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Febrifugine. Group: Biochemicals. Grades: Plant Grade. CAS No. 24159-07-7. Pack Sizes: 20mg. Molecular Formula: C16H19N3O3, Molecular Weight: 301.34. US Biological Life Sciences.
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Febrifugine
Febrifugine is a quinazolinone alkaloid found in the roots and leaves of Dichroa febrifuga , with antimalarial activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 24159-07-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N2384.
Febrifugine dihydrochloride is a quinazolinone alkaloid found in the roots and leaves of Dichroa febrifuga , with antimalarial activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 32434-42-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N2384A.
Febrifugine dihydrochloride
Febrifugine is a quinazolinone alkaloid isolated from the Chinese herb Dichroa febrifuga. Synonyms: (+)-Febrifugine dihydrochloride. Grades: > 95%. CAS No. 32434-42-7. Molecular formula: C16H21Cl2N3O3. Mole weight: 374.26.
(-)-Deoxyhalofebrifugine Dihydrobromide
(-)-Deoxyhalofebrifugine is an analog of Halofuginone (H102500, HCl salt), a halogenated derivative of Febrifugine (F228500). Halofuginone is used as an antiprotozoal. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C16H19Br3ClN3O2, Molecular Weight: 560.51. US Biological Life Sciences.
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(+)-Deoxyhalofebrifugine Dihydrobromide
(+)-Deoxyhalofebrifugine is an analog of Halofuginone (H102500, HCl salt), a halogenated derivative of Febrifugine (F228500). Halofuginone is used as an antiprotozoal. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C16H19Br3ClN3O2, Molecular Weight: 560.51. US Biological Life Sciences.
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rac-Febrifugine Dihydrochloride
rac-Febrifugine dihydrochloride is the salt of Febrifugine, a bioactive constituent of a Chinese medicinal herb that is characterized by its therapeutic activity regarding malaria, cancer, fibrosis and inflammatory diseases. Group: Biochemicals. Alternative Names: rel-3-[3-[(2R,3S)-3-Hydroxy-2-piperidinyl]-2-oxopropyl]-4(3H)quinazolinone Dihydrochloride; rel-Febrifugine Dihydrochloride. Grades: Highly Purified. CAS No. 32434-42-7. Pack Sizes: 1mg, 10mg. US Biological Life Sciences.
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1, 1, 1-tri methyl -N- (tri phenylphosphoranylide ne ) silanamine
1, 1, 1-tri methyl -N- (tri phenylphosphoranylide ne ) silanamine is a reagent used in the synthesis of febrifugine derivatives and in the development of effective and safer tetrahydroquinazoline-type antimalarial. Group: Biochemicals. Grades: Highly Purified. CAS No. 13892-06-3. Pack Sizes: 100mg, 500mg. Molecular Formula: C21H24NPSi, Molecular Weight: 349.48. US Biological Life Sciences.
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Allyl Bromoridane
Allyl Bromoridane is used as an anticoccidial agent. Allyl Bromoridane is an intermediate of Febrifugine and Halofuginone. Group: Biochemicals. Alternative Names: trans-2-(3-Bromo-2-oxopropyl)-3-methoxy-1-piperidinecarboxylic Acid 2-Propenyl Ester. Grades: Highly Purified. CAS No. 117348-70-6. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Bromoridane Hydrobromide
Bromoridane is a piperidylpropanone derivative having anti-coccidiosis activity. Bromoridane is an intermediate of Febrifugine and Halofuginone. Group: Biochemicals. Alternative Names: trans-. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Halofuginone
Halofuginone (RU-19110), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K i of 18.3 nM [1] [2]. Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Natural products. Alternative Names: RU-19110. CAS No. 55837-20-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1584.
Halofuginone
Halofuginone (RU-19110), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM. Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity. Halofuginone is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca2+ channels. Halofuginone has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 7-bromo-6-chloro-3-[3-[(2r,3s)-3-hydroxy-2-piperidyl]-2-oxopropyl]-4(3h)-quinazolinone;HALOFUGINONE;4(3h)-quinazolinone,7-bromo-6-chloro-3-(3-(3-hydroxy-2-piperidinyl)-2-oxopropy;7-Bromo-6-chloro-3[3-(3-hydroxy-2-piperidi-nyl)-2-oxopropyl]-4(3H)-quinzolinone;trans-7-bromo-6-chloro-3-(3-(3-hydroxy-2-piperidinyl)-2-oxopropyl)-4(3h)-qui;trans-l);7-Bromo-6-chloro-3-(3-(3-hydroxypiperidin-2-yl)-2-oxopropyl)quinazolin-4(3H)-one;7-Bromo-6-chlorofebrifugine Hydrochloride. Product Category: Inhibitors. Appearance: Solid. CAS No. 55837-20-2. Molecular formula: C16H17BrClN3O3. Mole weight: 414.68. Purity: 0.9978. Canonical SMILES: O=C1N(CC(C[C@@H]2NCCC[C@H]2O)=O)C=NC3=C1C=C(Cl)C(Br)=C3. Product ID: ACM55837202. Alfa Chemistry ISO 9001:2015 Certified.
Halofuginone hydrobromide
Halofuginone (RU-19110) hydrobromid, a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K i of 18.3 nM [1] [2]. Halofuginone hydrobromid is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone hydrobromid is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone hydrobromid has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Natural products. Alternative Names: RU-19110 hydrobromide. CAS No. 64924-67-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-N1584A.
Halofuginone lactate
Halofuginone lactate, a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a K i of 18.3 nM [1] [2]. Halofuginone lactate is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone lactate is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca 2+ channels. Halofuginone lactate has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RU-19110 lactate. CAS No. 82186-71-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1584C.
Halofuginone lactate
Halofuginone lactate is a halogenated derivative of febrifugine. Halofuginone inhibits prolyl-tRNA synthetase in an ATP-dependent manner with a Ki of 18.3 nM. Grades: >95%. CAS No. 82186-71-8. Molecular formula: C19H23BrClN3O6. Mole weight: 504.76.
Halofuginone (Standard)
Halofuginone (Standard) is the analytical standard of Halofuginone. This product is intended for research and analytical applications. Halofuginone (RU-19110), a Febrifugine derivative, is a competitive prolyl-tRNA synthetase inhibitor with a Ki of 18.3 nM [1] [2]. Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activity [3] [4]. Halofuginone is also a potent pulmonary vasodilator by activating Kv channels and blocking voltage-gated, receptor-operated and store-operated Ca2+ channels. Halofuginone has anti-malaria, anti-inflammatory, anti-cancer, anti-fibrosis effects [5]. Uses: Scientific research. Group: Natural products. CAS No. 55837-20-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1584R.
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