Alcohols and polyols
4-Chloro-1-butanol, tech. 85%
CAS: 928-51-8 Molecular Formula: C4H9ClO Molecular Weight (g/mol): 108.57 MDL Number: MFCD00002967 InChI Key: HXHGULXINZUGJX-UHFFFAOYSA-N Synonym: 4-chloro-1-butanol,4-chlorobutanol,1-butanol, 4-chloro,tetramethylene chlorohydrin,4-chloro-1-butane-ol,4-chlorbutan-1-ol,unii-42ei3i5ay0,4-chlorbutan-1-ol german,ccris 7507,4-chloro-butan-1-ol PubChem CID: 13569 ChEBI: CHEBI:87310 IUPAC Name: 4-chlorobutan-1-ol SMILES: OCCCCCl
1,2,3-Butanetriol 90.0+%, TCI America™
CAS: 4435-50-1 Molecular Formula: C4H10O3 Molecular Weight (g/mol): 106.121 MDL Number: MFCD00059662 InChI Key: YAXKTBLXMTYWDQ-UHFFFAOYSA-N Synonym: 1,2,3-Trihydroxybutane PubChem CID: 20497 IUPAC Name: butane-1,2,3-triol SMILES: CC(C(CO)O)O
cis-1,2-Cyclohexanedimethanol 97.0+%, TCI America™
CAS: 15753-50-1 Molecular Formula: C8H16O2 Molecular Weight (g/mol): 144.21 MDL Number: MFCD00062987,MFCD16660860,MFCD22572336,MFCD19300921,MFCD22572336,MFCD09260493 InChI Key: XDODWINGEHBYRT-UHFFFAOYNA-N Synonym: cis-1,2-Bis(hydroxymethyl)cyclohexane PubChem CID: 2724019 IUPAC Name: [2-(hydroxymethyl)cyclohexyl]methanol SMILES: OCC1CCCCC1CO
1-(p-Tolyl)ethanol 97.0+%, TCI America™
CAS: 536-50-5 Molecular Formula: C9H12O Molecular Weight (g/mol): 136.194 MDL Number: MFCD00016860 InChI Key: JESIHYIJKKUWIS-UHFFFAOYSA-N Synonym: 1-4-methylphenyl ethanol,1-p-tolyl ethanol,bilagen,galinex,norbilan,tomobil,methyl-p-tolylcarbinol,p-tolylmethylcarbinol,1-4-tolyl ethanol,1-p-tolyl-1-ethanol PubChem CID: 10817 IUPAC Name: 1-(4-methylphenyl)ethanol SMILES: CC1=CC=C(C=C1)C(C)O
Medchemexpress LLC Proanthocyanidins | 20347-71-1 | 50 MG
Proanthocyanidin (Procyanidin) is a class of polyphenolic compounds widely distributed in higher plants, consisting of an electrophilic flavanyl unit. It can be used as an antioxidant and anti-cancer agent. Additionally, Proanthocyanidin exhibits anti-inflammatory, cardioprotective, antibacterial, and antifungal properties, making it useful in treating chronic venous insufficiency, capillary fragility, sunburn, and retinopathy.
- Antioxidant
- Anti-cancer agent
- Anti-inflammatory
- Cardioprotective
- Antibacterial
- Antifungal properties
- Can inhibit P-fimbriated *E. coli* from adhering to uroepithelial cells
- Shows strong antimutagenic effects
- Inhibits rat pancreatic carcinogenesis in the initiation stage
Medchemexpress LLC JH295 50mg | 1311143-71-1 | 50 MG
JH295 is an irreversible, cysteine-targeted inhibitor of NIMA-related kinase 2 (Nek2) used for biochemical and cellular studies. It irreversibly alkylates Cys22, shows an IC50 of approximately 770 nM, and contains an alkyne functional group suitable for copper-catalyzed azide-alkyne cycloaddition (click chemistry).
- Irreversible Nek2 inhibitor; IC50 ≈ 770 nM.
- Cysteine-targeted covalent mechanism (alkylation of Cys22).
- Contains an alkyne handle for click chemistry applications.
- Molecular weight 320.35; formula C18H16N4O2.
- High reported purity (98.66%).
- Solid, yellow to orange appearance.
Medchemexpress LLC Alfuzosin hydrochloride | 81403-68-1 | 99.7% | 50 MG
Alfuzosin hydrochloride is an orally active, selective and competitive α1-adrenoceptor antagonist. It relaxes the muscles of the prostate and bladder neck, aiding in urination. This compound can be used in the study of benign prostatic hyperplasia (BPH).
- Orally active
- Selective and competitive α1-adrenoceptor antagonist
- Relaxes the muscles of the prostate and bladder neck
- Aids in urination
- Can be used in the study of benign prostatic hyperplasia (BPH)
Medchemexpress LLC Imidapril (hydrochloride) | 89396-94-1 | 99.9% | 50 MG
Imidapril hydrochloride (TA-6366) is an orally active angiotensin-converting enzyme (ACE) and MMP-9 inhibitor. It suppresses the conversion of angiotensin I to angiotensin II, reducing total peripheral resistance and systemic blood pressure. It is used for research related to hypertension, type 1 diabetic nephropathy, and chronic heart failure.
