Fatty alcohol esters
Medchemexpress LLC Ziconotide acetate (SNX-111 acetate) | 914454-03-8 | 99.2% | 2639.13 (free base) | 1 MG
Ziconotide acetate (SNX-111 acetate) | 914454-03-8 | 99.2% | 2639.13 (free base) | 1 MG
Medchemexpress LLC Orbofiban acetate | 163250-91-7 | 98.1% | 421.45 g/mol | C19H27N5O6 | 50 MG
Orbofiban acetate is an orally active platelet GPIIb/IIIa antagonist used in research to inhibit platelet aggregation. It is supplied as a purified acetate salt for laboratory and preclinical studies, with accompanying documentation to support safe handling and compound characterization.
- Orally active GPIIb/IIIa antagonist that inhibits platelet aggregation.
- High purity (98.13%) suitable for research applications.
- Molecular weight 421.45 g/mol; chemical formula C19H27N5O6.
- Supplied in a 50 mg quantity for laboratory use.
- Documentation available: datasheet, certificate of analysis, and safety data sheet.
Medchemexpress LLC BIO-11006 acetate 10mM 1mL | 10MM 1ML
BIO-11006 acetate an analog of the MANS peptide is a MARCKS (myristoylated alanine-rich C kinase substrate) inhibitor[1
Medchemexpress LLC Orbofiban acetate | 163250-91-7 | 98.1% | 421.45 g/mol | C19H27N5O6 | 10 MG
Orbofiban acetate is an orally active platelet GPIIb/IIIa antagonist used in research to inhibit platelet aggregation. It is supplied as the acetate salt for laboratory research use only and is not for human or clinical use.
- Orally active GPIIb/IIIa antagonist that inhibits platelet aggregation.
- Supplied as acetate salt with reported purity of 98.13%.
- Available in multiple small research package sizes (5-500 mg) suitable for in vitro and in vivo studies.
- Soluble in DMSO, facilitating preparation of concentrated stock solutions for assays.
- Used to study platelet aggregation, thrombosis models, and GPIIb/IIIa receptor function.
Medchemexpress LLC Alisol A 24-acetate | 18674-16-3 | 98.0% | 532.75 | C32H52O6 | 10 MG
Alisol A 24-acetate is a naturally occurring prototerpene-type triterpenoid supplied as a high-purity research chemical for biochemical and pharmacological studies. It is provided as a solid or as a ready-to-use DMSO solution for assay applications and is intended for research use only.
- high purity: 98.0% by analytical specification
- small-scale quantities suitable for screening and pilot studies
- available as a solid and as a 10 mM solution in DMSO
- molecular formula: C32H52O6; molecular weight: 532.75
- provided with datasheet, certificate of analysis, and safety data sheet
TARGETMOL CHEMICALS INC GLATIRAMER ACETATE 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Glatiramer acetate (GA) is a synthetic amino acid copolymer that is approved for treatment of relapsing remitting multiple sclerosis (RRMS) and clinically isolated syndrome (CIS). purity: 98%
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.
Medchemexpress LLC Talfirastide acetate | 2855063-75-9 | 99.8% | 959.06 | C43H66N12O13 | 10MM 1ML
Talfirastide acetate is the acetate salt of the endogenous heptapeptide angiotensin-(1-7), used in research on the renin-angiotensin system and studies of cardiovascular, anti-inflammatory, and anti-fibrotic pathways. It is provided as a 10 mM solution (1 mL) or as a powder for reconstitution; sequence is Asp-Arg-Val-Tyr-Ile-His-Pro (DRVYIHP).
- Heptapeptide angiotensin-(1-7) acetate (sequence DRVYIHP).
- Supplied as 10 mM, 1 mL solution; powder available for reconstitution.
- Molecular weight 959.06; chemical formula C43H66N12O13.
- Purity reported as 99.8%.
- Storage: powder sealed at -80°C (2 years) or -20°C (1 year); in solvent -80°C (6 months) or -20°C (1 month).
- Intended for research use only.
