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| Product | Description | |
|---|---|---|
| Y-1005 | Y-1005 is a quinone antibiotic isolated from Fusiform yeast stiain BY1. It is effective against gram-positive and -negative bacteria, as well as yeast. Molecular formula: C16H16O6. Mole weight: 304.29. |  |
| Y11 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Y11 | Y11 inhibits FAK1 autophosphorylation by blocking phosphorylation of Y397 and decreases tumor growth [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1086639-59-9. Pack Sizes: 1 mg. Product ID: HY-103471. |  |
| Y 11 | Y 11 is a potent inhibitor of focal adhesion kinase (FAK); Y 11 prevents FAK autophosphorylation at the Y397 site (IC50 ~ 50 nM in an in vitro kinase assay). Displays selectivity for FAK over a panel of other kinases (concentration used in assay = 1uM). Y 11 decreases cell viability in a number of cancer cell lines; blocks colony formation in SW620 and BT474 cell lines. Group: Biochemicals. Alternative Names: 1-(2-Hydroxyethyl)-3, 5, 7-triaza-1-azoniatricyclo[3. 3. 1. 13, 7]decane Bromide. Grades: Highly Purified. CAS No. 1086639-59-9. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Y 134 | Y 134. Group: Biochemicals. Grades: Purified. CAS No. 849662-80-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Y15 | Y15 is a potent and specific inhibitor of focal adhesion kinase (FAK) that inhibits its autophosphorylation activity, decreases the viability of cancer cells, and blocks tumor growth. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FAK Inhibitor 14. CAS No. 4506-66-5. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12444. | |
| Y15 | Y15. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,2,4,5-benzenetetramine tetrahydrochloride. Product Category: Amide & Amine Monomers. Appearance: Light Green to Green Solid Powder. CAS No. 4506-66-5. Molecular formula: C6H14Cl4N4. Mole weight: 284.01 g/mol. Purity: 0.98. Product ID: ACM-MO-4506665. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Y15 hydrochloride | Y15 hydrochloride, also known as FAK Inhibitor 14, is a direct FAK autophosphorylation inhibitor, blocking phosphorylation of Y397 with an IC50 value of about 1 μM. Y15 decreases viability, clonogenicity, and cell attachment in thyroid cancer cell lines and synergizes with targeted therapeutics. Y15 was shown to decrease cancer growth in vitro and in vivo. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Y15 hydrochloride; Y15 tetrahydrochloride; Y 15; Y-15. FAK Inhibitor 14. Product Category: Inhibitors. Appearance: Light green to green solid powder. CAS No. 4506-66-5. Molecular formula: C6H14Cl4N4. Mole weight: 284.01. Purity: >97%. IUPACName: 1,2,4,5-benzenetetramine tetrahydrochloride. Canonical SMILES: NC1=CC(N)=C(N)C=C1N.[H]Cl.[H]Cl.[H]Cl.[H]Cl. Product ID: ACM4506665. Alfa Chemistry ISO 9001:2015 Certified. | |
| Y16 | Y16 is a specific inhibitor of Leukemia-associated Rho guanine nucleotide exchange factor (LARG) with a K d value of 76 nM. Y16 is active in blocking the interaction of LARG and related G-protein-coupled Rho GEFs with RhoA. Y16 shows no detectable effect on other diffuse B-cell lymphoma (Dbl) family Rho GEFs, Rho effectors, or a RhoGAP [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 429653-73-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-12649. | |
