「Aldehyde」の共起表現(1語右で並び替え)

「Aldehyde」の共起表現一覧(1語右で並び替え)

Aldehyde

1語右で並び替え

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The 3 substrates of this enzyme are aldehyde, acceptor, and H2O, whereas its two products
Primary alcohols will only be oxidised to the aldehyde and not on to carboxylic acids.
ed alcohol is susceptible to oxidation to the aldehyde and carboxylic acid.
experiments indicated close proximity of the aldehyde and the aryl ring.
An aldol or aldol adduct (from " Aldehyde alcohol") is a beta-hydroxy ketone or aldehyd
Fischer believed he had synthesized an aldehyde, and therefore he gave the product a name tha
Two related compounds are caffeyl aldehyde and caffeic acid, the latter also being a min
s the chemical reaction of an aniline with an aldehyde and pyruvic acid to form quinoline-4-carboxyl
The colouration is specific to this aldehyde and is not produced from other organic specie
ol and acceptor, whereas its two products are aldehyde and reduced acceptor.
t used to differentiate between water-soluble aldehyde and ketone functional groups, and as a test f
d O2, whereas its two products are long-chain aldehyde and H2O.
ni reaction is an organic reaction between an aldehyde and the sulfonamide N-hydroxybenzenesulfonami
choline and H2O, whereas its two products are aldehyde and sn-glycero-3-phosphocholine.
amphor, safrole and methyleugenol or cinnamic aldehyde and eugenol depending on the chemical variety
using solvent-free conditions: resorcinol, an aldehyde, and p-toluenesulfonic acid are ground togeth
of the iridoid backbone and oxidation of the aldehyde at C4 of epi-iridotrial produced 8-epiloganic
As an unsaturated aldehyde, crotonaldehyde is a versatile intermediate i
This enzyme is also called aldehyde dehydrogenase (acceptor).
In enzymology, an aldehyde dehydrogenase (NAD+) (EC 1.2.1.3)
In enzymology, an aldehyde dehydrogenase [NAD(P)+] (EC 1.2.1.5)
Pristanal is oxidized by aldehyde dehydrogenase to form pristanic acid (which c
e are more genes in the family of alcohol and aldehyde dehydrogenase genes.
Other names in common use include aldehyde dehydrogenase [NAD(P)+], and ALDH.
In enzymology, an aldehyde dehydrogenase (FAD-independent) (EC 1.2.99.7)
In enzymology, an aldehyde dehydrogenase (pyrroloquinoline-quinone) (EC
Aldehyde dehydrogenase 1 family, member A3 also known
Aldehyde dehydrogenase isozymes are thought to play a
Aldehyde dehydrogenase 1 family, member L2 also known
alcohol dehydrogenase (QADH) and quinoprotein aldehyde dehydrogenase (QALDH) from Glucanobacter subo
ciated with a deficiency of the enzyme "fatty aldehyde dehydrogenase".
r names in common use include CoA-independent aldehyde dehydrogenase, m-methylbenzaldehyde dehydroge
There is a mutant form of aldehyde dehydrogenase, termed ALDH2*2, where a lysine
ALDH1L2 is an aldehyde dehydrogenase.
Not to be confused with aldehyde dehydrogenase.
intolerance, caused by the genetic absence of aldehyde dehydrogenase.
cal School on kinetic studies with the enzyme aldehyde dehydrogenase.
y disulfiram (Antabuse), due to inhibition of aldehyde dehydrogenase.
y disulfiram (Antabuse), due to inhibition of aldehyde dehydrogenase.
omplex is effective in catalyzing a number of aldehyde Diels-Alder reactions.
eveloped a practical Diels-Alder catalyst for aldehyde dienophiles.
n (3) occurs, followed by oxidation (4) to an aldehyde directly followed by further hydroxylation (5
Other names in common use include aldehyde dismutase, and cannizzanase.
In this NAD(P)+ dependent reaction, the aldehyde enters the active site through a channel loca
In enzymology, an aldehyde ferredoxin oxidoreductase (EC 1.2.7.5) is an
Enzymes of the aldehyde ferredoxin oxidoreductase (AOR) family contai
H), FMNH2, and O2, whereas its 4 products are aldehyde, FMN, sulfite, and H2O.
The aldehyde form of glucose
The compound can exist in a monocyclic aldehyde form or in a bicyclic hemiacetal (lactol) for
ction of a number of aldehydes, including the aldehyde form of glucose, and is thereby implicated in
lan fibres, elaunin fibres stain with orcein, aldehyde fuchsin and resorcin fuchsin without prior ox
roxyl function of the terminal carbon and the aldehyde function of the first carbon have been fully
It is a monoterpenoid containing an aldehyde functional group.
ontaining five carbon atoms, and including an aldehyde functional group.
ccharide with five carbon atoms and having an aldehyde functional group.
