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| Product | Description | |
|---|---|---|
| Gibberellin A95 | Gibberellin A95 is a derivative of Gibberelic Acid. It is a stereoisomer of Gibberelin A5. Synonyms: 4a,1-(Epoxymethano)-7,9a-methanobenz[a]azulene, gibb-3-ene-1,10-dicarboxylic Acid Deriv.; GA95; NSC 224287. Grades: > 95%. CAS No. 78259-50-4. Molecular formula: C19H22O5. Mole weight: 330.38. |  |
| gibberellin A9 O-methyltransferase | The enzyme also methylates gibberellins A20 (95%), A3 (80%), A4 (69%) and A34 (46%) with significant activity. Group: Enzymes. Synonyms: GAMT1. Enzyme Commission Number: EC 2.1.1.275. 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-1881; gibberellin A9 O-methyltransferase; EC 2.1.1.275; GAMT1. Cat No: EXWM-1881. |  |
| gibberellin β-D-glucosyltransferase | Acts on the plant hormone gibberellin GA3 and related compounds. Group: Enzymes. Synonyms: uridine diphosphoglucose-gibberellate 7-glucosyltransferase; uridine diphosphoglucose-gibberellate 3-O-glucosyltransferase. Enzyme Commission Number: EC 2.4.1.176. CAS No. 99775-14-1,94489-97-1. 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-2401; gibberellin β-D-glucosyltransferase; EC 2.4.1.176; 99775-14-1,94489-97-1; uridine diphosphoglucose-gibberellate 7-glucosyltransferase; uridine diphosphoglucose-gibberellate 3-O-glucosyltransferase. Cat No: EXWM-2401. | |
| Gibbestatin B | It is produced by the strain of Streptomyces sp. C39. Gibbestatin B inhibits the expression of α-amylase induced by gibberellin in De-embryoned rice and barley (IC50 is 25-50 ppm, IC100 is 100-200 ppm), and has no anti-bacterial, anti-yeast and anti-fungal effects at 100 ppm (MIC, agar dilution method using bouillon agar for bacteria and Sabouraud agar for yeast and fungi). Synonyms: Antibiotic 2-11-B. CAS No. 89687-34-3. Molecular formula: C22H26O6. Mole weight: 386.44. | |
| Gibbestatin C | It is produced by the strain of Streptomyces sp. C39. It is a bioactive substance. Gibberellin C of 200 ppm has no inhibitory effect on α-amylase. It also has no anti-bacterial, anti-yeast and anti-fungal effects at 100 ppm (MIC, agar dilution method using bouillon agar for bacteria and Sabouraud agar for yeast and fungi). Synonyms: 2-Hydroxypenyl Gibbestatin B. Molecular formula: C28H30O7. Mole weight: 478.53. | |
| Giberellin A68 | Giberellin A68. Group: Biochemicals. Alternative Names: 4a,1-(Epoxymethano)-7,9a-methanobenz[a]azulene Gibb-3-ene-1,10-dicarboxylic Acid Deriv.; GA68. Grades: Highly Purified. CAS No. 71177-41-8. Pack Sizes: 2.5mg. Molecular Formula: C19H22O6, Molecular Weight: 346.37. US Biological Life Sciences. |  Worldwide |
| GIBH-130 | GIBH-130 is an effective inhibitor of neuroinflammation. GIBH-130 significantly suppresses theIL-1βsecretion by activated microglia (IC50=3.4 nM). GIBH-13 constitutes a unique chemical probe for pathogenesis research and drug development of AD, and it also suggests microglia-based phenotypic screenings that target neuroinflammation as an effective and feasible strategy to identify novel anti-AD agents. Synonyms: (4-methyl-6-phenylpyridazin-3-yl)-(4-pyrimidin-2; -ylpiperazin-1-yl)methanone; (4-methyl-6-phenylpyridazin-3-yl)(4-(pyrimidin-2-yl)piperazin-1-yl)methanone; GIBH-130; GIBH130; GIBH 130. CAS No. 1252608-59-5. Molecular formula: C20H20N6O. Mole weight: 360.41. | |
| Gidazepam | Gidazepam is an agonist of GABA receptor channels ( GABA RCs ). Uses: Scientific research. Group: Signaling pathways. Alternative Names: Gidasepam; Hidazepam; Hydazepam. CAS No. 129186-29-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-U00315. |  |