| Y16 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Y1 receptor antagonist 1 | Y1 receptor antagonist 1 (H 409-22 isomer) is a neuropeptide Y1 receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: H 409-22 (isomer). CAS No. 221697-09-2. Pack Sizes: 1 mg. Product ID: HY-101704. | |
| Y-20XP | Y-20XP. Group: Polymers. |  |
| Y-25130 hydrochloride | Y-25130 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 123040-16-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Y-25X | Y-25X. Group: Polymers. | |
| Y-26763 | Y-26763. Group: Biochemicals. Grades: Purified. CAS No. 127408-31-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Y-27152 | Y-27152. Group: Biochemicals. Grades: Purified. CAS No. 127408-30-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Y-27632 | Y-27632 Inhibitor. Uses: Scientific use. Product Category: T1725. CAS No. 129830-38-2. |  |
| Y-27632 | Y-27632 is an orally active, ATP-competitive inhibitor of ROCK-I and ROCK-II , with K i s of 220 and 300 nM, respectively. Y-27632 attenuates Doxorubicin-induced apoptosis of human cardiac stem cells. Y-27632 also suppresses dissociation-induced apoptosis of murine prostate stem/progenitor cells. Y-27632 primes human induced pluripotent stem cells (hIPSCs) to selectively differentiate towards mesendodermal lineage via epithelial-mesenchymal transition-like modulation [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. CAS No. 146986-50-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-10071. | |
| Y-27632 - CAS 146986-50-7 | Y-27632A, CAS 146986-50-7, is a cell-permeable, reversible, inhibitor of Rho kinases (Ki = 140 nM for p160ROCK). Enhances survival & cloning efficiency of ESC without affecting their pluripotency. Group: Fluorescence/luminescence spectroscopy. | |
| Y-27632-d4 Dihydrochloride Hydrate (ROCK Inhibitor) | A labeled Rho kinase inhibitor (ROCK) for the treatment of ischemia-reperfusion disorders. Group: Biochemicals. Alternative Names: trans-4-[(1R)-1-Aminoethyl]-N-4-pyridinyl-cyclohexanecarboxamide-d4 Dihydrochloride Monohydrate. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Y-27632 dihydrochloride | Y-27632 dihydrochloride is an orally active and ATP-competitive ROCK ( Rho-kinase ) inhibitor (ROCK-I K i =220 nM; ROCK-II K i =300 nM). Y-27632 dihydrochloride shows antiepileptic effects [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 129830-38-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10583. | |
| Y-27632 dihydrochloride | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Y-27632 Dihydrochloride | Y-27632 is a selective inhibitor of Rho-associated coiled-coil forming protein serine/threonine kinase (ROCK) family of protein kinases that selectively competes with ATP for binding to the catalytic site. It is reported to diminish dissociation-induced apoptosis, increase cloning efficiency, and facilitate subcloning after gene transfer in human embryonic stem cells (hES). Group: Biochemicals. Alternative Names: trans-4- [ (1R) -1-Aminoethyl] -N-4-pyridinylcyclohexane carboxamide Dihydrochloride; (+) - (R) -trans-4- (1-aminoethyl) -N- (4-pyridyl) cyclohexanecarboxamide Dihydrochloride; (+) -trans-N- (4-Pyridyl) -4- [ (R) -1-aminoethyl] cyclohexanecarboxamide Dihydrochloride. Grades: Highly Purified. CAS No. 129830-38-2. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C??H??N?O; 2(HCl), Molecular Weight: 320.3. US Biological Life Sciences. | Worldwide |
