Chromatography Standards
Sigma Aldrich Fine Chemicals Biosciences Dexamethasone United States Pharmacopeia (USP) Reference Standard | 50-02-2 | MFCD00064136 | 125MG
Dexamethasone United States Pharmacopeia (USP) Reference Standard | Mol Wt: 392.46 | 50-02-2 | MFCD00064136 | 125MG
Cayman Chemical Mogroside IIIE, Purity: ≥98%, CAS: 88901-37-5, 25 mg
A cucurbitane glycoside with anti-inflammatory activity; inhibits LPS-induced secretion of IL-1β, IL-6, and TNF-α from, as well as LPS-induced increases in TLR4 levels in, RAW 264.7 macrophages at 50 µM; reduces increases in BALF levels of IL-1β, IL-6, and TNF-α, and increases in lung tissue Mpo activity in a mouse model of LPS-induced acute lung injury at 20 mg/kg; decreases lung fibrosis and inflammation, as well as increases animal survival and reduced lung levels of MMP-9, in a mouse model of bleomycin-induced pulmonary fibrosis at 20 mg/kg per day
Sigma Aldrich Fine Chemicals Biosciences Naproxen sodium | 26159-34-2 | MFCD00058507 | 5g
Naproxen sodium | Mol Wt: 252.24 | 26159-34-2 | MFCD00058507 | 5g
Medchemexpress LLC Carboprost tromethamine | 58551-69-2 | 99.9% | C25H47NO8 | 25 MG
Carboprost tromethamine is the synthetic 15-methyl analogue of prostaglandin F2α. It effectively promotes uterine contraction and significantly reduces bleeding during and after delivery. It is for research use only and not sold to patients. It has been reported to be 84-96% successful in treating persistent hemorrhage due to uterine atony.
- Synthetic 15-methyl analogue of prostaglandin F2α
- Effectively promotes uterine contraction
- Significantly reduces bleeding during and after delivery
- Intended for research purposes only
- 84-96% successful in treating persistent hemorrhage due to uterine atony
Cayman Chemical Metronidazole Impurity G, Purity: ≥95%, CAS: 1010-93-1, 10 mg
A potential impurity found in commercial preparations of metronidazole; an inactive metabolite of metronidazole
Medchemexpress LLC Raloxifene hydrochloride | 82640-04-8 | 99.8% | 510.04 | 25 MG
Raloxifene hydrochloride is a second-generation, selective, and orally active estrogen receptor modulator. It exhibits estrogen-agonistic effects on bone and lipid metabolism, while demonstrating estrogen-antagonistic effects on uterine endometrium and breast tissue.
- Activates TGF beta 3 promoter as a full agonist
- Inhibits estrogen response element-containing vitellogenin promoter expression
- Acts as a potent uncompetitive inhibitor of human liver aldehyde oxidase
- Functions as a noncompetitive inhibitor of aldehyde oxidase-catalyzed reduction reactions
- Decreases viability in mouse mammary carcinoma cells
- Demonstrates estrogenic activity on bone resorption and serum cholesterol in ovariectomized rats
- Increases bone mineral density in ovariectomized rats
- Reduces serum cholesterol in ovariectomized rats
- Suppresses tumor volumes and decreases lymph node metastasis in mice
Sigma Aldrich Fine Chemicals Biosciences Aleuritic acid United States Pharmacopeia (USP) Reference Standard | 533-87-9 | MFCD00135596 | 50MG
Aleuritic acid United States Pharmacopeia (USP) Reference Standard | Mol Wt: 304.42 | 533-87-9 | MFCD00135596 | 50MG
Echelon Biosciences Research Labs Ins(1,4,5)P3 500 ug
Inositol phosphates are important signaling molecules involved in numerous cellular functions. Inositol 1,4,5-trisphosphate (Ins(1,4,5)P3), aka IP3, is a second messenger produced by phospholipase C catalyzed hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2). IP3 binds to the IP3-receptor on the endoplasmic reticulum causing calcium to be released through the opening of a tetrameric ion channel. IP3 is rapidly metabolized by a specific series of inositol phosphatases and kinases. This item is non returnable
Apexbio Technology LLC Itraconazole(Synonyms: Sporanox, Orungal, R51211, Lozanoc, Triasporin, Fungitraxx, Onmel, Itranox, Sporal, Itrizole, Candistat), 1g, CAS: 84625-61-6.
Itraconazole (CAS 84625-61-6) is a triazole-based antifungal compound that functions primarily by inhibiting cytochrome P450 enzymes particularly CYP3A4 As both a substrate and inhibitor of CYP3A4 itraconazole undergoes oxidative metabolism into hydroxylated keto- and N-dealkylated derivatives all with demonstrated inhibitory activities comparable or superior to the parent compound In addition to antifungal effects itraconazole inhibits the hedgehog signaling pathway and angiogenesis Due to its affinity for mammalian CYP-P450 enzymes itraconazole is frequently employed in drug interaction studies assessing CYP3A-mediated metabolism
Medchemexpress LLC Itacitinib adipate | 1334302-63-4 | 99.2% | 699.66 | 50 MG
Itacitinib adipate is an orally bioavailable and selective JAK1 inhibitor which has been tested for efficacy and safety in a phase II trial in myelofibrosis.
- Orally bioavailable and selective JAK1 inhibitor.
- Evaluated in phase II clinical trials for myelofibrosis.
- Available in various quantities and solution formats.
- High purity.
- Involved in numerous clinical trials for various conditions including Acute Lymphoblastic Leukemia, Systemic Sclerosis, Graft-versus-host Disease, and various cancers.
Sigma Aldrich Fine Chemicals Biosciences L-Arabinitol European Phar
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. for further information and support please go to the website of the issuing Pharmacopoeia.
Selleck Chemical LLC Diltiazem HCl 10mg 33286-22-5 RG 83606 HCl
Diltiazem (Tiazac, RG 83606) HCl is a benzothiazepine derivative with vasodilating action due to its antagonism of the actions of the calcium ion in membrane functions. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Mogroside IV | 89590-95-4 | 100 MG
Mogroside IV is a triterpenoid glycoside isolated from the extracts of Luo Han Guo, acting as a nonsugar sweetener. Mogrosides are known to be sweeter than sucrose and exhibit antioxidant, antidiabetic, and anticancer activities.
- Triterpenoid glycoside
- Nonsugar sweetener
- Sweeter than sucrose
- Exhibits antioxidant, antidiabetic, and anticancer activities
- Isolated from Luo Han Guo extracts
- Useful in food and metabolic disease research
Sigma Aldrich Fine Chemicals Biosciences Carmustine Related Compound A United States Pharmacopeia (USP) Reference Standard | 2214-72-4 | 25MG
Carmustine Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 185.05 | 2214-72-4 | 25MG