Alcohols and polyols
- (1)
- (55)
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- (1)
- (25)
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- (1)
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- (1)
- (463)
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- (46)
- (10)
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- (1)
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- (145)
- (116)
- (7)
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- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
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- (1)
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- (30)
- (1)
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- (1)
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- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
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- (6)
- (2)
- (1)
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- (4)
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- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
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- (4)
- (2)
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- (4)
- (17)
- (15)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (3)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (2)
- (1)
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- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
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- (1)
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- (1)
- (3)
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- (1)
- (1)
- (2)
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- (2)
- (2)
- (3)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
- (2)
- (2)
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- (1)
- (1)
- (2)
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- (1)
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- (27)
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- (1)
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- (1)
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- (1)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (82)
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- (1)
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- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
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- (40)
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- (1)
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- (1)
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- (21)
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- (1)
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- (1)
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- (1)
- (6)
- (278)
- (28)
- (2)
- (25)
- (2)
- (3)
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- (2)
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- (2)
- (3)
- (48)
- (3)
- (418)
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- (3)
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- (5)
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- (3)
- (1)
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- (21)
- (16)
- (2)
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- (1)
- (8)
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- (733)
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- (3)
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Filtered Search Results
Medchemexpress LLC Dyclonine hydrochloride | 536-43-6 | 99.3% | 10 G
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Dyclonine hydrochloride is an orally effective ALDH covalent inhibitor that crosses the blood-brain barrier. It functions as a local anesthetic, capable of suppressing or relieving pain by blocking nerve impulse transmission. It also exhibits sensitizing activities for targeted cancer cells and possesses antibacterial and fungicidal properties, demonstrating significant activity against various bacteria and fungi.
- Orally effective ALDH covalent inhibitor
- Crosses the blood-brain barrier
- Functions as a local anesthetic
- Sensitizes cancer cells to cysteine and GSH deficiency
- Demonstrates bactericidal and fungicidal activity
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Carbamic acid, n-[2-[(r)-(3-chlorophenyl)...methyl ester, hydrochloride | 1264191-73-2 | MFCD19443251 | 98.2% | 561.54 | C26H42Cl2N4O5 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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VTP-27999 Hydrochloride is the hydrochloride salt of an alkyl amine renin inhibitor supplied for preclinical research into hypertension and related end-organ diseases. Supplied as a purified solid with high aqueous solubility, it is intended for use in in vitro and in vivo studies.
- High purity (≈98.2%) suitable for research applications.
- Hydrochloride salt form for improved stability and handling.
- Water solubility ≥ 100 mg/mL enabling convenient dosing and formulation.
- Available in small package sizes for early-stage studies.
- Store sealed and away from moisture to preserve stability.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC RPR132595A hydrochloride | 185304-42-1 | MFCD18252420 | 99.5% | 555.02 g/mol | C28H31ClN4O6 | 1 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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RPR132595A hydrochloride is the hydrochloride salt of RPR132595A (NPC), an active metabolite of irinotecan (CPT-11) formed by cytochrome P-450 3A4 (CYP3A4) and primarily excreted in urine. It is supplied as a research reagent and reference standard for metabolic, pharmacokinetic, and analytical studies.
- Active metabolite of irinotecan produced by cytochrome P-450 3A4.
- Hydrochloride salt form for improved stability and handling.
- High purity suitable for use as a reference standard in analytical assays.
- Soluble in DMSO at experimental concentrations.
- Available in research-scale quantities for laboratory studies.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC SKF-34288 hydrochloride | 320386-54-7 | 98.6% | 10 MM * 1 ML
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SKF-34288 (3-Mercaptopicolinic acid) hydrochloride is an orally active phosphoenolpyruvate carboxykinase (PEPCK) inhibitor with a Ki of 2-9 μM. It acts as a potent hypoglycemic agent by inhibiting glucose synthesis. Additionally, it inhibits Asn metabolism and leads to an increase in amino acids and amides. It is intended for research use only.
