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ChemicalBook >> CAS DataBase List >> ROQUEFORTINE C

ROQUEFORTINE C

ROQUEFORTINE C price.
  • $80 - $555
  • Product name: ROQUEFORTINE C
  • CAS: 58735-64-1
  • MF: C22H23N5O2
  • MW: 389.45
  • EINECS:
  • MDL Number:MFCD00133802
  • Synonyms:10b-(1,1-dimethyl-2-propenyl)-6,10b,11,11a-tetrahydro-3-(1H-imidazol-4-ylmethylene)-2H-pyrazino(1,2:1,5)pyrrolo(2,3-b)indole-1,4(3H,5aH)-dione, Isoroquefortine C, Roquefortin, Roquefortine C;(3E,5aS,5aβ)-10bβ-(1,1-Dimethyl-2-propenyl)-3-(1H-imidazol-4-yl)methylene-6,10b,11,11aα-tetrahydro-2H-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4(3H,5aH)-dione;(5aS)-3-[(E)-(1H-Imidazole-4-yl)methylene]-10bβ-(1,1-dimethyl-2-propenyl)-1,3,4,5aβ,6,10b,11,11aα-octahydro-2H-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4-dione;2H-Pyrazino[1',2':1,5]pyrrolo[2,3-B]indole-1,4(3H,5ah)-dione, 10B-(1,1-dimethyl-2-propenyl)-6,10B,11,11A-tetrahydro-3-(1H-imidazol-4-ylmethylene)-, (3Z)-;Aids031208;Aids-031208;Nsc292134;2H-Pyrazino[1′,2′:1,5]pyrrolo[2,3-b]indole-1,4(3H,5aH)-dione, 10b-(1,1-dimethyl-2-propen-1-yl)-6,10b,11,11a-tetrahydro-3-(1H-imidazol-5-ylmethylene)-,(3E,5aS,10bR,11aS)-
8 prices
Selected condition:
Brand
  • Adipogen Life Sciences
  • Cayman Chemical
  • Sigma-Aldrich
  • TRC
  • Usbiological
Package
  • 500ug
  • 500μg
  • 1mg
  • ManufacturerAdipogen Life Sciences
  • Product numberBVT-0425-C500
  • Product descriptionRoquefortine C ≥98%(HPLC,NMR)
  • Packaging500μg
  • Price$80
  • Updated2021-12-16
  • Buy
  • ManufacturerAdipogen Life Sciences
  • Product numberBVT-0425-M001
  • Product descriptionRoquefortine C ≥98%(HPLC,NMR)
  • Packaging1mg
  • Price$125
  • Updated2021-12-16
  • Buy
  • ManufacturerCayman Chemical
  • Product number15376
  • Product descriptionRoquefortine C ≥98%
  • Packaging500μg
  • Price$171
  • Updated2024-03-01
  • Buy
  • ManufacturerCayman Chemical
  • Product number15376
  • Product descriptionRoquefortine C ≥98%
  • Packaging1mg
  • Price$305
  • Updated2024-03-01
  • Buy
  • ManufacturerSigma-Aldrich
  • Product numberSML0406
  • Product descriptionRoquefortine C ≥98% (HPLC), from Penicillium roqueforti
  • Packaging500μg
  • Price$555
  • Updated2024-03-01
  • Buy
  • ManufacturerTRC
  • Product numberR700875
  • Product descriptionRoquefortine C
  • Packaging1mg
  • Price$545
  • Updated2021-12-16
  • Buy
  • ManufacturerUsbiological
  • Product number207386
  • Product descriptionRoquefortine C
  • Packaging500ug
  • Price$316
  • Updated2021-12-16
  • Buy
  • ManufacturerUsbiological
  • Product numberR2999-45
  • Product descriptionRoquefortine C
  • Packaging500ug
  • Price$523
  • Updated2021-12-16
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Adipogen Life Sciences BVT-0425-C500 Roquefortine C ≥98%(HPLC,NMR) 500μg $80 2021-12-16 Buy
Adipogen Life Sciences BVT-0425-M001 Roquefortine C ≥98%(HPLC,NMR) 1mg $125 2021-12-16 Buy
Cayman Chemical 15376 Roquefortine C ≥98% 500μg $171 2024-03-01 Buy
Cayman Chemical 15376 Roquefortine C ≥98% 1mg $305 2024-03-01 Buy
Sigma-Aldrich SML0406 Roquefortine C ≥98% (HPLC), from Penicillium roqueforti 500μg $555 2024-03-01 Buy
TRC R700875 Roquefortine C 1mg $545 2021-12-16 Buy
Usbiological 207386 Roquefortine C 500ug $316 2021-12-16 Buy
Usbiological R2999-45 Roquefortine C 500ug $523 2021-12-16 Buy

Properties

Melting point :202-205℃
Boiling point :768.3±60.0 °C(Predicted)
Density :1.37±0.1 g/cm3(Predicted)
storage temp. :-20°C
solubility :chloroform: soluble1mg/mL
form :White to off-white solid.
pka :11.10±0.40(Predicted)
Stability :Hygroscopic

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.

Description

Roquefortine C is a mycotoxin that was first isolated from a strain of P. roqueforti, a species of Penicillium commercially used to ripen blue-veined cheeses. It has also been isolated from other members of the Penicillium genus found in contaminated food products where it displays neurotoxic properties. It has been shown to both activate a P-glycoprotein transport system involved in the efflux of xenobiotics and to inhibit cytochrome P450 3A detoxification enzymes. It has also been used as a biomarker for penitrem A intoxication.

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