Reference Standards
Material, sufficiently homogeneous and stable with respect to one or more specified properties, and the uses include the calibration of a measurement system, assessment of a measurement procedure, assigning values to other materials, and quality control and so on.
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Reference Standards Verwandte Produkte (11757)
Verwandte Produkte (11757)
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tert-Butyl 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate (Standard)
0 ImagesArt. -Nr.: HY-W101675RCAS. Nr.: 289042-12-2tert-Butyl 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate (Standard) is the analytical standard of tert-Butyl 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate. This product is intended for research and analytical applications.
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ABT-702 dihydrochloride (Standard)
0 ImagesArt. -Nr.: HY-103161RCAS. Nr.: 1188890-28-9ABT-702 dihydrochloride (Standard) is the analytical standard of ABT-702 dihydrochloride (HY-103161). This product is intended for research and analytical applications. ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor (IC50=1.7 nM).
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Sennidin A (Standard)
0 ImagesSennidin A (Standard) is the analytical standard of Sennidin A. This product is intended for research and analytical applications. Sennidin A, isolated from the leaves of Cassia angustifolia, inhibits HCV NS3 helicase, with an IC50 of 0.8 μM. Sennidin A induces phosphorylation of Akt and glucose transporter 4 (GLUT4) translocation. Sennidin A stimulates the glucose incorporation.
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Fesoterodine impurity 1 (Standard)
0 ImagesArt. -Nr.: HY-I0104RCAS. Nr.: 250214-69-82-[3-[Bis(1-methylethyl)amino]-1-phenylpropyl]-4-(methoxymethyl)phenol (Standard) is the analytical standard of 2-[3-[Bis(1-methylethyl)amino]-1-phenylpropyl]-4-(methoxymethyl)phenol. This product is intended for research and analytical applications.
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Perfluoropentanoic acid (Standard)
0 ImagesSynonyms: PFPeA (Standard); Perfluorovaleric acid (Standard)Perfluoropentanoic acid (Standard) (PFPeA (Standard)) is the analytical standard of Perfluoropentanoic acid (HY-21193). This product is intended for research and analytical applications. Perfluoropentanoic acid (PFPeA), a short-chain perfluorinated compound, serves as an important indicator of perfluorinated compound pollution in ecosystems. Perfluoropentanoic acid exhibits certain toxicity to mice.
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PR5-LL-CM01 (Standard)
0 ImagesArt. -Nr.: HY-109963RCAS. Nr.: 1005307-86-7PR5-LL-CM01 (Standard) is the analytical standard of PR5-LL-CM01 (HY-109963). This product is intended for research and analytical applications. PR5-LL-CM01 is a potent protein arginine methyltransferase 5 (PRMT5) inhibitor (IC50= 7.5 μM). Anti-tumor activies.
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(S)-3-(4-(5-Bromo-2-chlorobenzyl)phenoxy)tetrahydrofuran (Standard)
0 Images(S)-3-(4-(5-Bromo-2-chlorobenzyl)phenoxy)tetrahydrofuran (Standard) is the analytical standard of (S)-3-(4-(5-Bromo-2-chlorobenzyl)phenoxy)tetrahydrofuran. This product is intended for research and analytical applications.
![(8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-8,9,10,11,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one (Hydrocortisone Impurity) (Standard)](https://file.medchemexpress.com/product_pic/hy-z8639r.gif "Click to View (8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-8,9,10,11,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one (Hydrocortisone Impurity) (Standard) Product Detail")
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Alrizomadlin (Standard)
0 ImagesArt. -Nr.: HY-101518RCAS. Nr.: 1818393-16-6Synonyms: APG-115 (Standard); AA-115 (Standard)Alrizomadlin (Standard) is the analytical standard of Alrizomadlin (HY-101518). This product is intended for research and analytical applications. Alrizomadlin (APG-115) is an orally active MDM2 protein inhibitor binding to MDM2 protein with IC50 and Ki values of 3.8 nM and 1 nM, respectively. Alrizomadlin blocks the interaction of MDM2 and p53 and induces cell-cycle arrest and apoptosis in a p53-dependent manner.
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N6-Cyclopentyladenosine (Standard)
0 ImagesArt. -Nr.: HY-103181RCAS. Nr.: 41552-82-3Synonyms: CPA (Standard); UK-80882 (Standard)N6-Cyclopentyladenosine (Standard) is the analytical standard of N6-Cyclopentyladenosine (HY-103181). This product is intended for research and analytical applications. N6-Cyclopentyladenosine (CPA) is a selective Adenosine A1 receptor agonist, with Ki values of 2.3 nM, 790 nM and 43 nM for human A1, A2A and A3 receptors, respectively. N6-cyclopentyladenosine increases Apoptosis. N6-Cyclopentyladenosine has antitumor activity against leukemia. N6-cyclopentyladenosine improves 5-fluorouracil (HY-90006)-induced hematopoietic damage, regulates sleep, and delays Aminophylline-induced clonic epileptic seizures.
