Alcohols and polyols
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- (1)
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- (462)
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- (1)
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- (1)
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- (1)
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- (1)
- (36)
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Filtered Search Results
Medchemexpress LLC Arg1-in-1 (hydrochloride) | 00-00-0 | 90.0% | 292.57 g·mol⁻1 | C11H22BClN2O4 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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ARG1-IN-1 hydrochloride is a small-molecule inhibitor of human arginase 1 with a reported IC50 of 29 nM. It is intended for research use in biochemical and cellular studies to probe arginase-related pathways. The hydrochloride form improves handling and aqueous compatibility for assay preparation.
- Potent arginase 1 inhibition (IC50 29 nM).
- Suitable for biochemical and cellular assays.
- Provided as a 5 mg quantity for small-scale research use.
- Molecular weight 292.57 g·mol⁻1; formula C11H22BClN2O4.
- Purity typically 90.0% as reported on the certificate of analysis.
- Store at -20°C under nitrogen and protect from moisture; in solvent store at -80°C for long-term.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Pargyline hydrochloride | 306-07-0 | MFCD00012492 | 99.91% | C11H14ClN | 100 MG
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Pargyline hydrochloride is an irreversible monoamine oxidase (MAO) inhibitor with antihypertensive and anticancer activities. It functions as a click chemistry reagent, containing an Alkyne group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Irreversible monoamine oxidase (MAO) inhibitor
- Exhibits antihypertensive activities
- Demonstrates anticancer activities
- Functions as a click chemistry reagent
- Contains an alkyne group for CuAAc reactions
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC VTP-27999 Hydrochloride | 1264191-73-2 | 98.18% | C26H42Cl2N4O5 | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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VTP-27999 Hcl is an alkyl amine Renin inhibitor useful for Hypertension and End-Organ Diseases, targeting Renin with an IC50 value.
- Alkyl amine Renin inhibitor
- Useful for hypertension and end-organ diseases
- Targets renin (IC50 value)
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Ansofaxine hydrochloride | 916918-84-8 | 417.97 | 25 MG
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Ansofaxine hydrochloride is a triple reuptake inhibitor designed to inhibit serotonin, dopamine, and norepinephrine reuptake. It demonstrates IC50 values of 723 nM, 491 nM, and 763 nM for these reuptake processes, respectively. This compound is intended for research use only.
- Triple reuptake inhibitor
- Inhibits serotonin, dopamine, and norepinephrine reuptake
- Intended for research use only
- Appears as a solid
- Color ranges from white to off-white
- Recommended storage for solid is 4°C, sealed and away from moisture
- For solutions, store at -80°C for up to 6 months, or -20°C for 1 month
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Medchemexpress LLC Nevanimibe hydrochloride | 133825-81-7 | MFCD00899568 | 99.5% | 458.08 g/mol | C27H40ClN3O | 1 ML
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Nevanimibe hydrochloride is the hydrochloride salt of nevanimibe, a selective acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) inhibitor supplied as a 10 mM solution in DMSO (1 mL) for in vitro research use.
- Selective ACAT1 inhibitor with low-nanomolar activity
- Supplied as a ready-to-use 10 mM solution in DMSO
- High purity (~99.5%) suitable for biochemical and cell-based assays
- Molecular weight 458.08 g/mol aids solution preparation calculations
- Available in solid and solution formats for flexibility in workflows
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Medchemexpress LLC VU0357017 hydrochloride | 1135242-13-5 | 98.63% | 369.89 | 1 ML
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VU0357017 hydrochloride is a potent, selective, and brain-penetrant allosteric agonist of the M1 muscarinic acetylcholine receptor, with an EC50 of 477 nM. It is highly selective for M1, showing no activity at M2-M5 receptors up to 30 μM. This compound is used in research for conditions such as Alzheimer's disease and schizophrenia.
- Potent and selective M1 muscarinic acetylcholine receptor agonist.
- Exhibits brain penetrant properties.
- Highly selective for M1 over M2-M5 receptors.
