Aminophenols
Cell Signaling Technology 5-Carboxylcytosine (5-caC) (D7S8U) Rabbit mAb 20 ul
5-Carboxylcytosine (5-caC) (D7S8U) Rabbit mAb 20 ul
Medchemexpress LLC SBI-810 hydrochloride | 2772746-58-2 | 99.6% | 483.05 | C27H35ClN4O2 | 10 MG
SBI-810 hydrochloride is a β-arrestin-biased allosteric modulator of the neurotensin receptor 1 (NTSR1) supplied as the hydrochloride salt for research use. Provided as a solid with high analytical purity, it is intended for in vitro pharmacology and preclinical signaling or analgesia studies.
- β-arrestin-biased NTSR1 allosteric modulator for receptor signaling studies.
- High purity; typically ≥99.5% by supplier assay.
- Molecular weight 483.05; formula C27H35ClN4O2.
- Available in small-mass pack sizes suitable for in vitro and preclinical work.
- Option for 10 mM solution in DMSO, ready for reconstitution.
- Store sealed at 4°C; in solution store at -80°C for long-term storage.
Medchemexpress LLC Imiloxan hydrochloride | 81167-22-8 | 98.5% | 280.75 | C14H17ClN2O2 | 10 MG
Imiloxan hydrochloride is a potent, selective α2B-adrenoceptor antagonist used in pharmacology research to probe adrenergic receptor subtype function. It is used in both in vitro receptor assays and in vivo models to study antagonist activity and physiological responses such as mydriasis reversal.
- Selective α2B-adrenoceptor antagonist.
- High purity suitable for research use.
- Molecular weight 280.75 g·mol⁻¹.
- Available in small, precise research quantities.
- Applicable to in vitro assays and in vivo pharmacology models.
Medchemexpress LLC Axc-715 hydrochloride | 2490497-93-1 | 99.5% | 347.89 g/mol | C18H26ClN5 | 5 MG
AXC-715 hydrochloride is the hydrochloride salt of a small-molecule TLR7/TLR8 dual agonist used in preclinical research as an immunostimulant and as a building block for antibody-adjuvant immunoconjugates. It is supplied as a high-purity solid suitable for in vitro and in vivo studies, with recommended storage conditions to maintain stability.
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 9mg 564356418 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 9mg 564356418 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC R 59-022 (hydrochloride) | 93076-98-3 | MFCD34676749 | 98.9% | 496.04 g·mol⁻¹ | C27H27ClFN3OS | 50 MG
R 59-022 hydrochloride is the hydrochloride salt of R 59-022, a research compound that acts as a diacylglycerol kinase (DGK) inhibitor (reported IC50 ≈ 2.8 μM). It is used in cellular and biochemical assays to modulate diacylglycerol/protein kinase C signaling and to probe 5-HT receptor-related pathways. The material is supplied as an off-white solid (CAS 93076-98-3) with formula C27H27ClFN3OS and molecular weight 496.04 g·mol⁻¹.
- DGK inhibitor with reported IC50 ≈ 2.8 μM.
- Modulates protein kinase C and diacylglycerol signaling in cells.
- Hydrochloride salt form for improved handling and solubility in polar solvents.
- High purity suitable for research applications.
- Soluble in DMSO for preparation of stock solutions.
Medchemexpress LLC HJC0416 hydrochloride | 2415263-08-8 | 98.7% | 429.32 g/mol | C18H18Cl2N2O4S | 10MM 1ML
HJC0416 hydrochloride is a small-molecule inhibitor of STAT3 supplied for laboratory research. It is provided as a 10 mM solution in DMSO (1 mL) and in solid forms, and is reported with CAS 2415263-08-8, molecular weight 429.32 g/mol, formula C18H18Cl2N2O4S, and purity 98.7%.
- Small-molecule STAT3 inhibitor for cellular assays.
- Provided as 10 mM solution in DMSO (1 mL) and as solids (5 mg, 10 mg, 25 mg, 50 mg).
- High reported purity (98.7%).
- Characterized by CAS 2415263-08-8 and MW 429.32 g/mol.
- Intended for in vitro research applications targeting STAT3 signaling.
