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ChemicalBook >> CAS DataBase List >> thielavin B

thielavin B

thielavin B price.
  • $364 - $1310
  • Product name: thielavin B
  • CAS: 71950-67-9
  • MF:
  • MW: 0
  • EINECS:
  • MDL Number:MFCD11111623
  • Synonyms:thielavin B;4-[(2,4-Dihydroxy-3,6-dimethylbenzoyl)oxy]-2-methoxy-3,5,6-trimethylbenzoic acid 4-carboxy-3-methoxy-2,5,6-trimethylphenyl ester
6 prices
Selected condition:
Brand
  • AK Scientific
  • Cayman Chemical
  • Sigma-Aldrich
  • Usbiological
Package
  • 500ug
  • 500μg
  • 1mg
  • 2.5mg
  • ManufacturerAK Scientific
  • Product number0747CB
  • Product descriptionThielavin B
  • Packaging2.5mg
  • Price$1310
  • Updated2021-12-16
  • Buy
  • ManufacturerCayman Chemical
  • Product number18770
  • Product descriptionThielavin B ≥95%
  • Packaging500μg
  • Price$364
  • Updated2024-03-01
  • Buy
  • ManufacturerCayman Chemical
  • Product number18770
  • Product descriptionThielavin B ≥95%
  • Packaging2.5mg
  • Price$1088
  • Updated2024-03-01
  • Buy
  • ManufacturerSigma-Aldrich
  • Product numberSMB00566
  • Product descriptionThielavin B ≥95% (LC/MS-UV)
  • Packaging1mg
  • Price$705
  • Updated2024-03-01
  • Buy
  • ManufacturerUsbiological
  • Product numberT5006-50A
  • Product descriptionThielavin B
  • Packaging500ug
  • Price$582
  • Updated2021-12-16
  • Buy
  • ManufacturerUsbiological
  • Product number467494
  • Product descriptionThielavin B
  • Packaging500ug
  • Price$644
  • Updated2021-12-16
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
AK Scientific 0747CB Thielavin B 2.5mg $1310 2021-12-16 Buy
Cayman Chemical 18770 Thielavin B ≥95% 500μg $364 2024-03-01 Buy
Cayman Chemical 18770 Thielavin B ≥95% 2.5mg $1088 2024-03-01 Buy
Sigma-Aldrich SMB00566 Thielavin B ≥95% (LC/MS-UV) 1mg $705 2024-03-01 Buy
Usbiological T5006-50A Thielavin B 500ug $582 2021-12-16 Buy
Usbiological 467494 Thielavin B 500ug $644 2021-12-16 Buy

Properties

storage temp. :-20°C
solubility :DMF: soluble; DMSO: soluble; Ethanol: soluble
form :White to off-white powder.

Safety Information

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

Description

Thielavin B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion of PGH2 to PGE2 in B is a fungal metabolite that contains O-substituted salicylic acid. It inhibits cyclooxygenase, blocking both the conversion of arachidonic acid to Prostaglandin H2 (PGH2) and the conversion

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