Alcohols and polyols
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- (21)
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- (1)
- (26)
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- (1)
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- (1)
- (462)
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- (11)
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- (1)
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- (145)
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- (1)
- (1)
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- (1)
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- (1)
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- (2)
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- (2)
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- (1)
- (28)
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- (7)
- (3)
- (5)
- (1)
- (36)
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- (2)
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- (33)
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- (8)
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- (7)
- (2)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (3)
- (1)
- (15)
- (12)
- (1)
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- (2)
- (7)
- (12)
- (1)
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- (24)
- (1)
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- (1)
- (2)
- (1)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
- (2)
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- (1)
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- (1)
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- (1)
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Filtered Search Results
BIOCHROM ULTRA NINHYDRIN KIT 8L NC
NC3968835 ULTRA NINHYDRIN KIT 8L NC
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Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | 99.9% | C14H11ClN4O | 50 MG
Small and Specialty Supplier Partner
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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Olprinone Hydrochloride is a potent phosphodiesterase (PDE) 3 inhibitor, showing IC50s of 0.35 μM for PDE3. It is utilized in research for heart failure due to its positive inotropic and vasodilative effects, and also demonstrates anti-inflammatory activity.
- Potent PDE3 inhibitor
- Used in research for heart failure
- Exhibits positive inotropic and vasodilative effects
- Demonstrates anti-inflammatory activity
- Modulates inflammation associated with myocardial ischemia-reperfusion injury
- Reduces pro-inflammatory cytokines such as TNF-α and IL-1β
- Decreases expression of adhesion molecules like ICAM-1 and P-Selectin
- Inhibits apoptosis related to myocardial injury
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC SCH-23390 (hydrochloride) | 125941-87-9 | 99.8% | 324.24 | 100 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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SCH-23390 (hydrochloride) | 125941-87-9 | 99.8% | 324.24 | 100 MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Befiradol hydrochloride | 2436760-81-3 | MFCD31731608 | 99.9% | 430.32 g/mol | C20H23Cl2F2N3O | 10 MG
Small and Specialty Supplier Partner
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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Befiradol hydrochloride is a selective 5-HT1A receptor agonist provided for research use. It modulates serotonergic and dopaminergic activity in cortical regions and is used in preclinical pharmacology studies to investigate 5-HT1A-mediated mechanisms and models of neurological disorders. The material is supplied with supporting documentation for analytical and safety purposes.
- Selective 5-HT1A receptor agonist for receptor pharmacology studies.
- Demonstrated activity on dorsal raphe and medial prefrontal cortex neurotransmission.
- High chemical purity suitable for analytical and in vivo research.
- Supplied with certificate of analysis and safety data sheet.
- Available in multiple pack sizes for small-scale and bulk use.
- Not for human or clinical use; for research use only.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Berubicin (hydrochloride) | 293736-67-1 | 95.08% | 670.10 | 5 MG
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Berubicin hydrochloride is a Doxorubicin analog capable of crossing the blood-brain barrier. It inhibits P-gp and MRP1-mediated efflux, suppressing glioblastoma multiforme (GBM). This compound exhibits toxic effects on leukemia cells by activating nuclear factor κB (NF-κB) and induces apoptosis in neuroblastoma cells. It is suitable for studying nervous system-related tumors.
- Can cross the blood-brain barrier
- Inhibits P-gp and MRP1-mediated efflux
- Suppresses glioblastoma multiforme (GBM)
- Exerts toxic effects on leukemia cells by activating nuclear factor κB (NF-κB)
- Induces apoptosis in neuroblastoma cells
- Useful in the study of nervous system-related tumors
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Medchemexpress LLC Verapamil hydrochloride | 152-11-4 | 100.0% | C27H39ClN2O4 | 1 ML
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Verapamil hydrochloride, also known as (±)-Verapamil hydrochloride, functions as a calcium channel blocker and is identified as a potent, orally active first-generation P-glycoprotein (P-gp) inhibitor. This compound also exhibits inhibitory effects on CYP3A4. It holds potential for research applications related to conditions such as high blood pressure, heart arrhythmias, and angina.
- Acts as a calcium channel blocker.
- Functions as a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor.
- Demonstrates inhibition of CYP3A4.
- Suitable for research concerning high blood pressure.