- Used for the research of Alzheimer's disease and schizophrenia.
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Medchemexpress LLC Thialysine hydrochloride | 4099-35-8 | 98.0% | 1 G
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Thialysine hydrochloride is the hydrochloride salt of thialysine, a cysteine-derived amino acid analog used for biochemical and protein-synthesis research.
- Purity 98.0%
- Molecular weight 200.69 g/mol
- Chemical formula C5H13ClN2O2S
- Appearance white to off-white solid
- Available pack sizes include 250 MG, 500 MG, 1 G, 5 G, 10 G
- Store sealed at -20°C; in solvent: -80°C (6 months), -20°C (1 month)
- Datasheet, COA, and SDS available
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Medchemexpress LLC AkaLumine hydrochloride | 2558205-28-8 | 99.9% | 338.85 | 10 MG
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AkaLumine hydrochloride is an analogue of D-luciferin that emits near-infrared (NIR) light (λmax=677 nm) when reacting with native firefly luciferase (Fluc) protein. It offers high tissue-penetration and increased detection sensitivity from deep-tissue targets.
- Near-infrared (NIR) emission allows for high tissue-penetration.
- Enhances detection sensitivity from deep-tissue targets.
- Functions similarly to D-luciferin with a specified Km for recombinant firefly luciferase.
- Can be used to detect Akaluc expression in vitro and for subcutaneous/orthotopic tumor mouse imaging in vivo.
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Medchemexpress LLC Ots186935 (hydrochloride) | 99.6% | 522.31 | 100 MG
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OTS186935 hydrochloride is a potent protein methyltransferase SUV39H2 inhibitor with an IC50 of 6.49 nM. It significantly inhibits tumor growth in mouse xenograft models without detectable toxicity and regulates the production of γ-H2AX in cancer cells. This compound has shown growth suppressive effects in human cancer cell line derived xenograft models.
- Potent SUV39H2 inhibitor
- Inhibits tumor growth in mouse xenograft models
- Regulates production of γ-H2AX in cancer cells
- Shows significant inhibition of tumor growth without detectable toxicity
- Inhibits A549 cell growth with an IC50 of 0.67 μM
- Exhibits growth suppressive effects in human cancer cell line derived xenograft models
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Medchemexpress LLC EPZ020411 hydrochloride | 2070015-25-5 | 98.2% | 50 MG
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EPZ020411 hydrochloride is a potent and selective inhibitor of protein arginine methyltransferase 6 (PRMT6) with an IC50 of 10 nM. It exhibits over 10-fold selectivity for PRMT6 compared to PRMT1 and PRMT8. This compound is valuable for cancer research and has demonstrated the ability to decrease H3R2 methylation in A375 cells, as well as reduce neomycin- and cisplatin-induced cell apoptosis, thereby increasing hair cell survival.
- Selective inhibitor of PRMT6
- IC50 of 10 nM for PRMT6
- Over 10-fold selectivity for PRMT6 over PRMT1 and PRMT8
- Can be used for cancer research
- Decreases H3R2 methylation in A375 cells
- Reduces neomycin- and cisplatin-induced cell apoptosis
- Increases hair cell survival
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Medchemexpress LLC Midodrine (hydrochloride) | 43218-56-0 | 99.9% | 25 MG
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Midodrine hydrochloride is a selective and orally active adrenergic α1-receptor agonist. It strengthens vascular contraction and can be used for research on cardiovascular diseases such as orthostatic hypotension.