Medchemexpress LLC Abiraterone acetate | 154229-18-2 | 99.9% | C26H33NO2 | 100 MG
Abiraterone acetate is an oral, potent, selective, and irreversible inhibitor of CYP17A1 with antiandrogen activity. It is an ester prodrug of Abiraterone, an anticancer agent that inhibits key enzymes involved in steroidogenesis.
- Potent, selective, and irreversible inhibitor of CYP17A1.
- Exhibits antiandrogen activity.
- Functions as an ester prodrug of Abiraterone.
- Inhibits 17,20-lyase and 17α-hydroxylase.
- Suppresses proliferation of AR-positive prostate cancer cell lines.
- Blocks synthesis of 5α-dione and DHT.
- Inhibits CRPC progression and prolongs survival in castration-resistant prostate cancer.
Abcam Octyl-beta-D-thioglucopyranoside, APG surfactant
MW 308.44 Da, Purity >98%. APG surfactant. Reagent for the solubilisation and isolation of membranes.
Medchemexpress LLC TAT-CBD3A6K acetate | 1505463-57-9 | 99.8% | 3249.83 (free base) | 10 MG
TAT-CBD3A6K acetate is a modified TAT-CBD3 peptide that reduces T- and R-type voltage-dependent calcium currents in dorsal root ganglion (DRG) neurons. It also exhibits anti-nociceptive effects in a model of AIDS-induced peripheral neuropathy by preventing CRMP-2-mediated enhancement of T- and R-type calcium channel function.
- Reduces T- and R-type voltage-dependent calcium currents
- Exhibits anti-nociceptive effects in AIDS-induced peripheral neuropathy models
- Prevents CRMP-2-mediated enhancement of T- and R-type calcium channel function
- Modified TAT-CBD3 peptide
Medchemexpress LLC BMP-4 acetate | 99.3% | 1308.52 | 10 MG
BMP-4 acetate is a penetrating heparin-binding peptide with anti-inflammatory and anti-chondrogenic functions. It regulates the iNOS-IFN-IL6 signaling pathway to inhibit the expression of inflammatory proteins such as iNOS, COX2, IFN, and IL6, effectively suppressing inflammation and alleviating various arthritis symptoms in murine chondrocytes and macrophages.
- Penetrating heparin-binding peptide
- Anti-inflammatory and anti-chondrogenic functions
- Regulates iNOS-IFN-IL6 signaling pathway
- Inhibits expression of inflammatory proteins
- Suppresses inflammation and alleviates arthritis symptoms
- Targets IL-6 and COX-2
- Appearance: White to off-white crystal
- Soluble in H2O and DMSO at 100 mg/mL (requires sonication)
Medchemexpress LLC TAT-CBD3A6K acetate | 99.8% | 3249.83 (free base) | 1 MG
TAT-CBD3A6K acetate is a modified TAT-CBD3 peptide that reduces T- and R-type voltage-dependent calcium currents in dorsal root ganglion (DRG) neurons. It shows anti-nociceptive effects in a model of AIDS-induced peripheral neuropathy by preventing CRMP-2-mediated enhancement of T- and R-type calcium channel function.
- Peptides and derivatives
- Inhibitors and substrates
- Neurological applications
- Eye or ear disease research
- Inhibits calcium channels
- Used in AIDS research
- Anti-nociceptive effects
- Peripheral neuropathy studies
- DRG studies
Medchemexpress LLC Vapreotide acetate | 849479-74-9 | 98.2% | 1191.42 | 50 MG
Vapreotide acetate, also known as RC-160 acetate, is a neurokinin-1 (NK1) receptor antagonist. It inhibits Substance P (SP)-triggered intracellular calcium increases and NF-κB activation, making it suitable for various research applications in cell signaling and disease models.
- Neurokinin-1 (NK1) receptor antagonist with an IC50 of 330 nM
- Inhibits Substance P (SP)-induced IL-8 and MCP-1 production
- Demonstrates activity against HIV-1 infection in human MDM in vitro
- Effective in decreasing collateral circulation blood flow in cirrhosis in vivo
- Reduces tumor volumes in prostate-cancer xenografts in nude mice