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| Product | Description | |
|---|---|---|
| Somatostatin monoacetate | Somatostatin monoacetate is a peptide hormone. It regulates the endocrine system and affects neurotransmission and cell proliferation by interaction with G protein-coupled somatostatin receptors and inhibition of the release of numerous secondary hormones. It inhibits insulin and glucagon secretion. Synonyms: Somatostatin (sheep), monoacetate (salt); H-Ala-Gly-Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Cys-OH.CH3CO2H (Disulfide bridge: Cys3-Cys14); L-alanyl-glycyl-L-cysteinyl-L-lysyl-L-asparagyl-L-phenylalanyl-L-phenylalanyl-L-tryptophyl-L-lysyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-cysteine (3->14)-disulfide acetic acid. Grades: 98%. CAS No. 54472-66-1. Molecular formula: C78H108N18O21S2. Mole weight: 1697.95. |  |
| Somatostatin (Sheep) | It is a growth hormone-release inhibiting factor used in the treatment of severe, acute hemorrhages of gastroduodenal ulcers. It's an experimental diabetes drug. Uses: Growth hormone-release inhibiting factor; treatment of severe, acute hemorrhage of gastroduodenal ulcers; experimental antidiabetic. Synonyms: SRIF-14; Somatostatin-14; H-Ala-Gly-Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Cys-OH (Disulfide bridge: Cys3-Cys14); Cyclic somatostatin; 15-28-Somatostatin-28 (sheep); 15:PN:WO2007081792 SEQID:30 claimed protein. Grades: >98%. CAS No. 38916-34-6. Molecular formula: C76H104N18O19S2. Mole weight: 1637.88. | |
| Sombrevin | Sombrevin. Group: Biochemicals. Alternative Names: 4-[2-(Diethylamino)-2-oxoethoxy]-3-methoxybenzeneacetic Acid Propyl Ester; 13245RP; 2180TH; BAY 1420; Epontol; FBA 1420; Fabantol; Fabontal; Propanidid; Propanidide; Propantan; Propyl 4- (N, N-Diethyl carbamidomethoxy) -3-methoxy-phenyl acetate; Propyl [4-[ (Diethylcarbamoyl) methoxy]-3-methoxyphenyl]acetate; TH 2180; WH 5668; [4-[ (Diethylcarbamoyl) methoxy]-3-methoxyphenyl]acetic Acid Propyl Ester. Grades: Highly Purified. CAS No. 1421-14-3. Pack Sizes: 500mg. Molecular Formula: C18H27NO5, Molecular Weight: 337.41. US Biological Life Sciences. |  Worldwide |
| Sombrevin-d7 | Sombrevin-d7. Group: Biochemicals. Alternative Names: 4-[2-(Diethylamino)-2-oxoethoxy]-3-methoxybenzeneacetic Acid Propyl Ester-d7; 13245RP-d7; 2180TH-d7; BAY 1420-d7; Epontol-d7; FBA 1420-d7; Fabantol-d7; Fabontal-d7; Propanidid-d7; Propanidide-d7; Propantan-d7; Propyl 4- (N, N-Diethyl carbamidomethoxy) -3-methoxy-phenyl acetate-d7; Propyl [4-[ (Diethylcarbamoyl) methoxy]-3-methoxyphenyl]acetate-d7; TH 2180-d7; WH 5668-d7; [4-[ (Diethylcarbamoyl) methoxy]-3-methoxyphenyl]acetic Acid Propyl Ester-d7. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C18H20D7NO5, Molecular Weight: 344.45. US Biological Life Sciences. | Worldwide |
| S-ω-Amino Acid Transaminase (Crude Enzyme) | This product with the indicated enzyme activity was briefly purified from engineered E. coli. Group: Enzymes. Enzyme Commission Number: EC 2.6.1.x. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. S-ω-Amino Acid Transaminase. Pack: 100ml. Cat No: NATE-1823. |  |
