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| Product | Description | |
|---|---|---|
| WB-3559B | WB-3559B is a fibrinolytic metabolite produced by Flavobacterium sp. Alternative Names: WB-3559 B; WB 3559 B. CAS No. 96053-96-2. Molecular formula: C37H68N2O7. Mole weight: 652.9. |  |
| WB-3559C | WB-3559C is a fibrinolytic metabolite produced by Flavobacterium sp. Alternative Names: WB-3559 C; WB 3559 C. CAS No. 96095-05-5. Molecular formula: C36H68N2O7. Mole weight: 640.9. | |
| WB-3559D | WB-3559D is a fibrinolytic metabolite produced by Flavobacterium sp. Alternative Names: WB-3559 D; WB 3559 D. CAS No. 96095-04-4. Molecular formula: C37H70N2O7. Mole weight: 655. | |
| WB 4101 hydrochloride | WB 4101 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 2170-58-3. Pack Sizes: 25mg. US Biological Life Sciences. |  Worldwide |
| WB436B | WB436B is a highly selective STAT3 inhibitor. WB436B can selectively inhibit STAT3-Tyr705 phosphorylation and the expression of STAT3 target genes, showing cytotoxic effects on pancreatic cancer cells and inducing apoptosis. WB436B can suppress tumor growth and metastasis in pancreatic cancer mouse models, extending the survival of tumor-bearing mice[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2248552-84-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-164546. |  |
| WBC100 | WBC100 (14-D-Valine-TPL) is a potent, selective, and orally active c-Myc molecule glue degrader. WBC100 is a c-Myc degrader and targets ubiquitin E3 ligase CHIP mediated 26S proteasome pathway. WBC100 is used for c-Myc overexpressing tumors research[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 14-D-Valine-TPL. CAS No. 2095780-08-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145898. | |
| WC/15Co | WC/15Co. Purity: 0.999. |  |
| WCA-80 | WCA-80. CAS No. 35430-88-7. | |
| WC-Co Alloy Powder | WC-Co alloy powder, the commonly used ratio is 90/10, 94/6, namely WC-6wt% Co and WC-10wt% Co. Purity: 99.9%. | |
| WCK-4234 | WCK-4234 is a diazabicyclooctane β-lactamase inhibitor and susceptibility restorer. WCK-4234 lacks direct antibacterial activity. WCK-4234 inhibits class A, C, D β-lactamases and extended-spectrum β-lactamases to potentiate Imipenem (HY-B1369A) and Meropenem (HY-13678) activity against Gram-negative pathogens. WCK-4234 can be used for the research of gram-negative bacterial infections and β-lactamase-mediated carbapenem-resistant bacterial infections[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1804915-68-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125604. | |
| WD6305 | WD6305 is a potent and selective METTL3-METTL14 PROTAC degrader. WD6305 has DC50 values of 140 nM and 194 nM for METTL3 and METTL14, respectively. WD6305 inhibits m6A modification and proliferation of AML cells, and induces apoptosis. WD6305 has antitumor activity[1].(Pink: UZH2 (HY-115717); Black: Linker; Blue: VHL ligand (HY-150803)). Uses: Scientific research. Category: Signaling pathways. CAS No. 3066823-45-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-160415. | |
| WDR5 0103 | WDR5 0103. Group: Biochemicals. Grades: Purified. CAS No. 890190-22-4. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| WDR5-0103 | WDR5-0103 (WD-Repeat Protein 5-0103) is a potent and selective WD repeat-containing protein 5 (WDR5) antagonist with a Kd of 450 nM. WDR5-0103 competitively binds to the peptide-binding pocket of WDR5, blocking the interaction between WDR5 and mixed-lineage leukemia (MLL) protein and inhibiting the methyltransferase activity of MLL. WDR5-0103 is mainly used in the research of cancer and neurodegenerative diseases[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: WD-Repeat Protein 5-0103. CAS No. 890190-22-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19347. | |
| WDR5 degrader-1 | WDR5 degrader-1 (compound 25) is a cereblon (CRBN)-recruiting WDR5 degrader. WDR5 degrader-1 selectively degraded WDR5 over the CRBN neo-substrate IKZF1[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3032434-45-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-162014. | |
| WDR5-IN-1 | WDR5-IN-1 is a potent and selective WD repeat domain 5 (WDR5) inhibitor, with a Kd of <0.02 nM. WDR5-IN-1 inhibits MLL1 histone methyltransferase (HMT) activity with an IC50 of 2.2 nM. WDR5-IN-1 diminishes MYC recruitment at WDR5-displaced genes and exhibits potent anti-proliferative effects in CHP-134 (neuroblastoma) and Ramos (Burkitts lymphoma) lines[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2408842-51-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133121. | |
