「aldehyde」の共起表現(1語右で並び替え)

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共起表現

「aldehyde」の共起表現一覧(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

共起表現

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「aldehyde」の共起表現一覧(1語右で並び替え)