Adenosylcobalamin
CAS No. 13870-90-1
Adenosylcobalamin( Coenzyme B12,Cobamamide,AdoCbl )
Catalog No. M22704 CAS No. 13870-90-1
Adenosylcobalamin is a biologically active form of vitamin B12 .It is a cofactor for methylmalonyl CoA mutase.?It belongs to the corrinoid group of compounds, which contain a corrin macrocycle, and is produced only by certain bacteria and archaea.?
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 37 | In Stock |
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| 100MG | 67 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameAdenosylcobalamin
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NoteResearch use only, not for human use.
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Brief DescriptionAdenosylcobalamin is a biologically active form of vitamin B12 .It is a cofactor for methylmalonyl CoA mutase.?It belongs to the corrinoid group of compounds, which contain a corrin macrocycle, and is produced only by certain bacteria and archaea.?
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DescriptionAdenosylcobalamin is a biologically active form of vitamin B12 .It is a cofactor for methylmalonyl CoA mutase.?It belongs to the corrinoid group of compounds, which contain a corrin macrocycle, and is produced only by certain bacteria and archaea.?It is a cofactor for various enzymes including mutases, eliminases, aminomutases, and a reductase.Adenosylcobalamin serves as the cofactor for a group of enzymes that catalyze unusual rearrangement or elimination reactions.(In Vitro):Adenosylcobalamin serves as the cofactor for a group of enzymes that catalyze unusual rearrangement or elimination reactions.
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In VitroAdenosylcobalamin serves as the cofactor for a group of enzymes that catalyze unusual rearrangement or elimination reactions.
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In Vivo——
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SynonymsCoenzyme B12,Cobamamide,AdoCbl
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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RecptorHuman Endogenous Metabolite
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Research Area——
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Indication——
Chemical Information
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CAS Number13870-90-1
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Formula Weight1578.57
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Molecular FormulaC72H99CoN18O17P
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Purity>98% (HPLC)
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SolubilityH2O:4 mg/mL(2.53 mM)
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SMILES[CH2-][C@H]1O[C@@H]([C@@H](O)[C@H]1O)n1cnc2c(N)ncnc12.[H][C@]12[C@H](CC(N)=O)[C@@](C)(CCC(=O)NC[C@@H](C)OP([O-])(=O)O[C@@H]3[C@@H](CO)O[C@@H]([C@@H]3O)n3cnc4cc(C)c(C)cc34)\C([N-]1[Co+3])=C(C)\C1=N\C(=C/C3=N/C(=C(C)\C4=N[C@]2(C)[C@@](C)(CC(N)=O)[C@@H]4CCC(N)=O)[C@@](C)(CC(N)=O)[C@@H]3CCC(N)=O)C(C)(C)[C@@H]1CCC(N)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Kumudha A, et al. Characterization of vitamin B12 in Dunaliella salina. J Food Sci Technol. 2016 Jan;53(1):888-94.
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