Alcohols and polyols
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- (395)
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- (1)
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- (1)
- (462)
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- (1)
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- (1)
- (36)
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- (1)
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- (1)
- (1)
- (1)
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- (1)
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- (3)
- (1)
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- (12)
- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379263 SECO RAPAMYCIN ETHYL 50MG
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Medchemexpress LLC Glycodeoxycholic acid-d4 | 1069132-37-1 | MFCD06658888 | 99.9% | 453.65 | C26H39D4NO5 | 1MG
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Glycodeoxycholic acid-d4 is the deuterium-labeled form of the endogenous bile acid glycodeoxycholic acid, provided as a stable isotope internal standard for quantitative analytical methods such as LC-MS and GC-MS. It is intended for use in metabolomics and bioanalytical assays where isotopically labeled standards are required; storage and solubility instructions are provided to preserve analytical integrity.
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Medchemexpress LLC Ginsenoside Rh2 | 78214-33-2 | MFCD00800712 | 622.87 | 50 MG
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Ginsenoside Rh2 induces the activation of caspase-8 and caspase-9. It induces cancer cell apoptosis in a multi-path manner, making it a promising candidate for anti-tumor drug development. Ginsenoside Rh2 triggers p53-dependent Fas expression, leading to caspase-8 activation, and also initiates a p53-independent caspase-9-mediated intrinsic pathway to cause cancer cell death.
- Induces activation of caspase-8 and caspase-9.
- Induces cancer cell apoptosis through multiple pathways.
- Triggers p53-dependent Fas expression.
- Activates p53-independent caspase-9-mediated intrinsic pathway.
- Demonstrates cytotoxic activity against various human cancer cell lines (HeLa, SK-HEP-1, SW480, PC-3, A549, B16, B16-F10, DU-145, HCT-116, HL-60, HepG2, Huh-7, Jurkat, K562, KG-1, Kasumi 1, LNCaP, MCF7, MDA-MB-231, REH, THP-1, U-937).
- Enhances antitumor immunological response in a melanoma mice model.
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Medchemexpress LLC Remogliflozin etabonate (GSK189075) | 442201-24-3 | 99.64% | 522.59 | 5 MG
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Remogliflozin etabonate (GSK189075) is an orally active, selective, and low-affinity sodium glucose cotransporter (SGLT2) inhibitor. It functions as a proagent derived from benzylpyrazole glucoside and is metabolized into its active form, Remogliflozin, within the body. This compound has demonstrated antidiabetic efficacy in rodent models.
- Orally active and selective SGLT2 inhibitor
- Functions as a proagent of Remogliflozin
- Exhibits antidiabetic efficacy in rodent models
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Medchemexpress LLC Notoginsenoside Fa | 88100-04-3 | MFCD29904542 | 99.0% | 1241.41 | C59H100O27 | 10 MG
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Notoginsenoside Fa is a protopanaxadiol (PPD)-type saponin isolated from Panax notoginseng. Supplied as a white to off-white solid for research use, it has been studied for potential neuroprotective activity, including activation and recovery of degenerated brain function.
- Purity: 99.0%
- Cas number: 88100-04-3
- Chemical formula: C59H100O27
- Molecular weight: 1241.41
- Appearance: white to off-white solid
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC Ginsenoside F4 | 181225-33-2 | 5 MG
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Ginsenoside F4 (GF4) is a ginseng saponin isolated from notoginseng or red ginseng. It demonstrates an inhibitory effect on human lymphocytoma JK cells by inducing apoptosis. GF4 also inhibits matrix metalloproteinase 13 (MMP 13) expression in IL-1β-treated chondrocytes and blocks cartilage breakdown in rabbit cartilage tissue culture, suggesting its therapeutic potential for preventing cartilage collagen matrix breakdown in diseased tissues.
- Isolated from notoginseng or red ginseng
- Induces apoptosis in human lymphocytoma JK cells
- Inhibits matrix metalloproteinase 13 (MMP 13) expression
- Blocks cartilage breakdown in rabbit cartilage tissue culture
- Shows therapeutic potential for preventing cartilage collagen matrix breakdown
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Medchemexpress LLC Prednisolone hemisuccinate | 2920-86-7 | 99.9% | 50 MG
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Prednisolone hemisuccinate is a synthetic glucocorticoid, a derivative of cortisol, used to treat various inflammatory and auto-immune conditions. It is for research use only and not sold to patients.
- Synthetic glucocorticoid
- Derivative of cortisol
- Used to treat inflammatory and auto-immune conditions
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Medchemexpress LLC Hydrocortisone-d4 (Cortisol-d4) | 73565-87-4 | 366.48 | 1 MG
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Hydrocortisone-d4 is the deuterium labeled Hydrocortisone, a steroid hormone or glucocorticoid secreted by the adrenal cortex. This compound is intended for research use only. Deuteration has gained attention due to its potential to affect the pharmacokinetic and metabolic profiles of drugs.
- Used as a tracer.
- Used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
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Medchemexpress LLC HY-12316 5mg Medchemexpress, 20(S)-Hydroxycholesterol CAS:516-72-3 Purity:>98%
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Medchemexpress, HY-12316 5mg 20(S)-Hydroxycholesterol CAS:516-72-3 20(S)-hydroxyCholesterol (20α-Hydroxycholesterol) is an allosteric activator of the oncoprotein smoothened (Smo) that activates the hedgehog (Hh) signaling pathway with an EC 50 of 3 μM in a gene transcription reporter assay using NIH3T3 cells [1] [2] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-15257A 2mg Medchemexpress, Mavoglurant (racemate) CAS:1636881-61-2 Purity:>98%
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Medchemexpress, HY-15257A 2mg Mavoglurant (racemate) CAS:1636881-61-2 Mavoglurant (racemate) is the racemate of mavoglurant. Mavoglurant is a novel, non-competitive mGlu5 receptor antagonist. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Gypenoside XLIX | 94987-08-3 | 1047.23 | 20 MG
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Gypenoside XLIX is a multifunctional bioactive compound isolated from Gynostemma pentaphyllum. It acts as a PPAR-α agonist and binds to SIRT1. It inhibits TLR4-mediated NF-κB signaling pathway activation, reduces ROS accumulation, and alleviates hepatic inflammatory injury. It targets SIRT1 to block YAP-NLRP3 activation, improving sepsis-induced cardiomyopathy. The compound is applicable to research related to acute liver injury, lung injury, cardiomyopathy, acute splenic injury, sepsis-associated encephalopathy, acute kidney injury, atherosclerosis, and chronic inflammation.
- Acts as a PPAR-α agonist
- Inhibits TLR4-mediated NF-κB signaling pathway
- Reduces ROS accumulation
- Alleviates hepatic inflammatory injury
- Targets SIRT1 to block YAP-NLRP3 activation
- Prevents acute kidney injury
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Medchemexpress LLC Ercalcidiol-d3 (25-Hydroxy Vitamin D2-d3) | 1217467-39-4 | 99.9% | 415.67 | 500 UG
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Ercalcidiol-d3 is the deuterium labeled Ercalcidiol, a metabolite of Vitamin D2. It can be used as an indicator of vitamin D status. Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, primarily as tracers for quantitation during the drug development process.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
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Medchemexpress LLC Ginsenoside Rk2 | 364779-14-6 | 1 MG
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Ginsenoside Rk2 is a dammarane glycoside isolated from processed ginseng. Intended for research use only, it has 99.25% purity and appears as an off-white to light yellow solid.
- Molecular weight: 604.86
- Formula: C36H60O7
- Source: Panax ginseng C. A. Meyer (Araliaceae plants)
- Storage: -20°C, protected from light. In solvent, -80°C for 6 months or -20°C for 1 month.
- In vitro solubility: Soluble in DMSO (50 mg/mL, 82.66 mM), requires sonication.
- In vivo solubility: Protocols for suspended (1.25 mg/mL in DMSO/PEG300/Tween-80/Saline) or clear solution (≥ 1.25 mg/mL in DMSO/Corn Oil).
- Cellular effect: IC50 > 10 μM against human A549, HL-60, MCF7, and SW480 cells.
- Classifications: Natural products, terpenoids, triterpenes, inflammation/immunology.
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Medchemexpress LLC Gypenoside L | 94987-09-4 | 5 MG
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Gypenoside L is a saponin found in Gynostemma pentaphyllum. It increases SA-β-galactosidase activity, promotes the production of senescence-associated secretory cytokines, and activates p38, ERK MAPK, and NF-κB pathways to induce senescence. It also exhibits anti-tumor and anti-inflammatory activities.
- Saponin derived from Gynostemma pentaphyllum
- Increases SA-β-galactosidase activity
- Promotes production of senescence-associated secretory cytokines
- Activates p38 and ERK MAPK pathways
- Activates NF-κB pathway
- Induces senescence
- Exhibits anti-tumor activity
- Exhibits anti-inflammatory activity
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Medchemexpress LLC Alisol B | 18649-93-9 | 472.70 | 1 MG
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Alisol B is a triterpene that exhibits diverse biological activities, making it valuable for various research applications. It is known to bind human soluble epoxide hydrolase (sEH) and reduce its activity. This compound also plays a role in inhibiting RANKL-induced JNK phosphorylation, osteoclast formation, and SERCA pump activity, while promoting calcium mobilization and autophagy. Alisol B can be used for research into conditions such as hypercalcemia, osteoporosis, rheumatoid arthritis, acute kidney injury, and breast cancer.
- Inhibits sEH activity
- Reduces osteoclast formation
- Induces calcium mobilization
- Activates CaMKK-AMPK-mTOR pathway
- Promotes autophagic flux and autophagosome formation
- Induces G1 phase cell cycle arrest
- Activates endoplasmic reticulum stress and unfolded protein responses
- Induces cancer cell apoptosis
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