| Sonedenoson | Sonedenoson is an adenosine A2 receptor agonist under the development of King Pharmaceuticals Research and Development. It can effectively promote rapid wound healing. By stimulating adenosine A2 receptor, Sonedenoson can increase angiogenesis by down-regulating production of the antiangiogenic matrix protein thrombospondin 1. In Feb 2008, Sonedenoson was still in Phase II trials for wound healing in the United States, and treatment for Diabetic foot ulcer was discontinued. Uses: Diabetic foot ulcer;wound healing. Synonyms: MRE0094; MRE-0094; MRE 0094; Sonedenoson ;(2R,3R,4S,5R)-2-(6-amino-2-(4-chlorophenethoxy)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol. Grades: 95%. CAS No. 131865-88-8. Molecular formula: C18H20ClN5O5. Mole weight: 421.83. | |
| Sonelokimab | Sonelokimab is a novel trivalent nanobody comprised of monovalent camelid-derived nanobodies specific to human interleukin IL-17A, IL-17F, and human serum albumin. Sonelokimab has been used in the research of plaque psoriasis. Synonyms: ALX 0761; M 1095. CAS No. 1414386-05-2. | |
| Sonelokimab | Sonelokimab (ALX 0761) is a trivalent bispecific nanobody composed of camel derived humanized IL-17F antibodies, IL-17A/F antibodies, and serum albumin VHH antibodies. Sonelokimab can prolong the plasma half-life by binding to human serum albumin. Sonelokimab can be used for research on rheumatoid arthritis and psoriasis [1] [2] [3] [4]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: ALX 0761; M 1095. CAS No. 1414386-05-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99397. |  |
| Sonepcizumab | Sonepcizumab (LT 1009) is a fully human anti- S1P monoclonal antibody. Sonepcizumab has the potential for the research of metastatic renal cell carcinoma (mRCC) [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: LT 1009; Anti-Human S1P Recombinant Antibody. CAS No. 1031360-18-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99318. | |
| Sonepiprazole | Sonepiprazole (PNU-101387G) is a selective D4 dopamine antagonist with K i s of 3.6, 10.1, 5147, and 7430 nM for rD4-Dopamine, hD4.2-Dopamine, rD2-Dopamine, and Histamine-H1 receptors, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PNU-101387G; U-101387G. CAS No. 170858-33-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14328. | |
| Sonepiprazole | Sonepiprazole is a selective, brain penetrating and orally bioactive antagonist for the rat and human dopamine D4 receptor (Ki = 10 nM) with low affinity at other monoamine receptors (Ki > 2000 nM). Sonepiprazole was shown to induce c-fos gene expression in medial prefrontal cortex in a similar manner to clozapine. Synonyms: 4-[4-[2-[(1S)-3,4-Dihydro-1H-2-benzopyran-1-yl)ethyl]-1-piperazinyl]-benzenesulfonamide. Grades: ≥98% by HPLC. CAS No. 170858-33-0. Molecular formula: C21H27N3O3S. Mole weight: 401.52. | |
| Sonepiprazole | A selective D4 dopamine antagonist that exhibits low affinity at other monoamine receptors (Ki > 2000 nM). Induces c-fos gene expression in medial prefrontal cortex in a similar manner to Clozapine. Group: Biochemicals. Alternative Names: 4- [4- [2- [ (1S) -3, 4-Dihydro-1H-2-benzopyran-1-yl] ethyl] -1-piperazinyl] benzenesulfonamide; PNU 101387; U 101387; (S) -4- [4- [2- (3, 4-Dihydro-1H-2-benzopyran-1-yl) ethyl] -1-piperazinyl] benzenesulfonamide; PF-05191680. Grades: Highly Purified. CAS No. 170858-33-0. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Sonepiprazole hydrate | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Sonepiprazole hydrochloride | Sonepiprazole hydrochloride is a selective dopamine D4 antagonist and displays low affinity for other dopamine receptors, and noradrenalin, serotonin and histamine receptor families (Ki > 2000 nM). Synonyms: PNU 101387 hydrochloride; PNU101387 hydrochloride; PNU-101387 hydrochloride; 4-[4-[2-[(1S)-3,4-Dihydro-1H-2-benzopyran-1-yl)ethyl]-1-piperazinyl]-benzenesulfonamide hydrochloride. Grades: 98%. CAS No. 170857-36-0. Molecular formula: C21H27N3O3S.HCl. Mole weight: 437.98. | |