| Y-27632 dihydrochloride (GMP) | Y-27632 dihydrochloride (GMP) is the GMP level of Y-27632 dihydrochloride (HY-10583). GMP guidelines are used to produce Y-27632 dihydrochloride (GMP). GMP small molecules works appropriately as an auxiliary reagent for cell research manufacture. Y-27632 dihydrochloride is an orally active and ATP-competitive ROCK (Rho-kinase) inhibitor with antiepileptic effect[1][2][3][4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 129830-38-2. Pack Sizes: 10 mg; 50 mg; 100 mg. Product ID: HY-10583G. | |
| Y-27632 (dihydrochloride) (Standard) | Y-27632 (dihydrochloride) (Standard) is the analytical standard of Y-27632 (dihydrochloride). Y-27632 dihydrochloride is an orally active and ATP-competitive ROCK ( Rho-kinase ) inhibitor (ROCK-I K i =220 nM; ROCK-II K i =300 nM). Y-27632 dihydrochloride shows antiepileptic effects [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 129830-38-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10583R. | |
| Y-29794 oxalate | Y-29794 oxalate. Group: Biochemicals. Grades: Purified. CAS No. 146794-84-5. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Y2O3 stabilized ZrO2 Nano Powder | Y2O3 stabilized ZrO2 Nano Powder. Group: Oxides nanoparticles. 99.95+%. | |
| Y-33075 | Y-33075 is a selective ROCK inhibitor derived from Y-27632, and is more potent than Y-27632, with an IC50 of 3.6 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Y-39983 free base. CAS No. 199433-58-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-10067. | |
| Yacon powder | Yacon powder is a brown powder, using fresh yacon, maximize the retention of nutrients. It has a fresh, vivid yacon unique flavor. Easy to use, mellow taste. Group: Others. Yacon powder. Cat No: EXTC-148. |  |
| yadanziolide A | Yadanziolide A is extracted from seeds of Brucea javanica. It has strong antiviral activity. Synonyms: yadanziolide A; 95258-14-3; (1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R)-2,3,12,15,16-Pentahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione; CHEMBL2037039; HY-N4210; AKOS040760154; AC-34985; DA-61914; MS-27518; CS-0032442; G18579; (1R,2R,3R,6R,8S,12S,13S,14R,15R,16S,17R)-2,3,12,15,16-pentahydroxy-17-(hydroxymethyl)-9,13-dimethyl-5,18-dioxapentacyclo[12.5.0.0(1),?.0(2),(1)?.0?,(1)(3)]nonadec-9-ene-4,11-dione. Grade: 98.0%. CAS No. 95258-14-3. Molecular formula: C23H30O9. Mole weight: 450.5. | |
| Yadanziolide C | Yadanziolide C is extracted from the seeds of Brucea javanica. It could induce differentiation with cultured HL-60 promyelocytic leukemia cells. Synonyms: (+)-13,20-Epoxy-1α,11β,12α,14,15β-pentahydroxypicrasa-3-ene-2,16-dione. Grade: 96.5%. CAS No. 95258-12-1. Molecular formula: C20H26O9. Mole weight: 410.41. | |
| Yadanzioside A | Yadanzioside A is extracted from the seeds of Brucea javanica. It is a biochemical chemical and shows antileukemic activity. Synonyms: methyl dihydroxy-dimethyl-(3-methylbutanoyloxy)-dioxo-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-[?]carboxylate; (11beta,12alpha,15beta)-13,20-Epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-(3-methyl-1-oxobutoxy)-3,16-dioxo-picras-1-en-21-oic acid methyl ester; Picras-1-en-21-oic acid, 13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-dihydroxy-15-((3-methyl-1-oxobutoxy)-3,16-dioxo-, methyl ester, (11-beta,12-alpha,15-beta)-. Grade: 98.0%. CAS No. 95258-15-4. Molecular formula: C32H44O16. Mole weight: 684.68. | |
