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Filtered Search Results
Ambeed 1 2Hydroxyethyl 1Hpyrrole2 5di
1-(2-Hydroxyethyl)-1H-pyrrole-2,5-dione, 1585-90-6, 97%
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Strem, An Ascensus Company CAS# 1585-90-6. 1g. N-(2-Hydroxyethyl)maleimide, 99%. MFCD00465266
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CAS# 1585-90-6. 1g. N-(2-Hydroxyethyl)maleimide, 99%. MFCD00465266. Molecular Weight: 141.13. Molecular Formula: C6H7NO3. Color/form: white pwdr. Strem# 07-1010. http://www.strem.com/catalog/v/07-1010/
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Innovative Research Inc Ms tPA Rcmb Act 100ug
Mouse tPA Recombinant Active 100ug - Mouse tPA Active Recombinant from Innovative Research has been recombinantly produced in insect cells and purified using affinity chromatography. This is a frozen liquid buffered in 0.4M HEPES; 0.1M NaCl; pH 7.4 and a purity of >95%. This product is useful as a positive control for ELISA and western blot and for a variety of in vitro applications including cell differentiation, cell signaling, clotting assays, fibrinolysis, plasminogen activation, protein-protein interactions, receptor binding, thromboelastography, and thrombolysis. >95% active. More Details Source Insect Cell Culture Purification Affinity purified Purity >95% Storage Conditions -70C
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Medchemexpress LLC HY-12600 5mg Medchemexpress, AZD5582 CAS:1258392-53-8 Purity:>98%
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Medchemexpress, HY-12600 5mg AZD5582 CAS:1258392-53-8 AZD5582 is an antagonist of the inhibitor of apoptosis proteins (IAPs), which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis. 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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Vector Laboratories CY5 5 MALEIMIDE-1MG
NC3877560 CY5 5 MALEIMIDE-1MG
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AdipoGen Bisindolylmaleimide II (5 mg)
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Chemical. CAS: 137592-45-1. Formula: C27H26N4O2. MW: 438.5. Protein kinase C (PKC) inhibitor. Binds with reversed orientation to protein kinase A (PKA).
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AdipoGen Bisindolylmaleimide I (5 mg)
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Chemical. CAS: 133052-90-1. Formula: C25H24N4O2. MW: 412.5. Cell permeable kinase inhibitor with improved selectivity for protein kinase C (PKC) (Ki = 10 nM). Competetive inhibitor for the ATP-binding site of PKC. Anti-inflammatory. Binds to P-glycoprotein. Telomerase activity inhibitor. Potent glycogen synthase kinase-3 (GSK-3) inhibitor. Necrosis inhibitor. Blocks hERG potassium channels. Promotes osteoblastogenesis in human mesenchymal stem cells.
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Enzo Life Sciences L-161-982 (5 mg). CAS: 147776-06-5
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A potent and selective prostaglandin EP4 receptor antagonist. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO (25 mg/ml). Long Term Storage: -20°C.
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Cayman Chemical 9 Z-TrIcosen 1g
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An insect pheromone used in pesticides; activates antennal basiconic Or7a receptors in Drosophila; produced by honey bees to communicate information about food sources
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Sigma Aldrich Fine Chemicals Biosciences N Ethylmaleimide crystalli100G
N Ethylmaleimide crystalli100G
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Medchemexpress LLC Doxorubicin-SMCC 25mg | 400647-59-8 | 762.76 | C39H42N2O14 | 25 MG
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Doxorubicin-SMCC is a drug-linker conjugate for antibody-drug conjugate (ADC) research that couples the anthracycline topoisomerase II inhibitor doxorubicin to a non-cleavable SMCC linker, producing a stable payload for bioconjugation and preclinical studies.
- Non-cleavable SMCC linker for stable conjugation.
- Acts as a DNA topoisomerase II inhibitor payload.
- Purity 98.8% and molecular weight 762.76.
- Orange to red solid physical form.
- Soluble in DMSO (125 mg/mL); ultrasonic recommended.
- CAS number 400647-59-8 for cross-referencing.
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569800 FLUORESCEIN-5-MALEIMIDE-10MG
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Cayman Chemical NArachidonyl Maleimide
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A potent inhibitor of monoacylglycerol lipase (IC50 = 140 nM in rat cerebellar membranes)
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Cayman Chemical 9 Z 11 E 13 EOctadecatrienoic
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A fatty acid agonist of PPARγ; activates PPARγ transcriptional activity in a reporter assay using RAW 264.7 cells at 10 µM; an inhibitor of DNA polymerase α, -β, -γ, -Δ, and -ε (IC50s = 10.7, 13.4, 10.6, 14, and 22 µM, respectively); an inhibitor of topoisomerase I and -II (IC50s = 20 and 5 µM, respectively); reduces the viability of, and induces apoptosis in, MCF-7 breast cancer cells in a concentration-dependent manner; induces ferroptosis in MDA-MB-231 breast cancer cells in an ACSL1-dependent manner; reduces clinical signs of disease in a model of DSS-induced IBD in PPARγ-expressing, but not PPARγ-knockout, mice
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Cayman Chemical BIsIndolylmaleImIde V 10mg
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A weak inhibitor of PKC demonstrating an IC50 value >100 µM; blocks the activation of mitogen-stimulated protein kinase p70s6k/p85s6k (S6K) in vivo with an IC50 value of 8 µM
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