| Songorine | Songorine. Group: Biochemicals. CAS No. 509-24-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Sonic Hedgehog from mouse | recombinant, expressed in E. coli, ?97% (SDS-PAGE), ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Sonic Hedgehog Peptide from mouse | ?97% (SDS-PAGE), recombinant, expressed in E. coli, Fused to a histidine tag at the C-terminus, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Sonidegib | Sonidegib is an orally bioavailable small-molecule Smoothened (Smo) antagonist with potential antineoplastic activity. It was approved by the FDA for treating basal-cell carcinoma in July 2015. Synonyms: Erismodegib; LDE225; NVP-LDE225; Odomzo; N-[6-[(2S,6R)-2,6-dimethylmorpholin-4-yl]pyridin-3-yl]-2-methyl-3-[4-(trifluoromethoxy)phenyl]benzamide. Grades: >98%. CAS No. 956697-53-3. Molecular formula: C26H26F3N3O3. Mole weight: 485.507. | |
| Sonidegib | Sonidegib (Erismodegib) is a potent and selective Smo antagonist with IC 50 of 1.3 nM and 2.5 nM for mouse and human Smo in binding assay, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Erismodegib; LDE225; NVP-LDE225. CAS No. 956697-53-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16582A. | |
| Sonlicromanol | Sonlicromanol (KH176) is an orally active reactive oxygen species (ROS) modulator for the study in mitochondrial disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KH176. CAS No. 1541170-75-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-121577. | |
| Sonlicromanol hydrochloride | Sonlicromanol (KH176) hydrochloride, a chemical entity derivative of Trolox, is a blood-brain barrier permeable ROS-redox modulator. Sonlicromanol (KH176) hydrochloride is used in the study for mitochondrial disorders [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KH176 hydrochloride. CAS No. 2162149-24-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120332. | |
| Sonoflora 1 | Sonoflora 1, a kind of PDT photosensitivizer, was once studied against breast cancer and the Phase I/II trial has been already discontinued by SonneMed. Synonyms: Sonoflora 1; Sonoflora1; Sonoflora-1; SF1; SF-1; SF 1; Stannate(3-)?, [N-[2-[(7S, ?8S)?-3-carboxy-7-(2-carboxyethyl)?-13-ethenyl-18-ethyl-2, ?8, ?12, ?17-tetramethyl-21H, ?23H-porphin-5-yl-κ N21, ?κ N22, ?κ N23, ?κ N24]?acetyl]?glycylglycinato(5-). Grades: 98%. CAS No. 1609250-37-4. Molecular formula: C38H42N6O10Sn. Mole weight: 861.48. | |
| Sonolisib | Sonolisib, also known as PX-866, is a small-molecule wortmannin analogue inhibitor of the alpha, gamma, and delta isoforms of phosphoinositide 3-kinase (PI3K) with potential antineoplastic activity. PI3K inhibitor PX-866 inhibits the production of the secondary messenger phosphatidylinositol-3,4,5-trisphosphate (PIP3) and activation of the PI3K/Akt signaling pathway, which may result in inhibition of tumor cell growth and survival in susceptible tumor cell populations. Activation of the PI3K/Akt signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K/Akt signaling may contribute to tumor resistance to a variety of antineoplastic agents. Uses: Potential anti-cancer agent. Synonyms: PX-866; PX866; PX 866. Grades: >98%. CAS No. 502632-66-8. Molecular formula: C29H35NO8. Mole weight: 525.59. | |
