Reaction Process: BioCyc:META_PWY-6688

thyronamine and iodothyronamine metabolism related metabolites

find 11 related metabolites which is associated with chemical reaction(pathway) thyronamine and iodothyronamine metabolism

3',5'-diiodothyronamine + A(H2) ⟶ 3'-iodothyronamine + A + H+ + iodide

Iodide

Trihydridoiodine

I- (126.904477)


Iodide can function as an antioxidant as it is a reducing species that can detoxify reactive oxygen species such as hydrogen peroxide. Over three billion years ago, blue-green algae were the most primitive oxygenic photosynthetic organisms and are the ancestors of multicellular eukaryotic algae (1). Algae that contain the highest amount of iodine (1-3 \\% of dry weight) and peroxidase enzymes, were the first living cells to produce poisonous oxygen in the atmosphere. Therefore algal cells required a protective antioxidant action of their molecular components, in which iodides, through peroxidase enzymes, seem to have had this specific role. In fact, iodides are greatly present and available in the sea, where algal phytoplankton, the basis of marine food-chain, acts as a biological accumulator of iodides, selenium, (and n-3 fatty acids) :; Antioxidant biochemical mechanism of iodides, probably one of the most ancient mechanisms of defense from poisonous reactive oxygen species:; An iodide ion is an iodine atom with a -1 charge. Compounds with iodine in formal oxidation state -1 are called iodides. This can include ionic compounds such as caesium iodide or covalent compounds such as phosphorus triiodide. This is the same naming scheme as is seen with chlorides and bromides. The chemical test for an iodide compound is to acidify the aqueous compound by adding some drops of acid, to dispel any carbonate ions present, then adding lead(II) nitrate, yielding a bright yellow precipitate of lead iodide. Most ionic iodides are soluble, with the exception of yellow silver iodide and yellow lead iodide. Aqueous solutions of iodide dissolve iodine better than pure water due to the formation of complex ions: [HMDB]. Iodide is found in many foods, some of which are breakfast cereal, star anise, annual wild rice, and peppermint. Iodide can function as an antioxidant as it is a reducing species that can detoxify reactive oxygen species such as hydrogen peroxide. Over three billion years ago, blue-green algae were the most primitive oxygenic photosynthetic organisms and are the ancestors of multicellular eukaryotic algae (1). Algae that contain the highest amount of iodine (1-3 \\% of dry weight) and peroxidase enzymes, were the first living cells to produce poisonous oxygen in the atmosphere. Therefore algal cells required a protective antioxidant action of their molecular components, in which iodides, through peroxidase enzymes, seem to have had this specific role. In fact, iodides are greatly present and available in the sea, where algal phytoplankton, the basis of marine food-chain, acts as a biological accumulator of iodides, selenium, (and n-3 fatty acids) :; Antioxidant biochemical mechanism of iodides, probably one of the most ancient mechanisms of defense from poisonous reactive oxygen species:; An iodide ion is an iodine atom with a -1 charge. Compounds with iodine in formal oxidation state -1 are called iodides. This can include ionic compounds such as caesium iodide or covalent compounds such as phosphorus triiodide. This is the same naming scheme as is seen with chlorides and bromides. The chemical test for an iodide compound is to acidify the aqueous compound by adding some drops of acid, to dispel any carbonate ions present, then adding lead(II) nitrate, yielding a bright yellow precipitate of lead iodide. Most ionic iodides are soluble, with the exception of yellow silver iodide and yellow lead iodide. Aqueous solutions of iodide dissolve iodine better than pure water due to the formation of complex ions:. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Hydrogen Ion

Hydrogen cation

H+ (1.0078246)


