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| Product | Description | |
|---|---|---|
| Ilaprazole | Ilaprazole is a proton pump inhibitor (PPI) used in the treatment of dyspepsia, peptic ulcer disease (PUD), gastroesophageal reflux disease (GORD/GERD) and duodenal ulcer. Group: Biochemicals. Grades: Highly Purified. CAS No. 172152-36-2. Pack Sizes: 10mg, 100mg. Molecular Formula: C19H18N4O2S, Molecular Weight: 366.44. US Biological Life Sciences. |  Worldwide |
| Ilaprazole | Ilaprazole (IY-81149) is an orally active proton pump inhibitor. Ilaprazole irreversibly inhibits H+/K+-ATPase in a dose-dependent manner with an IC50 of pump inhibitory activity of 6 μM in rabbit parietal cell preparation. Ilaprazole is used for the research of gastric ulcers. Ilaprazole is also a potent TOPK (T-lymphokine-activated killer cell-originated protein kinase) inhibitor. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ilaprazole;2-[[(4-Methoxy-3-methyl-2-pyridinyl)methyl]sulfinyl]-6-(1H-pyrrol-1-yl)-1H-benzimidazole. Product Category: Inhibitors. Appearance: Solid. CAS No. 172152-36-2. Molecular formula: C19H18N4O2S. Mole weight: 366.44. Purity: 0.9926. Canonical SMILES: O=S(C1=NC2=CC=C(N3C=CC=C3)C=C2N1)CC4=NC=CC(OC)=C4C. Product ID: ACM172152362. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Ilaprazole-d3 | Ilaprazole-d3 is labelled Ilaprazole (I266400) which is a proton pump inhibitor (PPI) used in the treatment of dyspepsia, peptic ulcer disease (PUD), gastroesophageal reflux disease (GORD/GERD) and duodenal ulcer. Group: Biochemicals. Grades: Highly Purified. CAS No. 10370969-17-3. Pack Sizes: 1mg. Molecular Formula: C19H15D3N4O2S, Molecular Weight: 369.46. US Biological Life Sciences. | Worldwide |
| Ilaprazole Impurity 1 | Grades: > 95%. Molecular formula: C19H18N4OS. Mole weight: 350.45. |  |
| Ilaprazole Impurity 10 | Grades: > 95%. Molecular formula: C19H18N4OS. Mole weight: 350.45. | |
| Ilaprazole Impurity 11 | Grades: > 95%. Molecular formula: C19H18N4O4S. Mole weight: 398.44. | |
| Ilaprazole Impurity 12 | Grades: > 95%. Molecular formula: C19H17ClN4O2S. Mole weight: 400.89. | |
| Ilaprazole Impurity 13 | Grades: > 95%. Molecular formula: C19H17ClN4O2S. Mole weight: 400.89. | |
| Ilaprazole Impurity 14 | Grades: > 95%. Molecular formula: C20H20N4OS. Mole weight: 364.47. | |
| Ilaprazole Impurity 14 | Ilaprazole Impurity 14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1018229-53-2. Molecular formula: C11H9N3O. Mole weight: 199.21. Catalog: APB1018229532. |  |
| Ilaprazole Impurity 15 | Grades: > 95%. Molecular formula: C16H20N2O4. Mole weight: 304.35. | |
| Ilaprazole Impurity 16 | Grades: > 95%. Molecular formula: C15H14N4O4S. Mole weight: 346.37. | |
| Ilaprazole Impurity 17 | Grades: > 95%. Molecular formula: C11H9N3O2S. Mole weight: 247.28. | |
| Ilaprazole Impurity 18 | Grades: > 95%. Molecular formula: C9H9N3OS. Mole weight: 207.26. | |
| Ilaprazole Impurity 19 | Grades: > 95%. Molecular formula: C9H9N3O3S. Mole weight: 239.25. | |
| Ilaprazole Impurity 2 | Grades: > 95%. Molecular formula: C27H27N5O3S. Mole weight: 501.61. | |
| Ilaprazole Impurity 20 | Grades: > 95%. Molecular formula: C8H9Cl2NO. Mole weight: 206.07. | |
| Ilaprazole Impurity 21 | Impurity of Ilaprazole. Synonyms: 2-Chloromethyl-3-methyl-4-nitro-pyridine. Grades: > 95%. Molecular formula: C7H7ClN2O2. Mole weight: 186.60. | |
| Ilaprazole Impurity 22 | Impurity of Ilaprazole. Synonyms: 2-(3-Methyl-pyridin-2-ylmethanesulfinyl)-5-pyrrol-1-yl-1H-benzoimidazole. Grades: > 95%. Molecular formula: C18H16N4OS. Mole weight: 336.42. | |