| Gidazepam | Gidazepam has a 3-fold higher affinity for MBR than for CBR (IC50= 710 and 2200 nmol/L, respectively). Uses: Anticonvulsants. Synonyms: 2-(7-bromo-2-oxo-5-phenyl-3H-1,4-benzodiazepin-1-yl)acetohydrazide; (1-hydrazinocarbonyl)-7-bromo-5-phenyl-1,2-dihydro-3H-1,4-benzodiazepine-2-one; gidazepam. CAS No. 129186-29-4. Molecular formula: C17H15BrN4O2. Mole weight: 387.23. | |
| Giemsa stain | Giemsa stain. Group: Biochemicals. Grades: Highly Purified. CAS No. 51811-82-6. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C14H14ClN3S. US Biological Life Sciences. | Worldwide |
| Giemsa stain | Giemsa stain can stain chromatin and nuclear membrane. Giemsa stain histopathologic detection of malaria and other microorganisms, such as Histoplasma, LeishmaniaToxoplasma, and Pneumocystis [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 51811-82-6. Pack Sizes: 1 g; 5 g. Product ID: HY-D0944. | |
| Giemsa Stain | 25g Pack Size. Group: Stains & Indicators. Formula: C14H14ClN3S. CAS No. 51811-82-6. Prepack ID 48872073-25g. Molecular Weight 291.8. See USA prepack pricing. |  |
| Giemsa Stain, Certified | Giemsa Stain, Certified. Group: Biochemicals. Grades: Certified Dye. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Gigantol | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Gilsonite 12002-43-6 | Gilsonite - Surface Coatings. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Gilteritinib | Gilteritinib (ASP2215) is a potent and ATP-competitive FLT3 / AXL inhibitor with IC 50 s of 0.29 nM/0.73 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ASP2215. CAS No. 1254053-43-4. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12432. | |
| Gilteritinib | Gilteritinib, also known as (ASP2215, is a potent FLT3/AXL inhibitor, which showed potent antileukemic activity against AML with either or both FLT3-ITD and FLT3-D835 mutations. In invitro, among the 78 tyrosine kinases tested, ASP2215 inhibited FLT3, LTK, ALK, and AXL kinases by over 50% at 1 nM with an IC50 value of 0.29 nM for FLT3, approximately 800-fold more potent than for c-KIT, the inhibition of which is linked to a potential risk of myelosuppression. ASP2215 inhibited the growth of MV4-11 cells, which harbor FLT3-ITD, with an IC50 value of 0.92 nM, accompanied with inhibition of pFLT3, pAKT, pSTAT5, pERK, and pS6. ASP2215 decreased tumor burden in bone marrow and prolonged the survival of mice intravenously transplanted with MV4-11 cells. ASP2215 may have potential use in treating AML. Synonyms: Gilteritinib; ASP2215; ASP-2215; ASP 2215. CAS No. 1254053-43-4. Molecular formula: C29H44N8O3. Mole weight: 552.724. | |
| Gilteritinib hemifumarate | Gilteritinib (ASP2215) hemifumarate is a potent and ATP-competitive FLT3/AXL inhibitor with IC50 of 0.29 nM/0.73 nM, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ASP2215 hemifumarate. CAS No. 1254053-84-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12432A. | |
| Gilteritinib hemifumarate | Gilteritinib hemifumarate. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1254053-84-3. Molecular formula: C33H48N8O7. Mole weight: 668.8. Catalog: APB1254053843. | |
| Gilvetmab | Gilvetmab is a potent caninized anti- PD-1 monoclonal antibody. gilvetmab blocks the interaction between PD-1 and its ligand PDL-1 [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 1808081-43-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99641. | |
