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Filtered Search Results
Medchemexpress LLC G4RGDSP, integrin-binding peptide | 774577-43-4 | 99.61% | 758.74 | 100 MG
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G4RGDSP, integrin-binding peptide is a cell integrin-binding peptide that targets integrin receptors. It is coupled to alginate to increase the viability of cells in the scaffold and can be used as an extrudable carrier for chondrocyte delivery for the study of 3D printing technology.
- Targets integrin receptors
- Increases viability of cells in scaffold
- Suitable for chondrocyte delivery studies
- Used in 3D printing technology research
- Increases expression of aggregin, collagen type II, and sox9 genes in HAC cells
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Medchemexpress LLC HY-B2156 100mg Medchemexpress, Menaquinone-4 CAS:863-61-6 Purity:>98%
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Medchemexpress, HY-B2156 100mg Menaquinone-4 CAS:863-61-6 Menaquinone-4 is a vitamin K, used as a hemostatic agent, and also a adjunctive therapy for the pain of osteoporosis. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC BI-2865 | 2937327-93-8 | C23H27N7O2S | 1 ML
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BI-2865 is a non-covalent pan-KRAS Inhibitor. It binds to wild-type and various mutant KRAS forms, including G12C, G12D, G12V, and G13D, inhibiting the proliferation of mutant KRAS expressing BaF3 cells. Characterized by a prolinol substituent and a pyrimidine linker, it forms specific interactions within the KRAS binding site. This product is for research use only.
- Binds to wild-type and various mutant KRAS forms
- Inhibits proliferation of mutant KRAS expressing BaF3 cells
- Features a prolinol substituent and a pyrimidine linker
- Demonstrates direct ionic interaction with E62
- Forms a water-mediated hydrogen bond network with R68 and Q61
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Medchemexpress LLC BI-2493 | 2937344-16-4 | C24H27N7OS | 50 MG
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BI-2493 is a structural analogue of BI-2865 and a highly selective and orally active pan-KRAS inhibitor. It is designed to attenuate tumor growth and is primarily used for cancer diseases research.
- Highly selective and orally active pan-KRAS inhibitor
- Attenuates tumor growth
- Used for cancer diseases research
- Inhibits proliferation of KRAS mutant cancer cell lines in a concentration-dependent manner
- Exhibits tumor-suppressive activity in xenograft mouse models
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Medchemexpress LLC Talibegron hydrochloride (ZD2079 hydrochloride) | 178600-17-4 | C18H22ClNO4 | 1 MG
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Talibegron hydrochloride (ZD2079 hydrochloride) is a potent β3-adrenoceptor agonist with a pD2 of 3.72 on phenylephrine-preconstricted rat mesenteric artery. It has a potent vasorelaxant effect.
- Potent β3-adrenoceptor agonist.
- Has potent vasorelaxant effect.
- Produces a concentration-dependent relaxation of phenylephrine-preconstricted isolated mesenteric arteries.
- Causes full relaxation with 1 mM.
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Medchemexpress LLC Alprenolol hydrochloride | 13707-88-5 | 99.8% | 500 MG
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Alprenolol hydrochloride is an orally active non-selective β-adrenoceptor antagonist and an antagonist of 5-HT1A and 5-HT1B receptors. It is used as an anti-hypertensive, anti-anginal and anti-arrhythmic agent.
- Orally active non-selective β-adrenoceptor antagonist.
- Antagonizes 5-HT1A and 5-HT1B receptors.
- Used as an anti-hypertensive, anti-anginal, and anti-arrhythmic agent.
- High purity of 99.76%.
- Soluble in DMSO (100 mg/mL) and water (50 mg/mL).
- Formulations available for oral and intraperitoneal injection.
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Medchemexpress LLC Givinostat hydrochloride | 199657-29-9 | MFCD28502062 | 98.1% | 457.95 | 100 MG
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Givinostat hydrochloride is a Histone Deacetylase (HDAC) inhibitor that can penetrate the blood-brain barrier (BBB). It is known to inhibit HDAC1 and HDAC3, and has shown efficacy in suppressing inflammatory responses and inhibiting cell proliferation in various studies.
- Inhibits HDAC1 (IC50: 198 nM) and HDAC3 (IC50: 157 nM)
- Penetrates the blood-brain barrier (BBB)
- Suppresses LPS-induced IL-1β production
- Decreases IL-6 secretion in PBMCs
- Inhibits JS-1 cell proliferation
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Medchemexpress LLC Irinotecan hydrochloride trihydrate | 136572-09-3 | 99.9% | 677.18 | 100 MG
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Irinotecan hydrochloride trihydrate is a topoisomerase I inhibitor with antitumor activity, used to treat colon and rectal cancer. It is for research use only and has been shown to inhibit the growth of various cancer cell lines, such as LoVo and HT-29.
- Inhibits topoisomerase I
- Demonstrates antitumor activity
- Suppresses proliferation of human umbilical vein endothelial cells
- Available for research use only
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Medchemexpress LLC Benzenesulfonamide, 4-[(6-amino-4-pyrimidinyl)amino]-, hydrochloride (1:1) | 21886-12-4 | 99.6% | 301.75 | 25 MG
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PNU112455A hydrochloride is an ATP-competitive inhibitor of CDK2 and CDK5. It binds to the ATP site of CDK2 and CDK5 with Kms of 3.6 and 3.2 μM, respectively. This product is for research use only and is not sold to patients.