| Sonrotoclax | Sonrotoclax is a potent, orally active Bcl2 inhibitor. Sonrotoclax has effective cell killing effect against a variety of lymphoma and leukemia cell lines [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BGB 11417. CAS No. 2383086-06-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-148026. | |
| Soot Carbon Black Nanopowder | Soot Carbon Black Nanopowder. Group: Metal nano dispersion. CAS No. 7440-44-0. Molecular formula: 12.011 g/mol. Mole weight: C. 98.9%. |  |
| SOP1812 | SOP1812 (QN-302) is a naphthalene diimide (ND) derivative with anti-tumor activity. SOP1812 binds to quadruplex arrangements (G4s), and down-regulates several cancer gene pathways. SOP1812 shows great affinity to hTERT G4 and HuTel21 G4 with KD values of 4.9 and 28.4 nM, respectively. SOP1812 can be used for the research of cancer[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: QN-302. CAS No. 2546091-70-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-148012. | |
| Sophocarpine | Sophocarpine is one of the significant alkaloid extracted from the traditional herb medicine Sophora flavescens which has many pharmacological properties such as anti-virus, anti-tumor, anti-inflammatory. Sophocarpine significantly inhibits the growth of gastric cancer (GC) cells through multiple mechanisms such as induction of autophagy , activation of cell apoptosis and down-regulation of cell survival PI3K/AKT signaling pathway. Sophocarpine has been demonstrated to have anti-tumor activity in various cancer cells, including hepatocellular carcinoma, prostate cancer and colorectal cancer [1]. Uses: Scientific research. Group: Natural products. CAS No. 6483-15-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg. Product ID: HY-N0103. | |
| Sophocarpine | Sophocarpine. Group: Biochemicals. Alternative Names: 13,14-Didehydromatridin-15-one, 9CI. Grades: Plant Grade. CAS No. 6483-15-4,145572-44-7. Pack Sizes: 20mg. Molecular Formula: C15H22N2O, Molecular Weight: 246.348. US Biological Life Sciences. | Worldwide |
| Sophocarpine monohydrate | Sophocarpine (monohydrate) is one of the significant alkaloid extracted from the traditional herb medicine Sophora flavescens which has many pharmacological properties such as anti-virus, anti-tumor, anti-inflammatory. Sophocarpine (monohydrate) significantly inhibits the growth of gastric cancer (GC) cells through multiple mechanisms such as induction of autophagy , activation of cell apoptosis and down-regulation of cell survival PI3K/AKT signaling pathway. Sophocarpine (monohydrate) has been demonstrated to have anti-tumor activity in various cancer cells, including hepatocellular carcinoma, prostate cancer and colorectal cancer [1]. Uses: Scientific research. Group: Natural products. CAS No. 145572-44-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0103A. | |
| Sophoflavescenol | Sophoflavescenol. Group: Biochemicals. Grades: Plant Grade. CAS No. 216450-65-6. Pack Sizes: 5mg. Molecular Formula: C21H20O6, Molecular Weight: 368.38. US Biological Life Sciences. | Worldwide |
