Fatty alcohol esters
Medchemexpress LLC Larixyl acetate | 4608-49-5 | 99.5% | 348.52 g/mol | C22H36O3 | 10 MG
Larixyl acetate is a diterpenoid research compound that acts as a potent, selective TRPC6 inhibitor with additional activity against TRPC3. It has reported protective effects in models of human papillomavirus impact and traumatic brain injury-induced endothelial dysfunction, and is supplied as a high-purity analytical standard for laboratory research.
- Potent TRPC6 inhibitor (IC50: 0.58 μM).
- Also inhibits TRPC3 (IC50: 6.83 μM).
- High purity, approximately 99.5%.
- Molecular weight 348.52 g/mol; formula C22H36O3.
- Stable as a powder at -20°C for up to 3 years.
- Provided as a 10 mg research-grade sample for analytical use.
Medchemexpress LLC Larazotide (acetate) | 881851-50-9 | MFCD31630844 | 99.7% | 785.89 g/mol | C34H59N9O12 | 100 MG
Larazotide acetate is an eight-amino-acid peptide zonulin antagonist supplied as a research reagent. It is used in studies of celiac disease and intestinal barrier dysfunction and has reported antiviral activity against varicella-zoster virus. For research use only; not for human therapeutic use.
- Eight-amino-acid peptide sequence: Gly-Gly-Val-Leu-Val-Gln-Pro-Gly.
- Orally active zonulin antagonist that modulates tight junctions.
- Reported in vitro antiviral activity versus varicella-zoster virus.
- Supplied as a powder; recommended sealed, cold storage to preserve stability.
- Well characterized molecular weight and formula for research applications.
Medchemexpress LLC Ulipristal acetate | 126784-99-4 | 99.9% | 475.62 | 50 MG
Ulipristal acetate (CDB-2914) is an orally active, selective progesterone receptor modulator (SPRM). It stimulates the autophagic response selectively in leiomyoma cells and has the potential for treating benign gynecological conditions such as uterine myoma.
- Orally active, selective progesterone receptor modulator (SPRM).
- Stimulates the autophagic response selectively in leiomyoma cells.
- Potential for benign gynecological conditions treatment, such as uterine myoma.
- Exhibits significant antiprogestational activity in vivo.
- Decreases incidences of fibroadenomas and adenocarcinomas in the mammary gland in all treated groups.
- Increases the frequency with which pathologists assessed the endometrium as being thickened in a dose-dependent manner.
Medchemexpress LLC BIO-11006 acetate | 00-00-0 | 99.9% | 1110.22 | C48H79N13O17 | 100 MG
BIO-11006 acetate is the acetate salt of BIO-11006, an analog of the MANS peptide that inhibits MARCKS (myristoylated alanine-rich C kinase substrate). Supplied for laboratory research use only, the peptide salt is provided with characterization data to support in vitro studies of MARCKS-related signaling and membrane interactions.
- High purity suitable for research (>99.9%).
- Acetate salt form for improved handling and stability.
- Relevant for in vitro studies of MARCKS-mediated signaling and peptide-membrane interactions.
- Available in laboratory-scale pack sizes to support assay development.
- Characterized molecular weight and formula provided for experimental planning.
Medchemexpress LLC Resomelagon acetate | 1809420-72-1 | 99.75% | 358.35 | 100 MG
Resomelagon (AP1189) acetate is a potent, orally active melanocortin receptor (MR) agonist, specific for MC1 and MC3. It induces ERK1/2 phosphorylation and Ca2+ mobilization. Resomelagon acetate also exhibits anti-inflammatory activity and can be used for obesity and chronic inflammation research.
- Potent, orally active melanocortin receptor (MR) agonist about MC1 and MC3.
- Induces ERK1/2 phosphorylation and Ca2+ mobilization.
- Possesses anti-inflammatory activity.
- Applicable for obesity and chronic inflammation research.