| Gilvocarcin E | It is produced by the strain of Streptomyces gilvotanareus, Str. anandii. It has anti-gram-positive bacterial activity and can inhibit sarcoma 180 and P388 leukemia cells. Synonyms: 8-Ethyl-4-(6-deoxy-α-L-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one; Anandimycin C; Toromycin C; dihydrotoromycin; 4-Fucofuranosyl-1-hydroxy-10,12-dimethoxy-8-ethyl-6H-benzo(d)naphtho(1,2b)pyran-6-one; 1,4-Anhydro-6-deoxy-1-(8-ethyl-1-hydroxy-10,12-dimethoxy-6-oxo-6H-benzo[d]naphtho[1,2-b]pyran-4-yl)hexitol. CAS No. 80937-34-4. Molecular formula: C27H28O9. Mole weight: 496.50. | |
| Gilvocarcin M | It is produced by the strain of Streptomyces gilvotanareus, Str. anandii. It has anti-gram-positive bacterial activity and can inhibit sarcoma 180 and P388 leukemia cells. Synonyms: 6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-; 4-(6-Deoxy-α-L-galactofuranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-6H-benzo[d]naphtho[1,2-b]pyran-6-one; Anandimycin B; ToroMycin B; Antibiotic 1072A. Grades: >95% by HPLC. CAS No. 77879-89-1. Molecular formula: C26H26O9. Mole weight: 482.48. | |
| Gilvocarcin M (Anandimycin B, Toromycin B, Antibiotic 1072A) | Gilvocarcin M is the minor analogue of a complex of C-glycoside antitumor actives isolated from a Streptomyces sp. Gilvocarcin M contains a methyl group in the 8-position and is less active than the vinyl analogue (gilvocarcin V), which is thought to act as an inhibitor of human topoisomerase II. Gilvocarcin M displays potent antibacterial, antifungal, antiviral and antitumor activity. Recent research on the gilvocarcins suggests that they act as photoactivated crosslinkers of DNA to histones. Group: Biochemicals. Alternative Names: Anandimycin B, Toromycin B, Antibiotic 1072A. Grades: Highly Purified. CAS No. 77879-89-1. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Gilvocarcin V | It is produced by the strain of Streptomyces gilvotanareus, Str. anandii. It has anti-gram-positive bacteria, negative bacteria, fungal activity and can inhibit sarcoma 180 and P388 leukemia cells. Synonyms: DC-38-V; Anandimycin A; Toromycin; Antibiotic 1072B; Antibiotic B21085; Antibiotic DC 38A; Antibiotic DC 38V; 4-(6-Deoxy-α-D-galactofuranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one; NSC 338943; NSC 348115. Grades: >95% by HPLC. CAS No. 77879-90-4. Molecular formula: C27H26O9. Mole weight: 494.49. | |
| Gilvocarcin V | Antibiotic. Antitumor compound. Weakly active against Gram-positive bacteria and fungi. Mediates a unique cross-linking reaction between DNA and histone H3 by light. Single strand scission and covalent binding to DNA after photoactivation. Source:Streptomyces sp. Gö 3592. Group: Biochemicals. Alternative Names: 4-(6-Deoxy-α-D-galactofuranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one; Antibiotic 1072B; NSC 338943; NSC 348115. Grades: Highly Purified. CAS No. 77879-90-4. Pack Sizes: 100ug, 250ug, 1mg. Molecular Formula: C??H??O?. US Biological Life Sciences. | Worldwide |
| Gilvocarcin V | Gilvocarcin V is an antibiotic with antibacterial activity and can be isolated from Actinomycete. Gilvocarcin V also has anti-tumor activity and can be used in cancer research [1]. Uses: Scientific research. Group: Natural products. CAS No. 77879-90-4. Pack Sizes: 100 μg; 250 μg. Product ID: HY-129307. | |