| Sophoflavescenol | Sophoflavescenol is a compound of the flavonoid class found in the roots of Sophora flavescens Ait. Sophoflavescenol is a PDE5 inhibitor with antioxidant and anti-inflammatory properties. Synonyms: 3,7-dihydroxy-2-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one. Grades: >98%. CAS No. 216450-65-6. Molecular formula: C21H20O6. Mole weight: 368.385. | |
| Sophorabioside | Sophorabioside is a compound of the flavonoid class found in the seeds of Sophora japonica. Synonyms: 3-[4-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5,7-dihydroxychromen-4-one. Grades: >98%. CAS No. 2945-88-2. Molecular formula: C27H30O14. Mole weight: 578.523. | |
| Sophorabioside | Sophorabioside. Group: Biochemicals. CAS No. 2945-88-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Sophoraflavanone G | Sophoraflavanone G (Kushenol F) is iaolated from Sophora flavescens and shows anti-tumor and anti-inflammatory properties. Sophoraflavanone G (Kushenol F) induces MDA-MB-231 and HL-60 cells apoptosis through suppression of MAPK-related pathways [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Kushenol F. CAS No. 97938-30-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg. Product ID: HY-N1231. | |
| Sophora Flavescens P.E. 5:1 | Sophora Flavescens P.E. 5:1. |  CA, FL & NJ |
| Sophoraflavonoloside | Sophoraflavonoloside. Group: Biochemicals. CAS No. 19895-95-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Sophora Japonica Extract Rutin 95%UV | Sophora Japonica Extract Rutin 95%UV. | CA, FL & NJ |
| Sophoramine | Sophoramine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 11,12,13,14-Tetrahydromatridin-15-one, Matridin-15-one, 11,12,13,14-tetrahydro-, 6682-66-2, AC1L4721, LS-89362, 1-(1,1,4,6,7-pentamethyl-2,3-dihydroinden-5-yl)ethanone, 1-(1,1,4,6,7-pentamethyl-2,3-dihydro-1H-inden-5-yl)ethanone. Product Category: Heterocyclic Organic Compound. CAS No. 6682-66-2. Molecular formula: C16H22O. Mole weight: 230.345280 [g/mol]. Purity: 0.96. IUPACName: 1-(1,1,4,6,7-pentamethyl-2,3-dihydroinden-5-yl)ethanone. Product ID: ACM6682662. Alfa Chemistry ISO 9001:2015 Certified. Categories: Sophoradin. |  |
| Sophoranol | Sophoranol is an alkaloid that can be isolated from S. flavescens, with antiviral activity. Sophoranol has anti-HBV (hepatitis B virus) activity. Sophoranol shows potent antiviral activities against respiratory syncytial virus (RSV)with an IC50 of 10.4 μg/mL. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-Hydroxymatridine-15-one. Product Category: Inhibitors. CAS No. 3411-37-8. Molecular formula: C15H24N2O2. Mole weight: 264.36. Purity: 95%+. Canonical SMILES: O=C1CCC[C@]2([H])[C@@]3([H])CCCN4[C@@]3([H])[C@](CCC4)(O)CN21. Density: 1.25. Product ID: ACM3411378. Alfa Chemistry ISO 9001:2015 Certified. Categories: Sophora molloyi. | |
| Sophora Root Extract | Sophora root extract is prepared from the sophora flavescens, a species of plant in the genus sophora. Matrine is the major alkaloid component found in sophora root extract. Sophora root extract is commonly used for the treatment of viral hepatitis, enteritis, cancer, viral myocarditis, gastrointestinal hemorrhage and skin diseases. Group: Others. Mole weight: 248.37. Sophora Root Extract; Sophora Flavescens Alt. Cat No: EXTC-019. | |
| Sophoricoside | Sophoricoside - Product ID: NST-10-40. Category: Flavonoids. Alternative Names: Genistein-4'-O-glucoside. Purity: 98%. Test method: HPLC. CAS No. 152-95-4. Pack Sizes: 10g, 20g, 50g, 100g. Appearance: White to beige coloured Powder. Molecular formula: C21H20O10. Mole weight: 432.38. Storage: +2 +8 °C. |  |
