NP-MRD: Showing NP-Card for Lycopsamine (NP0045599)

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Record Information

Version

2.0

Created at

2022-03-17 19:32:30 UTC

Updated at

2022-03-17 19:32:30 UTC

NP-MRD ID

NP0045599

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lycopsamine

Description

Lycopsamine is found in Ageratina conyzoides, Ageratum conyzoides, Ageratum houstonianum, Amsinckia hispida, Amsinckia intermedia, Amsinckia menziesii, Amsinckia vernicosa, Anchusa arvensis , Anchusa caerulea, Anchusa officinalis , Arnebia decumbens, Brickellia grandiflora, Chromolaena odorata, Critonia morifolia, Critonia portoricensis, Cynoglossum amabile, Cynoglossum creticum, Cynoglossum furcatum, Cynoglossum germanicum, Cynoglossum officinale , Cynoglossum pictum Ait., Danaus plexippus, Echium horridum, Echium humile, Echium vulgare, Eupatorium altissimum, Eupatorium cannabinum , Eupatorium cannabium, Eupatorium chinense, Eupatorium compositifolium, Eupatorium fortunei, Eupatorium maculatum, Eupatorium portoricense Urban, Eupatorium serotinum, Heliotropium amplexicaule, Heliotropium arborescens, Heliotropium circinatum, Heliotropium indicum , Heliotropium megalanthum, Heliotropium steudneri, Heliotropium supinum, Heliotropium transalpinum, Lappula myosotis, Liatris punctata, Lindelofia angustifolia, Lindelofia stylosa, Lithospermum canescens, Lithospermum canesens, Mertensia bakeri, Tournefortia argentea, Messerschmidia sibirica, Neatostema apulum, Oreocarya virgata, Paracaryum rugulosum, Paracynoglossum imeretinum, Parsonsia eucalyptophylla, Parsonsia straminea, Praxelis clematidea, Pulmonaria obscura, Rindera austroechinata, Rindera baldschuanica, Solenanthus circinatus, Symphytum x uplandicum, Symphytum asperum, Symphytum bohemium, Symphytum caucasicum, Symphytum caucasium, Symphytum grandiflorum, Symphytum ibericum, Symphytum officinale , Symphytum officinalis, Symphytum peregrinum, Symphytum tanaiense, Symphytum tuberosum, Symphytum uplandicum and Trichodesma africanum.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241212572D          

 24 25  0  0  0  0            999 V2000
   -4.6054    1.3465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0903    0.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6054    0.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0361    1.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8207    1.0915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8207    0.2665    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0361    0.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5512    0.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7812    2.1311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742    2.3026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7193    3.0872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9123    3.2587    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2713    3.7003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6574    4.0434    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3603    2.6457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1496    4.2149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2094    4.6565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1672    2.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6152    1.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4467    2.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6574    4.8684    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8207    1.9165    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4023    1.5600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0179    2.0609    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  5  1  0  0  0  0
  2  3  1  0  0  0  0
  3  6  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  6  1  0  0  0  0
  4  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
 11 13  2  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  1  0  0  0
 14 16  1  6  0  0  0
 14 17  1  0  0  0  0
 12 18  1  6  0  0  0
 15 19  1  0  0  0  0
 15 20  1  0  0  0  0
 14 21  1  1  0  0  0
  5 22  1  6  0  0  0
  1 23  1  1  0  0  0
  1 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0045599

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@](C)(O)[C@@](O)(C(C)C)C(=O)OCC1=CCN2CC[C@@]([H])(O)[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H25NO5/c1-9(2)15(20,10(3)17)14(19)21-8-11-4-6-16-7-5-12(18)13(11)16/h4,9-10,12-13,17-18,20H,5-8H2,1-3H3/t10-,12+,13+,15-/m0/s1

> <INCHI_KEY>
SFVVQRJOGUKCEG-ZGFBFQLVSA-N

> <FORMULA>
C15H25NO5

> <MOLECULAR_WEIGHT>
299.3627

> <EXACT_MASS>
299.173272915

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
31.74697694699978

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,7aR)-1-hydroxy-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl]methyl (2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate

> <ALOGPS_LOGP>
0.41

> <JCHEM_LOGP>
-0.291114993666667

> <ALOGPS_LOGS>
-0.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.31270179754289