| Gilvocarcin V (Anandimycin A, Toromycin B, Antibiotic 1072B) | Gilvocarcin V is the major analogue of a complex of C-glycoside antitumor actives isolated from a Streptomyces sp. Gilvocarcin V contains a vinyl group in the 8-position and is the most potent analogue of the complex. It is thought to act as an inhibitor of the catalytic activity of human topoisomerase II. The metabolite displays potent antibacterial, antifungal, antiviral and antitumor activity. Recent research on the gilvocarcins suggests that they act as photoactiviated crosslinkers of DNA to histones. Group: Biochemicals. Alternative Names: Anandimycin A, Toromycin B, Antibiotic 1072B. Grades: Highly Purified. CAS No. 77879-90-4. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Gilvusmycin | It is produced by the strain of Streptomyces sp. It is an antibiotic with strong anti-tumor activity. It can inhibit P388, K562, A431 and MKN28 cells with IC50 (ng/mL) of 0.08, 0.86, 0.72 and 0.75, respectively. Synonyms: 6-({6-[(6-acetyl-5-hydroxy-4-methoxy-3,6,7,8-tetrahydropyrrolo[3,2-e]indol-2-yl)carbonyl]-5-hydroxy-4-methoxy-3,6,7,8-tetrahydropyrrolo[3,2-e]indol-2-yl}carbonyl)-3-methyl-4,4a,5,6-tetrahydrocyclopropa[c]pyrrolo[3,2-e]indol-8(1H)-one. CAS No. 195052-09-6. Molecular formula: C38H34N6O8. Mole weight: 702.71. | |
| Gimatecan | Gimatecan is an orally bioavailable, semi-synthetic lipophilic analogue of camptothecin, a quinoline alkaloid extracted from the Asian tree Camptotheca acuminate, with potential antineoplastic and antiangiogenic activities. Gimatecan binds to and inhibits the activity of topoisomerase I, stabilizing the cleavable complex of topoisomerase I-DNA, which inhibits the religation of single-stranded DNA breaks generated by topoisomerase I; lethal double-stranded DNA breaks occur when the topoisomerase I-DNA complex is encountered by the DNA replication machinery, DNA replication is disrupted, and the tumor cell undergoes apoptosis. Although the mechanism of its antiangiogenic activity has yet to be full elucidated, this agent may inhibit endothelial cell migration, tumor neovascularization, and the expression of proangiogenic basic fibroblast growth factor (bFGF). Synonyms: ST1481; 1H-Pyrano(3',4':6,7)indolizino(1,2-b)quinoline-11-carboxaldehyde, 4-ethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-, 11-(O-(1,1-dimethylethyl)oxime), (C(E),4S)-; 7-t-Butoxyiminomethylcamptothecin; (4S)-11-((E)-((1,1-DImethylethoxy)imino)methyl)-4-ethyl-4-hydroxy-1,12-dihydro-14H-pyrano(3',4':6,7)indolizino(1,2-b)quinoline-3,14(4H)-dione; NSC793724. Grades: ≥98%. CAS No. 292618-32-7. Molecular formula: C25H25N3O5. Mole weight: 447.48. | |
| Gimatecan | Gimatecan (ST1481) is a potent topoisomerase I inhibitor. Gimatecan is an orally bioavailable camptothecin analogue with antitumor activity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: LBQ707; LBQ 707; LB-Q707; ST1481; ST1481; ST-1481; CPT 1847; CPT-1847; CPT1847; Gimatecan. Product Category: Inhibitors. Appearance: Solid powder. CAS No. 292618-32-7. Molecular formula: C25H25N3O5. Mole weight: 447.4831 g/mol. Purity: ≥98%. IUPACName: (4S)-11-((E)-((1,1-Dimethylethoxy)imino)methyl)-4-ethyl-4-hydroxy-1,12-dihydro-14H-pyrano(3,4:6,7)indolizino(1,2-b)quinoline-3,14(4H)-dione. Canonical SMILES: O=C1[C@](O)(CC)C2=C(CO1)C(N3CC4=C(/C=N/OC(C)(C)C)C5=CC=CC=C5N=C4C3=C2)=O. Product ID: ACM292618327. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Gimeracil | Gimeracil, a component of an oral fluoropyrimidine derivative S-1, inhibits DNA DSB repair and is a potent inhibitor of DPYD (dihydropyrimidine dehydrogenase, DPD) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Gimestat. CAS No. 103766-25-2. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-17469. | |
