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ChemicalBook > Product Catalogue >API >Circulatory system drugs >Antihypertensive drugs >Ketanserin

Ketanserin

Ketanserin Structure
  • ₹5400 - ₹14600
  • Product name: Ketanserin
  • CAS: 74050-98-9
  • MF: C22H22FN3O3
  • MW: 395.43
  • EINECS:277-680-2
  • MDL Number:MFCD00083392
  • Synonyms:B(p51A);B(p51B);EEC3;OFC8;p53CP;p63, GST tagged human;p73H;p73L
2 prices
Selected condition:

Brand

  • TCI Chemicals (India)

Package

  • 200MG
  • 1G
  • ManufacturerTCI Chemicals (India)
  • Product numberK0051
  • Product descriptionKetanserin
  • Packaging200MG
  • Price₹5400
  • Updated2022-05-26
  • Buy
  • ManufacturerTCI Chemicals (India)
  • Product numberK0051
  • Product descriptionKetanserin
  • Packaging1G
  • Price₹14600
  • Updated2022-05-26
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
TCI Chemicals (India) K0051 Ketanserin 200MG ₹5400 2022-05-26 Buy
TCI Chemicals (India) K0051 Ketanserin 1G ₹14600 2022-05-26 Buy

Properties

Melting point :227-235°C
Density :1.280±0.06 g/cm3(Predicted)
storage temp. :Sealed in dry,2-8°C
solubility :DMF: 10 mg/mL, clear, colorless
form :Solid
pka :7.5(at 25℃)
color :White to Off-White
Merck :14,5296
CAS DataBase Reference :74050-98-9(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P270 Do not eat, drink or smoke when using this product.

Description

Ketanserin is reported to have a high affinity for multiple G protein-coupled receptors, such as serotonin receptors. Ketanserin is a selective serotonin 5-HT2/5-HT1C antagonist. It has been used to distinguish between 5-HT1D and 5-HT1B receptor subtypes. Additional studies have noted that Ketanserin is able to differentiate between recombinant human forms of these receptors with a higher affinity for 5-HT1Dα receptors compared to 5-HT1Dβ receptors.

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