Alcohols and polyols
- (1)
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- (1)
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- (1)
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- (33)
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- (1)
- (1)
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- (1)
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- (12)
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- (1)
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- (24)
- (1)
- (8)
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- (1)
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- (1)
- (17)
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- (5)
- (2)
- (1)
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- (3)
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- (24)
- (5)
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- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
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- (11)
- (2)
- (7)
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- (1)
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Filtered Search Results
Medchemexpress LLC Asiaticoside B | 125265-68-1 | 5 MG
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Asiaticoside B is a 9,19-cycloartane triterpene glycoside found in Actaea asiatica. It exhibits cytotoxicity against HepG2 and MCF-7 cancer cells with IC50 values of 9.74 μM and 8.32 μM, respectively.
- Purity: 99.46%
- Molecular weight: 975.12
- Formula: C48H78O20
- Appearance: Solid
- Color: White to off-white
- Structure classification: Terpenoids, triterpenes
- Initial source: Plants (Compositae, Tagetes lucida Cav., Umbelliferae)
- Storage: 4°C, protect from light. In solvent: -80°C for 6 months; -20°C for 1 month (protect from light)
- Solubility (in vitro): DMSO: 100 mg/mL (102.55 mM; requires ultrasonic; hygroscopic DMSO has a significant impact on solubility, use newly opened DMSO)
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eMolecules D-epi-4-Inosose | 33471-33-9 | | 10mg
Oakwood Chemical | D-epi-4-Inosose | 10mg | 537710416 | 103801 | | 33471-33-9 | | 178.140 | C6H10O6
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Medchemexpress LLC Abiraterone decanoate | 2486052-18-8 | 99.7% | C34H49NO2 | 50 MG
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Abiraterone decanoate is a potent Abiraterone proagent that provides controlled release of Abiraterone and long-acting CYP17 inhibition via intramuscular (IM) delivery. This solid, white to off-white laboratory chemical is intended for research use only.
- Potent abiraterone proagent
- Provides controlled release of abiraterone
- Offers long-acting CYP17 inhibition
- Suitable for intramuscular (IM) delivery
- Targets CYP17
- Appears as a white to off-white solid
- Used in the manufacture of substances
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000285208 -PHENYLETHYL -D-GL 5MG
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Medchemexpress LLC Phenethyl acetate 50g
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Phenethyl acetate (Phenethyl alcohol) is a natural product[1]
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Medchemexpress LLC Taurochenodeoxycholic acid | 516-35-8 | 499.70 | 100 MG
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Taurochenodeoxycholic acid (12-Deoxycholyltaurine) is identified as one of the primary bioactive components found in the bile acid of animals. This substance is known for its ability to induce apoptosis and exhibits significant anti-inflammatory and immune regulation properties.
- Induces apoptosis
- Shows obvious anti-inflammatory properties
- Exhibits immune regulation properties
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Medchemexpress LLC Isoforskolin | 64657-21-2 | 1 MG
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Isoforskolin is the principal active component of C. forskohlii, native to China. It functions as an anti-inflammatory agent by reducing the secretion of lipopolysaccharide (LPS)-induced cytokines, specifically TNF-α, IL-1β, IL-6, and IL-8, in human mononuclear leukocytes. It is used for the treatment of Lyme arthritis.
- Principal active component of C. forskohlii.
- Reduces LPS-induced cytokine secretion (TNF-α, IL-1β, IL-6, and IL-8).
- Acts as an anti-inflammatory agent.
- Potentially treats Lyme arthritis.
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Medchemexpress LLC PhiKan 083 hydrochloride | 1050480-30-2 | 99.3% | 274.79 | 10 MG
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PhiKan 083 hydrochloride is a carbazole derivative designed to bind to the surface cavity and stabilize the Y220C p53 mutant, with a binding affinity (Kd) of 167 μM. It effectively slows down the thermal denaturation rate of the p53 mutant and has been shown to reduce cell viability in engineered variants of Ln229 cells. When used in combination with NSC 123127, it enhances pro-apoptotic activity across multiple Ln229 cell variants.