| Gimeracil | Gimeracil is an antitumor agent. Gimeracil is a potent inhibitor of dihydropyrimidine dehydrogenase (DPD). Group: Biochemicals. Alternative Names: 5-Chloro-4-hydroxy-2(1H)-pyridinone; 5-Chloro-2,4-dihydroxypyridine; 5-Chloro-4-hydroxy-2-pyridone; Gimestat; CDHP. Grades: Highly Purified. CAS No. 103766-25-2. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
| Gimeracil | 5-Chloro-4-hydroxy-2(1H)-pyridinone,5-chloro-2,4-pyridinediol. Grades: CAS No. 103766-25-2. Product ID: 8-04513. Molecular formula: C5H4NO2Cl. Mole weight: 140.55. |  |
| Gimeracil | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopyenzyme activators, inhibitors & substrates. | |
| Gimeracil-13C3 | Antitumor agent. A potent inhibitor of dihydropyrimidine dehydrogenase (DPD). Group: Biochemicals. Alternative Names: 5-Chloro-4-hydroxy-2(1H)-pyridinone-13C3; 5-Chloro-2,4-dihydroxypyridine-13C3; 5-Chloro-4-hydroxy-2-pyridone-13C3; Gimestat-13C3; CDHP -13C3. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Gimeracil (CDHP) | Cas No. 103766-25-2. | |
| Gimeracil Impurity 1 | Synonyms: Gimeracil; 103766-25-2; gimestat; 5-Chloro-2,4-dihydroxypyridine; 5-chloropyridine-2,4-diol; 5-Chloro-4-hydroxy-2(1H)-pyridone; 5-Chloro-4-hydroxy-2(1H)-pyridinone; Gimeracil [INN]; 5-Chloro-4-hydroxy-1H-pyridin-2-one; 5-Chloro-2,4-pyridinediol; 5-CHLORO-4-HYDROXYPYRIDIN-2(1H)-ONE; 5-chloro-2-hydroxypyridin-4(1H)-one; 2(1H)-Pyridinone, 5-chloro-4-hydroxy-; 5-CHLORO-4-HYDROXY-2-PYRIDONE. Grades: > 95%. Molecular formula: C9H10ClNO3. Mole weight: 215.64. | |
| Gimeracil Impurity 10 | Grades: > 95%. Molecular formula: C14H14Cl2N2O5. Mole weight: 361.18. | |
| Gimeracil Impurity 2 | Grades: > 95%. Molecular formula: C5H5ClN2O2. Mole weight: 160.56. | |
| Gimeracil impurity 3 | Gimeracil impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1227600-22-7. Molecular formula: C6H6ClNO3. Mole weight: 159.57. Catalog: APB1227600227. | |
| Gimeracil Impurity 3 | Grades: > 95%. Molecular formula: C4H5N3O5. Mole weight: 175.10. | |
| Gimeracil Impurity 5 | Synonyms: 5-Chloro-4-hydroxy-1-methylpyridin-2(1H)-one; Gimeracil Impurity 5; 5-chloro-4-hydroxy-1-methyl-1,2-dihydropyridin-2-one; 5-chloro-4-hydroxy-1-methylpyridin-2-one; 5-Chloro-O-demethyl-3-decyanoRicinine; CN1C(C=C(C(=C1)Cl)O)=O; MFCD19687930; AT19250; 5-Chloro-O-demethyl-3-decyano Ricinine; EN300-6496558; Z1258976765. Grades: > 95%. CAS No. 1379260-15-7. Molecular formula: C6H6ClNO2. Mole weight: 159.57. | |
| Gimeracil Impurity 6 | Grades: > 95%. Molecular formula: C16H18Cl2N2O9. Mole weight: 453.24. | |
| Gimeracil Impurity 7 | Synonyms: Gimeracil Impurity 7; 1227600-22-7; 5-chloro-2-hydroxy-4-methoxypyridine5-chloro-4-methoxy-1H-pyridin-2-one. Grades: > 95%. CAS No. 1227600-22-7. Molecular formula: C6H6ClNO2. Mole weight: 159.57. | |
| Gimeracil Impurity 8 | Grades: > 95%. CAS No. 17902-24-8. Molecular formula: C8H9ClN2O3. Mole weight: 216.63. | |
| Gimeracil Impurity 9 | Grades: > 95%. Molecular formula: C3H3N3O2. Mole weight: 113.08. | |
| Ginger | Ginger. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ginger;Ginger oil. Product Category: Heterocyclic Organic Compound. CAS No. 8007-8-7. Product ID: ACM2230756. Alfa Chemistry ISO 9001:2015 Certified. | |
| Ginger CO2 Extract | Ginger CO2 Extract (Oleoresin). CAS No. 84696-15-1. FEMA No. 2521. Kosher: Y. VIGON Item # 503776. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Ginger CO2 Extract | Ginger CO2 Extract. CAS No. 84696-15-1. FEMA No. 2521. Kosher: Y. VIGON Item # 504502. Categories: Speciality Ingrdients Suppliers, Flavors, Aromatherapy, Essetial Oils. | America & Internationally |
