Acyl bromides
AdipoGen 4-ITCB-MPO-pyridinium bromide
Chemical. CAS 155862-90-1. Formula C23H18BrN3O2S. MW 480.38. Synthetic. New class of highly photostable, water soluble fluorescent labels with large Stokes shift, high QY in aqueous media and pH tolerance. Major disadvantage rel. low extinction coefficient.
Cayman Chemical N-a-Benzoyl-L-ArgInInamIdeh 5g
A synthetic nonapeptide sedative increases EEG delta activity and induces orthodox slow-wave sleep in free-moving rabbits at 30 nmol/kg i v increases NREM and total sleep in free-moving rats
Cayman Chemical p-Benzoyl-L-phenylalnIn 500mg
A polyether ionophore antibiotic selectively binds to monovalent cations over divalent cations active against Gram-positive bacteria (MICs 0 9-125 Ug/ml) reduces the viability of asexual and gametocyte P falciparum parasites (EC50s 1 3 and 14 8 nM respectively) reduces P berghei transmission in a mouse model of malaria at 4 and 8 mg/kg reduces the severity of lesions and completely protects chicks against mortality in a model of E tenella-induced coccidiosis at 5-10 ppm in the diet
Cayman Chemical p-Benzoyl-L-phenylalnIn 1g
Source Active recombinant human C-terminal His-tagged Bcl-2 expressed in E coli Amino acids MW 24 7 kDa
TARGETMOL CHEMICALS INC Pipecuronium bromide 10MG
Also available in 1 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Pipecuronium bromide (RGH-1106) is a selective and potent nAChR antagonist that also acts as a non-depolarising steroidal neuromuscular blocker, causing muscle relaxation, often in conjunction with antibiotics. Purity 100%
Sigma Aldrich Fine Chemicals Biosciences Ipratropium bromide Relate5MG
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
TARGETMOL CHEMICALS INC KRN2 BROMIDE 5MG
Also available in 2mg 10mg 25mg 50mg 100mg 500mg and bulk. Please contact Fisher for quotes. KRN2 bromide is a potent selective inhibitor of nuclear factor of activated T cells (NFAT5 IC50= 0.1 μM). purity: 99%
TARGETMOL CHEMICALS INC DEMECARIUM BROMIDE 50MG
Also available in 2 mg 5 mg 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Demecarium bromide (BC-48) is a potent cholinesterase inhibitorand is treatment glaucoma agent. purity: 98%
TARGETMOL CHEMICALS INC UMECLIDINIUM BROMIDE 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Umeclidinium bromide (GSK573719A) is a novel mAChR antagonist. purity: 99%
eMolecules 5-(Bromoacetyl)-3-(3,4-dichlorophenyl)isoxazole (tech) | 175277-38-0 | MFCD00173899 | 1g
Oakwood Chemicals | 5-(Bromoacetyl)-3-(3,4-dichlorophenyl)isoxazole (tech) | 1g | 480113864 | 017228 | | 175277-38-0 | MFCD00173899 | 334.980 | C11H6BrCl2NO2
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Cayman Chemical N4-benzoyl-2-DeoxycytIdIn 25g
A BD2 bromodomain inhibitor inhibits BD2 in BRD2 BRD3 and BRD4 (IC50s 0.08 0.05 and 0.02 UM respectively) and is selective for BD2 over BD1 (IC50s 3.76 2.34 and 1.16 UM for BRD2 BRD3 and BRD4 respectively) as well as CREBBP and p300 (IC50s 50 UM for both) decreases levels of the mRNAs encoding IL-6 and VCAM-1 in primary synovial fibroblasts isolated from patients with rheumatoid arthritis at 10 and 30 UM It prevents LPS-induced increases in IL-6 and Ifn-Y serum levels in a mouse model of LPS-induced endotoxemia at 75 mg/kg inhibits collagen-induced increases in ankle and knee diameter cartilage damage the ankle tissue levels of mRNAs encoding IL-1B Mmp-3 Mmp-13 and Rankl and ankle joint protein levels of IL-6 and VCAM-1 in a rat model of collagen-induced rheumatoid arthritis at 25 50 and 75 mg/kg twice per day improves gait and mobility and reverses body w8 loss as well as decreases the number of spinal cord inflammatory foci and apoptotic cells
Cayman Chemical N4-benzoyl-2-DeoxycytIdIn 10g
A BD2 bromodomain inhibitor inhibits BD2 in BRD2 BRD3 and BRD4 (IC50s 0.08 0.05 and 0.02 UM respectively) and is selective for BD2 over BD1 (IC50s 3.76 2.34 and 1.16 UM for BRD2 BRD3 and BRD4 respectively) as well as CREBBP and p300 (IC50s 50 UM for both) decreases levels of the mRNAs encoding IL-6 and VCAM-1 in primary synovial fibroblasts isolated from patients with rheumatoid arthritis at 10 and 30 UM It prevents LPS-induced increases in IL-6 and Ifn-Y serum levels in a mouse model of LPS-induced endotoxemia at 75 mg/kg inhibits collagen-induced increases in ankle and knee diameter cartilage damage the ankle tissue levels of mRNAs encoding IL-1B Mmp-3 Mmp-13 and Rankl and ankle joint protein levels of IL-6 and VCAM-1 in a rat model of collagen-induced rheumatoid arthritis at 25 50 and 75 mg/kg twice per day improves gait and mobility and reverses body w8 loss as well as decreases the number of spinal cord inflammatory foci and apoptotic cells