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| Product | Description | |
|---|---|---|
| Traumatic Acid | Traumatic Acid is a wound healing agent and a cytokinin (phytohormone). Traumatic Acid enhances the biosynthesis of collagen in cultured human skin fibroblasts. Traumatic Acid inhibits MCF-7 breast cancer cells viability and enhances apoptosis and oxidative stress. Traumatic Acid can be used in studies of cancer, circulatory disorders (including arterial hypertension), and skin diseases associated with oxidative stress and impaired collagen biosynthesis [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 6402-36-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-119358. |  |
| Traumatic Acid | Traumatic Acid, is the product of a biosynthetic pathway from a physiological role of alpha-ketol fatty acids in plant lipid hydroperoxide lyase metabolism. This compound is also used in would healing as it stimulates cell division to form a protective callus around the wound site. Group: Biochemicals. Grades: Highly Purified. CAS No. 6402-36-4. Pack Sizes: 100mg, 500mg. Molecular Formula: C12H20O4, Molecular Weight: 228.28. US Biological Life Sciences. |  Worldwide |
| Levacetylleucine | Levacetylleucine, an orally bioavailable and brain-penetrant endogenous metabolite, is an acetylated derivative of amino acid leucine. Levacetylleucine is the active form of N-acetyl-leucine (NAL). Levacetylleucine attenuates neuronal death and neuroinflammation in the cortical tissue of mice. Levacetylleucine also potentially improves ameliorates lysosomal and metabolic dysfunction. Levacetylleucine improves compensation of postural symptoms after unilateral chemical labyrinthectomy (UL) in rats. Levacetylleucine is promising for research of neurological manifestations of Niemann-Pick disease type C, traumatic brain injury and neurodegeneration prevention [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 1188-21-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-59291. | |
| Talampanel | Talampanel, also known as LY300164 and GYKI-53773, is a glutamate receptor inhibitor with anti-seizure activity. Talampanel is also an orally active, potent and selective AMPA-receptor antagonist, and can noncompetitively bind to the AMPA subtype of glutamate excitatory amino acid receptors and may inhibit the growth of gliomas by interfering with neurotransmitters involved in brain tumor growth. This agent may also protect against traumatic brain injury. Talampanel (GYKI 53405) is being investigated for the treatment of epilepsy, malignant gliomas and amyotrophic lateral sclerosis (ALS). As of May 2010, results from the trial for ALS have been found negative. Synonyms: LY300164; LY 300164; LY-300164; GYKI-53773; Gyki 53405; Gyki53405; Gyki-53405; LY293606; LY-293606; LY 293606. Grades: >98%. CAS No. 161832-65-1. Molecular formula: C19H19N3O3. Mole weight: 337.37. |  |
| ZJ 43 | ZJ 43 is a potent inhibitor of glutamate carboxypeptidase II and III (GCP II and III/NAAG peptidase/NAALADase) (Ki = 0.8 and 23 nM, respectively). It inhibits the hydrolysis of NAAG (IC50 = 2.4 nM) and decreases the deleterious effects of excessive extracellular glutamate. ZJ 43 has been shown to reduce neuronal degeneration in a rat model of traumatic brain injury (TBI) and reduce locomotor activity in the PCP-model of schizophrenia. Synonyms: ZJ 43; ZJ43; ZJ-43; N-[[[(1S)-1-Carboxy-3-methylbutyl]amino]carbonyl]-L-glutamic acid; (2S) -2- [ [ (1S) -1-carboxy-3-methylbutyl] carbamoylamino] pentanedioic acid. CAS No. 723331-20-2. Molecular formula: C12H20N2O7. Mole weight: 304.3. | |
| Meclocycline Sulfosalicylate Salt | Meclocycline Sulfosalicylate Salt. Group: Biochemicals. Alternative Names: 2-Hydroxy-5-sulfo-benzoic Acid (4S, 4aR, 5S, 5aR, 12aS) -7-Chloro-4- (di methyl amino) -1, 4, 4a, 5, 5a, 6, 11, 12a-octahydro-3, 5, 10, 12, 12a-pentahydroxy-6- methyl ene -1, 11-dioxo-2-naphthacene carboxamide; Meclan; Meclan Cream; Mecloderm; Meclosorb; Meclutin; Traumatociclina. Grades: Highly Purified. CAS No. 73816-42-9. Pack Sizes: 100mg. Molecular Formula: C22H21ClN2O8 C7H6O6S, Molecular Weight: 695.05. US Biological Life Sciences. | Worldwide |
| (R)-CPPene ((R)-4-[(2E)-3-Phosphono-2-propenyl]-2-piperazinecarboxylic Acid, SDZ EAA 494, Midafotel) | A highly potent competitive antagonist of NMDA receptors (ED50 = 39 nM; pA2 = 6.8). Biologically active admitted systemically. Frequently used in assessing the functional roles of NMDA receptors mediated neurotransmissions in a variety of research areas, such as excitotoxic cell death, apoptosis, bipolar disorders, ischemia, traumatic brain injury, epilepsy, and neuropathic pain. Group: Biochemicals. Grades: Highly Purified. CAS No. 117414-74-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
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