Fatty alcohol esters
TARGETMOL CHEMICALS INC Felypressin acetate 25MG
Also available in 5 mg, 10 mg, 50 mg, 100 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Felypressin acetate (PLV-2) is an agonist of vasopressin 1 and acts on all arginine vasopressin receptors 1AS. Felypressin acetate can be used in dental procedures. Purity 97.06%
TARGETMOL CHEMICALS INC Bazedoxifene acetate 50MG
Also available in 1 mL, 5 mg, 10 mg, 25 mg, 100 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Bazedoxifene acetate (WAY-TES 424) is a novel selective estrogen receptor modulator (SERM). Purity 98%
TARGETMOL CHEMICALS INC Icatibant Acetate 5MG
Also available in 1 mL, 1 mg, 2 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Icatibant Acetate, an antagonist of the bradykinin B2 receptor, is used in the treatment of hereditary angioedema. Purity 98%
TARGETMOL CHEMICALS INC Lanreotide acetate 25MG
Also available in 1 mL, 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Lanreotide acetate (BIM 23014 acetate) is a somatostatin analogue with antineoplastic activity, used for carcinoid syndrome Purity 100%
Medchemexpress LLC Ulipristal acetate (CDB-2914) | 126784-99-4 | 99.9% | 475.62 | 1 ML
Ulipristal acetate (CDB-2914) is an orally active, selective progesterone receptor modulator (SPRM). It stimulates the autophagic response selectively in leiomyoma cells and has potential for treating benign gynecological conditions like uterine myoma.
- Orally active.
- Selective progesterone receptor modulator (SPRM).
- Stimulates autophagic response in leiomyoma cells.
- Potential for treating uterine myoma.
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 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