Bioactive Small Molecules
Medchemexpress LLC (S)-Pro-xylane | 868156-46-1 | MFCD32067869 | >99.0% | 192.21 g/mol | C8H16O5 | 1 ML
A ready-to-use 10 mM solution of (S)-Pro-xylane in DMSO supplied for biochemical and cosmetic research. (S)-Pro-xylane is a bioactive C-glycoside that stimulates glycosaminoglycan biosynthesis in fibroblasts, supports dermal extracellular matrix stability, and promotes collagen and hyaluronic acid production to improve skin hydration and elasticity.
- Stimulates glycosaminoglycan synthesis in fibroblasts.
- Promotes collagen and hyaluronic acid production.
- Improves skin hydration and elasticity in topical models.
- Supplied as a 10 mM solution in DMSO for immediate use.
- Eco-friendly and biodegradable profile.
![Medchemexpress LLC N-[(1S)-3-[(2Z)-2-[(4R)-3,4-dimethyl-1,3-thiazolidin-2-ylidene]hydrazinyl]-1-(oxan-4-yl)-2,3- | 868273-90-9 | 99.6% | 438.58 g·mol⁻¹ | C21H34N4O4S | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000243024.png-250.jpg)
Medchemexpress LLC N-[(1S)-3-[(2Z)-2-[(4R)-3,4-dimethyl-1,3-thiazolidin-2-ylidene]hydrazinyl]-1-(oxan-4-yl)-2,3- | 868273-90-9 | 99.6% | 438.58 g·mol⁻¹ | C21H34N4O4S | 100 MG
Small-molecule research compound originally developed as a cathepsin K inhibitor for the treatment of osteoporosis; now used in preclinical studies to probe cathepsin K biology and investigate antiviral activity. Supplied as a solid powder for in vitro and animal research use only, not for human therapeutic use.
- Potent, selective cathepsin K inhibitor.
- Intended for in vitro and preclinical research.
- Solid powder form, off-white to light yellow.
- High purity (≈99.6%), batch-dependent.
- Molecular formula C21H34N4O4S; molecular weight 438.58 g·mol⁻¹.
- CAS registry number 868273-90-9.
Medchemexpress LLC Ganaplacide hydrochloride | 2751586-94-2 | 98.2% | 447.91 g/mol | C22H24ClF2N5O | 25 MG
Ganaplacide hydrochloride is the hydrochloride salt of ganaplacide (KAF156), an investigational antimalarial research compound supplied as a white to yellow solid for laboratory use. It has molecular formula C22H24ClF2N5O, molecular weight 447.91 g/mol, CAS 2751586-94-2, and a reported purity of 98.22%.
- High purity suitable for research applications.
- Hydrochloride salt form, solid and stable for handling and storage.
- Suitable for in vitro and in vivo antimalarial pharmacology studies.
- Characterized molecular weight and formula for analytical work.
- Available in small research packaging for dosing flexibility.
Medchemexpress LLC 1-((2-(2,4-difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole methanesulfonate | 86386-77-8 | MFCD13184268 | 100g
1-((2-(2 4-Difluorophenyl)oxiran-2-yl)methyl)-1H-1 2 4-triazole methanesulfonate (Efinaconazole Impurity) is a biological molecule
![Medchemexpress LLC Potassium [(cyanomethyl)thio]acetate | 52069-54-2 | MFCD09842532 | 500mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000269724.png-250.jpg)
Medchemexpress LLC Potassium [(cyanomethyl)thio]acetate | 52069-54-2 | MFCD09842532 | 500mg
Cefmetazole impurity 1 is an impurity of Cefmetazole (HY-B1595)
Medchemexpress LLC 4-(3-fluoro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl methanone | 845614-11-1 | MFCD18251496 | 543.46 g/mol | C21H20F7N3O4S | 10 MG
Bitopertin is a research reagent that acts as a potent, selective inhibitor of the glycine transporter 1 (GlyT1). It reduces glycine reuptake at human GlyT1 with a reported IC50 of 25 nM and is supplied as a solid powder intended for research and analytical use.
- Potent, selective GlyT1 inhibitor with reported IC50 of 25 nM.
- Noncompetitive mechanism of action.
- Suitable for in vitro research and analytical applications.
- Provided as a solid powder with recommended storage guidance.
- Molecular formula C21H20F7N3O4S and molecular weight 543.46 g/mol.
- CAS number 845614-11-1 for unambiguous identification.
Selleck Chemical LLC PF 429242 947303-87-9
PF 429242 is known as a S1P inhibitor with an IC50 of 170 nM, showing no significant inhibition of trypsin, elastase, proteinase K, plasmin, kallikren, factor XIa, thrombin, or furin at concentrations up to 100 ?M and only modest inhibition of urokinase (IC50 = 50 ?M) and factor Xa (IC50 = 100 ?M). *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC N-(3,4-difluorophenyl)-7-methoxy-6-nitroquinazolin-4-amine | 2119689-75-5 | 50mg
Dacomitinib impurity 8 is an impurity of Dacomitinib (HY-13272)
Selleck Chemical LLC N-Desmethyl tamoxifen HCl E2368-5MG
N-Desmethyltamoxifen hydrochloride (N-Desmethyl tamoxifen HCl) the primary metabolite of tamoxifen is an estrogen response modifer and protein kinase C inhibitor with IC50 of 25 M
Selleck Chemical LLC ONO-AE3-208 E2986-5MG
ONO-AE3-208(AE 3-208) is a selective and orally active EP4 receptor antagonist with a Ki of 1 3 nM less potent to EP3 FP and TP receptors with Ki of 30 nM 790 nM and 2400 nM respectively
Selleck Chemical LLC p38-MAPK-IN-1 E2372-25MG
p38- MAPK-IN-1 is an inhibitor of p38- with IC50 value of 2300 nM in EFC displacement assay and 5500 nM in HTRF assay
Selleck Chemical LLC Vignae Semen Extract E3093-5MG
Vignae Semen Extract is extracted from Vignae Semen that induces diuresis to relieve edema evacuate pus and eliminate toxin
Selleck Chemical LLC Gramicidin E2970-100MG
Gramicidin from Bacillus aneurinolyticus (Bacillus brevis) is an antimicrobial peptide that destroys gram-positive bacteria It inhibits the growth of bacteria by forming pores and channels in the cell wall which increase its permeability to monovalent cations
Selleck Chemical LLC Ruthenium Red E2993-50MG
Ruthenium red (Ammoniated ruthenium oxychloride) is a polycationic dye which is a L-type calcium current (ICa) blocker It is widely used for electron microscopy (EM) of cells tissues and vegetative bacteria Ruthenium red strongly reacts with phospholipids and fatty acids and binds to acidic mucopolysaccharides