| Sophoricoside | Sophoricoside is an isoflavone glycoside isolated from Sophora japonica and has anti-inflammatory, anti-cancer and immunosuppressive effects. Uses: Scientific research. Group: Natural products. CAS No. 152-95-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N0423. | |
| Sophoricoside | Sophoricoside. Group: Biochemicals. Alternative Names: Genistein 4?-glucoside. Grades: Plant Grade. CAS No. 152-95-4. Pack Sizes: 20mg. Molecular Formula: C21H20O10, Molecular Weight: 432.377999999999. US Biological Life Sciences. | Worldwide |
| Sophoridine | Sophoridine. Group: Biochemicals. Grades: Plant Grade. CAS No. 6882-68-4. Pack Sizes: 20mg. Molecular Formula: C15H24N2O, Molecular Weight: 248.36. US Biological Life Sciences. | Worldwide |
| Sophorose monohydrate | Sophorose (2-O-beta-D-Glucopyranosyl-D-glucopyranose) monohydrate is the disaccharide component of microbial glycolipids, which are often used as biosurfactants due to their hydrophobicity. Sophorolipids also exhibit antibacterial, antifungal, spermicidal, virucidal, and anticancer activities. In studies of Trichoderma reesei fermentation, sophorose monohydrate has been identified as a potent inducer of cellulase gene expression [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 2-O-beta-D-Glucopyranosyl-D-glucopyranose monohydrate. CAS No. 140686-17-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-119445A. | |
| Sopropylated naphthalene) | Sopropylated naphthalene). Uses: Designed for use in research and industrial production. Additional or Alternative Names: Naphthalene, 2-isopropyl-, 2-ISOPROPYLNAPHTHALENE, beta-Isopropylnaphthalene, 2-iso-Propylnaphthalene, 2-(1-Methylethyl)naphthalene, Naphthalene, 2-(1-methylethyl)-, 2-propan-2-ylnaphthalene, Naphthalene, isopropylated. beta.-Isopropylnaphthalene, HSDB 5863, EINECS 217-976-0, TVYVQNHYIHAJTD-UHFFFAOYSA-, MolPort-002-501-657, NSC 166466, CID16238, BRN 1099059, NSC166466, SBB007801, FR-0361, LS-94718. Product Category: Heterocyclic Organic Compound. CAS No. 68442-08-0. Molecular formula: C13H14. Mole weight: 170.250260 [g/mol]. Purity: 0.96. IUPACName: 2-propan-2-ylnaphthalene. Product ID: ACM68442080. Alfa Chemistry ISO 9001:2015 Certified. | |
| Soquelitinib | Soquelitinib (CPI-818) is an orally active and highly selective covalent interleukin-2-inducible kinase ( ITK ) inhibitor. Soquelitinib is active in six different models of T cell-mediated inflammatory and immune disease, including acute and chronic asthma, pulmonary fibrosis, systemic sclerosis (scleroderma), psoriasis, and acute graft versus host disease with Th2 cytokine product inhibition. Soquelitinib increases tumor infiltration of normal CD8 + cells that possess enhanced T effector function [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CPI-818. CAS No. 2226636-04-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-150298. | |
| Sorafenib | Sorafenib Inhibitor. Uses: Scientific use. Product Category: T0093L. CAS No. 284461-73-0. |  |
| Sorafenib | Sorafenib (Bay 43-9006) is a potent and orally active Raf inhibitor with IC 50 s of 6 nM and 20 nM for Raf-1 and B-Raf , respectively. Sorafenib is a multikinase inhibitor with IC 50 s of 90 nM, 15 nM, 20 nM, 57 nM and 58 nM for VEGFR2 , VEGFR3 , PDGFRβ , FLT3 and c-Kit , respectively. Sorafenib induces autophagy and apoptosis. Sorafenib has anti-tumor activity. Sorafenib is a ferroptosis activator [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bay 43-9006. CAS No. 284461-73-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 1 g. Product ID: HY-10201. | |
