A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
BAL27862 is a novel synthetic potent inhibitor of tubulin polymerization that induces cancer cell death. BAL27862 is a novel microtubule-destabilizing drug that is currently undergoing phase I clinical evaluation as the prodrug BAL101553. Synonyms: Avanbulin; BAL-27862; BAL 27862. Grades: 98%. CAS No. 798577-91-0. Molecular formula: C20H17N7O2. Mole weight: 387.40.
b-Ala-b-Ala-OH 98+% (TLC)
b-Ala-b-Ala-OH 98+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g. US Biological Life Sciences.
Worldwide
Balaglitazone
The Rs for the separations were 3.5 for balaglitazone enantiomers, 3.5 for pioglitazone enantiomers, and 3.7 for rosiglitazone. The squared correlation coefficients (r2) were found to be 0.999 for all three compounds. Balaglitazone treated groups shown significantly reduce of HbA1c (%), FSG (mmol/L), postprandial glucose as comparison to pioglitazone. Balaglitazone 10 mg and 20 mg show the similar magnitudes of the effects which comparable to the effects seen in the pioglitazone 45 mg group. The incidence of fluid retention and fat accumulation fewer than those observed with pioglitazone 45 mg. Sixty male dio induced obese rats were divided into five categories: vehicle, pioglitazone 10 mg/kg, pioglitazone 30 mg/kg, balaglitazone 5 mg/kg, balaglitazone 10 mg/kg. At day -7, 21 and 42 fasting serum samples were collected and whole body tissue composition was evaluated by MR scanning. Synonyms: DRF-2593; NN-2344; DRF2593; NN2344; DRF 2593; NN 2344. Grades: >98%. CAS No. 199113-98-9. Molecular formula: C20H17N3O4S. Mole weight: 395.43.
Balaglitazone
Balaglitazone is a selective partial PPARγ agonist with an EC 50 of 1.351 μM for human PPAR&gamma. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DRF 2593; NN 2344. CAS No. 199113-98-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16086.
b-Alanine-2,2,3,3-d4
Heterocyclic Organic Compound. Alternative Names: BETA-ALANINE-2,2,3,3-D4;B-ALANINE-2,2,3,3-D4. CAS No. 116173-67-2. Molecular formula: C3H3D4NO2. Mole weight: 93.117827112. Purity: 98 atom % D. IUPACName: 3-amino-2,2,3,3-tetradeuteriopropanoicacid. Canonical SMILES: C(CN)C(=O)O. Density: 1.22 g/cm³. Catalog: ACM116173672.
b-Alanine-2-chlorotrityl resin
b-Alanine-2-chlorotrityl resin. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
b-Alaninol 2-chlorotrityl resin. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Balanol
It is produced by the strain of Streptomyces sp. Tu 4128. Balanol, a fungal metabolite, is a potent ATP-competitive inhibitor of Protein Kinase C (PKC) and Protein Kinase A (PKA). It is an important target in oncology. Synonyms: 4-(2-Carboxy-6-hydroxybenzoyl)-3,5-dihydroxybenzoic Acid (3R,4R)-Hexahydro-3-[(4-hydroxybenzoyl)amino]-1H-azepin-4-yl Ester; (3R-trans)-Balanol; (-)-Balanol; Azepinostatin; Ophiocordin. Grades: >95%. CAS No. 63590-19-2. Molecular formula: C28H26N2O10. Mole weight: 550.53.
Balapiravir
Balapiravir is the prodrug of a nucleoside analogue inhibitor of the hepatitis C virus (HCV) RNA-dependent RNA polymerase. It is the tri-isobutyrate ester prodrug of R1479 under clinical development to improve exposure of R1479 upon oral administration. It was discontinued for safety reasons in 28-36% of patients and the percentage of patients with serious adverse events was dose related. Synonyms: R1626; R-1626; R 1626; RO4588161; RO-4588161; RO 4588161; Balapiravir. Grades: >98%. CAS No. 690270-29-2. Molecular formula: C21H30N6O8. Mole weight: 494.5.
