Hydroxy acids and derivatives
Medchemexpress LLC Sodium Tartrate | 868-18-8 | 99.0% | 10 MG
Sodium Tartrate is a pH-regulating agent that also exhibits antioxidant activity. It is particularly effective at retarding hydrolysis when heated at high temperatures, which helps increase the acid values (AVs) of vegetable oils.
- Functions as a pH-regulating agent
- Exhibits antioxidant activity
- Retards hydrolysis during high-temperature heating of vegetable oils
- A white to off-white solid
- Soluble in H2O at 100 mg/mL (requires sonication)
![eMolecules 304-59-6 | Potassium sodium tartrate | Ambeed | MFCD00065391 | 210.158 | C4H4KNaO6 | 99.000 | [Na+].[K+].O[C@H]([C@@H](O)C([O-])=O)C([O-])=O | 500g | 536765806](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000472141.jpg-250.jpg)
eMolecules 304-59-6 | Potassium sodium tartrate | Ambeed | MFCD00065391 | 210.158 | C4H4KNaO6 | 99.000 | [Na+].[K+].O[C@H]([C@@H](O)C([O-])=O)C([O-])=O | 500g | 536765806
Potassium sodium tartrate | Ambeed | 304-59-6 | MFCD00065391 | 210.158 | C4H4KNaO6 | 99.000 | [Na+].[K+].O[C@H]([C@@H](O)C([O-])=O)C([O-])=O | 500g | 536765806
Apexbio Technology LLC Tylosin tartrate 74610-55-2 1g
Tylosin tartrate (CAS 74610-55-2) is a small-molecule inhibitor targeting the bacterial 50S ribosomal subunit It is designed to inhibit bacterial protein synthesis thereby disrupting peptide elongation during translation Tylosin tartrate exerts its biological activity primarily through reversible binding to the 50S ribosomal subunit In microbiological assays tylosin tartrate demonstrates antibacterial activity with IC50 values typically ranging from 0 01 to 0 1 g/mL against mycoplasma strains depending on strain sensitivity Based on these pharmacological properties tylosin tartrate holds research potential in the investigation of antimicrobial mechanisms resistance profiles and bacterial physiology associated with poultry and livestock infections
Medchemexpress LLC Ifenprodil (tartrate) | 23210-58-4 | 99.9% | 100 MG
Ifenprodil tartrate (NP-120) is a cerebral vasodilator and a noncompetitive NMDA receptor antagonist. It shows high affinity for NR1A/NR2B receptors and acts as an α1 adrenergic receptor antagonist, inhibiting GIRK (Kir3) to reduce inward currents. It exhibits reliable inhibitory effects against A/H1N1 strains and possesses neuroprotective, anticonvulsant, and antinociceptive properties.
- Cerebral vasodilator
- Noncompetitive NMDA receptor antagonist
- High affinity for NR1A/NR2B receptors
- Acts as an α1 adrenergic receptor antagonist
- Inhibits GIRK (Kir3) activity
- Exhibits inhibitory effects against A/H1N1 strains
- Possesses neuroprotective, anticonvulsant, and antinociceptive properties
- Useful for studying cerebrovascular diseases and peripheral arterial obliterative disease
Cusabio Technology LLC Beta-Hydroxybutyric Acid B-OHB
The Bovine Beta-Hydroxybutyric Acid (B-OHB) ELISA Kit is designed for the quantitative detection of B-OHB in bovine serum and plasma samples using a competitive ELISA method This kit detects B-OHB with a sensitivity of 9 5 nmol/mL and provides a broad detection range from 50 nmol/mL to 800 nmol/mL making it suitable for monitoring ketosis and metabolic disorders in cattle The assay requires a sample volume of 50-100 L and delivers results within 1 to 5 hours Measurements are performed at an absorbance wavelength of 450 nm ensuring reliable and accurate quantification Ideal for veterinary research and clinical diagnostics this kit offers a standardized protocol for efficient analysis of B-OHB levels supporting metabolic health assessments in bovine populations
Apexbio Technology LLC Tolterodine tartrate 124937-52-6 10mM (in 1mL DMSO)
Tolterodine tartrate (CAS 124937-52-6) is the tartrate salt form of tolterodine a small molecule that acts as a competitive antagonist at muscarinic acetylcholine receptors By selectively inhibiting these receptors particularly subtypes involved in urinary bladder contraction tolterodine tartrate reduces detrusor muscle activity This mechanism underlies its utility in studies related to bladder function muscarinic receptor pharmacology and disorders characterized by overactive bladder The compound is commonly employed in preclinical and clinical research investigating the modulation of cholinergic signaling in urological and neurological contexts
Apexbio Technology LLC Lasofoxifene (tartrate) 190791-29-8 50mg
Lasofoxifene tartrate (CAS 190791-29-8) is a small-molecule selective estrogen receptor modulator (SERM) targeting estrogen receptor-alpha (ER- ) and acting as a selective inverse agonist at the cannabinoid receptor subtype CB2 It is designed to modulate estrogen receptor signaling in a tissue-dependent manner thereby regulating estrogen-related biological pathways Lasofoxifene tartrate exerts its biological activity through dual estrogen agonist antagonist actions depending on tissue context In preclinical studies using ovariectomized rat models Lasofoxifene tartrate prevents estrogen deficiency-associated bone loss reduces serum cholesterol and body mass without inducing uterine hypertrophy Based on these pharmacological properties Lasofoxifene tartrate holds research potential in the management of osteoporosis breast cancer and cardiovascular health in postmenopausal women
Medchemexpress LLC Pyrantel (tartrate) | 33401-94-4 | 98.7% | 356.39 | 500 MG
Pyrantel tartrate is an orally active anthelmintic and an agonist of the nicotinic acetylcholine receptor (nAChR). It induces spasmodic muscle paralysis in parasites, making it useful for studying parasitic infections like ascariasis, hookworm infections, intestinal worms (pinworm infections), and trichinosis.