| Yadanzioside F | Yadanzioside F is extracted from the seeds of Brucea javanica. It is a biochemical chemical and shows antileukemic activity. Synonyms: Picras-1-en-21-oic acid, 15-(acetyloxy)-11,12-dihydroxy-3,16-dioxo-13,20-epoxy-2-(beta-D-glucopyranosyloxy)-, methyl ester, (11-beta,12-alpha,15-beta)-. Grade: 98.0%. CAS No. 95258-11-0. Molecular formula: C29H38O16. Mole weight: 642.60. | |
| Yadanzioside I | Yadanzioside I is extracted from the seeds of Brucea javanica. It has strong antiviral activity. Synonyms: Yadanzioside I; 99132-95-3; AKOS040762515; DA-68760; B0005-267620. Grade: 96.0%. CAS No. 99132-95-3. Molecular formula: C29H38O16. Mole weight: 642.6. | |
| Yadanzioside K | Yadanzioside K is extracted from the seeds of Brucea javanica. Synonyms: Picras-3-en-21-oicacid, 15-[[(2E)-4-(acetyloxy)-3,4-dimethyl-1-oxo-2-pentenyl]oxy]-13,20-epoxy-3-(b-D-glucopyranosyloxy)-11,12-dihydroxy-2,16-dioxo-, methyl ester, (11b,12a,15b)- (9CI). Grade: 97.0%. CAS No. 101559-98-2. Molecular formula: C36H48O18. Mole weight: 768.76. | |
| Yadanzioside M | Yadanzioside M is extracted from the seeds of Brucea javanica. It has antitumor activity. Synonyms: Methyl benzoyloxy-dihydroxy-dimethyl-dioxo-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-[?]carboxylate; Picras-1-en-21-oic acid, 15-(benzoyloxy)-13,20-epoxy-2-(beta-D-glucopyranosyloxy)-11,12-di- hydroxy-3,16-dioxo-, methyl ester, (11beta,12alpha,15beta)-. Grade: 97.0%. CAS No. 101559-99-3. Molecular formula: C34H40O16. Mole weight: 704.68. | |
| Yaddle1 | Yaddle1 is an agonist of the mechano-activated ion channel (Piezo1) with a half-maximal effective concentration (MEC50) of 0.40 ?M. Yaddle1 can significantly trigger Ca2+ inflow in T cells and induce T cell activation response. Yaddle1 can be used in the study of vaccine adjuvants[1]. Uses: Scientific research. Group: Signaling pathways. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-162501. | |
| YAG Dispersion | YAG Dispersion. Group: Oxide nano dispersion. CAS No. 12005-21-9. Molecular formula: 593.62g/mol. Mole weight: Y3Al5O12. 99.5+%. | |
| Yam Extract | Yam extract contains diosgenin, which has anti-fatigue, anti-inflammatory, anti-stress. Yam extract is antispasmodic, and could be helpful for nausea of pregnant women (morning sickness), spasmodic hiccough and asthma. Group: Others. Mole weight: 414.63. Wild Yam Extract; Rhizoma Dioscoreae. Cat No: EXTC-017. | |
| Yamogenin | Yamogenin is a sapogenin compound found in the plant amber fenugreek, with steroid framework, that maintains antidiabetogenic activity. They also provide framework for the synthesis of a potential inhibitor of metallo- β-lactamase-1 which is a major target in the treatment of diseases involving gram-negative bacteria. Group: Biochemicals. Alternative Names: (22R,25S)-(20α)-Spirost-5-en-3 β-ol; Jamogenin; NSC 226132; (25S)-Spirost-5-en-3 β-ol; Neodiosgenin; (3 β,25S)-Spirost-5-en-3-ol. Grades: Highly Purified. CAS No. 512-06-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Yamogenin | Yamogenin (Neodiosgenin) is a diastereomer of diosgenin. Yamogenin (Neodiosgenin) antagonizes the activation of the liver X receptor (LXR) in luciferase ligand assay. Yamogenin (Neodiosgenin) inhibits triacylglyceride (TG) accumulation through the suppression of gene expression of fatty acid synthesis in HepG2 hepatocytes [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Neodiosgenin. CAS No. 512-06-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N2078. | |