| Sorafenib 2-Chloro Isomer | An impurity of Sorafenib. Sorafenib is a small inhibitor of several tyrosine protein kinases, such as VEGFR, PDGFR and Raf family kinases, for the treatment of primary kidney cancer, advanced primary liver cancer and radioactive iodine resistant advanced thyroid carcinoma. Synonyms: 4- [4- [ [ [ [2-Chloro-3- (trifluoromethyl) ?phenyl] ?amino] ?carbonyl] ?amino] ?phenoxy] ?-N-methyl-2-pyridinecarboxamide; 4-Deschloro-2-chloro-Sorafenib. Grades: > 95%. CAS No. 1431697-81-2. Molecular formula: C21H16ClF3N4O3. Mole weight: 464.83. | |
| Sorafenib-beta-D-Glucuronide | Sorafenib-beta-D-Glucuronide is one of Sorafenib metabolites. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Synonyms: N-[4-Chloro-3-(trifluoromethyl)phenyl]-N-[(4-{[2-(methylcarbamoyl)pyridin-4-yl]oxy}phenyl)carbamoyl]-beta-D-glucopyranuronosylamine; 1- [ [4-Chloro-3- (trifluoroMethyl) phenyl] [ [ [4- [ [2- [ (MethylaMino) carbonyl] -4-pyridinyl] oxy] phenyl] aMino] carbonyl] aMino] -1-deoxy-Beta-D-glucopyranuronic Acid; Sorafenib Beta-D-Glucuronide. Grades: ≥95%. CAS No. 1130164-93-0. Molecular formula: C27H24ClF3N4O9. Mole weight: 640.95. | |
| Sorafenib-d3 | Cas No. 1130115-44-4. | |
| Sorafenib ?-D-Glucuronide | Sorafenib ?-D-Glucuronide. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1130164-93-0. Molecular formula: C27H24ClF3N4O9. Mole weight: 640.95. Catalog: APB1130164930. | |
| Sorafenib Hemitosylate | Sorafenib Hemitosylate is the salt of Sorafenib, which is a kinase inhibitor drug used for the treatment of primary kidney cancer (advanced renal cell carcinoma), advanced primary liver cancer (hepatocellular carcinoma), FLT3-ITD positive AML and radioactive iodine resistant advanced thyroid carcinoma. Synonyms: 4-[4-[[[[4-chloro-3- (trifluoromethyl) phenyl]amino]carbonyl]amino] phenoxy]-N-methyl-2-pyridinecarboxamide, 4-methylbenzenesulfonate (2:1). CAS No. 2056030-06-7. Molecular formula: C21H16ClF3N4O3.1/2(C7H8O3S). Mole weight: 550.92. | |
| Sorafenib Impurity 1 | Sorafenib Impurity 1 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Molecular formula: C28H25N7O6. Mole weight: 555.54. | |
| Sorafenib Impurity 10 | Sorafenib Impurity 10 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Synonyms: SORAFENIB IMPURITY 10; 2206827-14-5; propan-2-yl N-[4-[2-(methylcarbamoyl)pyridin-4-yl]oxyphenyl]carbamate; SORAFENIBIMPURITY10; EN300-6494528; Z3064469246; Isopropyl 4-[[2-(N-Methylcarbamoyl)-4-pyridyl]oxy]phenylcarbamate; propan-2-yl N-(4-{[2-(methylcarbamoyl)pyridin-4-yl]oxy}phenyl)carbamate. Molecular formula: C24H24F3N5O4. Mole weight: 503.47. | |
| Sorafenib Impurity 4 | Sorafenib Impurity 4 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Molecular formula: C7H7NO2. Mole weight: 137.14. | |
| Sorafenib Impurity 5 | Sorafenib Impurity 5 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Molecular formula: C14H13ClN4O2. Mole weight: 304.73. | |
| Sorafenib Impurity 7 | Sorafenib Impurity 7 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Synonyms: 4-Hydroxy-phenylhydroxylamine. Grades: ≥ 95%. CAS No. 3505-87-1. Molecular formula: C6H7NO2. Mole weight: 125.13. | |