| Ilaprazole Impurity 23 | Impurity of Ilaprazole. Synonyms: 2-(4-Chloro-3-methyl-pyridin-2-ylmethanesulfinyl)-5-pyrrol-1-yl-1H-benzoimidazole. Grades: > 95%. Molecular formula: C18H15ClN4OS. Mole weight: 370.86. | |
| Ilaprazole Impurity 24 | Impurity of Ilaprazole. Synonyms: 1-Methyl-8-pyrrol-1-yl-10-thioxo-10H-4a,5,9b-triaza-indeno[2,1-a]inden-2-one. Grades: > 95%. Molecular formula: C18H12N4OS. Mole weight: 332.39. | |
| Ilaprazole Impurity 25 | Impurity of Ilaprazole. Synonyms: 1-Methyl-8-pyrrol-1-yl-10-thioxo-10H-4a,5,9b-triaza-indeno[2,1-a]inden-2-one. Grades: > 95%. Molecular formula: C18H12N4OS. Mole weight: 332.39. | |
| Ilaprazole Impurity 3 | Grades: > 95%. Molecular formula: C27H27N5O3S. Mole weight: 501.61. | |
| Ilaprazole Impurity 4 | Grades: > 95%. Molecular formula: C19H17N4O3SNa. Mole weight: 404.43. | |
| Ilaprazole Impurity 5 | Grades: > 95%. Molecular formula: C19H17N4O3SNa. Mole weight: 404.43. | |
| Ilaprazole Impurity 55 | Ilaprazole Impurity 55. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1508282-87-8. Molecular formula: C18H14N4O3. Mole weight: 334.34. Catalog: APB1508282878. | |
| Ilaprazole Impurity 6 | Grades: > 95%. Molecular formula: C19H16ClN4O2SNa. Mole weight: 422.87. | |
| Ilaprazole Impurity 7 | Grades: > 95%. Molecular formula: C27H27N5O2S. Mole weight: 485.61. | |
| Ilaprazole Impurity 73 | Ilaprazole Impurity 73. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1508282-92-5. Molecular formula: C19H18N4O3S. Mole weight: 382.44. Catalog: APB1508282925. | |
| Ilaprazole Impurity 8 | Grades: > 95%. Molecular formula: C27H27N5O2S. Mole weight: 485.61. | |
| Ilaprazole Impurity 9 | Grades: > 95%. Molecular formula: C19H18N4O3S. Mole weight: 382.44. | |
| Ilaprazole Impurity HCl | Ilaprazole Impurity HCl is pyridine derivative used in the preparation of anti-ulcerative agents and other pharmaceutical compounds. Synonyms: 2-(Chloromethyl)-4-methoxy-3-methylpyridine HCl; Pyridine, 2-(chloromethyl)-4-methoxy-3-methyl-, hydrochloride. Grades: > 95%. CAS No. 86604-74-2. Molecular formula: C8H11Cl2NO. Mole weight: 208.09. | |
| Ilaprazole sodium | Ilaprazole (IY-81149) sodium is an orally active proton pump inhibitor. Ilaprazole sodium irreversibly inhibits H + /K + -ATPase in a dose-dependent manner with an IC 50 of 6 μM in rabbit parietal cell preparation. Ilaprazole sodium is used for the research of gastric ulcers. Ilaprazole sodium is also a potent TOPK (T-lymphokine-activated killer cell-originated protein kinase) inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IY-81149 sodium. CAS No. 172152-50-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B2145. |  |
| Ilaprazole sodium | Ilaprazole sodium is the sodium salt form of ilaprazole, a novel proton pump inhibitor (PPI) used in the treatment of duodenal ulcers. Synonyms: IY-81149 sodium. CAS No. 172152-50-0. Molecular formula: C19H17N4NaO2S. Mole weight: 388.42. | |
| Ilaprazole sodium hydrate | Ilaprazole (IY-81149) sodium hydrate is an orally active proton pump inhibitor. Ilaprazole sodium hydrate irreversibly inhibits H + /K + -ATPase in a dose-dependent manner with an IC 50 of 6 μM in rabbit parietal cell preparation. Ilaprazole sodium hydrate is used for the research of gastric ulcers. Ilaprazole sodium hydrate is also a potent TOPK (T-lymphokine-activated killer cell-originated protein kinase) inhibitor [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: IY-81149 sodium hydrate. CAS No. 2322264-11-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B2145A. | |