Balapiravir
Balapiravir (Ro 4588161; R1626) is an orally active proagent of a nucleoside analogue inhibitor of the RNA-dependent RNA polymerase (RdRp) of HCV (R1479; 4'-Azidocytidine). Balapiravir has anti- HCV activity [1] [2] [3]. Balapiravir is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 4588161; R1626. CAS No. 690270-29-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10443.
b-Ala-pNA·HBr 99+% (TLC)
b-Ala-pNA·HBr 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
Balcinrenone
Balcinrenone (AZD9977) is a potent, selective, and orally active mineralocorticoid receptor (MR) modulator. Balcinrenone is used for heart failure, and chronic kidney disease research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AZD9977. CAS No. 1850385-64-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-120274.
Balhimycin
It is produced by the strain of Amycolatopsis sp. 8621022. Balhimycin has the activity of congela-positive bacteria (including MRSA) similar to vancomycin. Synonyms: DB04111; balhimycin. CAS No. 140932-79-2. Molecular formula: C66H73Cl2N9O24. Mole weight: 1447.23.
Balicatib
The cathepsin K inhibitor AAE-581 (balicatib) as the most advanced of them passed Phase II clinical trials in 2005. Eighty adult female Macaca fascicularis underwent bilateral ovariectomies and were dosed twice daily by oral gavage with balicatib at 0, 3, 10, and 50 mg/kg for 18 months (groups O, L, M, H, respectively). Approximately 1 month after treatment initiation, the 50 mg/kg dose was decreased to 30 mg/kg. Twenty animals underwent sham-ovariectomies (group S). Bone mass was measured at 3-6 month intervals. At 18 months, vertebra and femur were collected for histomorphometry. Synonyms: AAE581; AAE-581; AAE 581. Grades: 0.98. CAS No. 354813-19-7. Molecular formula: C23H33N5O2. Mole weight: 411.54.
Balipramine Hydrochloride-d6 (Impurity)
Balipramine Hydrochloride-d6 (Impurity). Group: Biochemicals. Alternative Names: N,N-Dimethyl--5H-dibenz[b,f]azepine-5-propanamine Hydrochloride-d6; G 31406 Hydrochloride-d6; 10,11-Dehydroimipramine Hydrochloride-d6; Depramine Hydrochloride-d6. Grades: Highly Purified. Pack Sizes: 2.5mg. Molecular Formula: C19H17D6N2Cl, Molecular Weight: 320.89. US Biological Life Sciences.
Worldwide
Balipramine Hydrochloride (Impurity)
Balipramine Hydrochloride (Impurity). Group: Biochemicals. Alternative Names: N,N-Dimethyl-5H-dibenz[b,f]azepine-5-propanamine Hydrochloride; G 31406 Hydrochloride; 10,11-Dehydroimipramine Hydrochloride, Depramine Hydrochloride. Grades: Highly Purified. CAS No. 58262-51-4. Pack Sizes: 500mg. Molecular Formula: C19H23N2Cl, Molecular Weight: 314.85. US Biological Life Sciences.
Worldwide
Ball Clay
Ball Clay. Group: Glass additives.
Ball Clay
Ball Clay. Uses: For analytical and research use. Group: Process materials, geological, cement & soils. Catalog: APS00931.
Balm Gilead Extract
Extract obtained from Commiphora Gileadensis (Balm of Gilead) plants. Contains 20% extract dissolved in water and glycerin. Has tonic and soothing properties. Especially suitable for use on irritated or sensitive skin. Uses: Creams, lotions, salves, toners and gels. Group: Skin actives. CAS No. 7732-18-5/56-81-5/122-99-6. Appearance: Light to medium amber liquid, herbal odor. Catalog: CI-SC-0951.
