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ChemicalBook >> CAS DataBase List >> azo analog I

azo analog I

azo analog I price.
  • $43 - $1415
  • Product name: azo analog I
  • CAS: 64192-56-9
  • MF: C20H32N2O2
  • MW: 332.48
  • EINECS:
  • MDL Number:
  • Synonyms:azo analog I;SRIZDZJPKIYUPZ-ACGFIOGVSA-N;5-Heptenoic acid, 7-[(1R,4S,5R,6R)-6-(1E)-1-octen-1-yl-2,3-diazabicyclo[2.2.1]hept-2-en-5-yl]-, (5Z)-;U-51605, PGI2 and TXA2 synthase inhibitor
4 prices
Selected condition:
Brand
  • Cayman Chemical
Package
  • 100μg
  • 500μg
  • 1mg
  • 5mg
  • ManufacturerCayman Chemical
  • Product number16465
  • Product descriptionU-51605 ≥98%
  • Packaging100μg
  • Price$43
  • Updated2024-03-01
  • Buy
  • ManufacturerCayman Chemical
  • Product number16465
  • Product descriptionU-51605 ≥98%
  • Packaging500μg
  • Price$187
  • Updated2024-03-01
  • Buy
  • ManufacturerCayman Chemical
  • Product number16465
  • Product descriptionU-51605 ≥98%
  • Packaging1mg
  • Price$332
  • Updated2024-03-01
  • Buy
  • ManufacturerCayman Chemical
  • Product number16465
  • Product descriptionU-51605 ≥98%
  • Packaging5mg
  • Price$1415
  • Updated2023-06-20
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Cayman Chemical 16465 U-51605 ≥98% 100μg $43 2024-03-01 Buy
Cayman Chemical 16465 U-51605 ≥98% 500μg $187 2024-03-01 Buy
Cayman Chemical 16465 U-51605 ≥98% 1mg $332 2024-03-01 Buy
Cayman Chemical 16465 U-51605 ≥98% 5mg $1415 2023-06-20 Buy

Properties

Boiling point :463.1±34.0 °C(Predicted)
Density :1.10±0.1 g/cm3(Predicted)
storage temp. :Store at -20°C
solubility :DMF: >100 mg/ml (from U-46619); DMSO: >100 mg/ml (from U-46619); Ethanol: >100 mg/ml (from U-46619); PBS pH 7.2: >2 mg/ml (from U-46619)
pka :4.76±0.10(Predicted)

Safety Information

Symbol(GHS): GHS hazard pictogramsGHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

U-51605 is a stable analog of the endoperoxide prostaglandin H2 (PGH2). It is an inhibitor of both prostacyclin (PGI) and thromboxane (TX) synthases with more selectivity towards PGI synthase. U-51605 is also a partial agonist at TP receptors. In human foreskin fibroblasts, U-51605 inhibits PGI synthase at a concentration of 2.8 μM, whereas, human platelet TX synthase is inhibited at a concentration of 5.6 μM. At concentrations up to 1 μM, U-51605 reduced the release of prostacyclin in SHR aorta elicited by the calcium ionophore A-23187 with no effect on TXA2 production and yet significantly increased PGE2 and PGF2α release.