- Orally active ACE inhibitor
- MMP-9 inhibitor
- Suppresses angiotensin I to angiotensin II conversion
- Reduces total peripheral resistance
- Reduces systemic blood pressure
- Used for hypertension research
- Used for type 1 diabetic nephropathy research
- Used for chronic heart failure research
Medchemexpress LLC Embramine hydrochloride | 13977-28-1 | 384.74 | 50 MG
Embramine hydrochloride is a monoethanolamine used as an antihistamine and anticholinergic.
- Antihistamine
- Anticholinergic
- For research use only
- Related to Histamine receptor research
Medchemexpress LLC Pholedrine (hydrochloride) | 877-86-1 | 99.6% | 50 MG
Pholedrine hydrochloride is the hydrochloride salt of pholedrine, a sympathomimetic amine that acts on adrenergic receptors and is used in cardiovascular and receptor signaling research. It is supplied for laboratory research use with accompanying safety documentation and a certificate of analysis.
- Hydrochloride salt form for improved stability and solubility.
- High purity: 99.6% (LCMS, per COA).
- Molecular formula C10H16ClNO; molecular weight 201.69 g/mol.
- Used in adrenergic receptor and cardiovascular pharmacology studies.
- Available as a 50 MG research pack.
Medchemexpress LLC (+)-1-(1-Naphthyl)ethylamine | 3886-70-2 | 99.99% | C12H13N | 50 G
(+)-1-(1-Naphthyl)ethylamine ((+)-1-(1-NEA)) is a chiral modifier utilized to introduce enantioselectivity in catalytic hydrogenation reactions. This compound, 1-NEA, can undergo H-D exchange with D2 in solution to form N-D bonds. This indicates that 1-NEA has the capability to complete Pt surface adsorption and protonation through amine N atoms, thereby potentially imparting enantioselectivity to Pt hydrogenation catalysts.
- Utilized to introduce enantioselectivity in catalytic hydrogenation reactions.
- Can undergo H-D exchange with D2 in solution to form N-D bonds.
- Capable of completing Pt surface adsorption and protonation through amine N atoms.
- Potentially imparts enantioselectivity to Pt hydrogenation catalysts.
Medchemexpress LLC Voreloxin Hydrochloride | 175519-16-1 | 99.58% | 437.90 | 50 MG
Voreloxin Hydrochloride is a first-in-class topoisomerase II inhibitor that intercalates DNA and induces site-selective DNA DSB, G2 arrest, and apoptosis.
- Inhibits topoisomerase II activity.
- Induces site-selective DNA DSB.
- Causes G2 arrest.
- Leads to apoptosis.
- Shows potent cytotoxic activity in AML cell lines.
- Exhibits additive or synergistic activity with cytarabine in acute leukemia cell lines.
- Reduces bone marrow cellularity in mice.
- Causes reversible decrease in myeloid and lymphoid cells in vivo.
Medchemexpress LLC Alosetron Hydrochloride | 122852-69-1 | 99.63% | C17H19ClN4O | 50 MG
Alosetron Hydrochloride is a potent and highly selective antagonist of the serotonin 5-HT3 receptor. It is researched for its application in irritable bowel syndrome (IBS). The compound effectively blocks the rapid 5HT3-mediated depolarization in guinea-pig myenteric and submucosal neurons, with an IC50 of approximately 55 nM. It also demonstrates an ability to lessen the visceral nociceptive effects of rectal distension in conscious or anesthetized dogs, and exhibits anti-inflammatory properties.
- Highly selective antagonist of the serotonin 5-HT3 receptor.
- Under investigation for irritable bowel syndrome.
- Blocks 5HT3-mediated depolarization.
- Attenuates visceral nociceptive effects.
- Exhibits anti-inflammatory effects.
Medchemexpress LLC BI-0115 | 4929-23-1 | 99.7% | 287.74 | 50 MG
BI-0115 is a selective inhibitor of LOX-1 (IC50=5.4 μM) that blocks cellular uptake of oxLDL. BI-0115 binding triggers receptor inhibition by formation of dimers of the homodimeric ligand binding domain.
- Selective inhibitor of LOX-1 (IC50=5.4 μM)
- Blocks cellular uptake of oxLDL
Medchemexpress LLC Bobcat339 hydrochloride | 2436747-44-1 | 99.6% | 334.20 | 50 MG
Bobcat339 hydrochloride is a potent and selective cytosine-based inhibitor of the TET enzyme, with IC50s of 33 μM and 73 μM for TET1 and TET2, respectively. It is useful in epigenetics and serves as a starting point for new therapeutics targeting DNA methylation and gene transcription.
- Potent and selective cytosine-based inhibitor of TET enzyme.
- Useful in epigenetics.
- Serves as a starting point for new therapeutics that target DNA methylation and gene transcription.