| WDR5-IN-5 | WDR5-IN-5 is an orally active and selective inhibitor of WIN site of WD repeat domain 5 (WDR5). WDR5-IN-5 exhibits anti-proliferative activity towards cancer cells and good pharmacokinetics profile in mice. WDR5-IN-5 shows high affinity to WDR5 and the binding affinity Ki value <0.02 nM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2417012-26-9. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg. Product ID: HY-150654. | |
| WDR5-IN-6 | WDR5-IN-6 is a WDR5 inhibitor, targeting to WBM site. WDR5-IN-6 inhibits cell proliferation of neuroblastoma cell lines with potent anti-tumor activity. WDR5-IN-6 shows high synergy with OICR-9429 (HY-16993), a WDR5 inhibitor targeting to WIN site. WDR5-IN-6 can be used for reasearch in neuroblastoma[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 326901-92-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-154949. | |
| WD repeat domain 16 (145-175) | WD repeat domain 16 (145-175). | |
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| Weat Gluten Processing Complex Enzyme (Food Grade) | This product is a compound enzyme which designed for the processing of weat gluten. Applications: 1.influencing on the non-starch polysaccharides(nps) ,the viscosity of starches is increased. 2.increase the yield of starches and vital wheat glutens. 3.reduce the consumption of materials,water and energy. Group: Enzymes. Synonyms: Wheat Gluten Processing Complex Enzyme; Complex Enzyme; Wheat Gluten Processing; starch processing enzymes; starch; Wheat Gluten; Food Grade. Starch enzyme. Activity: 8,000,000u/ml. Storage: Should be stored in a cool place avoiding high temperature. Liquid: 3 months at 25°C, activity remain >90%; 6 months, activity remains >80%. Increase dosage after shelf life. Form: Liquid. Wheat Gluten Processing Complex Enzyme; Complex Enzyme; Wheat Gluten Processing; starch processing enzymes; starch; Wheat Gluten; Food Grade. Pack: 25kgs/drum, 1.125kgs/drum. Cat No: ASE-001. |  |
| WEB 2086 | WEB 2086. Group: Biochemicals. Grades: Purified. CAS No. 105219-56-5. Pack Sizes: 1mg, 10mg. US Biological Life Sciences. | Worldwide |
| Weck's Etchant | Weck's tint etch for Ti and alloys. | |
| Wedelialactone A | Wedelialactone A is isolated from the herbs of Wedelia trilobata. Alternative Names: Wedelialactone A; 175862-40-5; [(3aR,4R,4aS,5R,8R,8aR,9S,9aR)-5,8-dihydroxy-5,8a-dimethyl-3-methylidene-4-(2-methylpropanoyloxy)-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-9-yl] (E)-2-methylbut-2-enoate; AKOS040762504. Grades: 97.0%. CAS No. 175862-40-5. Molecular formula: C24H34O8. Mole weight: 450.53. | |
| Wedelolactone | Wedelolactone Inhibitor. Uses: Scientific use. Product Category: T3384. CAS No. 524-12-9. |  |
| Wedelolactone | Wedelolactone isolated from the herbs of Eclipta prostrata. It could significantly inhibit the activation of LX-2 cells. Uses: Anti-cancer. Alternative Names: 1,8,9-Trihydroxy-3-methoxy-6H-benzofuro[3,2-c][1]benzopyran-6-one. Grades: 98.5%. CAS No. 524-12-9. Molecular formula: C16H10O7. Mole weight: 314.3. | |
| Wedelolactone | Wedelolactone suppresses LPS-induced caspase-11 expression by directly inhibits the IKK Complex. Wedelolactone also inhibits 5-lipoxygenase (5-Lox) with an IC50 of 2.5 μM. Wedelolactone induces caspase-dependent apoptosis in prostate cancer cells via downregulation of PKCε without inhibiting Akt. Wedelolactone can extract from Eclipta alba, and it can be used for the research of cancer[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 524-12-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0551. | |
| Wedelolactone | Wedelolactone. Group: Biochemicals. Alternative Names: 5,11,12-Trihydroxy-7-methoxycoumestan. Grades: Plant Grade. CAS No. 524-12-9. Pack Sizes: 20mg. Molecular Formula: C16H10O7, Molecular Weight: 314.245999999999. US Biological Life Sciences. | Worldwide |
| WEE1-IN-4 | WEE1-IN-4 (compound 15) is a pyrrolocarbazole-1,3(2H,6H)-dione derivative and Wee1 kinase inhibitor with an IC50 value of 11 nM.WEE1-IN-4 can be used for the research of cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 622855-37-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108343. | |
| WEHI-345 | WEHI-345 is a potent and selective RIPK2 kinase inhibitor with an IC50 of 0.13 μM, which delays RIPK2 ubiquitylation and NF-κB activation on oligomerization domain (NOD) stimulation[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1354825-58-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18937. | |
