「isomer」の共起表現一覧(1語右で並び替え)
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The fourth | isomer, alpha-chlorotoluene (benzyl chloride), consis |
This | isomer also occurs in kuromoji oil. |
isomers may differ in the parent anthraquinone | isomer and/or of the three hydroxyl groups. |
Despite being the trans | isomer, angelic acid has a lower melting point and hi |
The notion of | isomer appears also in other fields such as chemistry |
which have varying properties, with the 2-(R) | isomer being a μ-opioid full agonist around 5 times m |
around the azetidine ring, with the (S,S)-(+) | isomer being the most active, slightly more potent th |
and so have two stereoisomers, with the dextro | isomer being the more potent in all cases, although b |
somers, both of which are active, although one | isomer blocks reuptake of only dopamine and noradrena |
hydrocarvone, c-dihydrocarvone, dihydrocarveol | isomer c-carveol and t-carveol. |
The chiral cis | isomer can be obtained by heating the trans isomer. |
The alpha phellandrene | isomer can form hazardous and explosive peroxides on |
The geometric | isomer, cis-glutaconic acid, has a noticeably lower m |
suppresses the formation of the 2-substituted | isomer compared to the use of borane. |
Double bonds may be in either a cis or a trans | isomer, depending on the geometry of the double bond. |
The alternative structural | isomer DOIP, with a 4-isopropyl substitution, is also |
The most highly branched | isomer DOTB was completely inactive in both animal an |
Shulgin speculates that the s-butyl | isomer DSBT may be more potent than the straight chai |
pecially the O-acetyl ester of the most active | isomer, EA-2233-2, were among the more promising non- |
the higher boiling point, the more rounded cis | isomer escapes easier, thus having a lower boiling po |
In the most significant | isomer, fluoren-9-ol or 9-hydroxyfluorene, the hydrox |
An all-trans beta | isomer has been described. |
The first | isomer has all three chlorines attached to one carbon |
The (-)-cis-CPCA | isomer has similar reinforcing effects to cocaine as |
a pharmacological standpoint is TMA-2, as this | isomer has been much more widely used as a recreation |
Stilbene derivatives especially E(trans) | isomer have estrogenic activity so used in making non |
a-meprodine and beta-meprodine, with the alpha | isomer having been more widely used. |
nimal drug discrimination assays, with the (R) | isomer having an ED50 of 33nmol/kg for producing drug |
The E | isomer, in which the two phenyl rings are cis to each |
The active | isomer is levcromakalim. |
The natural | isomer is D-erythrose. |
The cis | isomer is found in an African orchid. |
Another double-bond | isomer is known as sabinene. |
The (3R,4R) | isomer is the agonist, while (3S,4S) is antagonist. |
The 2,3-chloro | isomer is subsequently isomerized to 3,4 isomer, whic |
The (-)-optical | isomer is one of the organic compounds responsible fo |
The unbranched | isomer is normal or n-heptadecane, CH3(CH2)15CH3. |
Another structural | isomer is the bicyclic compound 5-methylenebicyclo[2. |
The trans- | isomer is reported to be more active than the racemat |
A less common chemically-related double-bond | isomer is known as β-thujene (or 2-thujene). |
The most common | isomer is 3-methylcholanthrene, although the methyl g |
The S-acid | isomer is believed to be more stable than the O-acid |
for the α,β-unsaturated ketone, only the trans | isomer is observed. |
The 3S,4S | isomer is extracted by the alcoholic beverage from so |
The (3S,4R) | isomer is extracted by the alchoolic beverage from so |
everal stereo isomers exist of which, only one | isomer is medically viable: cilazapril ((1S,9S)-9-[(2 |
The lifetime of the hafnium | isomer is long enough for tractable amounts of materi |
s, a polarimeter can be used to identify which | isomer is present in a sample - if it rotates polariz |
Its non-planar | isomer is called "hexaethynyl-carbo-[6]trannulene" - |
s are a pair of enantiomers, whereas the 2R,3S | isomer is a meso compound and thus optically inactive |
This | isomer is a pigment in African marigolds (Tagetes spp |
te is a specimen example of where the unwanted | isomer is usually not separated so that profits can b |
This is particularly true if the unrequired | isomer is simply an inactive "dummy" and does not add |
