Alcohols and polyols
- (1)
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- (25)
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- (1)
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- (1)
- (463)
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- (10)
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- (1)
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- (13)
- (148)
- (114)
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- (1)
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- (1)
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- (1)
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- (20)
- (10)
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- (15)
- (1)
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- (1)
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- (1)
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- (1)
- (36)
- (5)
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- (2)
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- (17)
- (14)
- (4)
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- (1)
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- (1)
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- (37)
- (4)
- (2)
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- (8)
- (2)
- (2)
- (9)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (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)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
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- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (1)
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- (1)
- (2)
- (9)
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- (12)
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- (1)
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- (1)
- (1)
- (1)
- (1)
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- (60)
- (5)
- (2)
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- (1)
- (30)
- (2)
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- (11)
- (81)
- (12)
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- (81)
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- (378)
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- (28)
- (2)
- (25)
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- (48)
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- (418)
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Medchemexpress LLC Embramine hydrochloride | 13977-28-1 | 384.74 | 10 MG
Small and Specialty Supplier Partner
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Embramine hydrochloride is a monoethanolamine used as an antihistamine and anticholinergic, with antihistamine and anticholinergic properties.
- Used as an antihistamine and anticholinergic
- Molecular weight: 384.74
- Formula: C18H23BrClNO
- Data sheet and handling instructions available
- For research use only; not for sale to patients
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC NNMT-IN-6 hydrochloride | 3031756-18-7 | 98.2% | 544.00 g/mol | C25H30ClN7O5 | 5 MG
Small and Specialty Supplier Partner
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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NNMT-IN-6 hydrochloride is a research-grade small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT). Supplied as the hydrochloride salt for improved solubility and handling, it has reported biochemical potency (IC50 = 1.41 μM; Kd = 5.6 μM). Molecular formula C25H30ClN7O5, molecular weight 544.00, with a COA-reported purity of 98.21%.
- Potent NNMT inhibitor with reported IC50 = 1.41 μM and Kd = 5.6 μM.
- Supplied as a hydrochloride salt for improved solubility.
- High chemical purity appropriate for biochemical and cellular assays.
- Small-molecule format compatible with standard assay workflows.
- Available in multiple package sizes to support screening and follow-up studies.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Ravidasvir (hydrochloride) | 1303533-81-4 | 99.9% | 835.82 g/mol | C42H52Cl2N8O6 | 10MM 1ML
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Ravidasvir hydrochloride is a pan-genotypic hepatitis C virus (HCV) NS5A inhibitor supplied for research use. It is provided as a ready-to-use 10 mM solution in DMSO (1 mL) and is intended for in vitro antiviral assays, medicinal chemistry, and analytical studies. The material is characterized by high purity and is supported by analytical documentation to aid reproducibility and assay development.
- Pan-genotypic HCV NS5A inhibitor for antiviral research.
- Provided as a 10 mM solution in DMSO, 1 mL vial.
- High purity suitable for biological and analytical assays.
- Characterized by supporting analytical documentation such as SDS and COA.
- Molecular weight 835.82 g/mol; chemical formula C42H52Cl2N8O6.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Sultopride hydrochloride | 23694-17-9 | 99.9% | 390.93 | 25 MG
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Sultopride hydrochloride is a selective antagonist of the dopamine D2 receptor.
- Selective antagonist of dopamine D2 receptor.
- Has shown higher levels of DOPAC and HVA in the striatum and nucleus accumbens in rats compared to sulpiride-treated rats.
- Available for research use only.
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Medchemexpress LLC Betaxolol hydrochloride | 63659-19-8 | 98.1% | 10 MM * 1 ML
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Betaxolol hydrochloride is a selective beta1 adrenergic receptor blocker that can be used for the research of hypertension and glaucoma. It is a cardioselective beta-adrenergic receptor blocking agent.
- Functions as a selective beta1 adrenergic receptor blocker
- Cardioselective beta-adrenergic receptor blocking agent
- Applicable for research in hypertension
- Applicable for research in glaucoma
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Medchemexpress LLC Dyclonine hydrochloride | 536-43-6 | 99.3% | 10 G
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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
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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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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.
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Medchemexpress LLC Olcegepant hydrochloride | 586368-06-1 | MFCD30738010 | 99.3% | 906.11 g/mol | C38H47Br2N9O5.HCl | 100 MG
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Olcegepant hydrochloride is a selective non-peptide antagonist of the calcitonin gene-related peptide 1 (CGRP1) receptor used in neuroscience and pharmacology research. Supplied as a stable solid with high reported purity, it is employed in assays to investigate CGRP signaling, receptor pharmacology, and migraine-related mechanisms.
- Selective CGRP1 receptor antagonist suitable for receptor studies.
- High purity appropriate for research applications.
- Suitable for in vitro and in vivo pharmacology studies.
- Available in multiple pack sizes for experimental flexibility.
- Provided as a stable solid powder for convenient storage and handling.
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Medchemexpress LLC Deterenol hydrochloride | 23239-36-3 | 99.7% | 231.72 g/mol | C11H18ClNO2 | 5 MG
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Deterenol hydrochloride is a selective β-adrenergic receptor agonist supplied for research use. It is reported to cause vasodepressor effects, anxiety, increased heart rate, hypotension, palpitations, and respiratory distress; handle with appropriate laboratory safety practices.