- ATP-competitive CDK2 and CDK5 inhibitor.
- Binds to the ATP site of CDK2 and CDK5.
- Purity: 99.56%.
- Available in various sizes and concentrations, including solid and solution forms.
- Soluble in DMSO and H2O.
- Provided with detailed solubility and storage information for both in vitro and in vivo applications.
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Apexbio Technology LLC Menadione, 10mM (in 1mL DMSO). Cas: 58-27-5 MFCD: MFCD00001681. precursor to vitamin K2
Menadione (vitamin K3), used as a nutritional supplement, is an inhibitor of mitochondrial DNA polymerase γ (pol γ), with an IC 50 value of 6 µM. Pol γ is responsible for all aspects of mitochondrial DNA synthesis, including all replication, recombination of the mitochondrial genome, and repair of mitochondrial DNA damage. Other sizes are available. Please inqury us for quote.
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Medchemexpress LLC Givinostat hydrochloride monohydrate | 732302-99-7 | 99.6% | 475.97 | 25 MG
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Givinostat hydrochloride monohydrate is a potent HDAC inhibitor, demonstrating IC50 values of 198 nM for HDAC1 and 157 nM for HDAC3. This compound is notable for its ability to penetrate the blood-brain barrier, making it suitable for a range of research applications.
- Potent HDAC inhibitor for HDAC1 and HDAC3
- Penetrates the blood-brain barrier
- Suppresses LPS-induced IL-1β and IL-6 production
- Inhibits JS-1 cell proliferation
- Reduces serum TNFα and IL-1β levels in vivo
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Medchemexpress LLC Xaliproden hydrochloride | 90494-79-4 | 98.4% | 417.89 | 1 ML
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Xaliproden hydrochloride (SR57746A) is a potent, selective, and orally active agonist of the 5-HT1A receptor, showing high affinity for 5-HT1A specific binding sites in the rat hippocampus (IC50=3 nM). It is also a selective antagonist of the dopamine D2 receptor, with moderate affinity (IC50=0.1-1 μM). Xaliproden hydrochloride exhibits anti-depression and anti-anxiety effects and may have therapeutic potential for the research of neurodegenerative diseases.
- Potent, selective, and orally active 5-HT1A receptor agonist
- High affinity for 5-HT1A specific binding sites (IC50=3 nM)
- Selective antagonist of the dopamine D2 receptor
- Moderate affinity for D2 receptor (IC50=0.1-1 μM)
- Exhibits anti-depression and anti-anxiety effects
- May have therapeutic potential for neurodegenerative disease research
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Medchemexpress LLC 5-pyrimidineacetic acid, 4,6-bis(dimethylamino)-2-[[4-[[4-(trifluoromethyl)benzoyl]amino]phenyl]methyl]- | 1093108-50-9 | 99.4% | 501.50 | 50 MG
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This product is a highly specific and potent antagonist of chemoattractant receptor-homologous molecule on Th2 cells (DP2/CRTH2), with IC50 values of 4.5 nM and 3.7 nM for PGD2 binding to CRTH2 in hCRTH2 and mCRTH2 transfected cells, respectively. It has potential for the treatment of poorly controlled asthma. It can also significantly inhibit AHR in mice and effectively block edema formation while reducing inflammatory infiltrate and skin pathology in drug vehicle-treated animals.
- Highly specific and potent antagonist of CRTH2.
- Demonstrates low nanomolar potency against human and mouse CRTH2 in transfected cells.
- Shows significant inhibition of airway hyperreactivity (AHR) in mice.
- Effectively blocks edema formation in animal models.
- Reduces inflammatory infiltrate and skin pathology.
- Potential for treating poorly controlled asthma.
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Apexbio Technology LLC BI 2536(Synonyms: BI-2536, BI2536, Plk1 inhibitor BI 2536), 50mg, CAS: 755038-02-9.
BI 2536 (CAS number 755038-02-9) is an ATP-competitive inhibitor selectively targeting human polo-like kinase 1 (PLK1) exhibiting an IC50 value of approximately 0 83 nM Comparatively BI 2536 shows substantially less affinity towards other kinases In vitro studies demonstrate that BI 2536 inhibits proliferation of various human tumor cell lines (EC50 values ranging from 2 to 25 nM) and induces G2/M cell cycle arrest accompanied by apoptosis as evidenced in HeLa cervical cancer cells In vivo data from xenograft tumor models indicate that BI 2536 administered intravenously on a weekly or biweekly schedule possesses antitumor efficacy
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Medchemexpress LLC PNU112455A hydrochloride | 21886-12-4 | 99.6% | 301.75 | 1 ML
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PNU112455A hydrochloride is an ATP-competitive inhibitor of CDK2 and CDK5. It binds to the ATP site of CDK2 and CDK5 with Km values of 3.6 μM and 3.2 μM, respectively. This product is intended for research use only and is not sold to patients.
- ATP-competitive CDK2 and CDK5 inhibitor.
- Binds to the ATP site of CDK2 and CDK5.
- Km for CDK2: 3.6 μM.
- Km for CDK5: 3.2 μM.
- Purity: 99.56%.
- Appearance: Solid, Light yellow to yellow.
- Shipping: Room temperature in continental US.
- Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C for 6 months; -20°C for 1 month.
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