| Yangonin | Yangonin exhibits affinity for the human recombinant cannabinoid CB1 receptor with an IC 50 and a K i of 1.79 μM and 0.72 μM, respectively. Uses: Scientific research. Group: Natural products. CAS No. 500-62-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0919. | |
| Yangonin | A lactone isolated from the Kava plant (Piper methysticum). Group: Biochemicals. Alternative Names: 4-Methoxy-6-[(1E)-2-(4-methoxyphenyl)ethenyl]-thoxy-α-pyrone. Grades: Highly Purified. CAS No. 500-62-9. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Yangonin-d3 | Yangonin-d3. Group: Biochemicals. Alternative Names: 4-Methoxy-6-[(1E)-2-(4-methoxyphenyl)ethenyl]-. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C16H15D3O4. US Biological Life Sciences. | Worldwide |
| yapsin 1 | In peptidase family A1 of pepsin, and weakly inhibited by pepstatin. Can partially substitute for kexin in a deficient strain of yeast. The homologous product of the Mkc7 gene (Saccharomyces cerevisiae) has similar catalytic activity and has been termed yapsin 2. Group: Enzymes. Synonyms: yeast aspartic protease 3; Yap3 gene product (Saccharomyces cerevisiae). Enzyme Commission Number: EC 3.4.23.41. CAS No. 205132-58-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4278; yapsin 1; EC 3.4.23.41; 205132-58-7; yeast aspartic protease 3; Yap3 gene product (Saccharomyces cerevisiae). Cat No: EXWM-4278. | |
| YAP/TAZ inhibitor-1 | YAP/TAZ inhibitor-1 is a YAP/TAZ inhibitor extracted from patent WO2017058716A1, Compound 1, has an IC50 of <0.100 ?? in firefly luciferase assay[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2093565-23-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-111429. | |
| YAP-TEAD Inhibitor 1 | YAP-TEAD Inhibitor 1 is a potent inhibitor of YAP-TEAD interaction with IC50 value of 25 nM. Synonyms: YAP-TEAD-IN-1; YAP-TEAD (Peptide 17). Grade: 98%. CAS No. 1659305-78-8. Molecular formula: C93H144ClN23O21S2. Mole weight: 2019.86. | |
| Yara Yara | Yara Yara (Nerolin Yara Yara). CAS No. 93-04-9. FEMA No. 4704. VIGON Item # 500961. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers. |  America & Internationally |
| Yarrow P.E. 4:1 & 10:1 | Yarrow P.E. 4:1 & 10:1. |  CA, FL & NJ |
| Yatakemycin | It is an antifungal antibiotic produced by the strain of Streptomyces sp. TP-A0356. Its anti-fungal activity against Aspergillus fumigatus, Aspergillus flavus, Aspergillus Niger, Candida albicans and Cryptococcus neoformans is stronger than Amphotericin B and Etraconazole (MIC is 0.0039-0.0156 μg/mL). It also has strong cytotoxicity to P388, HeLa, HEL and other tumor cells (IC50 is 0.01-0.33 μg/mL). Synonyms: (+)-yatakemycin; Ethanethioic acid, S-(6-(((7bR,8aS)-1,2,4,5,8,8a-hexahydro-2-((6-hydroxy-5-methoxy-1H-indol-2-yl)carbonyl)-4-oxocyclopropa(c)pyrrolo(3,2-e)indol-6-yl)carbonyl)-3,6,7,8-tetrahydro-5-hydroxy-4-methoxybenzo(1,2-b:4,3-b')dipyrrol-2-yl) ester. CAS No. 606136-98-5. Molecular formula: C35H29N5O8S. Mole weight: 679.70. | |
| Yatein | Yatein is a lignan isolated from A. chilensis, with antiproliferative activity. Yatein suppresses herpes simplex virus type 1 (HSV-1 ) replication by interruption the immediate-early gene expression. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (3R)-3α-(3,4,5-Trimethoxybenzyl)-4β-(1,3-benzodioxole-5-ylmethyl)tetrahydrofuran-2-one. Product Category: Inhibitors. Appearance: Powder. CAS No. 40456-50-6. Molecular formula: C22H24O7. Mole weight: 400.4. Purity: 0.98. IUPACName: (3R,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one. Canonical SMILES: COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4. Density: 1.266±0.06 g/ml. Product ID: ACM40456506. Alfa Chemistry ISO 9001:2015 Certified. Categories: Yatinuwara Polling Division. | |