TARGETMOL CHEMICALS INC Ciraparantag acetate 25MG
Also available in 1 mL, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Ciraparantag acetate, an anticoagulant reversal agent, is a small molecule specifically designed to bind noncovalently by charge-charge interaction to unfractionated heparin and low-molecular-weight heparin.It shows binding characteristics that are similar to those of direct oral anticoagulants (DOACs). Purity 99.65%
Selleck Chemical LLC Methylprednisolone Acetate
Methylprednisolone (NSC-19987 Medrol) acetate is a synthetic glucocorticoid receptor agonist used to achieve prompt suppression of inflammation Methylprednisolone activates ACE2 and reduces IL-6 levels thus improves severe or critical COVID-19 Methylprednisolone markedly reduces autophagy and apoptosis
AdipoGen Ulipristal acetate
Chemical. CAS 126784-99-4. Formula C30H37NO4. MW 475.62. Synthetic. Ulipristal acetate is a selective progesterone receptor modulator SPRM that binds to the human progesterone receptors PR-A and PR-B EC50s=8.5 and 7.7nM, respectively, rabbit uterine PR EC50=13.6nM, and rabbit thymic glucocorticoid receptor GR EC50=15.4nM. It is selective for human progesterone receptors over the human estrogen receptor ER EC50>10,000nM. It inhibits growth of IGROV-1 and SKOV3 human ovarian cancer cells IC50s=15.5 and 31.5µM, respectively even after resistance to combined cisplatin and paclitaxel treatment has developed. Ulipristal acetate reverses the proliferative effect of progesterone on patient-derived germline mutant BRCA1 breast tissue xenografts in ovariectomized athymic mice. Formulations containing ulipristal acetate have been used as emergency contraceptives and to treat uterine fibroids.
AdipoGen Isoeugenyl acetate
Chemical. CAS 93-29-8. Formula C12H14O3. MW 206.2. Isoeugenol is used as a fragrance material in perfumes and perfumed products. It is a moderate to strong skin allergen and a frequent cause of contact allergy. Isoeugenyl acetate has been used as a substitute for Isoeugenol, but is probably easily hydrolysed in the skin to produce isoeugenol. Isoeugenyl acetate is a useful building block and has antibacterial and antifungal properties. Compound can be used as analytical reference material.
AdipoGen Isoeugenyl acetate
Chemical. CAS 93-29-8. Formula C12H14O3. MW 206.2. Isoeugenol is used as a fragrance material in perfumes and perfumed products. It is a moderate to strong skin allergen and a frequent cause of contact allergy. Isoeugenyl acetate has been used as a substitute for Isoeugenol, but is probably easily hydrolysed in the skin to produce isoeugenol. Isoeugenyl acetate is a useful building block and has antibacterial and antifungal properties. Compound can be used as analytical reference material.
AdipoGen Ulipristal acetate
Chemical. CAS 126784-99-4. Formula C30H37NO4. MW 475.62. Synthetic. Ulipristal acetate is a selective progesterone receptor modulator SPRM that binds to the human progesterone receptors PR-A and PR-B EC50s=8.5 and 7.7nM, respectively, rabbit uterine PR EC50=13.6nM, and rabbit thymic glucocorticoid receptor GR EC50=15.4nM. It is selective for human progesterone receptors over the human estrogen receptor ER EC50>10,000nM. It inhibits growth of IGROV-1 and SKOV3 human ovarian cancer cells IC50s=15.5 and 31.5µM, respectively even after resistance to combined cisplatin and paclitaxel treatment has developed. Ulipristal acetate reverses the proliferative effect of progesterone on patient-derived germline mutant BRCA1 breast tissue xenografts in ovariectomized athymic mice. Formulations containing ulipristal acetate have been used as emergency contraceptives and to treat uterine fibroids.
Apexbio Technology LLC Guanabenz Acetate 23256-50-0 10mM (in 1mL DMSO)
Guanabenz Acetate (CAS 23256-50-0) is a small molecule that acts as a selective agonist of the 2-adrenergic receptor subtypes It exhibits notable affinity for the 2a-adrenergic receptor (pEC50 8 25) with moderate activity at the 2b-adrenergic receptor (pEC50 7 01) and lower potency at the 2c-adrenergic receptor (pEC50 5) Through activation of these receptors Guanabenz Acetate modulates adrenergic neurotransmission making it a valuable tool for investigating the physiological and pharmacological functions of 2-adrenergic signaling in biomedical research
TARGETMOL CHEMICALS INC ULIPRISTAL ACETATE 50MG
Also available in 5 mg 10 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Ulipristal acetate (CDB-2914) is an orally bioavailable acetate salt of ulipristal a selective progesterone receptor modulator with anti-progesterone activity. Ulipristal binds to the progesterone receptor (PR) thereby inhibiting PR-mediated gene expression and interfering with progesterone activity in the reproductive system. As a result this agent may suppress the growth of uterine leiomyomatosis. Furthermore by inhibiting or delaying ovulation and effecting endometrial tissue ulipristal can be used as an emergency contraception. purity: 100%