>
116.99119999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.84e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3aR,4S,6aR)-1,4-bis(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan

> <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       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.465  -0.476   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.894   2.235   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.388   2.555   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.088   4.019   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.942   5.164   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.449   4.844   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.924   3.379   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.479   5.988   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.985   5.668   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.466   6.629   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.497   7.773   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.595   4.340   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.071   5.804   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.834   0.294   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.204  -0.476   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.775  -3.186   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.281  -3.507   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.757  -4.971   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.727  -6.116   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.220  -5.795   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.744  -4.331   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.190  -6.940   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.684  -6.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.203  -7.580   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.709  -7.900   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.264  -5.291   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.739  -6.756   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
CONECT    1    2   32                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   16                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    4                                                       
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    7   13                                                       
CONECT   13   12                                                            
CONECT   14    6   15                                                       
CONECT   15   14                                                            
CONECT   16    3   17   32                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   30                                                  
CONECT   23   22   24   28                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24   20                                                       
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   23   29                                                       
CONECT   29   28                                                            
CONECT   30   22   31                                                       
CONECT   31   30                                                            
CONECT   32   19    1   16                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
(1S-(1alpha,3Aalpha,4alpha,6aalpha))-isomer OF epiyangambin	MeSH
Epi-yangambin	MeSH
Yangambin	MeSH

Chemical Formula

C₂₄H₃₀O₈

Average Mass

446.4960 Da

Monoisotopic Mass

446.19407 Da

IUPAC Name

(1R,3aR,4S,6aR)-1,4-bis(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan

Traditional Name

(1R,3aR,4S,6aR)-1,4-bis(3,4,5-trimethoxyphenyl)-hexahydrofuro[3,4-c]furan

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1OC)[C@H]1OC[C@H]2[C@@H]1CO[C@H]2C1=CC(OC)=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C24H30O8/c1-25-17-7-13(8-18(26-2)23(17)29-5)21-15-11-32-22(16(15)12-31-21)14-9-19(27-3)24(30-6)20(10-14)28-4/h7-10,15-16,21-22H,11-12H2,1-6H3/t15-,16-,21-,22+/m0/s1

InChI Key

HRLFUIXSXUASEX-WWLNLUSPSA-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
Achillea holosericea	LOTUS Database	35616633
Artemisia absinthium	LOTUS Database	35616633
Artemisia arborescens	LOTUS Database	35616633
Artemisia argentea	LOTUS Database	35616633
Hernandia nymphaeifolia	Plant	KNApSAcK
Hernandia ovigera	Plant	KNApSAcK
Leucophyllum frutescens	Plant	KNApSAcK
Ocotea duckei	Plant	KNApSAcK
Virola elongata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoid lignans. These are lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Not Available

Direct Parent

Furanoid lignans

Alternative Parents

Substituents

Furanoid lignan
Furofuran lignan skeleton
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Furofuran
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Oxolane
Oxacycle
Dialkyl ether
Ether
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
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	2.76	ALOGPS
logP	2.25	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	73.84 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	116.99 m³·mol⁻¹	ChemAxon
Polarizability	46.79 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	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00007197

Chemspider ID

8224785

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10049223

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gu JQ, Park EJ, Totura S, Riswan S, Fong HH, Pezzuto JM, Kinghorn AD: Constituents of the twigs of Hernandia ovigera that inhibit the transformation of JB6 murine epidermal cells. J Nat Prod. 2002 Jul;65(7):1065-8. doi: 10.1021/np020042w. [PubMed:12141878 ]
Sultan MH, Zuwaiel AA, Moni SS, Alshahrani S, Alqahtani SS, Madkhali O, Elmobark ME: Bioactive Principles and Potentiality of Hot Methanolic Extract of the Leaves from Artemisia absinthium L "in vitro Cytotoxicity Against Human MCF-7 Breast Cancer Cells, Antibacterial Study and Wound Healing Activity". Curr Pharm Biotechnol. 2020;21(15):1711-1721. doi: 10.2174/1389201021666200928150519. [PubMed:32988347 ]
Moni SS, Hadi Sultan M, Makeen HA, Jabeen A, Sanobar S, Siddiqui R, Ur Rehman Z, Alam MS, Ahmad S, Elmobark ME, Moochikkal R: Phytochemical and spectral analysis of the methanolic extracts of leaves of Murraya koenigii of Jazan, Saudi Arabia. Nat Prod Res. 2021 Aug;35(15):2569-2573. doi: 10.1080/14786419.2019.1679137. Epub 2019 Oct 21. [PubMed:31631708 ]
Radulovic NS, Mladenovic MZ, Ethordevic ND: Chemotypification of Astrantia major L. (Apiaceae): essential-oil and lignan profiles of fruits. Chem Biodivers. 2012 Jul;9(7):1320-37. doi: 10.1002/cbdv.201100430. [PubMed:22782878 ]

Showing NP-Card for (+)-Epiyangambin (NP0054877)

MOL for NP0054877 ((+)-Epiyangambin)

3D MOL for NP0054877 ((+)-Epiyangambin)

3D SDF for NP0054877 ((+)-Epiyangambin)

3D-SDF for NP0054877 ((+)-Epiyangambin)

PDB for NP0054877 ((+)-Epiyangambin)

3D PDB for NP0054877 ((+)-Epiyangambin)

SMILES for NP0054877 ((+)-Epiyangambin)

INCHI for NP0054877 ((+)-Epiyangambin)

Structure for NP0054877 ((+)-Epiyangambin)

3D Structure for NP0054877 ((+)-Epiyangambin)