| Ile-Gly-Gly-OH | Ile-Gly-Gly-OH. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Ile-Gly-OH | Ile-Gly-OH. Group: Biochemicals. Alternative Names: L-Isoleucyl-glycine. Grades: Highly Purified. CAS No. 868-28-0. Pack Sizes: 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Ile-Gly-OH | Synonyms: L-Isoleucyl-glycine. Grades: ≥ 98% (HPLC). CAS No. 868-28-0. Molecular formula: C8H16N2O3. Mole weight: 188.23. | |
| Ile-Gly-OH 99+% | Ile-Gly-OH 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 868-28-0. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences. | Worldwide |
| Ile-His | Isoleucyl-histidine is a dipeptide composed of isoleucine and histidine. It is an incomplete breakdown product of protein digestion or protein catabolism. Synonyms: Isoleucyl-Histidine; L-Ile-L-His. Grades: ≥95% by HPLC. CAS No. 97284-12-3. Molecular formula: C12H20N4O3. Mole weight: 268.31. | |
| Ile-Ile-OH | Ile-Ile-OH. Group: Biochemicals. Alternative Names: L-Isoleucyl-L-isoleucine. Grades: Highly Purified. CAS No. 42537-99-5. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Ile-Ile-OH | Synonyms: L-Isoleucyl-L-isoleucine. Grades: ≥ 98% (HPLC). CAS No. 42537-99-5. Molecular formula: C12H24N2O3. Mole weight: 244.33. | |
| Ile-Ile-OH 98+% (HPLC) | Ile-Ile-OH 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Ile-Phe | Ile-Phe and similar dipeptides may serve as models for studying the first steps of the aggregation/fibrillation of amyloid peptides. Synonyms: Isoleucyl-Phenylalanine; L-Ile-L-Phe; L-Phenylalanine,L-isoleucyl-. CAS No. 22951-98-0. Molecular formula: C15H22N2O3. Mole weight: 278.35. | |
| Ile-Pro-Ile | ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Ile-Pro-Pro | Synonyms: H-Ile-Pro-Pro-OH; IPP, ACE-I Inhibitor. Grades: >98%. CAS No. 26001-32-1. Molecular formula: C16H27N3O4. Mole weight: 325.4. | |
| Ile-Tyr-OH | ACE inhibitor. Synonyms: L-Isoleucyl-L-tyrosine. Grades: ≥ 99% (HPLC). CAS No. 38579-21-4. Molecular formula: C15H22N2O4. Mole weight: 294.35. | |
| Ile-Tyr-OH | Ile-Tyr-OH. Group: Biochemicals. Alternative Names: L-Isoleucyl-L-tyrosine. Grades: Highly Purified. CAS No. 38579-21-4. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Ile-Tyr-OH 99+% (TLC) | Ile-Tyr-OH 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg. US Biological Life Sciences. | Worldwide |
| Ilexgenin A | Botanical Source: Group: Biochemicals. Alternative Names: Myriaboric acid. Grades: Plant Grade. CAS No. 108524-94-3. Pack Sizes: 10mg, 20mg. US Biological Life Sciences. | Worldwide |
| Ilexhainanoside D | Ilexhainanoside D. Group: Biochemicals. CAS No. 1137648-52-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ilexoside D | Ilexoside D. Group: Biochemicals. CAS No. 109008-27-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ilexoside K | Ilexoside K. Group: Biochemicals. CAS No. 109008-26-6. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ilexsaponin A | Ilexsaponin A, isolated from the root of Ilex pubescens, attenuates ischemia-reperfusion-induced myocardial injury through anti-apoptotic pathway. Ilexsaponin A can reduce myocardial infarct size, lower the serum levels of LDH, AST and CK-MB, increase cellular viability and inhibit apoptosis in hypoxia/reoxygenation cardiomyocytes. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Powder. CAS No. 108524-93-2. Molecular formula: C36H56O11. Mole weight: 664.83. Purity: 0.98. IUPACName: (3S,4R,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-3,12-dihydroxy-4,6a,6b,11,12,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid. Canonical SMILES: CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O. Product ID: ACM108524932. Alfa Chemistry ISO 9001:2015 Certified. Categories: Ilexsaponin A1. | |