- Applicable for studies on heart arrhythmias.
- Used in angina research.
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Medchemexpress LLC Azasetron hydrochloride | 123040-16-4 | 99.8% | C17H21Cl2N3O3 | 100 MG
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Azasetron hydrochloride is a benzamide derivative that functions as a potent and selective antagonist of the 5-HT3 receptor, demonstrating an IC50 of 0.33 nM against this target. It has been investigated for its potential in studies related to chemotherapy-induced nausea and vomiting (CINV) and has shown the ability to penetrate the skin and enter systemic circulation in in vivo models.
- Mechanism of action: Potent and selective 5-HT3 receptor antagonist.
- Target affinity: IC50 of 0.33 nM for 5-HT3 receptor.
- Chemical classification: Benzamide derivative.
- Molecular formula: C17H21Cl2N3O3.
- Molecular weight: 386.27.
- Purity: 99.76%.
- Physical characteristics: White to off-white solid.
- Solubility: Soluble in water (20 mg/mL) and DMSO (2.22 mg/mL).
- Research application: Used in CINV studies.
- Pharmacokinetic property: Penetrates skin and enters systemic circulation in animal models.
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Medchemexpress LLC Donepezil Hydrochloride | 120011-70-3 | 99.9% | C24H30ClNO3 | 500 MG
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Donepezil Hydrochloride (E2020) is a reversible, selective AChE inhibitor with an IC50 of 6.7 nM for AChE activity. It shows high selectivity for AChE over BuChE and exhibits a neuroprotective effect on Aβ42 neurotoxicity. Its neuroprotective mechanism is related to the enhanced phosphorylation of Akt and GSK-3β and reduced phosphorylation of tau and glycogen synthase.
- Reversible, selective AChE inhibitor
- Shows high selectivity for AChE over BuChE
- Exhibits neuroprotective effect on Aβ42 neurotoxicity
- Neuroprotective mechanism is related to enhanced phosphorylation of Akt and GSK-3β
- Reduced phosphorylation of tau and glycogen synthase
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Medchemexpress LLC Pargyline hydrochloride | 306-07-0 | 99.9% | C11H14ClN | 1 ML
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Pargyline hydrochloride is an irreversible monoamine oxidase (MAO) inhibitor with Kis of 13 μM for MAO-A and 0.5 μM for MAO-B. It exhibits antihypertensive and anticancer activities. Pargyline (hydrochloride) is also a click chemistry reagent, containing an Alkyne group, which can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules that have Azide groups.
- Irreversible monoamine oxidase (MAO) inhibitor
- Inhibits MAO-A with a Ki of 13 μM
- Inhibits MAO-B with a Ki of 0.5 μM
- Demonstrates antihypertensive activities
- Exhibits anticancer activities
- Functions as a click chemistry reagent
- Contains an Alkyne group for CuAAc reactions
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Medchemexpress LLC Prasugrel hydrochloride | 389574-19-0 | C20H21ClFNO3S | 500 MG
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Prasugrel hydrochloride (PCR 4099 hydrochloride) is a thienopyridine and a proagent that inhibits platelet function. It is an orally active and potent P2Y12 receptor antagonist, which works by inhibiting ADP-induced platelet aggregation. In rat platelets, the active metabolite of Prasugrel hydrochloride inhibits in vitro platelet aggregation induced by adenosine ADP (10μM) with an IC50 value of 1.8 μM.
- Exhibits faster and significantly more potent antiplatelet effects in vivo compared to Clopidogrel.
- Requires in vivo metabolic processing as an inactive prodrug to generate its active antiplatelet metabolite.
- Rapidly absorbed from the gut following oral administration.
- Achieves maximum plasma levels of active metabolite within 1 hour.
- Leads to effective, maximum inhibition of platelet aggregation within 1-2 hours.
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Medchemexpress LLC PRT062607 hydrochloride (P505-15 hydrochloride) | 1370261-97-4 | C19H24ClN9O | 1 ML
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PRT062607 Hydrochloride (P505-15 Hydrochloride) is an orally available Syk inhibitor with an IC50 of 1 nM. It inhibits inflammation and induces apoptosis, demonstrating potent antitumor activity in tumor xenograft mouse models. In vitro, it also exhibits significant activity against a variety of kinases, including Fgr, MLK1, Yes, Flt3, PAK5, Lyn, cSRC, Lck, Pyk, and FAK.
