Page last updated: 2024-11-12

cobamamide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

cobamamide : A member of the class of cobalamins that is vitamin B12 in which the cyano group is replaced by a 5'-deoxyadenos-5'-yl moiety. It is one of the two metabolically active form of vitamin B12. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID91820207
MeSH IDM0040899

Synonyms (20)

Synonym
cobamamid
5'-deoxy-5'-adenosylcobalamin
adenosylcob(iii)alamin
dibencozide
cobamamide
5'-deoxyadenosylcobalamin
(5,6-dimethylbenzimidazolyl)cobamide coenzyme
5,6-dimethylbenzimidazolyl-co-5'-deoxyadenosylcobamide
ADENOSYLCOBALAMIN ,
cobamide coenzyme
5,6-dimethylbenzimidazolyl-5-deoxyadenosyl-cobamide
(5'-deoxy-5'-adenosyl)cobamide coenzyme
calomide
13870-90-1
5'-deoxyadenosyl-5,6-dimethylbenzimidazolylcobamide
cobalamin coenzyme
deoxyadenosylcobalamin
funacomide
5'-deoxyadenosyl vitamin b12
coenzyme b12

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" It is also suggested that dibencozide could be useful in clinical practice for reducing the dosage of opioids."( Depressive effects of mu and delta opioid receptor agonists on activities of dorsal horn neurones are enhanced by dibencozide.
Bing, Z; Bouhassira, D; Le Bars, D; Villanueva, L, 1991
)
0.28
" Dosage guidelines are inadequate, and quality control is poor."( Efficacy of nutritional supplements used by athletes.
Beltz, SD; Doering, PL, 1993
)
0.29
" The dose-response curve also shows a lower effectivity of OHCbl with respect to stabilization, with an AC(50) of 7 microM."( Thermolability of mutant MMACHC protein in the vitamin B12-responsive cblC disorder.
Froese, DS; Gravel, RA; Healy, S; Kochan, G; McDonald, M; Niesen, FH; Oppermann, U, 2010
)
0.36
" Dose-response parameters including fold-change and half-maximal effective concentration were easily modulated and amplified simply by changing the promoter strength."( Novel Hybrid Input Part Using Riboswitch and Transcriptional Repressor for Signal Inverting Amplifier.
Jang, S; Jung, GY; Lim, HG; Noh, MH, 2018
)
0.48
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Pathways (36)

PathwayProteinsCompounds
(S)-propane-1,2-diol degradation618
tetrachloroethene degradation113
L-glutamate degradation VII (to butanoate)1036
pyruvate fermentation to propanoate I618
ethylmalonyl-CoA pathway1228
conversion of succinate to propanoate310
pyrimidine deoxyribonucleotides de novo biosynthesis I3034
3-hydroxypropanoate/4-hydroxybutanate cycle1840
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)1335
pyrimidine deoxyribonucleotides de novo biosynthesis III1130
propanoyl CoA degradation I1213
ethanolamine utilization1336
superpathway of L-lysine degradation33112
3,8-divinyl-chlorophyllide a biosynthesis II (anaerobic)934
2-oxobutanoate degradation I1028
adenosylcobalamin biosynthesis from adenosylcobinamide-GDP I512
adenosylcobalamin biosynthesis from adenosylcobinamide-GDP II212
superpathway of nicotinate degradation1254
L-lysine fermentation to acetate and butanoate857
anaerobic energy metabolism (invertebrates, mitochondrial)1342
superpathway of anaerobic energy metabolism (invertebrates)1660
L-leucine degradation II010
nicotinate degradation III1241
glycerol degradation III613
1,3-propanediol biosynthesis (engineered)1535
L-ornithine degradation II (Stickland reaction)1043
superpathway of bacteriochlorophyll a biosynthesis2270
L-arginine degradation (Stickland reaction)1254
L-glutamate degradation VI (to pyruvate)214
superpathway of glycerol degradation to 1,3-propanediol826
methyl tert-butyl ether degradation1425
superpathway of L-methionine salvage and degradation2869
adenosylcobalamin biosynthesis from cobyrinate a,c-diamide I626
adenosylcobalamin salvage from cobinamide I419
adenosylcobalamin salvage from cobalamin14
adenosylcobalamin biosynthesis II (aerobic)060

Research

Studies (557)

TimeframeStudies, This Drug (%)All Drugs %
pre-199097 (17.41)18.7374
1990's128 (22.98)18.2507
2000's199 (35.73)29.6817
2010's118 (21.18)24.3611
2020's15 (2.69)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials8 (1.38%)5.53%
Reviews63 (10.86%)6.00%
Case Studies14 (2.41%)4.05%
Observational0 (0.00%)0.25%
Other495 (85.34%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]