| Ilexsaponin A | Ilexsaponin A. Group: Biochemicals. CAS No. 108524-93-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ilexsaponin A1 | Botanical Source: Group: Biochemicals. Alternative Names: Ilexsaponina A. Grades: Plant Grade. CAS No. 108524-93-2. Pack Sizes: 10mg, 20mg. US Biological Life Sciences. | Worldwide |
| Iliac Artery Endothelial Cells, Human (Frozen) | Passage 3 cells are shipped in proliferating culture with a confluence of >90%. ENDO-Growth medium containing 5% serum and growth supplement is recommended for culture. Cells have an average population doubling level of >16 when cultured. Group: Biologicals. Grades: Cell Culture Grade. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| Iliac Artery Endothelial Cells, Human (T-25 flask) | Passage 3 cells are shipped in proliferating culture with a confluence of >90%. ENDO-Growth medium containing 5% serum and growth supplement is recommended for culture. Cells have an average population doubling level of >16 when cultured. Group: Biologicals. Grades: Cell Culture Grade. Pack Sizes: T-25 flask. US Biological Life Sciences. | Worldwide |
| Ilicicolin A | Ilicicolin A is originally isolated from Cylinddrocladium ilicicola MFC-870. It inhibited Bacillus carbonifera with the concentration of 6 μg/mL and its toxic concentration to Hela cells was 0.2 μg/mL. Synonyms: LL-Z 1272-alpha; 3-chloro-4,6-dihydroxy-2-methyl-5-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)benzaldehyde. Grades: >98%. CAS No. 22581-06-2. Molecular formula: C23H31ClO3. Mole weight: 390.94. | |
| Ilicicolin B | Ilicicolin B is originally isolated from Cylinddrocladium ilicicola MFC-870. It inhibited Bacillus carbonifera with the concentration of 6 μg/mL and its toxic concentration to Hela cells was 0.3 μg/mL. Synonyms: 2,4-Dihydroxy-6-methyl-3-((2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl)benzaldehyde; LL-Z1272beta. Grades: >98%. CAS No. 22581-07-3. Molecular formula: C23H32O3. Mole weight: 356.50. | |
| Ilicicolin C | Ilicicolin C is originally isolated from Cylinddrocladium ilicicola MFC-870. It inhibits Bacillus carbonifera with the concentration of 6 μg/mL and its toxic concentration to Hela cells is 0.2 μg/mL. Synonyms: LL-Z 1272delta; 3-Chloro-4,6-dihydroxy-2-methyl-5-((2E)-3-methyl-5-((1S,2R,6R)-1,2,6-trimethyl-3-oxocyclohexyl)-2-pentenyl)benzaldehyde. Grades: >95%. CAS No. 22562-67-0. Molecular formula: C23H31ClO4. Mole weight: 406.94. | |
| Ilicicolin F | ?98% (HPLC), from Verticillium hemipterigenum. Group: Fluorescence/luminescence spectroscopy. | |
| Ilimaquinone | Cytoplasmic microtubule inhibitor. Cell permeable, antimicrobial, anti-inflammatory, antimitotic and cytotoxic compound. Induces a complete and reversible breakdown/disruption of Golgi membranes into smaller vesicular structures. Blocks the association of the ADP-ribosylation factor and beta-COP to the Golgi membrane. Blocks protein transport to the plasma membrane and inhibits gap junctional communication. HIV-1 inhibitor. Blocks the cytotoxicity of ricin and diphtheria toxin. S-Adenosylhomocysteinase hydrolase inhibitor and cellular methylations inhibitor. DNA polymerase beta lyase activity inhibitor. Anti-cancer compound. Source:Isolated from Anthelia sp. Group: Biochemicals. Grades: Highly Purified. CAS No. 71678-03-0. Pack Sizes: 100ug. Molecular Formula: C22H30O4. US Biological Life Sciences. | Worldwide |