- Binds to and stabilizes Y220C p53 mutant
- Slows down thermal denaturation rate of p53 mutant
- Reduces cell viability in engineered variants of Ln229 cells
- Enhances pro-apoptotic activity when combined with NSC 123127
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Medchemexpress LLC Benzoylpaeoniflorin | 38642-49-8 | 584.57 | 50 MG
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Benzoylpaeoniflorin | 38642-49-8 | 584.57 | 50 MG
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Medchemexpress LLC Pseudoginsenoside RT1 | 98474-74-9 | 99.5% | 927.08 | C47H74O18 | 10 MG
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Pseudoginsenoside RT1 is a natural saponin isolated from the fruit of Randia siamensis and is supplied as a research-grade reference standard. It exhibits reported acute ichthyotoxic activity and is intended for analytical and laboratory use only.
- Natural saponin isolated from Randia siamensis.
- Reported acute ichthyotoxic activity.
- High purity (≈99.5%).
- Molecular formula C47H74O18; molecular weight 927.08.
- CAS number 98474-74-9.
- Available in small analytical pack sizes (e.g., 10 MG).
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Chemscene CHEMSCENE
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5000577684 TERT-BUTYL CIS-4-HYDROXYCY 25G
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Medchemexpress LLC Clorgyline hydrochloride | 17780-75-5 | 99.9% | C13H16Cl3NO | 50 MG
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Clorgyline hydrochloride is an irreversible and selective inhibitor of monoamine oxidase A (MAO-A) used in scientific research. It has minimal effect on conjugated dopamine (DA) amounts in superfusates of rat striatum slices. This compound contains an Alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Irreversible and selective inhibitor of monoamine oxidase A (MAO-A)
- Structurally related to Pargyline
- Contains an Alkyne group for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Azide groups
- Increases nicotine infusions and motivation to obtain nicotine in rats at 2 mg/kg daily for 28 days
- Pretreatment with 1 mg/kg intravenously for 1 hour has little effect on the efflux of conjugated dopamine (DA) and p-tyramine-evoked release of conjugated DA from slices of rat striatum
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Electron Microscopy Sciences Propylene Glycol, 85%, Aqueous 500 ML
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References: AFIP Manual of Histologic Staining Methods, Ed. L. Luna, 3rd ed., New York, McGraw-Hill Publications, c. 1968, p. 140.
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Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | 99.9% | C14H11ClN4O | 25 MG
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Olprinone Hydrochloride, also known as Loprinone Hydrochloride, is a potent phosphodiesterase (PDE) 3 inhibitor with an IC50 of 0.35 μM. It is utilized in research for heart failure due to its positive inotropic and vasodilative effects, and it also demonstrates anti-inflammatory activity.
- Potent PDE3 inhibitor (IC50 of 0.35 μM)
- Used in research for heart failure
- Exhibits positive inotropic and vasodilative effects
- Demonstrates anti-inflammatory activity
- Modulates inflammation associated with myocardial ischemia-reperfusion injury in rats
- Reduces histological evidence of myocardial injury
- Decreases pro-inflammatory cytokines (TNF-α and IL-1β)
- Reduces adhesion molecules (ICAM-1 and P-Selectin)
- Decreases nitrotyrosine formation and NF-κB expression
- Reduces PAR formation and apoptosis
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Medchemexpress LLC Leelamine hydrochloride | 16496-99-4 | 98.10% | 321.93 | 1 ML
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Leelamine hydrochloride is a tricyclic diterpene molecule extracted from the bark of pine trees. It acts as a cannabinoid receptor type 1 (CB1) agonist and an inhibitor of SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, independent of androgen receptor status. It also suppresses the transcriptional activity of the androgen receptor, which regulates fatty acid synthesis.
- Acts as a cannabinoid receptor type 1 (CB1) agonist
- Inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells
- Suppresses the transcriptional activity of the androgen receptor
- Extracted from the bark of pine trees
- Appears as a white to off-white solid
- Store at -20°C in sealed conditions, away from moisture
- For storage in solvent, store at -80°C for 6 months, or -20°C for 1 month in sealed conditions, away from moisture
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