- Potent phosphoenolpyruvate carboxykinase (PEPCK) inhibitor
- Inhibits glucose synthesis
- Increases amino acids and amides by inhibiting Asn metabolism
- Inhibits C2C12 cell proliferation
- Induces myogenic differentiation of C2C12 cells
- Reduces mRNA expression of Pck2 and genes associated with serine biosynthesis
- Reduces blood glucose in starved rats
- Neutralizes Salbutamol-mediated hyperglycaemia in rabbits
- Reduces pyruvate-induced blood glucose level in rats
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Medchemexpress LLC Vimirogant hydrochloride | 1802678-42-7 | 98.4% | C27H35F3N4O3S·XHCl | 10 MG
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Potent, selective RORγt inhibitor supplied as the hydrochloride salt for research use. It demonstrates low-nanomolar biochemical potency and cellular activity against IL-17A secretion and Th17 differentiation.
- Potent RORγt inhibition (Ki = 3.5 nM; IC50 = 17 nM).
- Reduces IL-17A secretion in human PBMCs (IC50 = 18 nM) and human whole blood (IC50 = 192 nM).
- Inhibits Th17 differentiation in mouse splenocytes (IC50 = 57 nM).
- High purity (98.4% by HPLC).
- Available in small research pack sizes, e.g., 10 MG.
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Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 g/mol | C16H22Cl2N2O2S | 5 MG
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W-7 isomer hydrochloride is the hydrochloride salt of an isomer of W-7, a selective calmodulin antagonist used in biochemical and cellular research to inhibit calmodulin-dependent signaling. Supplied as a powdered research reagent with specified purity and handling instructions, it is intended for laboratory research use only.
- Selective calmodulin antagonist for biochemical and cellular assays.
- High purity suitable for analytical and experimental applications.
- Supplied as a stable powder for convenient storage and handling.
- Available in small research quantities for assay development.
- Refer to safety data and handling instructions for proper use.
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Medchemexpress LLC Taltobulin hydrochloride | 228266-40-8 | 99.3% | 510.11 g/mol | C27H44ClN3O4 | 50 MG
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Taltobulin hydrochloride is a synthetic analogue of the tripeptide hemiasterlin and a potent antimicrotubule agent used in research. It inhibits tubulin polymerization, disrupts microtubule organization, and induces mitotic arrest and apoptosis.
- Potent tubulin inhibitor for research applications
- High purity (typically 99.34%)
- Supplied as a white to off-white solid
- Available in multiple pack sizes, including 50 mg
- Used in vitro and in vivo to assess antimitotic activity
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Medchemexpress LLC Tandutinib hydrochloride | 2438900-70-8 | 99.3% | 599.16 g/mol | C31H43ClN6O4 | 1 ML
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Tandutinib hydrochloride is a small-molecule tyrosine kinase inhibitor selective for FLT3, with additional activity against c-Kit and PDGFR. It is used as a research reagent in biochemical and cell-based assays to probe signaling pathways and assess antiproliferative effects in oncology studies. The compound has defined physicochemical properties and is suitable for preparing stock solutions for in vitro workflows.
- Potent FLT3 inhibition (IC50 ≈ 0.22 μM).
- Also inhibits c-Kit and PDGFR, supporting broader kinase profiling.
- High purity suitable for research applications (>99% by HPLC).
- Suitable for preparing accurate stock solutions for assays (e.g., 10 mM).
- Provided with datasheet information for safe handling and solubility guidance.
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Medchemexpress LLC Topotecan hydrochloride | 119413-54-6 | MFCD00866235 | 99.9% | 457.91 g/mol | C23H24ClN3O5 | 5 MG
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Topotecan hydrochloride is the hydrochloride salt of topotecan, a potent topoisomerase I inhibitor used in oncology research. It induces DNA damage and apoptosis in tumor cells and is supplied for research use only. Typical solvent compatibility includes DMSO.
- Potent topoisomerase I inhibitor with antineoplastic activity.
- Hydrochloride salt form for improved stability and handling.
- High purity suitable for cellular and molecular studies.
- Soluble in DMSO for assay and dosing preparations.
- Used to induce DNA damage, cell cycle arrest, and apoptosis in tumor models.
- Intended for research use only; not for human or diagnostic applications.