| Ginger Constituent Mixture | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Ginger extract | Ginger extract exhibits anti-cancer, anti-inflammatory and chemotherapeutic effects in vivo [1]. Uses: Scientific research. Group: Natural products. CAS No. 84696-15-1. Pack Sizes: 50 mg. Product ID: HY-N9451. | |
| Ginger Extract | Ginger Extract. Applications: Ginger extract can be used in functional food, drinks, health care products and pharmaceuticals. Group: Others. Purity: 5:1 10:1 20:1 or as customers requirements. Appearance: Yellowish-brown Powder. Source: Ginger (Zingiber officinale) is a flowering plant, in the family Zingiberaceae whose rhizome, ginger root or simply ginger, is widely used as a spice or a folk medicine. Ginger Extract; Zingiber officinale Rosc. Cat No: EXTC-183. | |
| Ginger Oil Chinese | Ginger Oil Chinese. CAS No. 8007-08-7. FEMA No. 2522. Kosher: Y. VIGON Item # 504286. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Ginger Oil - CO2 | Ginger CO2 is extracted in such a way that it also contains gingerols and shogaol, compounds that contribute to the sharp, pungent smell and taste of fresh ginger. The aroma of Ginger CO2 extract is spicy and warm, very dense and more complex than that of distilled Ginger - it smells just like the freshly harvested root. Ginger CO2 is a pale yellow to greenish yellow oil and is quite potent, so it is best to use it in low percentages. Traditionally used for its warming action, Ginger Root CO2 Total Extract aids digestion, stimulates blood flow and helps relieve a queasy stomach and menstrual discomfort. When added to a carrier oil or lotion, it helps joint and muscle aches associated with the wear and tear of normal aging. Uses: Aromatherapy, Flavour, Cosmetic and Care. Group: Plant Extracts. INCI Names: Zingiber Officinale (Ginger) Root Oil. Grades: FOOD GRADE. CAS No. 84696-15-1; 8007-08-7. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: FG-003. Olfactive Profile: Warm, spicy, pungent, woody, earthy, aromatic, sweet, citrus. EC No: 283-634-2. FEMA No: 2522. Origin: Indonesia. |  New Jersey |
| Ginger Oil Cochin | Ginger Oil Cochin. CAS No. 8007-08-7. FEMA No. 2522. VIGON Item # 509114. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Cosmetics, Aromatherapy, Essetial Oils. | America & Internationally |
| Gingerol | Cas No. 23513-14-6. | |
| Ginger Oleoresin African | Ginger Oleoresin African. CAS No. 84696-15-1. FEMA No. 2521. Kosher: Y. VIGON Item # 501251. Categories: Speciality Ingrdients Suppliers, Flavors. | America & Internationally |
| Ginger Powder | Ginger powder is made from fresh ginger, the underground stem, or rhizome, of the plant zingiber officinale. Ginger powder is be valued around the world as an important cooking spice and is believed to help the common cold, flu-like symptoms, headaches, and even painful menstual periods. Ginger powder also possesses a special efficacy of relieving seasick and carsick. Group: Others. Ginger Powder; Zingiber Officinale Roscoe. Cat No: EXTC-108. | |
| Ginger Root Powder | Ginger Root Powder. |  CA, FL & NJ |
| Ginger SFE | Ginger SFE. CAS No. 8007-08-7. FEMA No. 2522. Kosher: Y. VIGON Item # 504601. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| gingipain K | Activity is stimulated by glycine. Known from the bacterium Porphyromonas gingivalis and contributes to the pathogenicity of the organism. In peptidase family C25. Group: Enzymes. Synonyms: Lys-gingipain; PrtP proteinase. Enzyme Commission Number: EC 3.4.22.47. CAS No. 159745-69-4. 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-4222; gingipain K; EC 3.4.22.47; 159745-69-4; Lys-gingipain; PrtP proteinase. Cat No: EXWM-4222. | |
