Fatty alcohol esters
Medchemexpress LLC Abiraterone acetate | 154229-18-2 | MFCD00934213 | 99.9% | 10 MG
Abiraterone acetate analytical standard is the acetate ester prodrug of abiraterone, used as a reference compound in research and analytical assays targeting CYP17A1 activity. It is provided as a highly pure material suitable for identity confirmation, method development, and quantitative analysis.
- intended for research and analytical applications.
- validated identity with CAS 154229-18-2.
- molecular formula C26H33NO2 and molecular weight 391.55.
- high purity suitable for use as a reference standard.
- compatible with chromatography and assay development workflows.
Medchemexpress LLC 4-(3-(2H-1,2,3-triazol-2-yl)phenylamino)-2-(2-aminocyclohexylamino)pyrimidine-5-carboxamide acetate | 1370261-98-5 | MFCD23105961 | 99.8% | 453.50 | C21H27N9O3 | 10 MG
PRT062607 acetate is a research-grade small-molecule inhibitor of spleen tyrosine kinase (Syk), provided as a high-purity solid or as DMSO solutions for laboratory use. It is used in cellular and animal studies to probe Syk-mediated signaling, inflammation, and apoptosis pathways, and is supplied with analytical data to support research applications.
- Potent and selective Syk inhibition (IC50 ≈ 1 nM).
- High analytical purity (99.83%).
- Available as solid powder and 10 mM DMSO solutions for flexibility.
- Suitable for in vitro and in vivo preclinical studies.
- Supplied with supporting analytical documentation (COA/SDS).
Medchemexpress LLC Roxatidine Acetate Hydrochloride | 93793-83-0 | 99.6% | 1 ML
Roxatidine Acetate Hydrochloride is a potent, selective, competitive, and orally active histamine H2-receptor antagonist. It has antisecretory potency against gastric acid secretion and can suppress inflammatory responses. This product can be used for gastric and duodenal ulcers research and exhibits antitumor activity.
- Potent, selective, competitive, and orally active histamine H2-receptor antagonist
- Exhibits antisecretory potency against gastric acid secretion
- Can suppress inflammatory responses
- Suitable for gastric and duodenal ulcers research
- Shows antitumor activity
Medchemexpress LLC Resomelagon acetate | 1809420-72-1 | 99.75% | 358.35 | 1 ML
Resomelagon acetate is a potent, orally active melanocortin receptor (MR) agonist targeting MC1 and MC3, suitable for research on obesity and chronic inflammation.
TARGETMOL CHEMICALS INC Ursolic acid acetate 5MG
Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Ursolic acid acetate (Acetylursolic acid) has cytotoxic activity, antimalarial activity, antitumor and anticancer activities. Acetylursolic acid has NO production inhibitory activities. Acetylursolic acid has inhibition against both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes. Purity 98.3%
Medchemexpress LLC (E, E)-Farnesyl bromide | 28290-41-7 | MFCD00054465 | 95% | 285.26 | 100 MG
Trans,trans-Farnesyl bromide was used in the preparation of S-trans, trans-farnesyl-L-cysteine methylester, a post translational modified amino acid. It is also a starting reagent for the synthesis of (±)-farnesiferol A and (±)-farnesiferol C prenylated peptides.
- Preparation of S-trans, trans-farnesyl-L-cysteine methylester
- Starting reagent for the synthesis of (±)-farnesiferol A and (±)-farnesiferol C prenylated peptides
Medchemexpress LLC RI-AG03 acetate | 98.2% | 2477.93 | 1 MG
RI-AG03 acetate is the acetate of RI-AG03 (HY-P10861), an orally active and BBB-penetrable Tau aggregation peptide inhibitor. It inhibits Tau aggregation and improves associated neurodegeneration and behavioral phenotypes in both in vivo and in vitro models, making it useful in the study of tauopathies such as Alzheimer's disease.
- Inhibits tau aggregation
- Improves associated neurodegeneration and behavioral phenotypes
- Orally active and BBB-penetrable
- Suitable for in vivo and in vitro studies
- Useful in the study of tauopathies
Medchemexpress LLC Farnesyl pyrophosphate (ammonium) | 116057-57-9 | 95.4% | 433.42 | 10 MG
Farnesyl pyrophosphate (Farnesyl diphosphate) ammonium is a metabolic intermediate in the mevalonate (MVA) pathway and acts as a TRP channel (TRPM2) agonist, triggering Ca2+ influx and cell death. This compound is a critical branch substrate for cholesterol synthesis, ubiquinone synthesis, protein farnesylation, and geranylgeranyl pyrophosphate (GGPP) synthesis. It is utilized in research concerning cerebral ischemia, neurodegenerative diseases, pancreatic cancer, inflammation, and autoimmune diseases.
- Metabolic intermediate in the mevalonate (MVA) pathway.
- TRP channel (TRPM2) agonist that triggers Ca2+ influx and cell death.
- Key branch substrate for cholesterol synthesis, ubiquinone synthesis, protein farnesylation, and geranylgeranyl pyrophosphate (GGPP) synthesis.
- Used in research on cerebral ischemia, neurodegenerative diseases, pancreatic cancer, inflammation, and autoimmune diseases.
Apexbio Technology LLC Megestrol Acetate 595-33-5 1g
Megestrol Acetate (CAS 595-33-5) is a synthetic progestin utilized to downregulate nuclear and cytoplasmic androgen receptor activity It modulates hormone receptor-mediated processes thereby impacting cellular metabolic and signaling pathways Megestrol Acetate exerts its biological activity primarily by inducing apoptosis and disrupting cell cycle progression In in vitro studies using HepG2 cell lines Megestrol Acetate demonstrates proliferation inhibition with an IC50 value of approximately 260 M Based on these pharmacological properties Megestrol Acetate holds research potential in studies of cancer cachexia hepatocellular carcinoma and the investigation of tumor growth mechanisms
Medchemexpress LLC AKN-028 acetate | 98.38% | 362.39 | 1 ML
AKN-028 acetate is a novel, potent, and orally active tyrosine kinase (TK) inhibitor. It specifically targets FMS-like receptor tyrosine kinase 3 (FLT3) with an IC50 value of 6 nM. This compound inhibits FLT3 autophosphorylation and induces a dose-dependent cytotoxic response. It also induces apoptosis through the activation of caspase 3, making it suitable for research in acute myeloid leukemia (AML).
- Potent and orally active tyrosine kinase inhibitor.
- Targets FLT3 with high specificity (IC50 = 6 nM).
- Induces dose-dependent cytotoxic response.
- Activates caspase 3, leading to apoptosis.
- Useful for acute myeloid leukemia (AML) research.
Medchemexpress LLC Cetrorelix Acetate | 145672-81-7 | 99.92% | 1491.09 | 10 MG
Cetrorelix Acetate, also known as SB-75 acetate, is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM. It is intended for research use only.
- Inhibits the growth of ES-2 cell line at 1000 ng/mL
- Shows comparable antiproliferative effects to GnRH-I agonists
- Utilized in research for conditions such as Polycystic Ovarian Syndrome and Infertility
Indofine Chemical 7-AMINO-4-METHYLCOUMARIN, Flavonoid & Coumarins, 26093-31-2, 98+%, 250 mg
7-AMINO-4-METHYLCOUMARIN, Flavonoid & Coumarins, 26093-31-2, 98+%, 250 mg