| YC-001 | YC-001 is an inverse agonist and antagonist of rod opsin. YC-001 reversibly binds rod opsin and stabilizes the rod opsin structure. YC-001 protects mice from bright light-induced retinal degeneration. YC-001 has the potential for the research of retinal degeneration[1]. Uses: Scientific research. Group: Natural products. CAS No. 748778-73-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-124717. | |
| YC 1 | YC 1. Group: Biochemicals. Grades: Highly Purified. CAS No. 170632-47-0. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| YC-1 | powder. Group: Fluorescence/luminescence spectroscopy. | |
| YC-1 | Nitric oxide (NO) independent, superoxide-sensitive soluble guanylyl cyclase (sGC) activator. Induces concentration-dependent increase in cGMP levels. Inhibits platelet adhesion to collagen. Thombosis inhibitor. Non-specific phosphodiesterase inhibitor. Na+ channel blocker. Anticancer compound. HIF-alpha inhibitor. Blocks angiogenesis. Tumor growth inhibitor. Apoptosis inducer. NK cell differentiation enhancer. Group: Biochemicals. Alternative Names: 1-Benzyl-3-(5-hydroxymethylfur-2-yl)indazole; Lificiguat, 3-(5'-Hydroxymethyl-2'-furyl)-1-benzylindazole. Grades: Highly Purified. CAS No. 170632-47-0. Pack Sizes: 1mg, 5mg, 25mg. Molecular Formula: C??H??N?O?, Method for Determining. US Biological Life Sciences. | Worldwide |
| YCT529 | YCT529 is a potent, selective and orally active RAR-α inhibitor [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2863670-67-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153122A. | |
| YD2 | Alfa Chemistry offers YD2 products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Dye-sensitized solar cell (dssc) materials phthalocyanine dyes, porphyrin dyes. Alternative Names: [5-[Bis(4-hexylphenyl)amino]-15-[2-(4-carboxyphenyl)ethynyl]-10,20-bis(3,5-di-tert-butylphenyl)porphyrinato]zinc(II). CAS No. 1201915-91-4. Product ID: zinc; 4-[2-[10,20-bis(3,5-ditert-butylphenyl)-15-(4-hexyl-N-(4-hexylphenyl)anilino)porphyrin-22,24-diid-5-yl]ethynyl]benzoic acid. Molecular formula: 1230.02. Mole weight: C81H89N5O2Zn. CCCCCCC1=CC=C (C=C1)N (C2=CC=C (C=C2)CCCCCC)C3=C4C=CC (=N4)C (=C5C=CC (=C (C6=NC (=C (C7=CC=C3[N-]7)C8=CC (=CC (=C8)C (C) (C)C)C (C) (C)C)C=C6)C#CC9=CC=C (C=C9)C (=O)O)[N-]5)C1=CC (=CC (=C1)C (C) (C)C)C (C) (C)C. [Zn+2]. InChI=1S/C81H90N5O2. Zn/c1-15-17-19-21-23-53-27-34-63 (35-28-53) 86 (64-36-29-54 (30-37-64) 24-22-20-18-16-2) 76-72-45-43-70 (84-72) 74 (57-47-59 (78 (3, 4) 5) 51-60 (48-57) 79 (6, 7) 8) 68-41-39-66 (82-68) 65 (38-31-55-25-32-56 (33-26-55) 7 | |
| YD23 | YD23 is a SMARCA2 PROTAC. YD23 induces degradation of SMARCA2, which is synthetic lethal to SMARCA4. Moreover, YD23 decreases chromatin accessibility at enhancers of a number of genes including cell cycle and cell growth regulatory genes. YD23 reduces chromatin accessibility only in SMARCA4 deficient cells mechanistically[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2951015-29-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153361. | |