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Medchemexpress LLC Eperisone hydrochloride | 56839-43-1 | MFCD00941459 | 100.0% | 500 MG
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Eperisone Hydrochloride ((±)-Eperisone hydrochloride) is an orally active antispastic agent with a vasodilator effect, used for the research of muscle stiffness and pain. It is a potent and selectively P2X7 receptor antagonist, and also shows antagonism for human P2X3. Eperisone Hydrochloride works by relaxing both skeletal muscles and vascular smooth muscles, demonstrating a variety of effects such as reduction of myotonia, improvement of circulation and suppression of the pain reflex.
- Orally active antispastic agent
- Vasodilator effect
- Used for research of muscle stiffness and pain
- Potent and selective P2X7 receptor antagonist
- Shows antagonism for human P2X3
- Relaxes both skeletal muscles and vascular smooth muscles
- Reduces myotonia
- Improves circulation
- Suppresses the pain reflex
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Medchemexpress LLC Noscapine hydrochloride | 912-60-7 | 99.9% | 449.88 | 500 MG
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Noscapine hydrochloride | 912-60-7 | 99.9% | 449.88 | 500 MG
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Medchemexpress LLC DC-BPi-11 (hydrochloride) | 97.0% | C20H24ClN5O2S | 100 MG
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DC-BPi-11 hydrochloride is an inhibitor of bromodomain PHD finger transcription factor (BPTF), showing an IC50 value of 698 nM. It demonstrates significant inhibition against leukemia cell proliferation in human leukemia MV-4-11 cells with an EC50 value of 120 nM, while having minimal effects on normal cells, suggesting a favorable safety profile.
- Inhibits bromodomain PHD finger transcription factor (BPTF)
- Significantly inhibits leukemia cell proliferation
- Decreases downstream oncogene expression
- Dose-dependently decreases c-Myc protein level
- Minimal effects on normal cells
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Medchemexpress LLC m-PEG-NH2 hydrochloride | 99.1% | 2000 Da (average) | Polydisperse PEG (repeating unit C2H4O) hydrochloride (no single chemical formula) | 25 MG
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Amine-terminated methoxy polyethylene glycol hydrochloride with an average molecular weight of 2000 Da. This polydisperse PEG reagent is used as a building block and barrier-permeation modifier for preparing hybrid gels and for size-exclusion applications in biochemical assays.
- Amine-terminated methoxy polyethylene glycol hydrochloride with average molecular weight 2000 Da.
- Polydisperse polymeric reagent suitable for gel and biochemical assay applications.
- Helps AdSEC gels separate from complex biological mixtures such as blood, urine, sweat, and tears.
- Reported purity 99.13%.
- Soluble in DMSO at 100 mg/mL (ultrasonic recommended).
- Store at -20°C and protect from light; in solvent store at -80°C for up to 6 months or -20°C for 1 month.
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Medchemexpress LLC Voreloxin hydrochloride | 175519-16-1 | 99.6% | 437.90 g/mol | C18H20ClN5O4S | 10 MG
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Voreloxin hydrochloride is a research-grade anticancer compound and a first-in-class topoisomerase II inhibitor. It intercalates into DNA and induces site-selective double-strand breaks (DSB), causing G2 cell-cycle arrest and apoptosis. Supplied as a hydrochloride salt for laboratory research use only.
- First-in-class mechanism: topoisomerase II inhibition through DNA intercalation.
- Triggers site-selective DNA double-strand breaks and G2 arrest.
- High purity suitable for biochemical and cell-based assays.
- Well-characterized chemical identity: molecular formula C18H20ClN5O4S, molecular weight 437.90 g/mol.
- Available in accurately weighed small pack sizes for precise dosing in experiments.
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Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 | C16H22Cl2N2O2S | 100 MG
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W-7 isomer hydrochloride is the hydrochloride salt of a W-7 isomer used as a selective calmodulin antagonist in biochemical and cell biology research. It is provided as a purified solid or as a DMSO solution for small-scale laboratory experiments and mechanistic studies of Ca2+/calmodulin-dependent processes.
- Selective calmodulin antagonist suitable for biochemical assays and cell signaling studies.
- High purity, 99.7%, for reproducible experimental results.
- Available as powder and as a 10 mM solution in DMSO for ready-to-use applications.
- Small pack sizes support pilot experiments and dose-response testing.
- Long-term stability when stored at recommended low temperatures.
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