Print…
You Searched For:
2 results were found
2-Fluoro-4-methyl-3-(methylthio)benzoic+acid
Catalog Number:
(101850-782)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041091-250MG , MDL Number: MFCD12028536
Supplier:
BeanTown Chemical
Description:
CAS: 14667-47-1; MDL No: MFCD00128872
Solid; Molecular Formula: C7H8N2O2; MW: 152.15
Melting Point: 82-86°
Supplier:
ALADDIN SCIENTIFIC
Description:
Product Description2-Amino-3-formylchromone (2-Amino-4-oxo-4H-1-benzopyran-3-carboxaldehyde) is a benzopyran derivative. It is a bicyclic heterocyclic molecule made up of a benzene ring fused to a heterocyclic pyran ring. It undergoes condensation with (R)-2-amino-2-phenylethanol to afford Schiff base ligand, which forms complexes with Cu(NO3)2 and Zn(NO3)2Product Application2-Amino-3-formylchromone may be used in the preparation of the following:• chiral Schiff base ligands (R)/(S)-2-amino-3-(((1-hydroxypropan-2-yl)imino)methyl)-4H-chromen-4-one• hydrazone derivatives, required for the synthesis of heterocyclic Schiff′s bases having antimicrobial activity[• N-{4-[(6-chloro-4-oxo-4H-chromen-3-ylmethylene)amino]phenyl}-3,5-dimethyl-benzofuran-2-carboxamide• N-{4-[(6-chloro-4-oxo-4H-chromen-3-ylmethylene)amino]phenyl}-1,4-dihydro-chromono [2,3-b]pyrrole-2-carboxamide• 6-chloro-3-{[4-(2-thioxo-3,6-dihydro-2H-1,3,4-thiadiazin-5-ylamino)phenylimino] methyl}- 4-oxo-4H -chromene• 3¬-(2-amino¬-4¬-oxo¬-4H¬-chromen¬-3-¬yl)methylidene)¬-6-¬ ethyl-¬2H-¬pyrano[3,2-¬c]quinolone-¬2,4,5(3H,6H)-trione
Supplier:
Bachem Americas
Description:
Synonym(s): EDAC · HCl#EDC · HCl#N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide · HCl#Water-soluble Carbodiimide#WSC
Supplier:
Matrix Scientific
Description:
MF=C8H18CLN3 MW=191.71 CAS=25952-53-8 MDL=MFCD00012503 100G
Catalog Number:
(77412-122)
Supplier:
APOLLO SCIENTIFIC
Description:
6-(Ethylsulfonyl)-2H-1,4-benzoxazin-3(4H)-one
Catalog Number:
(101919-462)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 059925-1G , MDL Number: MFCD09878605
Catalog Number:
(101818-952)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 024809-25G , MDL Number: MFCD03840433
Catalog Number:
(101850-758)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041079-250MG , MDL Number: MFCD12028524
Supplier:
AMBEED, INC
Description:
7-(5-((4-(4-(N,N-Dimethylsulfamoyl)piperazin-1-yl)phenoxy)methyl)-1,3-dimethyl-1H-pyrazol-4-yl)-1-(2-morpholinoethyl)-3-(3-(naphthalen-1-yloxy)propyl)-1H-indole-2-carboxylic acid, Purity: 98%, CAS Number: 1668553-26-1, Appearance: White to light yellow powder or crystals, Sealed in dry, Size: 5mg
Supplier:
Adipogen
Description:
XL765 is active against class I PI3K (IC(50) = 39, 113, 9 and 43nM for p110alpha, beta, gamma and delta, respectively). XL765 also inhibits DNA-PK (IC(50) = 150nM) and mTOR (IC(50) = 157nM)
Catalog Number:
(AA12231-A1)
Supplier:
Thermo Scientific Chemicals
Description:
Application in luminous paints, preparation of bismuth salts
Supplier:
MP Biomedicals
Description:
Chloroquine Diphosphate salt is member of quinolone family, Chloroquine is a lysosomotropic agent (accumulate inside the acidic parts of the cell), this accumulation leads to inhibition of lysosomal enzymes that require an acidic pH, and prevents fusion of endosomes and lysosomes. Standard anti-malarial drug. Substrate for MRP in multidrug resistant cell line and inhibits photoaffinity labeling of MRP by quinoline-based photoactive drug IAAQ (N-[4-[1-hydroxy-2-(dibutylamino)ethyl]quinolin-8-yl]-4-azidosalicylamide).
Catalog Number:
(76483-192)
Supplier:
AAT BIOQUEST INC
Description:
This cell-permeant coumarin Ca2+ indicator BTC, AM exhibits a shift in excitation maximum from about 480 nm to 400 nm upon binding Ca2+, enabling ratiometric calcium measurements.
Supplier:
Adipogen
Description:
pan-Akt inhibitor targeting Akt1, 2, 3 with IC50 values of 2, 13 and 9 nM, respectively. Inhibits AMPK, DAPK3, PAK4, 5 and 6, as well as members of the AGC kinase family including PKA, PrkX and PKC isoforms (IC50 <lt/> 100 nM). Occupies the ATP binding pocket of the kinase domain and competes with ATP. Anti-cancer compound both in vitro and in vivo. Blocks the phosphorylation of downstream targets of ATK in a dose-dependent manner, which leads to antiproliferative and apoptotic effects in tumor cell lines. Induces hyperglycemia related to peripheral insulin resistance, increased gluconeogenesis, and/or hepatic glycogenolysis.
Supplier:
ALADDIN SCIENTIFIC
Description:
Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. Target: NRTIs; HBV Adefovir Dipivoxil works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body. Adefovir Dipivoxil is used for treatment of hepatitis B and herpes simplex virus infection [1-3]. Adefovir Dipivoxil is approved for the treatment of chronic hepatitis B in adults with evidence of active viral replication and either evidence of persistent elevations in serum aminotransferases (primarily ALT) or histologically active disease. Adefovir Dipivoxil is a failed treatment for HIV[3, 4]. Catalyst employed in the Sharpless Asymmetric Dihyroxylation of (E,E)- or (E,Z)-1,3-dienoates.1 Also used in the preparation of ?-hydroxy-γ-lactones from ?,γ-unsaturated esters.2Product Introduction:Adefovir dipivoxil, an adenosine analogue, is an oral proagent of the nucleoside reverse transcriptase inhibitor Adefovir. Adefovir dipivoxil inhibits both the wild type and HBV Lamivudine-resistant strains. Adefovir dipivoxil shows anti-orthopoxvirus activity.
Inquire for Price
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
 is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
|
|||||||||
List View
