Fatty alcohol esters
Medchemexpress LLC Prt062607 (acetate) | 1370261-98-5 | C21H27N9O3 | 50 MG
PRT062607 acetate is a chemical compound suitable for laboratory use and the manufacture of substances. This product is stable under recommended storage conditions and is not classified as a hazardous substance or mixture. It is provided in solid form and is intended for research use only.
- Solid appearance
- Stable under recommended storage conditions
- Not classified as a hazardous substance or mixture
- Intended for research use only
- Recommended storage at 4°C, sealed, away from moisture
Medchemexpress LLC Vapreotide acetate | 849479-74-9 | 98.2% | 1191.42 | 10 MG
Vapreotide acetate is a neurokinin-1 (NK1) receptor antagonist with an IC50 of 330 nM. It is intended for research use only.
- Attenuates Substance P (SP)-triggered intracellular calcium increases and NF-κB activation.
- Inhibits SP-induced IL-8 and MCP-1 production.
- Inhibits HIV-1 infection of human MDM in vitro.
- Inhibits GH-, PRL, and/or alpha-subunit release by human GH-secreting pituitary adenoma cells.
- Exhibits affinities for SSTR2, -3, and -5.
- Reduces tumor volumes and weights in androgen-independent prostate cancer xenografts.
- Decreases collateral circulation blood flow in cirrhosis and attenuates its development.
Medchemexpress LLC Vanillin acetate | 881-68-5 | 99.9% | 194.19 | 10 G
Vanillin acetate | 881-68-5 | 99.9% | 194.19 | 10 G
Medchemexpress LLC Lysipressin acetate | 83968-49-4 | 99.8% | 1116.27 | 2 MG
Lysipressin (Lysine vasopressin) acetate is an antidiuretic hormone found in pigs and some marsupial families. It induces contraction of the rabbit urinary bladder smooth muscle and activates adenylate-cyclase. This product is suitable for laboratory use and research.
- Induces contraction of rabbit urinary bladder smooth muscle
- Activates adenylate-cyclase
- White to off-white solid appearance
- High purity of 99.8%
Medchemexpress LLC Atic-in-1 acetate | 3067165-96-9 | C23H37N7O7 | 100 MG
ATIC-IN-1 acetate (compound 14) is an inhibitor targeting Aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC) dimerization with a Ki value of 685 nM. This enzyme catalyzes de novo purine biosynthesis, and ATIC dimerization is crucial for its aminoimidazole carboxamide ribonucleotide (AICAR) transformylase activity. ATIC-IN-1 acetate exhibits anti-tumor activity by reducing cell numbers and cell division rates.
- Acts as a specific inhibitor and shows non-specific aggregate mechanism in the presence of 1 mg/mL and 10 mg/mL BSA.
- Inhibits the proliferation of MCF-7 cells.
- Leads to a reduction in cell division rather than an increase in cell death.
Medchemexpress LLC Incensole Acetate | 34701-53-6 | 1 MG
Incensole Acetate, a main constituent of Boswellia carterii resin, demonstrates neuroprotective effects against neuronal damage from traumatic and ischemic head injury. It has been shown to reduce Aβ25-35-triggered apoptosis in hOBNSCs and, in in vitro studies, significantly ameliorates Aβ25-35-induced cell death.
- Demonstrates neuroprotective effects against neuronal damage
- Reduces Aβ25-35-triggered apoptosis in hOBNSCs
- Ameliorates Aβ25-35-induced cell death in in vitro studies
- High purity of 99.08%
- Soluble in DMSO
Medchemexpress LLC JMV 449 acetate | 141863-45-8 | 99.7% | 807.03 | 10 MG
JMV 449 acetate is a potent neurotensin receptor agonist. It shows an IC50 of 0.15 nM for inhibition of 125I-neurotensin binding to neonatal mouse brain and an EC50 of 1.9 nM in contracting the guinea-pig ileum. It also has highly potent and long-lasting hypothermic and analgesic effects in the mouse.
- Potent neurotensin receptor agonist
- IC50 of 0.15 nM for inhibition of 125I-neurotensin binding to neonatal mouse brain
- EC50 of 1.9 nM in contracting the guinea-pig ileum
- Highly potent and long-lasting hypothermic and analgesic effects in the mouse
Medchemexpress LLC SOR-C13 acetate | 1187852-48-7 | 99.12% | 1565.81 | 1 MG
SOR-C13 is a carboxy-terminal truncated peptide and a high-affinity TRPV6 antagonist with an IC50 value of 14 nM. TRPV6 is a non-voltage gated calcium channel associated with malignancy and poor prognosis in breast cancer. SOR-C13 demonstrates anticancer activity. This product is the acetate form.
- High-affinity TRPV6 antagonist
- Associated with anticancer activity
- Available in various quantities
- Also available in other forms
Medchemexpress LLC A11 (acetate) | 98.5% | 2767.16 (free base) | 10 MG
A11 acetate is an ANXA1-derived 11 amino acid-long peptide that functions as an ANXA1-EphA2 interaction blocker peptide. It has a molecular weight of 2767.16 (free base) and a purity of 98.5%. This peptide is suitable for laboratory research applications.
- Functions as an ANXA1-EphA2 interaction blocker peptide
- 11 amino acid-long peptide
- High purity (98.5%)
- Recommended storage conditions for powder and in solvent
Medchemexpress LLC L57 acetate | 99.0% | 2483.87 (free base) | 1 MG
L57 acetate is a Low-density lipoprotein receptor-related protein 1 (LRP1)-binding peptide. It has high affinity to LRP1 with a Ki of 45 nM. It can cross the blood-brain barrier (BBB) and is stable in plasma.
- High affinity to LRP1 (Ki of 45 nM)
- Crosses the blood-brain barrier (BBB)
- Stable in plasma
- Suitable as a carrier for CNS drug delivery
Medchemexpress LLC S961 acetate | 99.8% | 4802.12 | 10 MG
S961 acetate is a high-affinity and selective insulin receptor (IR) antagonist with IC50s of 0.048 nM for HIR-A and 0.027 nM for HIR-B. It also exhibits high affinity for Rat IR and Pig IR. This compound is intended for research use only.
- High-affinity and selective insulin receptor (IR) antagonist
- IC50s of 0.048 nM for HIR-A
- IC50s of 0.027 nM for HIR-B
- Also targets human insulin-like growth factor I receptor (HIGF-IR)
- High affinity for rat IR and pig IR
- Chemical formula: C211H295N55O71S2.xC2H4O2
- Appears as a white to off-white solid
Medchemexpress LLC Sifuvirtide acetate | 4727.98 (free base) | 10 MG
Sifuvirtide (SFT) acetate is a powerful HIV fusion inhibitor that prevents HIV-1 mediated cell fusion in a dose-dependent manner. It demonstrates high potency against both primary and laboratory-adapted HIV-1 isolates across various genotypes, making it suitable for anti-HIV drug research.
- Potent HIV fusion inhibitor.
- Inhibits HIV-1 mediated cell fusion in a dose-dependent manner.
- Highly potent against infection by primary and laboratory-adapted HIV-1 isolates of multiple genotypes.
- Can be used in the research of anti-HIV drugs.