| YD2, 97% | YD2, 97%. Group: other glass and ceramic materials. CAS No. 1201915-91-4. Product ID: zinc; 4-[2-[10,20-bis(3,5-ditert-butylphenyl)-15-(4-hexyl-N-(4-hexylphenyl)anilino)porphyrin-22,24-diid-5-yl]ethynyl]benzoic acid. Molecular formula: 1230g/mol. Mole weight: C81H89N5O2Zn. CCCCCCC1=CC=C (C=C1)N (C2=CC=C (C=C2)CCCCCC)C3=C4C=CC (=N4)C (=C5C=CC (=C (C6=NC (=C (C7=CC=C3[N-]7)C8=CC (=CC (=C8)C (C) (C)C)C (C) (C)C)C=C6)C#CC9=CC=C (C=C9)C (=O)O)[N-]5)C1=CC (=CC (=C1)C (C) (C)C)C (C) (C)C. [Zn+2]. InChI=1S/C81H90N5O2. Zn/c1-15-17-19-21-23-53-27-34-63 (35-28-53) 86 (64-36-29-54 (30-37-64) 24-22-20-18-16-2) 76-72-45-43-70 (84-72) 74 (57-47-59 (78 (3, 4) 5) 51-60 (48-57) 79 (6, 7) 8) 68-41-39-66 (82-68) 65 (38-31-55-25-32-56 (33-26-55) 77 (87) 88) 67-40-42-69 (83-67) 75 (71-44-46-73 (76) 85-71) 58-49-61 (80 (9, 10) 11) 52-62 (50-58) 81 (12, 13) 14; /h25-30, 32-37, 39-52H, 15-24H2, 1-14H3, (H2-, 82, 83, 84, 85, 87, 88) ; /q-1; +2/p-1. UUCNKZFNPQUPQT-UHFFFAOYSA-M. | |
| YE 120 | YE 120. Group: Biochemicals. Grades: Highly Purified. CAS No. 383124-82-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| YE6144 | YE6144 is a prototypical interferon regulatory factor 5 (IRF5) inhibitor. YE6144 selectively suppresses IRF5 activity through inhibition of IRF5 phosphorylation[1]. Uses: Scientific research. Group: Signaling pathways. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-150095. | |
| Yeast Beta Glucan (1,3/1,6) 70% & 85% | Yeast Beta Glucan (1,3/1,6) 70% & 85%. | CA, FL & NJ |
| Yeast Brewers | Debittered, BioReagent, suitable for insect cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Yeast, Brewer's, Powder, Laboratory Grade, 500 g | Brewer's Yeast, Powder, Laboratory Grade, 500 g. Grades: chem-grade laboratory. Product ID: 898900. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Yeast extract | 1kg Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials. Formula: N/A. CAS No. 8013-1-2. Prepack ID 35752308-1kg. See USA prepack pricing. |  |
| Yeast extract | 100g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials. Formula: N/A. CAS No. 8013-1-2. Prepack ID 35752308-100g. See USA prepack pricing. | |
| Yeast extract | Yeast extract. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Yeast extract;Yeast extract, paste;Yeast extract, powder. Product Category: Heterocyclic Organic Compound. CAS No. 8013-1-2. Product ID: ACM2232731. Alfa Chemistry ISO 9001:2015 Certified. | |
| Yeast extract | Yeast extract is a concentrate of the soluble part of yeast, especially Saccharomyces cerevisiae. The main nutritional components of yeast extract include partly hydrolyzed protein with 35-40% of free amino acid, and it also contain B vitamins and some trace elements. Yeast extract can be used as nutrients for bacterial culture media [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 8013-1-2. Pack Sizes: 50 g; 100 g. Product ID: HY-153126. | |
| Yeast Extract Polar | Yeast Extract Polar. Group: Others. Stability: 3 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; natural lipids; natural; synthetic lipid; synthetic; modified lipids; headgroup modified lipids; fatty acid modified lipids; singnal transduction; cell pathways; Yeast Extract Polar; Yeast Polar Lipid Extract (S. cerevisiae). Cat No: NSMZ-048. | |
| Yeast Extract Total | Yeast Extract Total. Group: Others. Stability: 3 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; natural lipids; natural; synthetic lipid; synthetic; modified lipids; headgroup modified lipids; fatty acid modified lipids; singnal transduction; cell pathways; Yeast Extract Total; Yeast Total Lipid Extract (S. cerevisiae). Cat No: NSMZ-047. | |
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