They have either an aldehyde functional group in position 1 (aldotetroses)
They have either an aldehyde functional group in position 1 (aldoheptoses)
it contains five carbon atoms and includes an aldehyde functional group.
y of sugar acids obtained by oxidation of the aldehyde functional group of an aldose to form a carbo
Oxidation of aldehyde group to carboxylic acid.
It has an aldehyde group and is an aldose.
An aldohexose is a hexose with an aldehyde group on one end.
btained by reduction of glucose, changing the aldehyde group to a hydroxyl group.
Viniferal is a hydroxystilbenoid with an aldehyde group found in Vitis vinifera (grapevine).
It has one aldehyde group and so is part of the aldose family.
The aldehyde group of the monosaccharide which normally fo
It has a terminal aldehyde group rather than a ketone in its linear chai
onosaccharide (a simple sugar) containing one aldehyde group per molecule and having a chemical form
In an aldose, the carbon of the aldehyde group is C1; in a ketose the carbon of the ke
n of its anion (by reaction with LDA ) to the aldehyde group in 8 to form 10 as a mixture of epimers
er, this enzyme does not exploit the reactive aldehyde group, but instead utilizes the phosphate gro
e group, it is a ketose and if it contains an aldehyde group, it is an aldose.
y to determine whether a compound contains an aldehyde group.
In it the aldehyde groups react with the sulfinic acid groups fo
olored liquid is the smallest dialdehyde (two aldehyde groups).
lose is formed by the bonding of two reducing aldehyde groups, it has no capacity to participate in
niferyl-aldehyde dehydrogenase uses coniferyl aldehyde, H2O, NAD+, and NADP+ to produce ferulate, NA
The 3 substrates of this enzyme are aldehyde, H2O, and acceptor, whereas its two products
The 3 substrates of this enzyme are abscisic aldehyde, H2O, and O2, whereas its two products are ab
The 4 substrates of this enzyme are coniferyl aldehyde, H2O, NAD+, and NADP+, whereas its 4 products
The 3 substrates of this enzyme are aldehyde, H2O, and oxidized ferredoxin, whereas its 3
It catalyzes the conversion of an aldehyde in the presence of oxygen and water to an aci
imple catalytic processes can hydrogenate the aldehyde into isobutanol, which can be used in motor f
The aldehyde is hydrogenated to give 1,3-propanediol.
Glycine betaine aldehyde is a short chain aldehyde and quaternary ammo
Protocatechuic aldehyde is a phenolic aldehyde, a compound released f
The fatty aldehyde is then further oxidized to the corresponding
Betaine aldehyde is a substrate for choline dehydrogenase (mit
Glycine betaine aldehyde is a component of glycine, serine and threoni
This aldehyde is a colourless oily liquid that is soluble i
Coniferyl aldehyde is a low molecular weight phenolic compound s
de will turn the solution an intense red when aldehyde is present.
ed to the decolorized Schiff reagent and when aldehyde is present a characteristic magenta or purple
Lilial (lily aldehyde) is a chemical compound which is used in cosm
the bridgehead hydrogens and approach of the aldehyde is blocked by the camphor moiety.
Perillaldehyde, or perilla aldehyde, is a natural organic compound found most abu
li (Cannizzaro reaction): one molecule of the aldehyde is reduced to the corresponding alcohol and a
Hexenal, also known as (Z)-3-hexenal and leaf aldehyde, is colorless liquid and an aroma compound wi
It is an aldehyde, isomeric with n-butyraldehyde (butanal).
kane, H2O, and O2, whereas its 4 products are aldehyde, ketone, nitrite, and H2O2.
aldehyde lyases (EC 4.1.2),
In particular, the fragility of the aldehyde meant that it collapsed to the alcohol and wa
e is an organic compound containing amine and aldehyde moieties which is used in Ehrlich's reagent f
s in common use include bacterial luciferase, aldehyde monooxygenase, luciferase, and Vibrio fischer
Aldehyde monosaccharides may be called aldoses; ketone
The 3 substrates of this enzyme are aldehyde, NAD+, and H2O, whereas its 3 products are ac
The 3 substrates of this enzyme are betaine aldehyde, NAD+, and H2O, whereas its 3 products are be
The 4 substrates of this enzyme are aldehyde, NAD+, NADP+, and H2O, whereas its 4 products
, NAD+, and NADP+, whereas its 4 products are aldehyde, NADH, NADPH, and H+.
iferyl alcohol and NADP+ to produce coniferyl aldehyde, NADPH, and H+.
nd NADP+, whereas its 3 products are aromatic aldehyde, NADPH, and H+.
d NADP+, whereas its 3 products are coniferyl aldehyde, NADPH, and H+.
e dehydrogenase (GAPDH) whose substrate is an aldehyde not an alcohol.