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Dinoprost tromethamine salt (Standard)
0 ImagesArt. -Nr.: HY-12956ARCAS. Nr.: 38562-01-5Synonyms: Prostaglandin F2α tromethamine salt (Standard); PGF2α THAM (Standard); Prostaglandin F2α THAM (Standard)Dinoprost (tromethamine salt) (Standard) is the analytical standard of Dinoprost (tromethamine salt). This product is intended for research and analytical applications. Dinoprost tromethamine salt (Prostaglandin F2α tromethamine salt) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost tromethamine salt is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost tromethamine salt plays a key role in the onset and progression of labour.
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PR-619 (Standard)
0 ImagesPR-619 (Standard) is the analytical standard of PR-619 (HY-13814). This product is intended for research and analytical applications. PR-619 is a broad-range and reversible DUB inhibitor with EC50s of 3.93, 4.9, 6.86, 7.2, and 8.61 μM for USP4, USP8, USP7, USP2, and USP5, respectively. PR-619 induces ER Stress and ER-Stress related apoptosis.
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Bufuralol (Standard)
0 ImagesArt. -Nr.: HY-105124RCAS. Nr.: 54340-62-4Synonyms: Ro 3-4787 (Standard)Bufuralol (Standard) is the analytical standard of Bufuralol (HY-105124). This product is intended for research and analytical applications. Bufuralol (Ro 3-4787) is a potent non-selective, orally active β-adrenoreceptor antagonist with partial agonist activity. Bufuralol hydrochloride is a CYP2D6 probe substrate.
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Lodoxamide (Standard)
0 ImagesArt. -Nr.: HY-14270RCAS. Nr.: 53882-12-5Synonyms: U-42585E free acid (Standard)Lodoxamide (Standard) is the analytical standard of Lodoxamide. This product is intended for research and analytical applications. Lodoxamide (U-42585E free acid) is an antiallergic compound acting as a mast-cell stabilizer for the treatment of asthma and allergic conjunctivitis.
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SCH529074 (Standard)
0 ImagesArt. -Nr.: HY-110088RCAS. Nr.: 922150-11-6SCH529074 (Standard) is the analytical standard of SCH529074 (HY-110088). This product is intended for research and analytical applications. SCH529074 is a potent and orally active p53 activator. SCH529074 binds specifically and conformation-dependently to p53 DBD ( DNA binding domain) with a Ki of 1-2 μM in a saturable manner. SCH529074 restores mutant p53 function and interrupts HDM2-mediated ubiquitination of wild Type p53. SCH529074 can be used for the study of non-small-cell lung carcinoma (NSCLC).
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RMC-7977 (Standard)
0 ImagesArt. -Nr.: HY-156498RCAS. Nr.: 2765082-12-8RMC-7977 (Standard) is the analytical standard of RMC-7977 (HY-156498). This product is intended for research and analytical applications. RMC-7977 is an orally active triple-complex RAS inhibitor that can simultaneously bind to cyclophilin A (CYPA) (Kd = 195 nM) and KRAS (G12V) (Kd = 292 μM). It exhibits broad-spectrum inhibitory activity against KRAS, NRAS, and HRAS proteins and their various wild-type and mutant variants. RMC-7977 induces apoptosis by inhibiting the phosphorylation of ERK, CRAF, and RSK, as well as increasing PARP cleavage. This leads to tumor regression, reduces resistance in KRASG12C cancer models, and demonstrates good tolerability across various RAS cancer models.
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GNE-049 (Standard)
0 ImagesArt. -Nr.: HY-108435RCAS. Nr.: 1936421-41-8GNE-049 (Standard) is the analytical standard of GNE-049 (HY-108435). This product is intended for research and analytical applications. GNE-049 is a highly potent and selective CBP inhibitor with an IC50 of 1.1 nM in TR-FRET assay. GNE-049 also inhibits BRET and BRD4(1) with IC50s of 12 nM and 4200 nM, respectively.
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Ropivacaine (Standard)
0 ImagesRopivacaine (Standard) is the analytical standard of Ropivacaine. This product is intended for research and analytical applications. Ropivacain is a potent sodium channel blocker. Ropivacain blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibrese. Ropivacaine is also an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM in COS-7 cell's membrane. Ropivacaine is used for the research of neuropathic pain management.
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2,2'-((1E,1'E)-Hydrazine-1,2-diylidenebis(methanylylidene))diphenol (Standard)
0 ImagesSynonyms: Salicylaldazine (Standard); Salicylaldehyde azine (Standard)Salicylaldehyde azine (Standard) is the analytical standard of Salicylaldehyde azine. This product is intended for research and analytical applications.
