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274694-98-3,MFCD00951284
Catalog No.:AA00BCGN

274694-98-3 | LE 300

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10mg
≥98%(HPLC)
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$443.00   $310.00
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA00BCGN
Chemical Name:
LE 300
CAS Number:
274694-98-3
Molecular Formula:
C20H22N2
Molecular Weight:
290.4021
MDL Number:
MFCD00951284
SMILES:
CN1CCc2ccccc2Cc2c(CC1)c1ccccc1[nH]2
Properties
Properties
 
Form:
Solid  
MP:
>91°C (dec.)  
Storage:
-20 ℃;Keep in dry area;  

Computed Properties
 
Complexity:
369  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
4.3  

Literature

Title: Chiral indolo[3,2-f][3]benzazecine-type dopamine receptor antagonists: synthesis and activity of racemic and enantiopure derivatives.

Journal: Journal of medicinal chemistry 20111027

Title: Residues at the indole-NH of LE300 modulate affinities and selectivities for dopamine receptors.

Journal: Archiv der Pharmazie 20110101

Title: Dopamine receptor ligands. Part 18: (1) modification of the structural skeleton of indolobenzazecine-type dopamine receptor antagonists.

Journal: Journal of medicinal chemistry 20100325

Title: Novel fused pyrrole heterocyclic ring systems as structure analogs of LE 300: Synthesis and pharmacological evaluation as serotonin 5-HT(2A), dopamine and histamine H(1) receptor ligands.

Journal: Archiv der Pharmazie 20100201

Title: Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum.

Journal: Nature chemical biology 20091001

Title: Modulation of AMPA currents by D(1)-like but not D(2)-like receptors in spinal motoneurons.

Journal: Neuroscience 20090218

Title: Dopamine/serotonin receptor ligands. Part 17: a cross-target SAR approach: affinities of azecine-styled ligands for 5-HT(2A) versus D1 and D2 receptors.

Journal: Bioorganic & medicinal chemistry letters 20080701

Title: Dopamine/serotonin receptor ligands. Part 15: Oxygenation of the benz-indolo-azecine LE 300 leads to novel subnanomolar dopamine D1/D5 antagonists.

Journal: Bioorganic & medicinal chemistry letters 20070301

Title: Dopamine/serotonin receptor ligands. 13: Homologization of a benzindoloazecine-type dopamine receptor antagonist modulates the affinities for dopamine D(1)-D(5) receptors.

Journal: Journal of medicinal chemistry 20061019

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: Dopamine/serotonin receptor ligands. 12(1): SAR studies on hexahydro-dibenz[d,g]azecines lead to 4-chloro-7-methyl-5,6,7,8,9,14-hexahydrodibenz[d,g]azecin-3-ol, the first picomolar D5-selective dopamine-receptor antagonist.

Journal: Journal of medicinal chemistry 20060323

Title: LE300--new results on its ability to antagonize the discriminative stimulus effects of cocaine.

Journal: Die Pharmazie 20060301

Title: Dopamine/serotonin receptor ligands. Part VIII: the dopamine receptor antagonist LE300 - modelled and X-ray structure plus further pharmacological characterization, including serotonin receptor binding, biogenic amine transporter testing and in vivo testings.

Journal: European journal of medicinal chemistry 20040601

Title: Pharmacological characterization of the benz[d]indolo[2,3-g]azecine LE300, a novel type of a nanomolar dopamine receptor antagonist.

Journal: Naunyn-Schmiedeberg's archives of pharmacology 20021201

Title: Dopamine/serotonin receptor ligands. Part IV [1]: synthesis and pharmacology of novel 3-benzazecines and 3-benzazonines as potential 5-HT2A and dopamine receptor ligands.

Journal: Archiv der Pharmazie 20021101

Title: Dopamine/serotonin receptor ligands, part III [1]: synthesis and biological activities of 7, 7'-alkylene-bis-6, 7, 8, 9, 14, 15-hexahydro-5H-benz[d]indolo[2, 3-g]azecines -- application of the bivalent ligand approach to a novel type of dopamine receptor antagonist.

Journal: Archiv der Pharmazie 20020801

Title: Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells.

Journal: The Journal of biological chemistry 20020419

Title: Synthesis and 5-HT2A antagonist activity of derivatives of the novel heterocycles indolo[3,2-d]pyrrolo[3,2-g]azecine and benzo[d]pyrrolo[3,2-g]azecine compared to the benz[d]indolo[2,3-g]azecine derivative LE 300.

Journal: Archiv der Pharmazie 20010701

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