- Strengthens vascular contraction
- Increases p-AMPK and PPARδ expression in C2C12, HL1, and HepG2 cells
- Increases Ca2+ in C2C12, HL1, and HepG2 cells
- Increases maximal mitochondrial oxidative phosphorylation and ATP content in C2C12 cells
- Reduces cellular lipid content in 3T3-L1 cells
- Reduces platelet-activating factor (Paf)-induced death in mice
- Shows anti-hypotensive effects in orthostatic hypotension rat models
- Relieves hypertension in spontaneously hypertensive rat models
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Medchemexpress LLC Iptacopan hydrochloride | 1646321-63-2 | 99.8% | 1 ML
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Iptacopan (LNP023) hydrochloride is an effective and orally-active highly selective factor B inhibitor with an IC50 value of 10 nM and KD of 7.9 nM. It prevents the destruction (hemolysis) of red blood cells in PNH and the damage of renal cells in IgAN and C3G by exerting a proximal effect in the complement cascade reaction. It can be used for the study of complement-mediated diseases, particularly paroxysmal nocturnal hemoglobinuria (PNH), primary immunoglobulin A nephropathy (IgAN), and complement 3 glomerulopathy (C3G).
- Effective and orally-active highly selective factor B inhibitor
- IC50 value of 10 nM and KD of 7.9 nM
- Prevents destruction (hemolysis) of red blood cells in PNH
- Prevents damage of renal cells in IgAN and C3G
- Used for the study of complement-mediated diseases
- Particularly paroxysmal nocturnal hemoglobinuria (PNH), primary immunoglobulin A nephropathy (IgAN), and complement 3 glomerulopathy (C3G)
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Medchemexpress LLC Tivozanib hydrochloride hydrate | 682745-41-1 | 99.8% | 509.34 | 50 MG
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Tivozanib hydrochloride hydrate is the hydrate hydrochloride form of Tivozanib. It is a selective, orally active inhibitor for vascular endothelial growth factor receptor (VEGFR)-1, 2, and 3, with IC50s of 30, 6.5, and 15 nM, respectively. It demonstrates antitumor efficacy.
- Selective, orally active inhibitor for VEGFR-1, 2, and 3
- Exhibits antitumor efficacy
- Inhibits phosphorylation of VEGFR-1, VEGFR-2, and VEGFR-3 with IC50s of 0.16-0.24 nM in vitro
- Inhibits VEGF-induced proliferation and migration of HUVECs in vitro
- Selectively inhibits VEGF-stimulated phosphorylation of MAPKs in endothelial cells in vitro
- Shows antitumor efficacy against breast, colon, hepatic, lung, ovarian, pancreatic, and prostate cancer in athymic mice models in vivo
- Reversibly suppresses vascular permeability and angiogenesis in Calu-6 tumor bearing rats in vivo
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Medchemexpress LLC Leelamine hydrochloride | 16496-99-4 | 98.10% | 321.93 | 1 ML
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Leelamine hydrochloride is a tricyclic diterpene molecule extracted from the bark of pine trees. It acts as a cannabinoid receptor type 1 (CB1) agonist and an inhibitor of SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, independent of androgen receptor status. It also suppresses the transcriptional activity of the androgen receptor, which regulates fatty acid synthesis.
- Acts as a cannabinoid receptor type 1 (CB1) agonist
- Inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells
- Suppresses the transcriptional activity of the androgen receptor
- Extracted from the bark of pine trees
- Appears as a white to off-white solid
- Store at -20°C in sealed conditions, away from moisture
- For storage in solvent, store at -80°C for 6 months, or -20°C for 1 month in sealed conditions, away from moisture
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Medchemexpress LLC SB-277011 hydrochloride | 215804-67-4 | 99.59% | 475.02 | 50 MG
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SB-277011 hydrochloride is a potent and selective dopamine D3 receptor (D3R) antagonist, demonstrating high oral bioavailability and brain penetrance. It exhibits significant selectivity over other dopamine receptors and possesses an excellent pharmacokinetic profile in rats. This compound has been shown to effectively reverse the effects of quinelorane and reduce cocaine self-administration in preclinical studies.
- Potent and selective D3 receptor antagonist
- High oral bioavailability and brain penetrance
- 80- to 100-fold selectivity over other dopamine receptors
- Excellent pharmacokinetic profile
- Reverses quinelorane effects in nucleus accumbens
- Reduces intravenous cocaine self-administration
- Inhibits basal and cocaine-enhanced locomotion
- Appearance: solid, off-white to light yellow
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