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.342357304233317

> <JCHEM_PKA_STRONGEST_BASIC>
7.816512056494238

> <JCHEM_POLAR_SURFACE_AREA>
90.23

> <JCHEM_REFRACTIVITY>
77.9425

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.08e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lycopsamine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -8.597   2.513   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.502   1.267   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.597   0.022   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.667   2.513   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.132   2.037   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -7.132   0.497   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -5.667   0.022   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.762   1.267   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.192   3.978   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -3.685   4.298   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.209   5.763   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.703   6.083   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.240   6.907   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.227   7.548   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.673   4.939   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.279   7.868   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.258   8.692   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.179   4.618   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.148   3.474   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.834   5.259   0.000  0.00  0.00           C+0
HETATM   21  H   UNK     0      -1.227   9.088   0.000  0.00  0.00           H+0
HETATM   22  H   UNK     0      -7.132   3.577   0.000  0.00  0.00           H+0
HETATM   23  O   UNK     0     -10.084   2.912   0.000  0.00  0.00           O+0
HETATM   24  H   UNK     0      -9.367   3.847   0.000  0.00  0.00           H+0
CONECT    1    2    5   23   24                                             
CONECT    2    1    3                                                       
CONECT    3    2    6                                                       
CONECT    4    5    8    9                                                  
CONECT    5    1    4    6   22                                             
CONECT    6    3    7    5                                                  
CONECT    7    6    8                                                       
CONECT    8    4    7                                                       
CONECT    9    4   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11   14   15   18                                             
CONECT   13   11                                                            
CONECT   14   12   16   17   21                                             
CONECT   15   12   19   20                                                  
CONECT   16   14                                                            
CONECT   17   14                                                            
CONECT   18   12                                                            
CONECT   19   15                                                            
CONECT   20   15                                                            
CONECT   21   14                                                            
CONECT   22    5                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
9-Viridiflorylretronecine	Kegg
Echinatine	MeSH
Indicine, (1S-(1alpha,7(2R,3S),7aalpha))-isomer	MeSH
Rinderine	MeSH
Indicine	MeSH
Indicine, (1R-(1alpha,7(2S,3S),7abeta))-isomer	MeSH
Indicine, (1R-(1alpha,7(2S,3R),7abeta))-isomer	MeSH
Indicine, (1S-(1alpha,7(2R,3R),7aalpha))-isomer	MeSH

Chemical Formula

C₁₅H₂₅NO₅

Average Mass

299.3627 Da

Monoisotopic Mass

299.17327 Da

IUPAC Name

[(1R,7aR)-1-hydroxy-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl]methyl (2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate

Traditional Name

lycopsamine

CAS Registry Number

10285-07-1

SMILES

[H][C@@](C)(O)[C@@](O)(C(C)C)C(=O)OCC1=CCN2CC[C@@]([H])(O)[C@@]12[H]

InChI Identifier

InChI=1S/C15H25NO5/c1-9(2)15(20,10(3)17)14(19)21-8-11-4-6-16-7-5-12(18)13(11)16/h4,9-10,12-13,17-18,20H,5-8H2,1-3H3/t10-,12+,13+,15-/m0/s1

