Methacrylyl-CoA: Difference between revisions

Revision as of 01:58, 20 November 2008 editThijs!bot (talk \| contribs)470,128 editsm robot Adding: ja:メタクリリルCoA ← Previous edit		Revision as of 05:33, 23 January 2009 edit undoChem-awb (talk \| contribs)Bots12,956 edits {{Chembox new --> {{Chembox, Replaced: {{chembox new → {{chembox using AWB Next edit →
Line 1:		Line 1:
	{{chembox ~~new~~		{{chembox
	\|ImageFile=Methacrylyl-CoA.png		\|ImageFile=Methacrylyl-CoA.png
	\|ImageSize=250px		\|ImageSize=250px
Line 27:		Line 27:

	'''Methacrylyl-CoA''' is an intermediate in the metabolism of ].		'''Methacrylyl-CoA''' is an intermediate in the metabolism of ].


⚫	{{organic-compound-stub}}

	{{Amino acid metabolism intermediates}}		{{Amino acid metabolism intermediates}}

	]		]


		⚫	{{organic-compound-stub}}

	]		]

Revision as of 05:33, 23 January 2009

Methacrylyl-CoA
Identifiers

CAS Number	6008-91-9
3D model (JSmol)	Interactive image
MeSH	methacrylyl-coenzyme+A
PubChem CID	877
CompTox Dashboard (EPA)	DTXSID00863677 DTXSID10975513, DTXSID00863677
SMILES O1(OP(O)(O)=O)(COP(OP(OCC(C)(C)(O)C(NCCC(NCCSC(C(C)=C)=O)=O)=O)(O)=O)(O)=O)O1N2C(N=CN=C3N)=C3N=C2
Properties
Chemical formula	C₂₅H₄₀N₇O₁₇P₃S
Molar mass	835.61 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Methacrylyl-CoA is an intermediate in the metabolism of valine.

lysine→	Saccharopine Allysine α-Aminoadipic acid 2-Oxoadipic acid Glutaryl-CoA Glutaconyl-CoA Crotonyl-CoA β-Hydroxybutyryl-CoA
leucine→	β-Hydroxy β-methylbutyric acid β-Hydroxy β-methylbutyryl-CoA Isovaleryl-CoA α-Ketoisocaproic acid β-Ketoisocaproic acid β-Ketoisocaproyl-CoA β-Leucine β-Methylcrotonyl-CoA β-Methylglutaconyl-CoA β-Hydroxy β-methylglutaryl-CoA
tryptophan→alanine→	N′-Formylkynurenine Kynurenine Anthranilic acid 3-Hydroxykynurenine 3-Hydroxyanthranilic acid 2-Amino-3-carboxymuconic semialdehyde 2-Aminomuconic semialdehyde 2-Aminomuconic acid Glutaryl-CoA

histidine→	Urocanic acid Imidazol-4-one-5-propionic acid Formiminoglutamic acid Glutamate-1-semialdehyde
proline→	1-Pyrroline-5-carboxylic acid
arginine→	Agmatine Ornithine Citrulline Cadaverine Putrescine
other	cysteine+glutamate→glutathione: γ-Glutamylcysteine

valine→	α-Ketoisovaleric acid Isobutyryl-CoA Methacrylyl-CoA 3-Hydroxyisobutyryl-CoA 3-Hydroxyisobutyric acid 2-Methyl-3-oxopropanoic acid
isoleucine→	2,3-Dihydroxy-3-methylpentanoic acid 2-Methylbutyryl-CoA Tiglyl-CoA 2-Methylacetoacetyl-CoA
methionine→	generation of homocysteine: S-Adenosyl methionine S-Adenosyl-L-homocysteine Homocysteine conversion to cysteine: Cystathionine α-Ketobutyric acid + Cysteine
threonine→	α-Ketobutyric acid
propionyl-CoA→	Methylmalonyl-CoA

phenylalanine→tyrosine→	4-Hydroxyphenylpyruvic acid Homogentisic acid 4-Maleylacetoacetic acid

Other

Cysteine metabolism	Cysteine sulfinic acid

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.