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Biotrend Chemicals AG

14

Basic Information

Company Name:Biotrend Chemicals AG

Business Type:Chemical manufacturer

Total NO.Employees:

Country/Region:Switzerland

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Year Established:

Introduction of Biotrend Chemicals AG

Web: www.biotrend.ch TEL:+41 (44) 805-7676 Fax:+41 (44) 805-7676 ex 77 Email:[email protected]

Products of Biotrend Chemicals AG

  • Chemical Name: SKF 81297
    CAS No.: 71636-61-8 Purity: Appearances: gray
    Brand: Synonyms: 6-chloro-1-phenyl-2,3,4,5-t... Quality Control & MSDS Files:
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  • Chemical Name: AM 404
    CAS No.: 198022-70-7 Purity: Appearances:
    Brand: Synonyms: N-(4-HYDROXYPHENYL)-5Z,8Z,1... Quality Control & MSDS Files:
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  • Chemical Name: DL-LAUROYLCARNITINE
    CAS No.: 7023-03-2 Purity: Appearances:
    Brand: Synonyms: DL-LAUROYLCARNITINE;(2-dode... Quality Control & MSDS Files:
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  • Chemical Name: DMAB-anabaseine (hydrochloride)
    CAS No.: 154149-38-9 Purity: Appearances:
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    Partial agonist at α7-containing neuronal nicotinic receptors and antagonist at α4β2 and other nicotinic receptors. Displays specific cognition-enhancing effects; improves long-term memory in rats.

  • Chemical Name: RX 801077 (hydrochloride)
    CAS No.: 89196-95-2 Purity: Appearances:
    Brand: Synonyms: 2 BFI hydrochloride;RX80107... Quality Control & MSDS Files:
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    High affinity I2 ligand (Ki = 9.8 nM). Putative I2 agonist; potentiates morphine antinociception. Produces ipsiversive rotational behavior in rats with a full 6-OHDA lesion of the nigrostriatal tract.

  • Chemical Name: N-Methylhistamine (dihydrochloride)
    CAS No.: 16503-22-3 Purity: Appearances:
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    Potent histamine agonist, particularly at H3 receptors (potency relative to histamine is 81, 185, and 270% at H1, H2 and H3 respectively). Also displays agonist properties at H4 receptors to which it binds with moderate affinity (Ki = 23 nM).

  • Chemical Name: CP 339818 HYDROCHLORIDE
    CAS No.: 185855-91-8 Purity: Appearances:
    Brand: Synonyms: N-[1-(PHENYLMETHYL)-4(1H)-Q... Quality Control & MSDS Files:
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    CP-339818 blocks both Kv1.3 and Kv1.4. CP-339818 is valuable for immune system studies, where the absence of Kv1.4 makes it functionally selective for Kv1.3, and it has shown suppression of T cell activation. Kv1.3 is expressed in the brain and in effector memory Tem (T) cells, and it is a member of the Shaker family of voltage-gated ...

  • Chemical Name: CY 208-243
    CAS No.: 100999-26-6 Purity: Appearances:
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    Centrally active dopamine D1 receptor agonist, selective over D2 receptor sites. Stimulates adenylate cyclase in rat striatal homogenates with an EC50 of 125 nM. Unlike SKF 38393 (Cat. No. 0922), it exerts antiParkinsonian activity in animal models.

  • Chemical Name: CGP46381
    CAS No.: 123691-14-5 Purity: Appearances:
    Brand: Synonyms: CGP 46381; CGP46381; CGP-46... Quality Control & MSDS Files:
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    Brain penetrant, selective GABAB receptor antagonist (IC50 = 4.9 μM).

  • Chemical Name: W 13 (hydrochloride)
    CAS No.: 88519-57-7 Purity: Appearances: white
    Brand: Synonyms: W-13 hydrochloride Quality Control & MSDS Files:
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    Calmodulin antagonist (inhibits calmodulin activated PDE activity with an IC50 of 68 μM). Inhibits growth of tamoxifen-resistant breast cancer cells.

  • Chemical Name: Salvinorin A
    CAS No.: 83729-01-5 Purity: Appearances:
    Brand: Synonyms: (-)-Salvinorin A; Divinorin... Quality Control & MSDS Files:
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    Potent naturally occuring non-nitrogenous κ-opioid selective agonist that displays high affinity at both native (Ki = 4.3 nM) and cloned (Ki = 16 nM) κ-opioid receptors. Also exhibits allosteric modulation of μ-opioid receptor binding. Reported to be brain-penetrant and displays psychoactive properties..

  • Chemical Name: Pirlindole (mesylate)
    CAS No.: 207572-66-5 Purity: Appearances:
    Brand: Synonyms: Pirlindole. Lifril, Pyrazidol, Quality Control & MSDS Files:
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    A highly selective reversible inhibitor of monoamine oxidase type A.

  • Chemical Name: Chromanol 293B
    CAS No.: 163163-23-3 Purity: Appearances: white
    Brand: Synonyms: Chromanol 239B Quality Control & MSDS Files:
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    Enantiomer that selectively inhibits the slow component of delayed rectifier K+ current (IKs). Block is use-dependent and 7-fold more potent than the (+)-(3S,4R) enantiomer (IC50 values are 1.36 and 9.6 μM respectively). Has negligible inhibitory action at KV11.1 (hERG) channels (IC50 > 30 μM). Racemate also available.

  • Chemical Name: SENKTIDE
    CAS No.: 106128-89-6 Purity: Appearances:
    Brand: Synonyms: [SUCCINYL-ASP6,ME-PHE8] SUB... Quality Control & MSDS Files:
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    NK3 tachykinin receptor agonist. Causes direct excitation of dopamine neurons; enhances dopaminergic function. Induces locomotor activity.