Balm Mint Extract
Extract obtained from Melissa Officinalis (Balm Mint) plants. Contains 20% extract dissolved in water and glycerin. Has soothing, rejuvenating and restorative properties. Uses: Creams, lotions, moisturizers, toners and bath and skin treatment products. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84082-61-1 / 122-99-6. Appearance: Medium amber colored liquid, characteristic odor. Catalog: CI-SC-0821.
Balofloxacin
Balofloxacin is a quinolone antibiotic, inhibiting the synthesis of bacterial DNA by interference with the enqyme DNA gyrase. Uses: Anti-bacterial agents. Synonyms: Balofloxacin; Balofloxacin [INN]; Q 35; UNII-Q022B63JPM; Q-35; Q35. Grades: >98%. CAS No. 127294-70-6. Molecular formula: C20H24FN3O4. Mole weight: 389.42.
Balofloxacin
Balofloxacin is a fluoroquinolone anti-bacterial agent. Group: Biochemicals. Alternative Names: (±) -1-Cyclopropyl-6-fluoro-1, 4-dihydro-8-methoxy-7-[3- (methylamino) piperidino]-4-oxo-3-quinolinecarboxylic Acid; 1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[3-(methylamino)-1-piperidinyl]-4-oxo-3-quinolinecarboxylic Acid; Balorain; Q 35; Q 35. Grades: Highly Purified. CAS No. 127294-70-6. Pack Sizes: 250mg, 500mg, 1g. Molecular Formula: C20H24FN3O4, Molecular Weight: 389.42. US Biological Life Sciences.
Worldwide
Balofloxacin Dihydrate
Fluorinated quinolone antibacterial. Group: Biochemicals. Alternative Names: (+/-)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[3-(methylamino)-1-piperidinyl]-4-oxo-3-quinolinecarboxylic Acid Dihydrate; Baloxin; Q 35. Grades: Highly Purified. CAS No. 151060-21-8. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Balovaptan
Balovaptan (RG7314) is an orally available, selective brain-penetrant vasopressin 1a (hV1a) receptor antagonist, with K i s of 1 and 39 nM for human (hV1a) and mouse (mV1a) receptors, and is used for the research of autism. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RG7314. CAS No. 1228088-30-9. Pack Sizes: 10 mM * 1ML; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109024.
Baloxavir
Baloxavir (Baloxavir acid), derived from the proagent Baloxavir marboxil, is a first-in-class, potent and selective cap-dependent endonuclease (CEN) inhibitor within the polymerase PA subunit of influenza A and B viruses. Baloxavir inhibits viral RNA transcription and replication and has potently antiviral activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Baloxavir acid; S-033447. CAS No. 1985605-59-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109025A.
Baloxavir
Baloxavir marboxil is a first-in-class, one-dose oral medicine with a novel proposed mechanism of action that has demonstrated efficacy in a wide range of influenza viruses, including in vitro activity against oseltamivir-resistant strains and avian strains (H7N9, H5N1) in non-clinical studies. Baloxavir is a polymerase acidic, cap-dependent, endonuclease inhibitor that is indicated for the treatment of acute uncomplicated influenza in patients aged 12 years and older who have been symptomatic for no more than 48 hours. It blocks viral proliferation by binding to one of two endonuclease binding sites, inhibiting the initiation of mRNA synthesis for both influenza A and influenza B strains. Baloxavir can interact with polyvalent cation-containing products, which can decrease its plasma concentration. Synonyms: Baloxavir acid; BXA; Xofluza; S-033447. Grades: ≥98%. CAS No. 1985605-59-1. Molecular formula: C24H19F2N3O4S. Mole weight: 483.49.
Baloxavir
Baloxavir. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-12-((S)-7,8-difluoro-6,11-dihydrodibenzo[b,e]thiepin-11-yl)-7-hydroxy-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione. CAS No. 1985605-59-1. Molecular Formula: C24H19F2N3O4S. Mole Weight: 483.49. Catalog: APB1985605591.