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 25mg 564356421 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 25mg 564356421 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC Ly266097 hydrochloride | 172895-39-5 | 99.6% | 407.33 g/mol | C21H24Cl2N2O2 | 5 MG
LY266097 hydrochloride is a research-grade selective 5-HT2B receptor antagonist supplied as the hydrochloride salt. It is a high-purity solid used in pharmacology and neuropharmacology studies to probe serotonin 5-HT2 receptor signaling and related behavioral and biochemical effects.
- Selective 5-HT2B antagonist with high affinity.
- High purity suitable for biochemical and cellular assays.
- Supplied as a stable solid for controlled storage.
- Well-characterized identifiers: CAS 172895-39-5; molecular weight 407.33 g/mol.
- Storage conditions compatible with long-term sample integrity.
Medchemexpress LLC Cgp71683 hydrochloride | 192322-50-2 | MFCD07783999 | ≥98.0% | 512.07 | C26H30ClN5O2S | 25 MG
CGP71683 hydrochloride is the hydrochloride salt of a selective, non-peptide antagonist of the neuropeptide Y (NPY) Y5 receptor, supplied for research use in receptor pharmacology and neuroscience studies. It is typically used in cellular assays and biochemical experiments to investigate Y5-mediated signaling pathways.
- Hydrochloride salt form improves solubility for assay preparation.
- High purity (>98% by HPLC) suitable for research applications.
- Potent Y5 receptor antagonism useful for pharmacological profiling.
- Offered in small lab-scale pack sizes for screening and method development.
- Characterized by CAS number 192322-50-2 and molecular formula C26H30ClN5O2S.
Medchemexpress LLC HY-117288 10mg Medchemexpress, S55746 CAS:1448584-12-0 Purity:>98%
Medchemexpress, HY-117288 10mg S55746 CAS:1448584-12-0 S55746 (BLC201) is a potent, orally active and selective BCL-2 inhibitor, with a Ki of 1.3 nM and a Kd of 3.9 nM. S55746 (BLC201) has antitumor activity with low toxicity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC AFM-30a (hydrochloride) | 99.8% | 502.97 | 25 MG
AFM-30a hydrochloride is a potent and selective protein arginine deiminase 2 (PAD2) inhibitor. It binds to PAD2 with an EC50 value of 9.5 μM and inhibits H3 citrullination with an EC50 value of 0.4 μM. It can be used for the research of certain cancers and various autoimmune diseases, including rheumatoid arthritis (RA), multiple sclerosis, lupus, and ulcerative colitis.
- Potent protein arginine deiminase 2 (PAD2) inhibitor
- Excellent PAD2-selectivity
- Inhibits H3 citrullination
- Low cytotoxicity for cells
- Suppresses NLRP3 signaling and decreases airway remodeling in PAD2-/-transgenic mice
- For research use only
Medchemexpress LLC CC-115 (hydrochloride) | 1300118-55-1 | 98.0% | 372.81 | 25 MG
CC-115 hydrochloride is a potent dual inhibitor of DNA-PK and mTOR kinase. It effectively blocks both mTORC1 and mTORC2 signaling pathways, with IC50 values of 13 nM and 21 nM respectively. This product is intended for research use only.
- Potent and dual DNA-PK and mTOR kinase inhibitor
- Blocks both mTORC1 and mTORC2 signaling
- Exhibits good in vivo PK profiles across multiple species
- Demonstrates significant tumor volume reductions in tested models
- Sustains inhibition for prolonged periods
- Available in various sizes, including solid and pre-made solutions
Medchemexpress LLC 1-myristoyl-sn-glycero-3-phosphatidylcholine-d7 | 95.4% | 474.62 | 1 MG
LysoPC(14:0/0:0)-d7 is a deuterium labeled lysophospholipid (LyP). It is a monoglycerophospholipid where a phosphorylcholine moiety occupies a glycerol substitution site. This product exhibits a potent antispasmodic effect and is for research use only.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Medchemexpress LLC Zymostenol-d7 | 2260669-19-8 | 99.9% | 393.70 | 1 MG
Zymostenol-d7 is deuterium labeled 5a-Cholest-8-en-3b-ol.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Deuterium substitution has the potential to affect the pharmacokinetic and metabolic profiles of drugs.