| Sorafenib Impurity 8 | Sorafenib Impurity 8 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Synonyms: Flucofuron; 370-50-3; Flucofuron [ISO]; TCMDC-137559; 1,3-bis[4-chloro-3-(trifluoromethyl)phenyl]urea; CHEBI:59242; 1,3-Bis(4-chloro-alpha,alpha,alpha-trifluoro-m-tolyl)urea; 1,3-bis(4-chloro-3-(trifluoromethyl)phenyl)urea; N,N'-bis[4-chloro-3-(trifluoromethyl)phenyl]urea; U3V3S70655; Mitin N; 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(4-chloro-3-(trifluoromethyl)phenyl)urea; N,N'-BIS(4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL)UREA. Molecular formula: C25H25F3N6O3. Mole weight: 514.50. | |
| Sorafenib Impurity 84 | Sorafenib Impurity 84. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1403469-80-6. Molecular formula: C7H6Cl2N2O. Mole weight: 205.04. Catalog: APB1403469806. | |
| Sorafenib Impurity 85 | Sorafenib Impurity 85. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1021077-12-2. Molecular formula: C7H6Cl2N2O. Mole weight: 205.04. Catalog: APB1021077122. | |
| Sorafenib Impurity 9 | Sorafenib Impurity 9 is one of Sorafenib impurities. Sorafenib is a polykinase inhibitor of Raf-1, B-Raf and VEGFR-2 and is an anti-tumor drug. Synonyms: 4- (4- (3- (4-Hydroxy-3- (trifluoromethyl) phenyl) ureido) phenoxy) -N-methylpicolinamide. CAS No. 862875-16-9. Molecular formula: C21H17F3N4O4. Mole weight: 446.38. | |
| Sorafenib Impurity C | An impurity of Sorafenib. Sorafenib is a small inhibitor of several tyrosine protein kinases, such as VEGFR, PDGFR and Raf family kinases, for the treatment of primary kidney cancer, advanced primary liver cancer and radioactive iodine resistant advanced thyroid carcinoma. Grades: > 95%. Molecular formula: C27H23N5O6. Mole weight: 513.51. | |
| Sorafenib Impurity G | Sorafenib Impurity G. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: ethyl (4-chloro-3-(trifluoromethyl)phenyl)carbamate. CAS No. 18585-06-3. Molecular formula: C10H9ClF3NO2. Mole weight: 267.63. Catalog: APB18585063. | |
| Sorafenib Impurity I | An impurity of Sorafenib. Sorafenib is a small inhibitor of several tyrosine protein kinases, such as VEGFR, PDGFR and Raf family kinases, for the treatment of primary kidney cancer, advanced primary liver cancer and radioactive iodine resistant advanced thyroid carcinoma. Synonyms: 1,3-bis-(4-Chloro-α,α,α-trifluoro-m-tolyl)urea. Grades: > 95%. CAS No. 370-50-3. Molecular formula: C15H8Cl2F6N2O. Mole weight: 417.13. | |
| Sorafenib Impurity INT-1-F | Sorafenib Impurity INT-1-F. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1065074-98-7. Molecular formula: C8H11N3O. Mole weight: 165.2. Catalog: APB1065074987. | |
| Sorafenib Impurity INT-1-N | Sorafenib Impurity INT-1-N. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1863331-80-9. Molecular formula: C9H13N3O. Mole weight: 179.22. Catalog: APB1863331809. | |
| Sorafenib-methyl-d3 | Labeled Sorafenib, a potent Raf kinase inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sorafenib N-oxide | Sorafenib N-oxide. Group: Biochemicals. Alternative Names: 4- [4- [ [ [ [4-Chloro-3- (trifluoromethyl) phenyl] amino] carbonyl] amino] phenoxy] -N-methyl-2-pyridinecarboxamide 1-oxide. Grades: Highly Purified. CAS No. 583840-03-3. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C21H16ClF3N4O4. US Biological Life Sciences. | Worldwide |
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