- Inhibits phosphorylation of ERK(Y204), AKT(S473), and SYK(Y352) in Ramos cells
- Inhibits BLNK Tyr84 phosphorylation
- Induces apoptosis in human whole blood
- Shows dose-dependent anti-inflammatory activity in rodent models of rheumatoid arthritis
- Inhibits B-cell activation
- Prevents tumor formation in mouse xenograft models
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Medchemexpress LLC Alosetron Hydrochloride | 122852-69-1 | 99.6% | C17H19ClN4O | 10 MM * 1 ML
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Alosetron Hydrochloride (GR 68755C) is a potent and highly selective serotonin 5-HT3 receptor antagonist, utilized for irritable bowel syndrome (IBS) research. It blocks 5-HT3-mediated depolarisation of guinea-pig myenteric and submucosal neurons (IC50 ~55 nM), attenuates visceral nociceptive effects, and demonstrates anti-inflammatory effects.
- Potent and highly selective serotonin 5-HT3 receptor antagonist.
- Used for research of irritable bowel syndrome.
- Blocks 5HT3-mediated depolarisation of neurons.
- Attenuates visceral nociceptive effects.
- Demonstrates anti-inflammatory effects.
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Medchemexpress LLC Alpelisib | 1217486-61-7 | C19H23ClF3N5O2S | 5 MG
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Alpelisib hydrochloride is a potent, orally active, and selective PI3Kα inhibitor with IC50s of 5 nM for p110α. It exhibits antineoplastic activity and potently inhibits Akt phosphorylation in cells transformed with PI3Kα.
- Potently inhibits PIK3CA somatic mutations (H1047R, E545K; IC50s~4 nM).
- Significantly reduces Akt phosphorylation in cells transformed with PI3Kα (IC50=74±15 nM).
- Inhibits cell growth of osteosarcoma cell lines.
- Induces G0/G1 phase cell cycle arrest in human and murine osteosarcoma cells.
- Reduces tumor volumes and deposition of ectopic bone matrix in animal models.
- Store powder at -20°C for 3 years or 4°C for 2 years.
- Store in solvent at -80°C for 2 years or -20°C for 1 year.
- Shipping can occur at room temperature if duration is less than 2 weeks.
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Medchemexpress LLC EPZ004777 hydrochloride | 1380316-03-9 | C28H42ClN7O4 | 25 MG
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EPZ004777 hydrochloride is an effective and selective DOT1L inhibitor with an IC50 of 0.4 nM. This compound reduces levels of H3K79me2 and H3K79me1, leading to a significant down-regulation of HOXA9 and MEIS1 expression. It selectively inhibits the proliferation of MLL rearrangement cells and promotes the differentiation and subsequent apoptosis of leukemia cells, making it suitable for leukemia research.
- Effective and selective DOT1L inhibitor
- Reduces H3K79me2 and H3K79me1 levels
- Down-regulates HOXA9 and MEIS1 expression
- Selectively inhibits MLL rearrangement cell proliferation
- Promotes differentiation and apoptosis of leukemia cells
- Potent DOT1L enzyme activity inhibition (IC50 of 400±100 pM)
- Demonstrates selectivity over other histone methyltransferases (HMTs)
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Medchemexpress LLC Dopexamine hydrochloride | 86484-91-5 | 429.42 | 5 MG
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Dopexamine hydrochloride is a β2 adrenergic receptor agonist and a dopamine analogue with agonist activity at β2 and dopaminergic receptors. It can attenuate systemic inflammatory response, reduce tissue leukocyte infiltration, and protect against organ injury at doses that do not alter global hemodynamics or regional microvascular flow. It also reduces the systemic inflammatory response to endotoxin, including cytokine release, endothelial adhesion molecules, and oxidative stress, without substantially changing systemic hemodynamics.
- β2 adrenergic receptor agonist
- Dopamine analogue with agonist activity at β2 and dopaminergic receptors
- Attenuates systemic inflammatory response
- Reduces tissue leukocyte infiltration
- Protects against organ injury
- Reduces systemic inflammatory response to endotoxin, including cytokine release, endothelial adhesion molecules, and oxidative stress
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