The (1R,cis)- | isomer is known as Cismethrin, but this is also not r |
The laevo | isomer is the source of the narcotic properties of th |
The cis | isomer is formed as a racemate, which can be resolved |
ce as active as the racemic mixture; the other | isomer is devoid of significant analgesic activity." |
The (1R,trans)- | isomer is also known as Bioresmethrin,(+)-trans-Resme |
[3,4-(methylenedioxy)phenyl]-1-propene) or its | isomer isosafrole via oxidation using the Wacker oxid |
Like the 'D-' | isomer, L-glucose usually occurs as one of four cycli |
+)-naloxone ("unnatural" | isomer, lacks opioid receptor affinity so selective f |
honokiol exists naturally with its structural | isomer magnolol, which differs from honokiol only by |
times less potent by weight than the 3-methoxy | isomer, making it around the same potency as ketamine |
ts associated with its better-known structural | isomer MDA. |
droxy- compounds can be derived from the other | isomer, namely 1,2-benzoquinone or ortho-benzoquinone |
existing data on rutherfordium-261 was for an | isomer, now designated rutherfordium-261a. |
One | isomer of lactic acid |
It is a structural | isomer of butalbital. |
Acridine is an | isomer of phenanthridine. |
It is an | isomer of lawsone. |
PrPSc is an | isomer of PrPC |
Enflurane is a structural | isomer of isoflurane. |
It is a | isomer of asymbescaline. |
Levomilnacipran (F2695) - The levo- | isomer of milnacipran. |
It closely resembles an | isomer of solasonine. |
It is an | isomer of cucurbitane. |
It is an | isomer of octane. |
It is an | isomer of propylamphetamine. |
It is an | isomer of xylene. |
It is an | isomer of o-xylene and p-xylene. |
Dihydroxyacetone, the simplest ketose, is an | isomer of glyceraldehyde. |
It is an | isomer of 2,6-xylidine and 3,4-xylidine. |
It is a structural | isomer of delta-valerolactone. |
(R)-PAC is the levo-rotating | isomer of phenylacetylcarbinol. |
It is the N-cyclopropyl | isomer of MDMA. |
It is the all-trans conformational | isomer of octadecatrienoic acid. |
methylbutane, also known as diisopropyl, is an | isomer of hexane. |
Theobromine is an | isomer of theophylline, as well as paraxanthine. |
It is also the N-allyl | isomer of MDA. |
It is an | isomer of isophthalic acid and terephthalic acid. |
It is also the N-butyl | isomer of MDA. |
It is an | isomer of o-phenylenediamine and p-phenylenediamine. |
Isobutyl cyanoacrylate is an | isomer of butyl cyanoacrylate. |
It is also the N-benzyl | isomer of MDA. |
It is a bicyclic sesquiterpene and an | isomer of guaiazulene. |
Isopropylbenzylamine is a structural | isomer of methamphetamine, and has the same molar mas |
2-hydroxyladenine is a purine base that is an | isomer of guanine. |
2-aminouracil is a pyrimidine base that is an | isomer of cytosine. |
It is an | isomer of the biologically important amino acid L-val |
This | isomer of coronaric acid was first definitively chara |
Pagodane is an | isomer of dodecahedrane and can be chemically convert |
It is an | isomer of mescaline, as well as an analog of TIM-2, T |
an omega-6 trans fatty acid and is a geometric | isomer of linoleic acid. |
It is the | isomer of the related cyanide (-C≡N), hence the prefi |
An | isomer of MaR1,was less potent, indicating stereosele |
Norleucine (abbreviated as Nle) is an | isomer of leucine, the α-amino acid 2-amino-hexanoic |
It is an | isomer of p-toluic acid and o-toluic acid. |
It is an | isomer of nicotinic acid, which has the carboxyl side |
It is a constitutional | isomer of m-xylene and p-xylene. |
The compound is an | isomer of indole and its reduced form is an isoindoli |
,3-trimethyl-2-norbornanol is a terpene and an | isomer of borneol. |
(reverse T3, or rT3) is a molecule that is an | isomer of triiodothyronine (T3). |
Structure of the Δ-(lel)3 (or Δ-(λλλ)) | isomer of [Co(en)3]3+. |
The “S” optical | isomer of MDA is more potent than the “R” optical iso |
1-decene is the only possible | isomer of decene that does not exist as a pair of dia |
glucose and turanose the latter of which is an | isomer of sucrose. |
It is an organic acid and an | isomer of isocyanic acid, discovered one year later b |
Levomoramide is the inactive | isomer of the opioid analgesic dextromoramide, invent |
