Synsets for "acid-forming"

Synset: acid-forming.s.01

Synonyms: acid-forming

Part of Speech: ADJECTIVE SATELLITE

Definition: yielding an acid in aqueous solution

Examples:

Lemmas: acid-forming

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L-amino-acid alpha-ligase This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). The systematic name of this enzyme class is L-amino acid:L-amino acid ligase (ADP-forming). Other names in common use include L-amino acid alpha-ligase, bacilysin synthetase, YwfE, and L-amino acid ligase.
Todorokite Todorokite is soluble in hydrochloric acid (HCl) with the evolution of chlorine (Cl), and in concentrated sulfuric acid (HSO) forming a purple-red solution. It is also soluble in nitric acid (HNO) forming a residue of manganese dioxide (MnO).
Boric acid Boric acid is soluble in boiling water. When heated above 170 °C, it dehydrates, forming "metaboric acid" (HBO):
Acid–base reaction Here, one molecule of water acts as an acid, donating an H and forming the conjugate base, OH, and a second molecule of water acts as a base, accepting the H ion and forming the conjugate acid, HO.
Benzoic acid Concern has been expressed that benzoic acid and its salts may react with ascorbic acid (vitamin C) in some soft drinks, forming small quantities of benzene.
Tubulin—tyrosine ligase This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). The systematic name of this enzyme class is alpha-tubulin:L-tyrosine ligase (ADP-forming).
Hydroxide Vanadic acid HVO shows similarities with phosphoric acid HPO though it has a much more complex vanadate oxoanion chemistry. Chromic acid HCrO, has similarities with sulfuric acid HSO; for example, both form acid salts A[HMO]. Some metals, e.g. V, Cr, Nb, Ta, Mo, W, tend to exist in high oxidation states. Rather than forming hydroxides in aqueous solution, they convert to oxo clusters by the process of olation, forming polyoxometalates.
Adenosylcobyric acid synthase (glutamine-hydrolysing) This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds carbon-nitrogen ligases with glutamine as amido-N-donor. The systematic name of this enzyme class is adenosylcobyrinic-acid-a,c-diamide:L-glutamine amido-ligase (ADP-forming). Other names in common use include CobQ, cobyric acid synthase, 5'-deoxy-5'-adenosylcobyrinic-acid-a,c-diamide:L-glutamine, amido-ligase, and Ado-cobyric acid synthase [glutamine hydrolyzing]. This enzyme participates in porphyrin and chlorophyll metabolism.
NOx Mono-nitrogen oxides eventually form nitric acid when dissolved in atmospheric moisture, forming a component of acid rain. This chemical reaction occurs when nitrogen dioxide reacts with water:
Succinate—CoA ligase (ADP-forming) This enzyme belongs to the family of ligases, specifically those forming carbon-sulfur bonds as acid-thiol ligases. The systematic name of this enzyme class is succinate:CoA ligase (ADP-forming). Other names in common use include succinyl-CoA synthetase (ADP-forming), succinic thiokinase, succinate thiokinase, succinyl-CoA synthetase, succinyl coenzyme A synthetase (adenosine diphosphate-forming), succinyl coenzyme A synthetase, A-STK (adenin nucleotide-linked succinate thiokinase), STK, and A-SCS. This enzyme participates in 4 metabolic pathways: Citric acid cycle, propanoate metabolism, c5-branched dibasic acid metabolism, and reductive carboxylate cycle (CO fixation).
Zinc nitrate Zinc nitrate is usually prepared by dissolving zinc in nitric acid, this reaction is concentration dependent, with a reaction in concentrated acid also forming ammonium nitrate:
Carnosine synthase This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). The systematic name of this enzyme class is 'L-histidine:beta-alanine ligase (AMP-forming)' (incorrect on AMP-forming). Other names in common use include 'carnosine synthetase', 'carnosine-anserine synthetase', 'homocarnosine synthetase', and 'carnosine-homocarnosine synthetase'.
Atropine The biosynthesis of atropine starting from "l"-phenylalanine first undergoes a transamination forming phenylpyruvic acid which is then reduced to phenyl-lactic acid. Coenzyme A then couples phenyl-lactic acid with tropine forming littorine, which then undergoes a radical rearrangement initiated with a P450 enzyme forming hyoscyamine aldehyde. A dehydrogenase then reduces the aldehyde to a primary alcohol making (−)-hyoscyamine, which upon racemization forms atropine.
Indoleacetate—lysine synthetase This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). The systematic name of this enzyme class is (indol-3-yl)acetate:L-lysine ligase (ADP-forming). This enzyme is also called indoleacetate:L-lysine ligase (ADP-forming).
Phenylboronic acid More C-C bond forming processes commonly use phenylboronic acid as a reagent. Alpha-amino acids can be generated using the uncatalyzed reaction between alpha-ketoacids, amines, and phenylboronic acid. Heck-type cross coupling of phenylboronic acid to alkenes and alkynes. This unique C-C bond forming reaction has the ability to couple a terminal olefin with boronic acid using a transition metal catalyst. Aryl azides and nitroaromatics can also be generated using phenylboronic acid. PhB(OH) can be used as a protecting group for diols and diamines. Phenylboronic acid can also be regioselectively halodeboronated using aqueous bromine, chlorine, or iodine.
Dimethylcadmium Dimethylcadmium is a weak Lewis acid, forming an adduct with bipyridine and with ether.
Hydrogen peroxide Hydrogen peroxide is a weak acid, forming hydroperoxide or peroxide salts with many metals.
Mycobacterium massiliense Strictly aerobic, nonmotile, non-spore forming, acid-fast, Gram-positive rods.
2,4-Dinitroanisole With iron and acetic acid DNAN nitro groups can be reduced to amines forming 2,4-diaminoanisole.
Zoledronic acid Zoledronic acid slows down bone resorption, allowing the bone-forming cells time to rebuild normal bone and allowing bone remodeling.