- Orally active anthelmintic
- Agonist of the nicotinic acetylcholine receptor (nAChR)
- Induces spasmodic muscle paralysis in parasites
- Useful for studying various parasitic infections
Apexbio Technology LLC Lasofoxifene (tartrate) 190791-29-8 25mg
Lasofoxifene tartrate (CAS 190791-29-8) is a small-molecule selective estrogen receptor modulator (SERM) targeting estrogen receptor-alpha (ER- ) and acting as a selective inverse agonist at the cannabinoid receptor subtype CB2 It is designed to modulate estrogen receptor signaling in a tissue-dependent manner thereby regulating estrogen-related biological pathways Lasofoxifene tartrate exerts its biological activity through dual estrogen agonist antagonist actions depending on tissue context In preclinical studies using ovariectomized rat models Lasofoxifene tartrate prevents estrogen deficiency-associated bone loss reduces serum cholesterol and body mass without inducing uterine hypertrophy Based on these pharmacological properties Lasofoxifene tartrate holds research potential in the management of osteoporosis breast cancer and cardiovascular health in postmenopausal women
Medchemexpress LLC Ifenprodil tartrate | 23210-58-4 | 99.9% | 1 ML
Ifenprodil tartrate is a cerebral vasodilator and a noncompetitive NMDA receptor antagonist, with high affinity for NR1A/NR2B receptors. It also acts as an α1 adrenergic receptor antagonist and inhibits GIRK (Kir3) activity. This compound shows inhibitory effects against A/H1N1 strains and offers neuroprotective, anticonvulsant, and antinociceptive properties, making it valuable for research into cerebrovascular diseases and peripheral arterial obliterative disease. This product is supplied as a 10 mM solution in 1 mL.
- Cerebral vasodilator
- Noncompetitive NMDA receptor antagonist
- High affinity for NR1A/NR2B receptors
- Acts as an α1 adrenergic receptor antagonist
- Inhibits GIRK (Kir3)
- Inhibits A/H1N1 strains
- Neuroprotective, anticonvulsant, and antinociceptive
- Used in cerebrovascular and peripheral arterial disease research
Medchemexpress LLC L-glyceric acid sodium | 146298-95-5 | MFCD28363841 | 99.0% | 128.06 g/mol | C3H5NaO4 | 5 MG
L-glyceric acid sodium is the sodium salt of L-glyceric acid, a urinary metabolite that accumulates in L-glyceric aciduria. Supplied as a high-purity analytical reference standard, it is intended for metabolic research and diagnostic applications requiring accurate reference material. The compound has formula C3H5NaO4, molecular weight 128.06 g/mol, and reported purity 99.0%.
- Purity of 99.0%.
- Molecular weight 128.06 g/mol.
- Chemical formula C3H5NaO4.
- Available in small milligram pack sizes for analytical use.
- Intended as an analytical reference for metabolic and diagnostic studies involving L-glyceric aciduria.
Apexbio Technology LLC Ketanserin tartrate 83846-83-7 100mg
Ketanserin tartrate (CAS 83846-83-7) is a selective antagonist of 5-HT2 receptors Experimental studies have demonstrated that it inhibits hERG potassium currents in a concentration-dependent manner exhibiting an IC50 of 0 11 M Due to its defined receptor selectivity and electrophysiological properties Ketanserin tartrate is widely employed in pharmacological studies and in research focused on cardiovascular system disorders
Apexbio Technology LLC Tylosin tartrate 74610-55-2 5g
Tylosin tartrate (CAS 74610-55-2) is a small-molecule inhibitor targeting the bacterial 50S ribosomal subunit It is designed to inhibit bacterial protein synthesis thereby disrupting peptide elongation during translation Tylosin tartrate exerts its biological activity primarily through reversible binding to the 50S ribosomal subunit In microbiological assays tylosin tartrate demonstrates antibacterial activity with IC50 values typically ranging from 0 01 to 0 1 g/mL against mycoplasma strains depending on strain sensitivity Based on these pharmacological properties tylosin tartrate holds research potential in the investigation of antimicrobial mechanisms resistance profiles and bacterial physiology associated with poultry and livestock infections
Medchemexpress LLC Tylosin tartrate | 74610-55-2 | 98.0% | 1 G
Tylosin tartrate is a macrolide antibiotic produced by *Streptomyces fradiae*. It demonstrates potent antimicrobial activity against Gram-positive bacteria and is used as a feed additive to promote animal growth. This compound is also utilized in veterinary medicine for treating bacterial dysentery and respiratory diseases in poultry, pigs, and cattle.
- Binds to 23S rRNA of bacterial ribosomal 50S subunit
- Prevents bacterial growth
- Suppresses elevated TNF-α and IL-1β levels in LPS-treated animals
- Increases IL-10 levels in LPS-treated animals