Phenols
Medchemexpress LLC Pirmenol hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g·mol⁻¹ | C22H31ClN2O | 100 MG
Pirmenol hydrochloride is an orally active antiarrhythmic research compound used in pharmacology and electrophysiology studies. It inhibits IK.ACh currents by blocking muscarinic acetylcholine receptors and is provided as a high-purity solid for laboratory research use.
- Orally active compound suitable for cellular and in vivo studies.
- Reported to inhibit IK.ACh with IC50 ≈ 0.1 μM.
- High purity solid for reproducible experimental results.
- Available in small-quantity packages appropriate for research workflows.
- Intended for laboratory research; not for human or diagnostic use.
eMolecules 38196-08-6 | (3-Amino-4-hydroxyphenyl)acetic acid | Apollo Scientific | MFCD04125028 | 167.164 | C8H9NO3 | 95.000 | Nc1cc(CC(O)=O)ccc1O | 250mg | 562446559
(3-Amino-4-hydroxyphenyl)acetic acid | Apollo Scientific | 38196-08-6 | MFCD04125028 | 167.164 | C8H9NO3 | 95.000 | Nc1cc(CC(O)=O)ccc1O | 250mg | 562446559
Apexbio Technology LLC ZM 39923 HCl 1021868-92-7 10mM (in 1mL DMSO)
ZM 39923 HCl (CAS 1021868-92-7) is a small molecule that selectively inhibits Janus kinases JAK1 and JAK3 displaying pIC50 values of 4 4 and 7 1 respectively As JAK family kinases play a pivotal role in cytokine-mediated signaling via the JAK-STAT pathway ZM 39923 HCl is frequently employed to investigate signal transduction mechanisms linked to hematological malignancies autoimmune conditions and inflammatory disorders The compound also inhibits tissue transglutaminase 2 (TGM2) with an IC50 of 10 nM and exhibits equivalent inhibition of EGFR In cellular studies ZM 39923 HCl modulates T cell proliferation and apoptosis and affects pathways involving VEGF and TGF 2 underscoring its utility in cytokine oncology and cell biology research
Medchemexpress LLC Tropisetron Hydrochloride | 105826-92-4 | 99.97% | C17H21ClN2O2 | 1 ML
Tropisetron Hydrochloride is an effective neuroprotective agent that acts as a 5-HT3 receptor antagonist, a calmodulin inhibitor, and an α7-nAChR receptor agonist, with an IC50 of 70.1 nM for the 5-HT3 receptor. It possesses anti-inflammatory properties and immune-regulating functions, effectively alleviating symptoms associated with chemotherapy and post-surgery. It also reduces Ab-induced hippocampal neuroinflammation.
- Neuroprotective agent
- 5-HT3 receptor antagonist
- Calmodulin inhibitor
- Α7-nAChR receptor agonist
- Anti-inflammatory properties
- Immune-regulating functions
- Alleviates symptoms associated with chemotherapy and post-surgery
- Reduces Ab-induced hippocampal neuroinflammation
![eMolecules 13682-77-4 | Potassium trifluoro(vinyl)borate | Advanced ChemBlocks | MFCD02093335 | 133.950 | C2H3BF3K | 97.000 | [K+].F[B-](F)(F)C=C | 25g | 728125555](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000164753.jpg-250.jpg)
eMolecules 13682-77-4 | Potassium trifluoro(vinyl)borate | Advanced ChemBlocks | MFCD02093335 | 133.950 | C2H3BF3K | 97.000 | [K+].F[B-](F)(F)C=C | 25g | 728125555
Potassium trifluoro(vinyl)borate | Advanced ChemBlocks | 13682-77-4 | MFCD02093335 | 133.950 | C2H3BF3K | 97.000 | [K+].F[B-](F)(F)C=C | 25g | 728125555
Medchemexpress LLC Zzw-115 hydrochloride | 10122-45-9 | 98.1 % | 573.97 | 5 MG
ZZW-115 hydrochloride is a potent NUPR1 inhibitor with a Kd of 2.1 μM. It induces tumor cell death through necroptosis and apoptosis, demonstrating anticancer activity. It is efficient in killing various cancer cells with IC50 values ranging from 0.42 μM to 4.93 μM. This compound also induces a decrease in ATP production and a ROS overproduction.
- Efficient in killing cancer cells with IC50 values ranging from 0.42 μM to 7.75 μM
- Induces tumor cell death via necroptosis and apoptosis
- Decreases ATP production and induces ROS overproduction
- Inhibits the growth of pancreatic xenografted tumors in vivo
- Demonstrates potent anticancer activity
Medchemexpress LLC Valecobulin hydrochloride | 1240321-53-2 | MFCD19311027 | 98.5% | 573.06 | 50 MG
Valecobulin hydrochloride (CKD-516 hydrochloride) is a valine proagent of S516 (HY-130233) and a vascular disrupting agent (VDA). It is a potent β-tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors.
- Valine proagent of S516
- Vascular disrupting agent (VDA)
- Potent β-tubulin polymerization inhibitor
- Marked antitumor activity against murine and human solid tumors
eMolecules 1118-68-9 | N-Me-Sar-OH | Ambeed | MFCD00004283 | 103.121 | C4H9NO2 | 98.000 | CN(C)CC(O)=O | 25g | 490553174
N-Me-Sar-OH | Ambeed | 1118-68-9 | MFCD00004283 | 103.121 | C4H9NO2 | 98.000 | CN(C)CC(O)=O | 25g | 490553174
Medchemexpress LLC 1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanamine | 253168-94-4 | 99.96% | 273.35 | 1 KG
1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanamine is a drug intermediate for the synthesis of various active compounds. It is for research use only.
- Purity: 99.96%
- Molecular weight: 273.35
- Formula: C12H19NO4S
- Cas no.: 253168-94-4
- Appearance: Solid
Medchemexpress LLC Capsaicin β-D-glucopyranoside | 153409-16-6 | C24H37NO8 | 1 MG
Capsaicin β-D-glucopyranoside is a glucoside converted by Capsaicin, the active ingredient of chili peppers responsible for their pungent flavor. This product is suitable for various research applications.
- Molecular weight: 467.55
- Appearance: Solid
- Color: White to off-white
- In vitro solubility: 100 mg/mL in DMSO (requires ultrasonication)
- Storage at -20°C, sealed, away from moisture and light
- In solvent storage at -80°C for 6 months or -20°C for 1 month
Medchemexpress LLC Guadecitabine sodium | 929904-85-8 | C18H23N9NaO10P | 1 MG
Guadecitabine sodium is a second-generation DNA methyltransferases (DNMT) inhibitor. It is utilized in research for acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS).
- Second-generation DNA methyltransferase (DNMT) inhibitor
- Inhibits DNA methylation
- Induces p16 expression
- Effective in reducing DNA methylation and retarding tumor growth
- Better tolerated than 5-Aza-CdR in vivo
eMolecules 1937210-90-6 | Ambeed | 2-Chloro-9-phenyl-110-phenanthroline | 1g | 660580711 | A1364363 | 290.75 | C18H11ClN2
Ambeed | 2-Carboxyquinoline 1-oxide | 250mg | 665578651 | A1503231 | 3297-64-1 | 189.170 | C10H7NO3
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