InChI Key

SFVVQRJOGUKCEG-ZGFBFQLVSA-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
Ageratina conyzoides	Plant	KNApSAcK
Ageratum conyzoides	LOTUS Database	35616633
Ageratum houstonianum	LOTUS Database	35616633
Amsinckia hispida	Plant	KNApSAcK
Amsinckia intermedia	Plant	KNApSAcK
Amsinckia menziesii	LOTUS Database	35616633
Amsinckia vernicosa	LOTUS Database	35616633
Anchusa arvensis	Plant	KNApSAcK
Anchusa caerulea	Plant	KNApSAcK
Anchusa officinalis	Plant	KNApSAcK
Arnebia decumbens	Plant	KNApSAcK
Borago officinalis	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases
Brickellia grandiflora	LOTUS Database	35616633
Chromolaena odorata	LOTUS Database	35616633
Critonia morifolia	Plant	KNApSAcK
Critonia portoricensis	LOTUS Database	35616633
Cynoglossum amabile	Plant	KNApSAcK
Cynoglossum creticum	LOTUS Database	35616633
Cynoglossum furcatum	Plant	KNApSAcK
Cynoglossum germanicum	LOTUS Database	35616633
Cynoglossum officinale	Plant	KNApSAcK
Cynoglossum pictum Ait.	Plant	KNApSAcK
Danaus plexippus	LOTUS Database	35616633
Echium horridum	LOTUS Database	35616633
Echium humile	LOTUS Database	35616633
Echium vulgare	LOTUS Database	35616633
Eupatorium altissimum	Plant	KNApSAcK
Eupatorium cannabinum	Plant	KNApSAcK
Eupatorium cannabium	Plant	KNApSAcK
Eupatorium chinense	LOTUS Database	35616633
Eupatorium compositifolium	Plant	KNApSAcK
Eupatorium fortunei	LOTUS Database	35616633
Eupatorium maculatum	Plant	KNApSAcK
Eupatorium portoricense Urban	Plant	KNApSAcK
Eupatorium serotinum	LOTUS Database	35616633
Heliotropium amplexicaule	Plant	KNApSAcK
Heliotropium arborescens	Plant	KNApSAcK
Heliotropium circinatum	Plant	KNApSAcK
Heliotropium indicum	Plant	KNApSAcK
Heliotropium megalanthum	Plant	KNApSAcK
Heliotropium steudneri	Plant	KNApSAcK
Heliotropium supinum	Plant	KNApSAcK
Heliotropium transalpinum	Plant	KNApSAcK
Lappula myosotis	LOTUS Database	35616633
Liatris punctata	LOTUS Database	35616633
Lindelofia angustifolia	Plant	KNApSAcK
Lindelofia stylosa	Plant	KNApSAcK
Lithospermum canescens	LOTUS Database	35616633
Lithospermum canesens	Plant	KNApSAcK
Mertensia bakeri	LOTUS Database	35616633
Messerschmidia argentea	LOTUS Database	35616633
Messerschmidia sibirica	Plant	KNApSAcK
Neatostema apulum	LOTUS Database	35616633
Oreocarya virgata	LOTUS Database	35616633
Paracaryum rugulosum	LOTUS Database	35616633
Paracynoglossum imeretinum	-	KNApSAcK
Parsonsia eucalyptophylla	Plant	KNApSAcK
Parsonsia straminea	Plant	KNApSAcK
Praxelis clematidea	LOTUS Database	35616633
Pulmonaria obscura	LOTUS Database	35616633
Rindera austroechinata	Plant	KNApSAcK
Rindera baldschuanica	Plant	KNApSAcK
Solenanthus circinatus	Plant	KNApSAcK
Symphytum x uplandicum	Plant	KNApSAcK
Symphytum asperum	Plant	KNApSAcK
Symphytum bohemium	Plant	KNApSAcK
Symphytum caucasicum	Plant	KNApSAcK
Symphytum caucasium	Plant	KNApSAcK
Symphytum grandiflorum	Plant	KNApSAcK
Symphytum ibericum	Plant	KNApSAcK
Symphytum officinale	Plant	KNApSAcK
Symphytum officinalis	Plant	KNApSAcK
Symphytum peregrinum	Plant	KNApSAcK
Symphytum tanaiense	Plant	KNApSAcK
Symphytum tuberosum	Plant	KNApSAcK
Symphytum uplandicum	Plant	KNApSAcK
Trichodesma africana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkaloids and derivatives. These are naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic properties. Also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Not Available

Sub Class

Not Available

Direct Parent

Alkaloids and derivatives

Alternative Parents

Substituents

Alkaloid or derivatives
Pyrrolizine
Beta-hydroxy acid
Fatty acid ester
Hydroxy acid
N-alkylpyrrolidine
Fatty acyl
Tertiary alcohol
Pyrroline
Pyrrolidine
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organonitrogen compound
Alcohol
Organic oxygen compound
Organooxygen compound
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Organic oxide
Amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

pyrrolizines (CHEBI:6598 )
Pyrrolizidine alkaloids (C10347 )

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	0.41	ALOGPS
logP	-0.29	ChemAxon
logS	-0.77	ALOGPS
pKa (Strongest Acidic)	11.34	ChemAxon
pKa (Strongest Basic)	7.82	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.23 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	77.94 m³·mol⁻¹	ChemAxon
Polarizability	31.75 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

FDB001505

KNApSAcK ID

C00002099

Chemspider ID

Not Available

KEGG Compound ID

C10347

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

107938

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Lycopsamine (NP0045599)

MOL for NP0045599 (Lycopsamine)

3D MOL for NP0045599 (Lycopsamine)

3D SDF for NP0045599 (Lycopsamine)

3D-SDF for NP0045599 (Lycopsamine)

PDB for NP0045599 (Lycopsamine)

3D PDB for NP0045599 (Lycopsamine)

SMILES for NP0045599 (Lycopsamine)

INCHI for NP0045599 (Lycopsamine)

Structure for NP0045599 (Lycopsamine)

3D Structure for NP0045599 (Lycopsamine)