| Ilimaquinone | Ilimaquinone, a marine sponge metabolite, displays anticancer activity via GADD153-mediated pathway. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-Epiilimaquinone. Product Category: Inhibitors. Appearance: Solid. CAS No. 71678-03-0. Molecular formula: C22H30O4. Mole weight: 358.5. Purity: 95%+. IUPACName: 3-[[(1R,2S,4aS,8aS)-1,2,4a-Trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl]-2-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione. Canonical SMILES: CC1CCC2(C(C1(C)CC3=C(C(=O)C=C(C3=O)OC)O)CCCC2=C)C. Density: 1.14±0.1 g/cm³. Product ID: ACM71678030. Alfa Chemistry ISO 9001:2015 Certified. | |
| Ilimaquinone | Ilimaquinone, a marine sponge metabolite, displays anticancer activity via GADD153-mediated pathway. Ilimaquinone can induce vesiculation of the Golgi apparatus [1]. Ilimaquinone exerts anti-HIV, anti-microbial, anti-inflammatory, and effects [2]. Uses: Scientific research. Group: Natural products. CAS No. 71678-03-0. Pack Sizes: 100 μg. Product ID: HY-119500. | |
| Ilimaquinone | Ilimaquinone is a marine sponge metabolite with antimicrobial, anti-HIV, anti-mitotic, and anti-inflammatory properties. Ilimaquinone significantly enhanced TRAIL-induced apoptosis in HCT 116 cells and sensitized colon cancer cells to TRAIL-induced apoptosis through increased caspase-8, -3 activation, PARP cleavage, and DNA damage. Ilimaquinone also reduced the cell survival proteins Bcl2 and Bcl-xL, while strongly up-regulating death receptor (DR) 4 and DR5 expression. Synonyms: ilimaquinone; 71678-03-0; Illimaquinone; UNII-5U0WAN3N8Q5U0WAN3N8Q. Grades: ≥98%. CAS No. 71678-03-0. Molecular formula: C22H30O4. Mole weight: 358.5. | |
| Ilimaquinone - CAS 71678-03-0 | A cell-permeable marine sponge metabolite with anti-microbial, anti-HIV, anti-inflammatory, and anti-mitotic properties. Group: Fluorescence/luminescence spectroscopy. | |
| ILK-IN-1 | ILK-IN-1, a ILK inhibitor, has been found to restrain the tumor cell growth through regulating signaling pathways related to oncogenesis and tumor progression. IC50: 0.6 μM. Uses: Ilk-in-1 is a ilk inhibitor that has been found to restrain the tumor cell growth through regulating signaling pathways related to oncogenesis and tumor progression. Synonyms: ILK-IN-1; CHEMBL1830587; GTPL8116; SCHEMBL8536228; BDBM50353484; CS-4936; ILK inhibitor 22(1,5); T315(1,5); OSU-T315 (1,5-regioisomer); OSUT315; OSU T315; OSU-T315. Grades: 98%. CAS No. 1333146-24-9. Molecular formula: C30H30F3N5O. Mole weight: 533.59. | |
| ILK Inhibitor, Cpd 22 (N-methyl-3- (1- (4- (piperazin-1-yl) phenyl) -5- (4'- (trifluoromethyl) biphenyl-4-yl) -1H-pyrazol-3-yl) propanamide) | A cell-permeable, tri-substituted pyrazol compound that acts as a potent and specific integrin-linked kinase (ILK) inhibitor (IC50=600nM). Shown to have high in vitro anti-proliferative potency against prostrate and breast cancer cell lines (IC50=1 to 2.5uM) while sparing normal epithelial cells. Its effect on cancer cells have been attributed to induction of autophagy and apoptosis. Suppresses ILK-mediated phosphorylation of Akt at Ser473 site, thereby down-regulating the downstream targets, such as GSK-3b and myosin light chain. Also causes a transcriptional repression of the transcription factor Y-Box binding protein 1 (YB-1). Exhibits minimum toxicity in mouse model. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C30H30F3N5O, Molecular Weight: 553.6. US Biological Life Sciences. | Worldwide |
| Illudin C2 | Illudin C2 is produced by the strain of Coprinus atramentarius ASI 20013. It has the effect of resisting bacterium and fungus, and the antibacterial activity is weak. Molecular formula: C15H20O3. Mole weight: 248.32. | |
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