
CAS 59461-30-2
:Cobinamide, Co-idrossi-, f-(dihidrogeno fosfato), sale interno, 3'-estere con (5,6-dimetil-1-α-D-ribofuranosil-1H-benzimidazolo-κN3), cloridrato (1:1)
Descrizione:
Cobinamide, Co-idrossi-, f-(dihidrogeno fosfato), sale interno, 3'-estere con (5,6-dimetil-1-α-D-ribofuranosil-1H-benzimidazolo-κN3), cloridrato (1:1) è un composto chimico complesso principalmente associato al metabolismo della vitamina B12. Presenta un ione di cobalto coordinato a una struttura di cobinamida, che è un derivato della cobalamina, e include un gruppo fosfato che ne migliora la solubilità e la biodisponibilità. La presenza del moiety 5,6-dimetil-1-α-D-ribofuranosil-1H-benzimidazolo indica il suo potenziale ruolo nei sistemi biologici, in particolare nel metabolismo degli acidi nucleici e nei processi energetici cellulari. Come sale cloridrato, è tipicamente più stabile e solubile in soluzioni acquose, rendendolo adatto per varie applicazioni farmaceutiche. La formazione di sale interno del composto suggerisce un arrangiamento strutturale unico che può influenzare la sua reattività e interazione con obiettivi biologici. In generale, i derivati della cobinamida sono di interesse in biochimica e chimica medicinale per i loro ruoli nelle reazioni enzimatiche e potenziali applicazioni terapeutiche.
Formula:C62H89CoN13O15P·ClH
InChI:InChI=1S/C62H90N13O14P.ClH.Co.H2O/c1-29-20-39-40(21-30(29)2)75(28-70-39)57-52(84)53(41(27-76)87-57)89-90(85,86)88-31(3)26-69-49(83)18-19-59(8)37(22-46(66)80)56-62(11)61(10,25-48(68)82)36(14-17-45(65)79)51(74-62)33(5)55-60(9,24-47(67)81)34(12-15-43(63)77)38(71-55)23-42-58(6,7)35(13-16-44(64)78)50(72-42)32(4)54(59)73-56;;;/h20-21,23,28,31,34-37,41,52-53,56-57,76,84H,12-19,22,24-27H2,1-11H3,(H15,63,64,65,66,67,68,69,71,72,73,74,77,78,79,80,81,82,83,85,86);1H;;1H2/q;;+3;/p-3
InChI key:InChIKey=KEHNCSYXYMMUCO-UHFFFAOYSA-K
SMILES:[OH-][Co+3]1234[N]=5C6(C)C7[N-]1C(C(C)(C7CC(N)=O)CCC(=O)NCC(C)OP(=O)([O-])OC8C(O)C(N9C=[N]2C=%10C9=CC(C)=C(C)C%10)OC8CO)=C(C)C%11=[N]3C(=CC%12=[N]4C(=C(C)C5C(CCC(N)=O)C6(CC(N)=O)C)C(CC(N)=O)(C)C%12CCC(N)=O)C(C)(C)C%11CCC(N)=O.Cl
Sinonimi:- Cobinamide, dihydroxide, dihydrogen phosphate (ester), inner salt, 3′-ester with 5,6-dimethyl-1-α-D-ribofuranosyl-1H-benzimidazole, monohydrochloride
- Cobinamide, Co-hydroxy-, f-(dihydrogen phosphate), inner salt, 3′-ester with (5,6-dimethyl-1-α-D-ribofuranosyl-1H-benzimidazole-κN3), hydrochloride (1:1)
- Cobinamide, Co-hydroxy-, f-(dihydrogen phosphate), inner salt, 3′-ester with (5,6-dimethyl-1-α-D-ribofuranosyl-1H-benzimidazole-κN3), monohydrochloride
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3 prodotti.
Hydroxocobalamin Chloride
CAS:Vitamin b12 (cyanocobalamin and related compounds with vitamin b12 activity) and its derivativesFormula:C62H89CoN13O15P·HClColore e forma:Red Brown Crystalline PowderPeso molecolare:1381.54374Hydroxocobalamin chloride
CAS:<p>Hydroxocobalamin chloride is a molecule that contains hydrochloric acid. It is used as a sample preparation reagent in the analysis of fatty acids, and as a chemical intermediate in the synthesis of magnesium salt. Hydroxocobalamin chloride reacts with an organic acid to form an ester or amide. The reaction mechanism for this process involves a nucleophilic attack by the hydroxyl group on the carbonyl carbon atom of the organic acid, followed by displacement of HCl from water. In analytical chemistry, Hydroxocobalamin chloride is used to determine the concentration of dehydroascorbic acid in a sample, which can be indicative of skin condition or dietary supplement intake. This compound also serves as an analytical method for measuring fatty acids and their derivatives (e.g., methyl esters). Symptoms associated with exposure to this compound include skin conditions such as dermatitis and eczema, together with symptoms such as fatigue and irritability that are related to high levels</p>Formula:C62H89CoN13O15P•HClPurezza:Min. 95%Colore e forma:PowderPeso molecolare:1,382.82 g/molhydroxocobalamin monohydrochloride
CAS:Formula:C62H90ClCoN13O15PPurezza:98%Peso molecolare:1382.8160609999993


