Lycopsamine

Base Information Edit

Chemical Name:Lycopsamine
CAS No.:10285-07-1
Molecular Formula:C₁₅H₂₅NO₅
Molecular Weight:299.367
Hs Code.:
European Community (EC) Number:683-135-3
UNII:UER4ET3OHI
DSSTox Substance ID:DTXSID60145542
Nikkaji Number:J15.603E
Wikidata:Q27107262
Metabolomics Workbench ID:68090
Mol file:10285-07-1.mol

Synonyms:echinatine;indicine;indicine pyrrolizidine;indicine, (1R-(1alpha,7(2S*,3R*),7abeta))-isomer;indicine, (1R-(1alpha,7(2S*,3S*),7abeta))-isomer;indicine, (1S-(1alpha,7(2R*,3R*),7aalpha))-isomer;indicine, (1S-(1alpha,7(2R*,3S*),7aalpha))-isomer;lycopsamine;rinderine

Suppliers and Price of Lycopsamine

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Medical Isotopes, Inc.
(+)-Lycopsamine
1 mg
$ 750.00

Biosynth Carbosynth
Lycopsamine
250 mg
$ 10650.00

Biosynth Carbosynth
Lycopsamine
100 mg
$ 4600.00

Biosynth Carbosynth
Lycopsamine
25 mg
$ 1600.00

Biosynth Carbosynth
Lycopsamine
50 mg
$ 2520.00

Biosynth Carbosynth
Lycopsamine
10 mg
$ 750.00

Arctom
Lycopsamine ≥98%
5mg
$ 488.00

American Custom Chemicals Corporation
LYCOPSAMINE 95.00%
5MG
$ 496.87

AK Scientific
Lycopsamine
50mg
$ 3452.00

AK Scientific
Lycopsamine
25mg
$ 2210.00

Total 13 raw suppliers

Chemical Property of Lycopsamine Edit

Chemical Property:

Vapor Pressure:1.57E-10mmHg at 25°C
Boiling Point:463.3°Cat760mmHg
Flash Point:234°C
PSA：90.23000
Density:1.26g/cm³
LogP:-0.38940
Storage Temp.:-20°C
Solubility.:Chloroform, Ethanol
XLogP3:-0.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:299.17327290
Heavy Atom Count:21
Complexity:436

Purity/Quality:

97% ^*data from raw suppliers

(+)-Lycopsamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O
Isomeric SMILES:C[C@@H]([C@@](C(C)C)(C(=O)OCC1=CCN2[C@H]1[C@@H](CC2)O)O)O
Description This amorphous pyrrolizidine alkaloid has been isolated from Arnsinckia hispida (Ruiz et Pav.) Johnst., A. interrnedia Fisch & Mey, and A. lycopsoides Lehm. It is dextrorotatory having [α]20D + 3.1 ° (c 5.98, EtOH). Alkaline hydrolysis yields retronecine and viridifloric acid.
Uses (+)-Lycopsamine, occurs in pyrrolizidine alkaloid-containing plants, which are the most common poisonous plants affecting livestock, wildlife, and humans. Thye are being known as hepatotoxins and tumorigens.It has been shown that pyrrolizidine Alkaloid-Derived DNA Adducts, are the common biological biomarker of pyrrolizidine alkaloid-induced liver tumor formation. (+)-Lycopsamine, occurs in pyrrolizidine alkaloid-containing plants, which are the most common poisonous plants affecting livestock, wildlife, and humans. Thye are being known as hepatotoxins and tumorigens. It has been shown that pyrrolizidine Alkaloid-Derived DNA Adducts, are the common biological biomarker of pyrrolizidine alkaloid-induced liver tumor formation.

Technology Process of Lycopsamine

There total 9 articles about Lycopsamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: