Tricarboxylic acids and derivatives
Selleck Chemical LLC Orphenadrine Citrate S2054-50mg
Orphenadrine Citrate is a skeletal muscle relaxant it acts in the central nervous system to produce its muscle relaxant effects
Medchemexpress LLC 5,8,11,14,17,20-hexaoxa-2-azadocosanedioic acid, 1-(9H-fluoren-9-ylmethyl) ester | 437655-96-4 | 99.4% | 561.62 | C29H39NO10 | 250 MG
Fmoc-NH-PEG6-CH2COOH is an Fmoc-protected polyethylene glycol (PEG6) linker with a terminal carboxylic acid, supplied for research use as a cleavable linker for antibody-drug conjugates and as a PEG-based PROTAC linker in targeted protein degradation research.
- Fmoc-protected amine with terminal carboxylic acid functionality.
- Suitable for ADC and PROTAC linker synthesis.
- Reported purity 99.4% and molecular weight 561.62.
- Molecular formula C29H39NO10.
- Available in small-scale pack sizes including 250 MG.
Medchemexpress LLC Mosapride citrate | 112885-42-4 | 99.9% | 1 ML
Mosapride citrate is an orally active gastroenterokinetic compound. It acts as a 5HT4 agonist and a CYP inducer. It exhibits a concentration-dependent inhibitory effect on Kv4.3, with an IC50 value of 15.2 μM. Mosapride citrate is used in the study of gastrointestinal diseases.
- Orally active gastroenterokinetic compound
- 5HT4 agonist
- CYP inducer
- Inhibitory effect on Kv4.3
- Useful for studying gastrointestinal diseases
Medchemexpress LLC (E/Z)-Zotiraciclib citrate | 1204918-73-9 | C29H32N4O8 | 50 MG
(E/Z)-Zotiraciclib citrate is a potent inhibitor targeting CDK2, JAK2, and FLT3. This compound is supplied as a solid, appearing off-white to light yellow, and is intended for research use only.
- Potent CDK2, JAK2, and FLT3 inhibitor
- High purity: 99.83%
- Molecular weight: 564.59
- Store at 4°C, sealed, away from moisture
Medchemexpress LLC Gefapixant citrate | 2310299-91-1 | 99.2% | 545.5 g/mol | C20H27N5O11S | 1 ML
Gefapixant citrate is a P2X3 receptor antagonist provided as a concentrated solution for laboratory research. The reagent is supplied at 10 mM in DMSO (1 mL) and is intended for in vitro pharmacology and biochemical studies, with analytical documentation available from the manufacturer.
- Ready-to-use 10 mM solution in DMSO, 1 mL.
- High purity (99.2%) suitable for research applications.
- Supports in vitro P2X3 receptor pharmacology and biochemical assays.
- Comes with data sheet, certificate of analysis, and safety data sheet.
- For research use only; not for human or diagnostic use.
Medchemexpress LLC cGAMP diammonium | 96.6% | 708.47 | 50 MG
cGAMP (Cyclic GMP-AMP) diammonium functions as an endogenous second messenger in metazoans and triggers interferon production in response to cytosolic DNA. It activates stimulator of interferon genes (STING), which activates a signaling cascade leading to the production of type I interferons and other immune mediators.
- Endogenous second messenger in metazoans.
- Triggers interferon production in response to cytosolic DNA.
- Activates stimulator of interferon genes (STING).
- Activates a signaling cascade leading to the production of type I interferons and other immune mediators.
- Promotes the antigen-specific proliferation capacity of spleen cells in mice.
- Directly activates murine and human dendritic cells *in vitro*.
eMolecules 23142-01-0 | Pentoxyverine citrate | MFCD00055697 | 1g
Ambeed | rel-(3R4S5S6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2345-tetraol | 1g | 649269182 | A1497324 | 54-17-1 | MFCD00063684 | 180.156 | C6H12O6
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Medchemexpress LLC DiMal-O-CH2COOH | 1620837-47-9 | 96.8% | 308.24 | C13H12N2O7 | 10 MG
This cleavable linker is designed for use in antibody-drug conjugate (ADC) construction and conjugation workflows, offering malemide-based chemistry for attaching payloads to antibodies or targeting moieties. It is provided at research-grade purity and supplied in small quantities suitable for method development and exploratory studies.
- Cleavable linker for ADC construction and conjugation workflows.
- Provides maleimide-based chemistry for reliable payload attachment.
- High purity (96.8%) suitable for research applications.
- Available in small research quantities; larger amounts available on request.
- Store at 4°C, protect from light; in solvent: -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC Tamoxifen (Citrate) | 54965-24-1 | 99.9% | 563.64 | 1 ML
Tamoxifen Citrate is an orally active, selective estrogen receptor modulator (SERM) that blocks estrogen action in breast cells while activating estrogen activity in other cells like bone, liver, and uterine cells. It functions as a potent Hsp90 activator, enhancing its molecular chaperone ATPase activity. Additionally, it can inhibit infectious EBOV Zaire and Marburg (MARV).
- Selective estrogen receptor modulator
- Blocks estrogen action in breast cells
- Activates estrogen activity in bone, liver, and uterine cells
- Potent Hsp90 activator
- Enhances Hsp90 molecular chaperone ATPase activity
- Inhibits infectious EBOV Zaire and Marburg (MARV)
- Activates autophagy
- Induces apoptosis
- Used to induce gene knockout in CreER transgenic mice
Medchemexpress LLC Cyclic GMP-AMP diammonium | 96.6% | 708.47 g/mol | C20H30N12O13P2 | 5 MG
cGAMP diammonium is a cyclic dinucleotide that functions as an endogenous second messenger and a potent activator of the stimulator of interferon genes (STING) pathway. Provided as the diammonium salt for research use, it induces type I interferon production and is used to study innate immune signaling.
- Activates STING and triggers type I interferon signaling.
- High purity (96.6%) suitable for research applications.
- Molecular formula C20H30N12O13P2; molecular weight 708.47 g/mol.
- Water-soluble; dissolves up to 100 mg/mL with ultrasonic assistance.
- Solid storage recommended at -20°C; solution storage guidance provided.
- Supplied in small quantities (e.g., 5 mg) for laboratory use.
eMolecules 123-04-6 | 3-(Chloromethyl)heptane | Ambeed | MFCD00018940 | 148.670 | C8H17Cl | 98.000 | CCCCC(CC)CCl | 25g | 599120951
3-(Chloromethyl)heptane | Ambeed | 123-04-6 | MFCD00018940 | 148.670 | C8H17Cl | 98.000 | CCCCC(CC)CCl | 25g | 599120951
Medchemexpress LLC ζ-Stat trisodium (NSC37044 trisodium) | 31894-34-5 | 97.0% | 450.31 | C10H5Na3O10S3 | 50MG
ζ-Stat trisodium is a small-molecule inhibitor of protein kinase C zeta (PKC-ζ) used in biochemical and cellular research. It is supplied as a light yellow to light brown solid with a reported purity of 97.0%, molecular formula C10H5Na3O10S3, and molecular weight 450.31 g/mol. The compound is typically provided in small, preweighed quantities suitable for laboratory studies.
- Inhibits protein kinase C zeta (PKC-ζ) activity.
- CAS number 31894-34-5.
- Purity 97.0%.
- Molecular formula C10H5Na3O10S3; molecular weight 450.31 g/mol.
- Solid, light yellow to light brown appearance.
- Available in multiple small research quantities (mg scale).
Medchemexpress LLC Zuclomiphene citrate | 7619-53-6 | MFCD00082252 | 99.8% | 598.1 g/mol | C32H36ClNO8 | 10 MG
Zuclomiphene citrate is the cis isomer of clomiphene citrate. It is orally active and exhibits antiestrogenic activity, and is used as a research reagent in studies of estrogen receptor modulation, endocrinology, and metabolic effects such as cholesterol regulation.
- Orally active antiestrogenic compound used in receptor modulation studies.
- Citrate salt form, provided as a solid for laboratory research.
- High purity: specification >95%, HPLC result 99.78% (reported).
- Molecular formula C32H36ClNO8; molecular weight 598.1 g/mol.
- Typically supplied in small research quantities such as 10 MG.
Selleck Chemical LLC Ixazomib Citrate (MLN9708) S4432-25mg
Ixazomib Citrate (MLN9708) is a prodrug of Ixazomib (MLN2238) which is a selective orally bioavailable inhibitor of 20S proteasome that inhibits the chymotrypsin-like proteolytic ( 5) site with IC50 of 3 4 nM and Ki of 0 93 nM respectively Ixazomib (MLN2238) also inhibits caspase-like ( 1) and trypsin-like ( 2) proteolytic sites with IC50 of 31 nM and 3500 nM respectively
Selleck Chemical LLC Zoledronic acid monohydrate S5244-1g
Zoledronic acid (Zoledronate CGP-4244) monohydrate a nitrogen-containing bisphosphonate is a potent osteoclast inhibitor which induces apoptosis in osteoclasts by inhibiting enzymes of the mevalonate pathway and preventing the isoprenylation of small GTP-binding proteins such as Ras and Rho