| gingipain R | A secreted endopeptidase from the bacterium Porphyromonas gingivalis. Strongly activated by glycine, and stabilized by Ca2+. Precursor molecule contains a hemagglutinin domain. Misleadingly described in some literature as "trypsin-like", being a cysteine peptidase, type example of family C25. Group: Enzymes. Synonyms: Arg-gingipain; gingipain-1; argingipain; Arg-gingivain-55 proteinase; Arg-gingivain-70 proteinase; Arg-gingivain-75 proteinase; arginine-specific cysteine protease; arginine-specific gingipain; arginine-specific gingivain; RGP-1; RGP. Enzyme Commission Number: EC 3.4.22.37. CAS No. 159745-71-8. 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-4212; gingipain R; EC 3.4.22.37; 159745-71-8; Arg-gingipain; gingipain-1; argingipain; Arg-gingivain-55 proteinase; Arg-gingivain-70 proteinase; Arg-gingivain-75 proteinase; arginine-specific cysteine protease; arginine-specific gingipain; arginine-specific gingivain; RGP-1; RGP. Cat No: EXWM-4212. | |
| Gingko Biloba Leaf Extract 24% Flavone Glycoside / 6% Terpene Lactones | Gingko Biloba Leaf Extract 24% Flavone Glycoside / 6% Terpene Lactones. | CA, FL & NJ |
| Ginisortamab | Ginisortamab (UCB6114) is a fully human IgG4P anti Gremlin-1 monoclonal antibody. Ginisortamab has the potential for the research of gastrointestinal (GI) tumors [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: UCB6114. CAS No. 2390147-17-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99643. | |
| Ginkbilobin | Ginkbilobin is a novel antifungal protein from Ginkgo biloba seeds with sequence similarity to embryo-abundant protein. The protein, designated ginkbilobin, exerted potent antifungal activity against a variety of fungi, including Botrytis cinerea, Mycosphaerella arachidicola, Fusarium oxysporum, Rhizoctonia solani, and Coprinus comatus. Ginkbilobin exhibited a moderate antibacterial action against Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli. It suppressed the activity of HIV-1 reverse transcriptase and the proliferation of murine splenocytes. | |
| Ginkgetin | Ginkgetin. Group: Biochemicals. Grades: Plant Grade. CAS No. 481-46-9. Pack Sizes: 10mg. Molecular Formula: C32H22O10, Molecular Weight: 566.51. US Biological Life Sciences. | Worldwide |
| Ginkgetin | Ginkgetin Inhibitor. Uses: Scientific use. Product Category: T4S2126. CAS No. 481-46-9. |  |
| Ginkgo biloba extract | Ginkgo biloba extract a natural product isolated from Ginkgo biloba, and can be used for Atherosclerosis and cardiovascular study [1]. Uses: Scientific research. Group: Natural products. CAS No. 90045-36-6. Pack Sizes: 50 mg; 100 mg. Product ID: HY-N12060. | |
| Ginkgo Biloba Extract | Ginkgo biloba extract is prepared from the leaves of Maidenhair Tree after Adiantum, which is a unique species of tree with no close living relatives. Ginkgo biloba leaf extract is used for the treatment of numerous conditions, many of which are under scientific investigation. The most powerful effect of ginkgo biloba extract is on the circulating system. Ginkgo biloba extract can be used to treat respiratory problems such as asthma and bronchitis. Group: Others. Mole weight: 408.4. Ginkgo Biloba Extract; Ginkgo Biloba Linn. Cat No: EXTC-009. | |
| Ginkgo Biloba Flavonoids Mix | 100 ?g/mL each component in methanol, ampule of 1.0 mL, certified reference material. Group: Herbal medicinal products standards. | |
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