Hydrogen ion, also known as proton or h+, is a member of the class of compounds known as other non-metal hydrides. Other non-metal hydrides are inorganic compounds in which the heaviest atom bonded to a hydrogen atom is belongs to the class of other non-metals. Hydrogen ion can be found in a number of food items such as lowbush blueberry, groundcherry, parsley, and tarragon, which makes hydrogen ion a potential biomarker for the consumption of these food products. Hydrogen ion exists in all living organisms, ranging from bacteria to humans. In humans, hydrogen ion is involved in several metabolic pathways, some of which include cardiolipin biosynthesis cl(i-13:0/a-25:0/a-21:0/i-15:0), cardiolipin biosynthesis cl(a-13:0/a-17:0/i-13:0/a-25:0), cardiolipin biosynthesis cl(i-12:0/i-13:0/a-17:0/a-15:0), and cardiolipin biosynthesis CL(16:1(9Z)/22:5(4Z,7Z,10Z,13Z,16Z)/18:1(11Z)/22:5(7Z,10Z,13Z,16Z,19Z)). Hydrogen ion is also involved in several metabolic disorders, some of which include de novo triacylglycerol biosynthesis TG(20:3(8Z,11Z,14Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)/22:5(7Z,10Z,13Z,16Z,19Z)), de novo triacylglycerol biosynthesis TG(18:2(9Z,12Z)/20:0/20:4(5Z,8Z,11Z,14Z)), de novo triacylglycerol biosynthesis TG(18:4(6Z,9Z,12Z,15Z)/18:3(9Z,12Z,15Z)/18:4(6Z,9Z,12Z,15Z)), and de novo triacylglycerol biosynthesis TG(24:0/20:5(5Z,8Z,11Z,14Z,17Z)/24:0). A hydrogen ion is created when a hydrogen atom loses or gains an electron. A positively charged hydrogen ion (or proton) can readily combine with other particles and therefore is only seen isolated when it is in a gaseous state or a nearly particle-free space. Due to its extremely high charge density of approximately 2×1010 times that of a sodium ion, the bare hydrogen ion cannot exist freely in solution as it readily hydrates, i.e., bonds quickly. The hydrogen ion is recommended by IUPAC as a general term for all ions of hydrogen and its isotopes. Depending on the charge of the ion, two different classes can be distinguished: positively charged ions and negatively charged ions . Hydrogen ion is recommended by IUPAC as a general term for all ions of hydrogen and its isotopes. Depending on the charge of the ion, two different classes can be distinguished: positively charged ions and negatively charged ions. Under aqueous conditions found in biochemistry, hydrogen ions exist as the hydrated form hydronium, H3O+, but these are often still referred to as hydrogen ions or even protons by biochemists. [Wikipedia])

   

4-[4-(2-Aminoethyl)-2-iodo-phenoxy]-2-iodo-phenol

4-[4-(2-Aminoethyl)-2-iodo-phenoxy]-2-iodo-phenol

C14H14I2NO2+ (481.9114024)


   

4-[4-(2-Aminoethyl)-2-iodo-phenoxy]-2,6-diiodo-phenol

4-[4-(2-Aminoethyl)-2-iodo-phenoxy]-2,6-diiodo-phenol

C14H13I3NO2+ (607.8080548)


   

2-[4-(4-Hydroxy-3-iodophenoxy)-3,5-diiodophenyl]ethylazanium

2-[4-(4-Hydroxy-3-iodophenoxy)-3,5-diiodophenyl]ethylazanium

C14H13I3NO2+ (607.8080548)


   

4-[4-(2-Aminoethyl)-2,6-diiodo-phenoxy]phenol

4-[4-(2-Aminoethyl)-2,6-diiodo-phenoxy]phenol

C14H14I2NO2+ (481.9114024)


   

4-[4-(2-Aminoethyl)phenoxy]-2-iodo-phenol

4-[4-(2-Aminoethyl)phenoxy]-2-iodo-phenol

C14H15INO2+ (356.01475)


   

2-(4-(4-Hydroxyphenoxy)-3-iodophenyl)ethanaminium chloride

2-(4-(4-Hydroxyphenoxy)-3-iodophenyl)ethanaminium chloride

C14H15INO2+ (356.01475)


   

4-[4-(2-Aminoethyl)phenoxy]-2,6-diiodo-phenol

4-[4-(2-Aminoethyl)phenoxy]-2,6-diiodo-phenol

C14H14I2NO2+ (481.9114024)


   

2-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]ethylazanium

2-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]ethylazanium

C14H12I4NO2+ (733.7047071999999)


   

2-[4-(4-Hydroxyphenoxy)phenyl]ethylazanium

2-[4-(4-Hydroxyphenoxy)phenyl]ethylazanium

C14H16NO2+ (230.1180976)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones