Fatty alcohol esters
Sigma Aldrich Fine Chemicals Biosciences Geranyl pyrophosphate ammonium salt 1 mg/mL in methanol (:aqueous 10 mM NH4OH (7:3)), >=95% (TLC) | 763-10-0 | MFCD00189726 | 1VL
Geranyl pyrophosphate ammonium salt 1 mg/mL in methanol (:aqueous 10 mM NH4OH (7:3)), >=95% (TLC) | Purity: >=95% (TLC) | Mol Wt: 365.3 | 763-10-0 | MFCD00189726 | 1VL
TARGETMOL CHEMICALS INC CETRORELIX ACETATE 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Cetrorelix Acetate is gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM. purity: 97%
Apexbio Technology LLC Bazedoxifene acetate 198481-33-3 50mg
Bazedoxifene acetate (CAS 198481-33-3) is a selective estrogen receptor modulator (SERM) targeting estrogen receptors (ER) It is designed to modulate ER activity thereby regulating estrogen-dependent cellular pathways Bazedoxifene acetate exerts its biological activity primarily through tissue-specific agonism and antagonism of ER In in vitro studies Bazedoxifene acetate demonstrates receptor modulation with reported affinities (Ki) of 26 nM for ER and 99 nM for ER Based on these pharmacological properties Bazedoxifene acetate holds research potential in osteoporosis and bone metabolism studies as well as in investigations of hormone-responsive cellular mechanisms and pancreatic cancer
Apexbio Technology LLC Atosiban acetate 914453-95-5 50mg
Atosiban acetate (CAS 914453-95-5) is a synthetic peptide functioning as a dual antagonist of the oxytocin receptor (OTR) and vasopressin receptors (V1aR V1bR V2R) It exhibits high affinity for human OTR (pKi 7 9) and V1aR (pKi 9 8) and effectively inhibits cell proliferation in MDCK and HEK293 cells stably expressing human OTR with IC50 values of 15 4 nM and 20 8 nM respectively In preclinical models Atosiban acetate suppresses uterine contractions and delays preterm labor Its application in research includes studies of receptor-mediated signaling uterine contractility and biased agonism Due to its peptide nature it is not suitable for oral or long-term use
Apexbio Technology LLC Guanabenz Acetate 23256-50-0 50mg
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
Cayman Chemical DL-Tryptophn octyl esterhy 5g
A stable, cell-permeable tryptophan derivative with an octyl ester protected COOH group
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%
eMolecules AstaTech / STEARYL BEHENATE / 0.1g / 718058767 / D93433 / 95.000 / 24271-12-3 / MFCD00048672 / 593.078 / C40H80O2
AstaTech / STEARYL BEHENATE / 0.1g / 718058767 / D93433 / 95.000 / 24271-12-3 / MFCD00048672 / 593.078 / C40H80O2
Apexbio Technology LLC Megestrol Acetate 595-33-5 10mM (in 1mL DMSO)
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 Farnesyl pyrophosphate-d2 triammonium | 00-00-0 | MFCD00010901 | 95.8% | 435.43 g/mol | C15H35D2N3O7P2 | 5 MG
Farnesyl pyrophosphate-d2 triammonium is a deuterium-labeled form of farnesyl pyrophosphate supplied as the triammonium salt. It functions as a metabolic intermediate in the mevalonate pathway, acts as a TRPM2 agonist in cellular assays, and is used as a tracer or internal standard for quantitative NMR, GC-MS, and LC-MS analyses in biochemical research related to cholesterol, ubiquinone, and protein prenylation pathways.
- Deuterium-labeled tracer for quantitative analysis.
- Suitable as an internal standard for NMR, GC-MS, and LC-MS.
- Acts as a TRPM2 agonist in cellular assays.
- High purity for reliable analytical results.
- Solid, white to off-white form for stable storage and handling.