Trimethobenzamide hydrochloride

CAS No. 554-92-7

Trimethobenzamide hydrochloride( Ro 2-9578 | Tribenzagan Hydrochloride )

Catalog No. M19813 CAS No. 554-92-7

Trimethobenzamide hydrochloride is a blocker of the D2 receptor. Trimethobenzamide is an antiemetic used to prevent nausea and vomiting.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 37 In Stock
25MG 37 In Stock
50MG 50 In Stock
100MG 75 In Stock
200MG Get Quote In Stock
500MG 154 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Trimethobenzamide hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Trimethobenzamide hydrochloride is a blocker of the D2 receptor. Trimethobenzamide is an antiemetic used to prevent nausea and vomiting.
  • Description
    Trimethobenzamide hydrochloride is a blocker of the D2 receptor. Trimethobenzamide is an antiemetic used to prevent nausea and vomiting.(In Vitro):Trimethobenzamide is a (non-phenothiazine) benzamide antiemetic that acts centrally to block D2 receptors, thereby inhibiting the medullary chemoreceptor trigger zone by blocking emetic impulses to the vomiting center.(In Vivo):The oral bioavailability of Trimethobenzamide is 60% to 100%. The time to peak is about 45 minutes after oral administration and; Intramuscular (I.M.) administration about 30 minutes after intramuscular administration.
  • In Vitro
    Trimethobenzamide is a (non-phenothiazine) benzamide antiemetic that acts centrally to block D2 receptors, thereby inhibiting the medullary chemoreceptor trigger zone by blocking emetic impulses to the vomiting center.
  • In Vivo
    The oral bioavailability of Trimethobenzamide is 60% to 100%. The time to peak is about 45 minutes after oral administration and; Intramuscular (I.M.) administration about 30 minutes after intramuscular administration.
  • Synonyms
    Ro 2-9578 | Tribenzagan Hydrochloride
  • Pathway
    GPCR/G Protein
  • Target
    Dopamine Receptor
  • Recptor
    D2
  • Research Area
    Others
  • Indication
    Nausea and vomiting

Chemical Information

  • CAS Number
    554-92-7
  • Formula Weight
    424.92
  • Molecular Formula
    C21H29ClN2O5
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:≥100 mg/mL (235.34 mM)
  • SMILES
    Cl.COc1cc(cc(OC)c1OC)C(=O)NCc1ccc(OCCN(C)C)cc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Smith HS et al. Dopamine receptor antagonists. Ann Palliat Med. 2012 Jul;1(2):137-42.
molnova catalog
related products
  • BL-1020

    BL-1020 is an ester of GABA and perphenazine, fuctions as orally-active antipsychotic agent and acts as a D2 antagonist and GABA agonist.

  • Medifoxamine

    Medifoxamine (LG 152) is a selective non-monoamine oxidase inhibitor that exhibits antidepressant activity through inhibition of 5 HT reuptake.Medifoxamine preferentially inhibits dopamine reuptake.

  • FAUC-365

    FAUC-365 is a D3 dopamine receptor agonist.