Drug Standards
Apexbio Technology LLC H1 histamine receptor antagonist. Clemizole hydrochloride 5mg. 728865-23-4. MFCD22665727
H1 histamine receptor antagonist. Clemizole hydrochloride 5mg. 728865-23-4. MFCD22665727
Apexbio Technology LLC Cobimetinib, 934660-93-2, MFCD22124461, 5 mg
MF: C21H21F3IN3O2, MW: 531.31, Solubility: 26.55 mg/mL in DMSO, 33.53 mg/mL in EtOH with gentle warming,insoluble in H2O. Cobimetinib is a selective inhibitor of mitogen-activated protein kinase kinase (MEK) with IC50 value of 0.9 nM.
Medchemexpress LLC Nevirapine 5mg | 129618-40-2 | 5MG
Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS with a Ki of 270 M[1
Sigma Aldrich Fine Chemicals Biosciences Perindopril Related Compound C United States Pharmacopeia (USP) Reference Standard | 129970-99-6 | 20MG
Perindopril Related Compound C United States Pharmacopeia (USP) Reference Standard | Mol Wt: 322.4 | 129970-99-6 | 20MG
Apexbio Technology LLC Fluvoxamine maleate 61718-82-9 10mM (in 1mL DMSO)
Fluvoxamine maleate (CAS 61718-82-9) is a selective serotonin reuptake inhibitor that acts by inhibiting the human serotonin (5-HT) transporter This action leads to increased extracellular serotonin concentrations Fluvoxamine maleate exhibits high binding affinity for the 5-HT transporter with a reported K sub i /sub of 1 6 nmol/l It is widely utilized in biomedical research to investigate serotonergic signaling pathways and to model mechanisms underlying antidepressant activity Fluvoxamine maleate is also available as part of the Serotonin Uptake Inhibitor Tocriset for experimental applications
U.S. Pharmacopeia Norphenylephrine hydrochloride, 4779-94-6, MFCD00012879, 25 mg
Linear Formula: HOC6H4CH(CH2NH2)OH · HCl, Molecular Weight: 189.64, mp: 162-164 °C, Synonym: α-Aminomethyl-3-hydroxybenzyl alcohol hydrochloride, 3,α-Dihydroxyphenethylamine hydrochloride, Norfenefrine hydrochloride.
Apexbio Technology LLC Betahistine 2HCl 5579-84-0 1g
Betahistine 2HCl (CAS 5579-84-0) is a small-molecule inhibitor targeting histamine H3 receptors exhibiting an inhibitory concentration (IC50) of 1 9 M By antagonizing H3 receptors betahistine modulates histaminergic neurotransmission which influences the release of various neurotransmitters in the central nervous system This compound is widely utilized in research focused on the physiological roles of histamine signaling particularly in studies of neurological and vestibular disorders as well as in the exploration of H3 receptor pharmacology and modulation
Apexbio Technology LLC Betahistine 2HCl 5579-84-0 100mg
Betahistine 2HCl (CAS 5579-84-0) is a small-molecule inhibitor targeting histamine H3 receptors exhibiting an inhibitory concentration (IC50) of 1 9 M By antagonizing H3 receptors betahistine modulates histaminergic neurotransmission which influences the release of various neurotransmitters in the central nervous system This compound is widely utilized in research focused on the physiological roles of histamine signaling particularly in studies of neurological and vestibular disorders as well as in the exploration of H3 receptor pharmacology and modulation
Apexbio Technology LLC Granisetron HCl 107007-99-8 100mg
Granisetron HCl (CAS 107007-99-8) is a selective antagonist of the serotonin 5-hydroxytryptamine type 3 (5-HT sub 3 /sub ) receptor By competitively inhibiting 5-HT sub 3 /sub receptor-mediated signaling Granisetron HCl suppresses serotonin-induced activation of the vomiting reflex pathway in both central and peripheral nervous systems This pharmacological activity underlies its utility in preventing and investigating the mechanisms of chemotherapy-induced and postoperative nausea and vomiting Granisetron HCl is widely employed in preclinical and clinical studies to elucidate 5-HT sub 3 /sub receptor function and to explore antiemetic strategies
Selleck Chemical LLC Pirfenidone 10mg 53179-13-8 S-7701,AMR-69
Pirfenidone (S-7701, AMR-69) is an inhibitor for TGF-? production and TGF-? stimulated collagen production, reduces production of TNF-? and IL-1?, and also has anti-fibrotic and anti-inflammatory properties. Pirfenidone attenuates chemokine (CC motif) ligand-2 (CCL2) and CCL12 production with anti-fibrotic activity. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Tenofovir alafenamide hemifumarate | 1392275-56-7 | C21H29N6O5P.1/2 C4H4O4 | 1 ML
Tenofovir alafenamide hemifumarate (GS-7340 hemifumarate) is an investigational oral proagent of Tenofovir. Tenofovir is an HIV-1 nucleotide reverse transcriptase inhibitor.
- Investigational oral proagent
- HIV-1 nucleotide reverse transcriptase inhibitor
- Amidate prodrug with good oral bioavailability
- Increased plasma stability
Selleck Chemical LLC Crenigacestat
Crenigacestat (LY3039478) is an oral Notch and gamma-secretase inhibitor with IC50 of 0 41 nM for Notch