CAS 15671-27-9: Sulfitocobalamin
Formula:C62H89CoN13O17PS
InChI:InChI=1S/C62H90N13O14P.Co.H2O3S/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;;1-4(2)3/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);;(H2,1,2,3)/q;+3;/p-3
InChI key:InChIKey=IUJJHFFFUXMHFY-UHFFFAOYSA-K
SMILES:[O-](S(=O)O)[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
Synonyms:- Cobalamin, sulfito-
- Cobalaminsulfonic acid
- Cobinamide, Co-(sulfito-κO)-, dihydrogen phosphate (ester), inner salt, 3′-ester with (5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosyl-1H-benzimidazole-κN<sup>3</sup>)
- Cobinamide, hydroxide sulfite (1:1) (salt), dihydrogen phosphate (ester), inner salt, 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosyl-1H-benzimidazole
- Cobinamide, sulfite (1:1) (salt), dihydrogen phosphate (ester), 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosylbenzimidazole
- Cobinamide, sulfite (1:1) (salt), dihydrogen phosphate (ester), inner salt, 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosyl-1H-benzimidazole
- Cobinamide, sulfite phosphate, 3′-ester with 5,6-dimethyl-1-α-<span class="text-smallcaps">D</span>-ribofuranosylbenzimidazole
- Sulfiotcobalamine
- Sulfitocobalamin
- Vitamin B<sub>12</sub>-sulfonic acid
- Cobinamide, Co-(sulfito-κO)-, dihydrogen phosphate (ester), inner salt, 3′-ester with (5,6-dimethyl-1-α-D-ribofuranosyl-1H-benzimidazole-κN3)
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Found 4 products.
Sulfitocobalamin sodium salt
CAS:Sulfitocobalamin sodium salt is a bacterial strain that is used as a probiotic. It has been shown to be biocompatible and can be used with human liver cells in laboratory studies. Sulfitocobalamin sodium salt is also effective in treating bowel disease, because it reduces the inflammatory response by inhibiting pro-inflammatory cytokine production and preventing the damage of mucosal cells. Sulfitocobalamin sodium salt has been shown to inhibit growth of infectious bacteria, such as Salmonella enterica serovar Typhimurium and Helicobacter pylori, which cause diseases like hepatitis and corrinosis. The molecule also has biological properties that are used for the treatment of inflammation, ulcerative colitis, and other diseases caused by infectious agents.Formula:C62H88CoN13NaO17PSPurity:Min. 95%Molecular weight:1,432.4 g/molSulfitocobalamin Sodium Salt
CAS:Applications Sulfitocobalamin Sodium Salt is a useful synthetic intermediate in the synthesis of Hydroxocobalamin Acetate (H826800); a physiological analog of vitamin B12 where the CN group is replaced with OH. Exists in aqueous solution as an equilibrium mixture of the hydroxy isomer and the ionic aqua isomer (aquacobalamin). Precursor of the coenzymes methylcobalamin and cobamamide. Coordination Compound. Vitamin (hematopoietic). References Kaczka, E.A., et al.: Science, 112, 354 (1950); Friedrich, W., et al.: Vitamins, 837 (1988); Forsyth, J.C., et al.: Clin. Toxicol., 31, 277 (1993)Formula:C62H88CoN13NaO17PSColor and Shape:NeatMolecular weight:1432.4