The 3 substrates of this enzyme are aromatic aldehyde, O2, and H2O, whereas its two products are ar
ls contain a chromophore (11-cis retinal, the aldehyde of Vitamin A1 and light-absorbing portion) bo
Glycine betaine aldehyde, often simply called betaine aldehyde, is an
Octanal can also be referred to as caprylic aldehyde or aldehyde C-8.
EC 2.2 includes enzymes that transfer aldehyde or ketone groups
iodic acid will cleave vicinal diols into two aldehyde or ketone fragments.
Reaction of a carbazide with aldehyde or ketone produces a carbazone.
imes can be synthesized by condensation of an aldehyde or a ketone with hydroxylamine.
transferases, specifically those transferring aldehyde or ketonic groups (transaldolases and transke
oreductases, specifically those acting on the aldehyde or oxo group of donor with NAD+ or NADP+ as a
oreductases, specifically those acting on the aldehyde or oxo group of donor with oxygen as acceptor
oreductases, specifically those acting on the aldehyde or oxo group of donor with an iron-sulfur pro
oreductases, specifically those acting on the aldehyde or oxo group of donor with a cytochrome as ac
oreductases, specifically those acting on the aldehyde or oxo group of donor with a disulfide as acc
oreductases, specifically those acting on the aldehyde or oxo group of donor with other acceptors.
l 4-reductase uses sinapaldehyde or coniferyl aldehyde or coumaraldehyde and NADPH to produce sinapy
further breakdown to hydrogen cyanide and an aldehyde or ketone is catalyzed by a hydroxynitrile ly
ldol moiety: When R3 is -H, it is a β-hydroxy aldehyde, otherwise it is a β-hydroxy ketone.
Aldehyde oxidase (EC 1.2.3.1)
Aldehyde oxidase is a candidate gene for amyotrophic l
Aldehyde oxidase produces hydrogen peroxide and, under
Aldehyde oxidase 1 is an enzyme that in humans is enco
The aldehyde oxidase and xanthine dehydrogenase, a/b hamme
Aldehyde oxidase is an enzyme which generates carboxyl
cofactor of xanthine dehydrogenase (XDH) and aldehyde oxidase (AOX1), which is required for their e
Other names in common use include aldehyde oxidase, aldehyde oxidoreductase, Mop, and AO
Other names in common use include betaine aldehyde oxidase, BADH, betaine aldehyde dehydrogenase
Other names in common use include abscisic aldehyde oxidase, AAO3, AOd, and AOdelta.
Not to be confused with aldehyde oxidase.
sulfite oxidase, xanthine oxidoreductase, and aldehyde oxidase.
n of acid chlorides to give the corresponding aldehyde product cannot proceed via LAH, since the lat
p in organic chemistry which is similar to an aldehyde, RC(O)H, in which a sulfur (S) atom replaces
Other names in common use include aldehyde reductase 1, prostaglandin 9-ketoreductase, x
ames in common use include retinal reductase, aldehyde reductase (NADPH/NADH), and alcohol dehydroge
orded 4 (after separation from regioisomers), aldehyde reduction (sodium borohydride) diol 5 and chl
8 hydroxyl was oxidized with PCC to give the aldehyde shown in structure 11.
ingaldehyde is a naturally occurring aromatic aldehyde soluble in alcohol.
Depending on the aldehyde starting material, the lower rim includes fou
The Grundmann aldehyde synthesis is a chemical reaction that produce
e other reactions are the Bodroux-Chichibabin aldehyde synthesis and the Chichibabin reaction.
Vilsmeier discovered the aldehyde synthesis reaction which bears his name in 19
on to the imine followed by hydrolysis to the aldehyde takes place in the Stephen aldehyde synthesis
al, also known as heliotropin, is an aromatic aldehyde that comes as transparent crystals, C8H6O3, a
stimulates the transformation of betaine aldehyde to glycine betaine.
Bourgeonal is an aromatic aldehyde used in perfumery.
the oxidation of an alcohol to a ketone or an aldehyde using chromium trioxide and pyridine.
Also, Pi stacking between the aryl group and aldehyde was suggested as an organizational feature wh
eoxyribose is converted to w-hydroxylevulinyl aldehyde, which reacts with the compound, diphenylamin
en an alpha, beta-unsaturated carbonyl and an aldehyde, which requires a nucleophilic catalyst, usua
e carbohydrate by sulfuric acid to produce an aldehyde, which condenses with two molecules of phenol
Cyanation of aldehyde with bisulfate
Octanal is an aldehyde with the chemical formula C8H16O.
Heptanal or heptanaldehyde is an alkyl aldehyde with a strong fruity odor which is used as an
tion) is the chemical reaction of a ketone or aldehyde with an α-haloester to form an α,β-epoxy este
(Oxidation of just the aldehyde yields an aldonic acid while oxidation of jus
rminal hydroxyl group instead of the terminal aldehyde yields a uronic acid, while oxidation of both