- Selective β-adrenergic agonist for pharmacology research.
- Reported physiological effects include vasodepression, tachycardia, hypotension, and anxiety.
- High stated purity: 99.7%.
- Off-white to light yellow solid suitable for small-scale assays.
- Typically supplied in milligram quantities and stored sealed at -20°C.
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ALADDIN SCIENTIFIC CORPORATION Ninhydrin, 5g
Used in the detection and assay of peptides amino acids amines and amino sugars yielding highly fluorescent ternary compounds with aldehydes and primary amines Reaction with sarcosine or proline gives azomethine ylides Application It can be used for the detection of peptides amino acids amino acids and amino sugars and can produce strong fluorescent ternary compounds with aldehydes and primary amines Reacts with sarcosine or proline to form methylimine Ylide Ninhydrin (ninhydrin hydrate) can be used as a reagent for the determination of amino acids and peptides by photometry and colorimetry It can also be used to prepare ninhydrin reagents by mixing ninhydrin with hydroninhydrin (reduced form of ninhydrin) in dimethyl sulfoxide This reagent can be used for the manual ninhydrin method to quantify amino acids It can be used to detect free amino groups in amino acids peptides and proteins
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Medchemexpress LLC Taltobulin hydrochloride | 228266-40-8 | 99.3% | 510.11 Da | C27H44ClN3O4 | 100 MG
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Taltobulin hydrochloride is a synthetic analogue of the tripeptide hemiasterlin and a potent antimicrotubule agent. It inhibits tubulin polymerization, disrupts microtubule organization, and induces mitotic arrest, and is supplied as a solid research reagent for in vitro and in vivo studies.
- Potent tubulin inhibitor with low-nanomolar activity in tumor cell lines.
- High purity suitable for research applications.
- Supplied as a solid powder for solution preparation in DMSO or aqueous buffers.
- Recommended solvent and formulation guidance provided for in vitro and in vivo use.
- Store sealed at 4°C; solutions stable at -80°C for long-term storage.
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Medchemexpress LLC Urea, N'-cyclohexyl-N-(phenylmethyl)-N-(4-piperidinylmethyl) hydrochloride | 2070014-88-7 | MFCD30377213 | 99.6% | 365.94 | C20H32ClN3O | 100 MG
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SRI-011381 hydrochloride is a research compound that functions as an orally active agonist of TGF-β/Smad signaling and has demonstrated neuroprotective effects in preclinical studies. It is supplied as a white to off-white solid and is characterized for both in vitro and in vivo research use.
- Orally active TGF-β signaling agonist with reported neuroprotective effects.
- High purity (~99.6%) suitable for research applications.
- White to off-white solid with validated physicochemical data.
- Soluble in DMSO and water; multiple in vivo formulation protocols available.
- Supplied in multiple sizes for dosing flexibility, including 100 mg.
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Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | MFCD01749474 | ≥98.0% | 286.72 g·mol⁻¹ | C14H11ClN4O | 5 MG
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Olprinone hydrochloride is a research-grade phosphodiesterase 3 (PDE3) inhibitor provided as an analytical standard for pharmacological and biochemical studies, commonly used in investigations of cardiac inotropy and vasodilation. The material is characterized for laboratory use and supplied in small pack sizes for precise dosing in experimental workflows.
- Research-grade analytical standard suitable for assay development and characterization.
- Selective phosphodiesterase 3 (PDE3) inhibitory activity relevant to cardiac function studies.
- Provided in small pack sizes for precise dosing and handling in the laboratory.
- Molecular formula C14H11ClN4O and molecular weight 286.72 g·mol⁻¹ for reproducible calculations.
- Available with high purity specifications to support reliable experimental results.
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Medchemexpress LLC 2-pyridinecarbonitrile, 5-[(4'-amino-5',8'-difluoro-spiroquinazoline)carbonyl] hydrochloride | 1781934-50-6 | 99.8% | 100 MG
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This hydrochloride salt is a potent, selective inducible nitric oxide synthase (iNOS) inhibitor with reported IC50 = 37 nM. Supplied as a high-purity research reagent suitable for in vitro and in vivo studies of iNOS-mediated pathways and inflammatory responses.
- High purity 99.8% as reported by manufacturer.
- Molecular weight 418.83.
- Chemical formula C19H17ClF2N6O.
- Hydrochloride salt form for improved solubility.
- Potent, selective iNOS inhibition (IC50 = 37 nM).
- Suitable for pharmacology and inflammation research applications.
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Medchemexpress LLC N4-(4-(2-bromo-4,5-difluorophenoxy)phenyl)-L-asparagine hydrochloride | 2450268-84-3 | MFCD28405312 | 99.8% | 451.65 g/mol | C16H14BrClF2N2O4 | 1 ML
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WAY-213613 hydrochloride is a potent, selective inhibitor of the human excitatory amino acid transporter 2 (EAAT2) used in central nervous system research. It inhibits EAAT2 with an IC50 of approximately 85 nM and is provided as a ready-to-use solution for pharmacological studies.
- Potent EAAT2 inhibition (IC50 = 85 nM).
- Selectivity over EAAT1 and EAAT3.
- Supplied as a 10 mM solution in DMSO (1 mL).
- High purity (≈99.8%).
- Suitable for central nervous system research and transporter pharmacology.
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