Despite being a positional | isomer of pipradrol, it is not a psychostimulant, and |
It is a positional | isomer of para-tyramine, and similarly to it, has eff |
It is a cycloalkane and an | isomer of the simplest diamondoid, adamantane, and li |
nt phentermine, and is the 2-chloro positional | isomer of chlorphentermine. |
ouabain may have been the 11 epimer, i.e., an | isomer of plant ouabain. |
Cannabidiol (CBD), an | isomer of THC and another major cannabinoid that is a |
It is a structural | isomer of LSD, with the two ethyl groups on the amide |
he 4-methylthio analogue of 2C-O, a positional | isomer of mescaline. |
One | isomer of HCA, known as (2S,3R)-HCA, inhibits pancrea |
Methylisopropyllysergamide is a structural | isomer of LSD, with the alkyl groups on the amide nit |
In the most common | isomer of terthiophene, two thienyl groups are connec |
This | isomer of triphos is more flexible and can bind to an |
is the pharmacologically active dextrorotatory | isomer of chlorpheniramine and seems to possess no ad |
reaction of dihydropentalene (pyrolysis of an | isomer of dicyclopentadiene) with n-butyllithium in s |
As an | isomer of octane, the boiling point is very close to |
The active | isomer of AP5 is considered to be the D configuration |
It is based on the observation that the R | isomer of citalopram can decrease the potency and inh |
A structural | isomer of JWH-193 with the methyl group on the indole |
tituted on the phenethyl ring) of the 3R,4S,βS | isomer of ohmefentanyl is one of the most potent opio |
en identified, varying mainly in whether a cis | isomer of a peptide bond is involved and on the dihed |
short duration of action, and is a structural | isomer of another potent dopamine reuptake inhibitor, |
This compound is a condensation | isomer of bisphenol A and acetone and of special impo |
by the Greek letter psi- Ψ) is the C-glycoside | isomer of the nucleoside uridine, and it is the most |
's uranyl phosphate sheet is a new geometrical | isomer of the group which differs in the orientation |
osphuranylite-type sheet in bergenite is a new | isomer of the group, with the uranyl phosphate tetrah |
vity, n-icosane (the straight-chain structural | isomer of icosane) is part of the paraffin group, and |
CB1 and 6.9nM at CB2. JWH-164 is a positional | isomer of the related compound JWH-081, but with a me |
a also revealed the formation of a short-lived | isomer of 262Rf (which undergoes spontaneous fission |
the following chemicals or the salt, optical | isomer, or salt of an optical isomer of the following |
ed transformation of an aldose into the ketose | isomer or vice versa, with a tautomeric enediol as re |
It is the main trans fatty acid | isomer present in milk fat. |
)-coniine (CAS 458-88-8), which is the natural | isomer present in hemlock and (R)-(-)-coniine (CAS 59 |
ubstituents will have a syn orientation in the | isomer referred to as "threo", and are anti in the is |
For the next steps to succeed, only the endo | isomer should form; this happens because the bromine |
It is a positional | isomer; the other two are m-cresol and o-cresol. |
1,6-phosphate has only one biologically active | isomer, the β-D-form. |
ficiency is accompanied by an increase of this | isomer; the Osbond/DHA ratio is thus a marker of diet |
menclature, the name refers exclusively to one | isomer, the straight-chain H3C(CH2)11CH3, also called |
butane refers only to the unbranched n-butane | isomer; the other one being called "methylpropane" or |
he compound trifluoracetonitrile (CF3CN) is an | isomer to trifluoromethylisocyanide. The nitrile is m |
ctural isomers, of which two are active, the γ | isomer trimeperidine, and the β isomer isopromedol. |
It can be produced from its | isomer verbenone in a photochemical rearrangement rea |
The trans | isomer was found to be around 591x more potent than m |
The 3,3 | isomer was formed in two steps by reaction of 1,4-bis |
wever, it can spontaneously shift into another | isomer which pairs with a different nucleobase, guani |
The double-bond | isomer with an exo-methylene group, β-copaene, was fi |
gen atom attached to carbon number 3 in the 5α | isomer with a hydroxyl group results in lanosterol, t |
The most compact and branched | isomer would be 3,3-di-tert-butyl-2,2,4,4-tetramethyl |
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