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Calystegine A3, a biomedically significant natural compound, displays remarkable potency in extensive biomedical research. Its distinct characteristics have been duly recognized for studying specific neurologic ailments, including the renowned Alzheimer's disease. Through meticulous analysis, Calystegine A3 is particularly noteworthy for its pronounced inhibitory properties targeting crucial enzymes associated with the development of neurodegenerative conditions. Synonyms: [1R-(2-endo,3-exo)]-8-Azabicyclo[3.2.1]octane-1,2,3-triol; Calystegin A3; (+)-Calystegine A3; 8-Azabicyclo[3.2.1]octane-1,2,3-triol, (1R,2S,3R,5R)-. Grades: ≥95%. CAS No. 131580-36-4. Molecular formula: C7H13NO3. Mole weight: 159.18.
Calystegine A5
Calystegine A5 is an extraordinary natural alkaloid obtained from diverse botanical sources, exhibiting remarkable potency in the suppression of glycosidases. This outstanding attribute renders Calystegine A5 a highly promising tool for the research of Type 2 diabetes. Synonyms: Calystegine A5; Calystegin A5; 165905-26-0; (1R,3S,4S,5R)-8-AZABICYCLO[3.2.1]OCTANE-1,3,4-TRIOL; 8-Azabicyclo(3.2.1)octane-1,3,4-triol, (1R,3S,4S,5R)-; CHEMBL3233943; AKOS040735614. CAS No. 165905-26-0. Molecular formula: C7H13NO3. Mole weight: 159.18.
Calystegine B1
Calystegine B1 is an exceedingly powerful naturally occurring alkaloid, garnering immense attention for its prowess in obstructing diverse enzymes. This compound has proven instrumental in studying an array of afflictions like cancer, neurodegenerative pathologies as well as viral invasions. Synonyms: Calystegine B1; 127414-86-2; (1R,2S,3R,5S,6R)-8-AZABICYCLO[3.2.1]OCTANE-1,2,3,6-TETROL; Calystegine B(1); 8-azabicyclo[3.2.1]octane-1,2,3,6-tetrol; DTXSID20925887; AKOS040736062; FS-6673; 8-Azabicyclo(3.2.1)octane-1,2,3,6-tetrol, (1R,2S,3R,5S,6R)-rel-. CAS No. 127414-86-2. Molecular formula: C7H13NO4. Mole weight: 175.18.
Calystegine B2
Calystegine B2 is a bioactive compound known for its potential therapeutic properties in studying neurodegenerative diseases, such as Alzheimer's and Parkinson's. Extensive research has revealed its ability to inhibit enzymes involved in the progression of these diseases, making it a promising candidate for drug development. Synonyms: (1R,2S,3R,4S,5R)-8-Azabicyclo[3.2.1]octane-1,2,3,4-tetrol; Nortropanoline. CAS No. 127414-85-1. Molecular formula: C7H13NO4. Mole weight: 175.19.
Calystegine b3
Calystegine b3. Uses: Designed for use in research and industrial production. CAS No. 178231-95-3. Molecular formula: C7H13NO4. Mole weight: 175.19. Purity: 0.96. Product ID: ACM178231953. Alfa Chemistry ISO 9001:2015 Certified.
Calystegine B3
Calystegine B3 is a highly potent natural inhibitor with widespread application encompassing the extensive research in targeting the debilitating neurodegenerative conditions, namely Alzheimer's and Parkinson's diseases. Synonyms: 8-Azabicyclo(3.2.1)octane-1,2,3,4-tetrol, (1R,2R,3R,4S,5R)-; 2-Epicalystegine B2; (+)-Calystegine B3; (1R,5R)-8-Azabicyclo[3.2.1]octane-1,2alpha,3alpha,4beta-tetrol; Calystegin B3; 8-Azabicyclo(3.2.1)octane-1,2,3,4-tetrol, (2-exo,3-exo,4-endo)-(+)-. Grades: >98%. CAS No. 178231-95-3. Molecular formula: C7H13NO4. Mole weight: 175.19.
Calystegine B4
Calystegine B4 is a potent natural compound found in various plants exhibiting promising applications in the study of neurodegenerative diseases, such as Alzheimer's and Parkinson's. Synonyms: Calystegine B4; 184046-85-3; (1R,2S,3R,4R,5R)-8-azabicyclo[3.2.1]octane-1,2,3,4-tetrol; CHEMBL3233945; 8-Azabicyclo(3.2.1)octane-1,2,3,4-tetrol, (1R,2S,3R,4R,5R)-; 8-Azabicyclo[3.2.1]octane-1,2,3,4-tetrol, (1R,2S,3R,4R,5R)-; (-)-Calystegine B4; Q29YLG74LW; Calystegine B4 - 90% min; DTXSID501317306; BDBM50002909; 8-Azabicyclo[3.2.1]octane-1,2,3,4-tetrol, (2-endo,3-exo,4-exo)-(-)-. CAS No. 184046-85-3. Molecular formula: C7H13NO4. Mole weight: 175.18.
Calystegine N1
Calystegine N1 is a highly potent inhibitor assuming a pivotal and indispensable function in the research of diverse ailments including cancer, viral infections and neurodegenerative afflictions.
tropinone reductase I
Also oxidizes other tropan-3α-ols, but not the corresponding β-derivatives. This enzyme along with EC 1.1.1.236, tropinone reductase II, represents a branch point in tropane alkaloid metabolism.Tropine (the product of EC 1.1.1.206) is incorporated into hyoscyamine and scopolamine whereas pseudotropine (the product of EC 1.1.1.236) is the first specific metabolite on the pathway to the calystegines. Both enzymes are always found together in any given tropane-alkaloid-producing species, have a common substrate, tropinone, and are strictly stereospecific. Group: Enzymes. Synonyms: tropine dehydrogenase; tropinone reductase (ambiguous); TR-I. Enzyme Commission Number: EC 1.1.1.206. CAS No. 118390-87-7. 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-0110; tropinone reductase I; EC 1.1.1.206; 118390-87-7; tropine dehydrogenase; tropinone reductase (ambiguous); TR-I. Cat No: EXWM-0110.
tropinone reductase II
This enzyme along with EC 1.1.1.206, tropine dehydrogenase, represents a branch point in tropane alkaloid metabolism.Tropine (the product of EC 1.1.1.206) is incorporated into hyoscyamine and scopolamine whereas pseudotropine (the product of EC 1.1.1.236) is the first specific metabolite on the pathway to the calystegines. Both enzymes are always found together in any given tropane-alkaloid-producing species, have a common substrate, tropinone, and are strictly stereospecific. Group: Enzymes. Synonyms: tropinone (ψ-tropine-forming) reductase; pseudotropine forming tropinone reductase; tropinone reductase (ambiguous); TR-II. Enzyme Commission Number: EC 1.1.1.236. CAS No. 136111-61-0. 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-0143; tropinone reductase II; EC 1.1.1.236; 136111-61-0; tropinone (ψ-tropine-forming) reductase; pseudotropine forming tropinone reductase; tropinone reductase (ambiguous); TR-II. Cat No: EXWM-0143.
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