| WEHI-345 | WEHI-345, a pyrazolo-pyridine derivative, is a RIPK2 inhibitor and has been found to influence the production of inflammatory cytokine. IC50: 0.13 μM. Uses: Wehi-345 is a ripk2 inhibitor and has been found to influence the production of inflammatory cytokine. Alternative Names: WEHI-345; WEHI345; WEHI 345. SCHEMBL10098386; CS-5045; HY-18937; CS 5045; HY 18937; CS5045; HY18937. Grades: 98%. CAS No. 1354825-58-3. Molecular formula: C22H23N7O. Mole weight: 401.46. | |
| WEHI-539 hydrochloride | WEHI-539 hydrochloride is a selective inhibitor of Bcl-XL with an IC50 of 1.1 nM. Uses: Scientific research. Category: Signaling pathways. CAS No. 2070018-33-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15607A. | |
| Weinreb linker | Weinreb linker. Group: Biochemicals. Alternative Names: Fmoc-N-methoxy-3-aminopropionic acid. Grades: Highly Purified. CAS No. 247021-90-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Weinreb Linker | Weinreb Linker. Alternative Names: 3-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methoxy)amino)propanoic acid; N-Fmoc-N-methoxy-3-aminopropionic acid; beta-Alanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methoxy-; N-Fmoc-N-methoxy-3-aminopropionicacid; PubChem11749; SCHEMBL1274753; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methoxy-Beta-alanine; Fmoc-N-methoxy-3-aminopropionic acid. Grades: > 97%. CAS No. 247021-90-5. Molecular formula: C19H19NO5. Mole weight: 341.36. | |
| Weinreb Resin | Weinreb Resin. Alternative Names: N-Fmoc-N-methoxy-beta-alanine, polymer bound. | |
| Welan gum | Welan gum is a natural polysaccharide produced by the bacterium Sphingomonas, known for its exceptional thickening and stabilizing properties. It is composed mainly of glucose, mannose, and rhamnose, with small amounts of glucuronic acid. Welan gum serves as a drug carrier in the pharmaceutical industry, improving the stability and controlled release of medications. Its high-efficiency thickening, combined with its temperature and salt resistance, shear-thinning properties, and biodegradability, make Welan gum a versatile and environmentally friendly choice for a wide range of applications. Alternative Names: BG 3810; Biozan; Bistop MN-W; Bistop W; Kelco Crete; Kelco Crete K 1C376; Kelco K 1A96; S 130; S 130 (gum); Wellan. CAS No. 96949-22-3. | |
| WESTON 430 | WESTON 430. Molecular formula: C12H27O9P. Mole weight: 346.31g/mol. IUPAC Name: tris[2-(2-hydroxyethoxy)ethyl] phosphite. SMILES: C(COCCOP(OCCOCCO)OCCOCCO)O. InChI: InChI=1S/C12H27O9P/c13-1-4-16-7-10-19-22(20-11-8-17-5-2-14)21-12-9-18-6-3-15/h13-15H,1-12H2. | |
| Weston EHDP | Weston EHDP. | |
| Weston PDDP | Weston PDDP. | |
| Weston TDP | Weston TDP. | |
| WESTREZ 5101P | WESTREZ 5101P. | |
| WEYIPNV | WEYIPNV is a ligand for SurA, specifically binding to the P1 domain of SurA (Kd: 1-14 μM). The binding of WEYIPNV promotes the release of the P1 domain from the core domain[1]. Uses: Scientific research. Category: Peptides. CAS No. 652969-14-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P10366. | |
| WF-10129 | WF-10129 is an angiotensin converting enzyme (ACE) inhibitor produced by Doratomyces putredinis, with IC50 of 1.4 X 10(-8) M. Alternative Names: WF 10129. CAS No. 109075-64-1. Molecular formula: C20H28N2O8. Mole weight: 424.4. | |
| WF11605 | WF11605 is an antagonist of leukotriene B4 (LTB4) isolated from the fungal strain F11605. It inhibited LTB4-induced chemotaxis of rabbit polymorphonuclear leukocytes (PMNLs) with an IC50 value of 1.7 x 10(-7) M and blocked 3H-LTB4 binding to PMNL membranes at 5.6 x 10(-6) M (IC50). It also inhibited LTB4-induced degranulation of rabbit PMNLs at 3.0 x 10(-6) M (IC50). Alternative Names: WF 11605; WF-11605. CAS No. 127475-47-2. Molecular formula: C38H60O11. Mole weight: 692.9. | |
| WF11899A | WF11899A is a lipopeptide antibiotic isolated from the culture broth of Coleophoma empetri F-11899. It shows antifungal activity against Candida spp. Alternative Names: WF-11899A. Molecular formula: C51H82N8O21S. Mole weight: 1175.3. | |
| WF11899B | WF11899B is a lipopeptide antibiotic isolated from the culture broth of Coleophoma empetri F-11899. It shows antifungal activity against Candida spp. Alternative Names: WF-11899B. Molecular formula: C51H82N8O20S. Mole weight: 1159.3. | |
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