Items 101 to 125 of 599 total

per page
  1. 3
  2. 4
  3. 5
  4. 6
  5. 7

Set Descending Direction
Catalog No. Product Name Application Product Information
A10145 SALE

Bimatoprost (Lumigan)

Bimatoprost is a prostaglandin analog/prodrug used topically (as eye drops) to control the progression of glaucoma and in the management of ocular hypertension
A11821 SALE


MCP inhibitor
Bindarit is an anti-inflammatory small molecule that modulates the NFκB pathway.
A10146 SALE

Biochanin A (4-Methylgenistein)


Biochanin A is an antiproliferative and anti-inflammatory agent that inhibits iNOS expression and lipopolysacharide (LPS)-induced nitric oxide production in macrophages. Additionally, Biochanin A displays the ability to block phosphorylation of IκBα and p38 MAPK, which prevents NF-κB activation. Furthermore, Biochanin A has been observed to suppress IL-6, IL-1β, and TNF-α production.


Biotin Hydrazide

Biotin hydrazide is a biotinyl derivative that can be used as a probe for the determination of protein carbonylation, which is a component of several diseases.


Biotin-X-NHS is a compound used to attach biotin to primary amines under alkaline conditions (pH~8-9).
A12908 SALE


DR5 activator
Bioymifi is a potent and selective small molecule agonist of DR5 that directly targets DR5, specifically binds the ECD of DR5 (Kd ~1.2 μM), and induces the formation of DR5 aggregates and DR5 activation.

Bleomycin hydrochloride

Bleomycin hydrochloride is an antitumor antibiotic which induces apoptosis.


BMPS is a short, sulfhydryl and amino reactive heterobifunctional crosslinking reagent.


Itk Inhibitor
The ITK inhibitor BMS-509744 disrupts several aspects of HIV replication.

BMS-806 (BMS 378806)

HIV Entry Inhibitor
BMS-806, also known as BMS-378806 , is a type of medicine called an entry inhibitor. Entry inhibitors work by blocking HIV from entering human cells. BMS-378806 (BMS-806) is a small molecule that blocks the binding of host-cell CD4 with viral gp120 protein and therefore inhibits the first steps of HIV-1 infection.
A13807 SALE


ATP-citrate lyase inhibitor
BMS303141 is a potent inhibitor of ATP citrate lyase (ACL). BMS303141 inhibits lipid synthesis in HepG2 cells with an IC50 of 8 μM, and lowers plasma triglycerides in a murine hyperlipdemia model.
A11765 SALE


Brinzolamide is a carbonic anhydrase inhibitor.

BTZ043 (BTZ038, BTZ044)

DprE1 inhibitor
BTZ043 (BTZ038, BTZ044) inhibits decaprenylphosphoryl-β-d-ribose 2?-epimerase, which is an enzyme which produces the cell wall of the pathogenic bacterium Mycobacterium tuberculosis.
A10166 SALE


Budesonide is a glucocorticoid steroid for the treatment of asthma, non-infectious rhinitis.
A10167 SALE


Bumetanide is a loop diuretic of the sulfamyl category to treat heart failure.
A10168 SALE

Bupivacaine HCl

Bupivacaine is a more potent inhibitor of cAMP production than are chemically related local anesthetics that are less prone to produce cardiovascular toxicity.
A10169 SALE

Busulfan (Myleran, Busulfex)

Busulfan is a cell cycle non-specific alkylating antineoplastic agent, in the class of alkyl sulfonates.
A11829 SALE

Butenafine HCl

Butenafine Hydrochloride is an antifungal which is used to control dermal fungal infections such as athletes foot and ring worm.
A10170 SALE

Butylscopolamine BR (Scopolamine butylbromide)

Butylscopolamine BR is an orally available bromide salt form of butylscopolamine which is a peripherally acting antimuscarinic, anticholinergic agent.


PRMT1 inhibitor
C7280948 is an inhibitor of histone arginine methyltransferase PRMT1 with IC50 values of 12.75 uM.
A11831 SALE


Microtubule Associated inhibitor
Cabazitaxel is a semi-synthetic derivative of a natural taxoid. Cabazitaxel in combination with prednisone is a treatment option for hormone-refractory prostate cancer following docetaxel-based treatment
A10171 SALE

Caffeic acid

Caffeic acid is an organic compound that is classified as hydroxycinnamic acid.
A11367 SALE


Calcifediol is a major circulating metabolite of vitamin D3 and acts as a competitive inhibitor with an apparent Ki of 3.9 μM. It also suppresses PTH secretion and mRNA (ED50=2 nM)


Calcipotriol is a low-calcemic vitamin D receptor (VDR) agonist.

Calcipotriol monohydrate

Calcipotriol hydrate is the hydrate form of vitamin D3 that displays minimal effects on calcium homeostasis.

Items 101 to 125 of 599 total

per page
  1. 3
  2. 4
  3. 5
  4. 6
  5. 7

Set Descending Direction