পারেন যৌগ (স্ফটিক বা অণু একজোড়া এক

Noun:

এনানসোমার,

enantiomer শব্দের বাংলা অর্থ এর উদাহরণ:

ওয়ারফারিন এর এনানসোমার CAS-Nummer: 5543-58-8 CAS-Nummer: 5543-57-7 ।

enantiomer's Usage Examples:

In chemistry, an enantiomer (/ɪˈnæntiəmər, ɛ-, -tioʊ-/ ə-NAN-tee-ə-mər; from Greek ἐνάντιος (enántios) 'opposite', and μέρος (méros) 'part') (also named.

ˈræsɪmeɪt/), is one that has equal amounts of left- and right-handed enantiomers of a chiral molecule.

(EC50 = 514 nM), while its (+)-enantiomer is a weak releaser of dopamine (EC50 = 1,457 nM) whereas its (−)-enantiomer is a weak reuptake inhibitor of.

some cases the (R)-enantiomer is the dextrorotary enantiomer, and in other cases the (R)-enantiomer is the laevorotary enantiomer.

contains one enantiomer in greater amounts than the other.

A racemic mixture has an ee of 0%, while a single completely pure enantiomer has an ee of 100%.

cyclopyrrolone derivatives are zopiclone (Imovane) and its active single-enantiomer component, eszopiclone (Lunesta), which are used to treat insomnia, and.

acts as a selective D1 agonist, with the (R)-enantiomer being a potent full agonist, while the (S) enantiomer retains its D1 selectivity but is a weak partial.

The [11C]-(+)-McN5652 enantiomer binds to the serotonin transporter.

so there are two enantiomers with quite different potency, the (R)-enantiomer having a Ki of 0.

27 nM at CB1 while the (S)-enantiomer has a much weaker.

Half of the optically active substance becomes its mirror image (enantiomer) referred as racemic mixtures (i.

In such reactions, the synthesis favors the formation of a specific enantiomer or diastereomer.

sources produce one enantiomer: the principal industrial source, citrus fruit, contains D-limonene ((+)-limonene), which is the (R)-enantiomer.

The name "theanine" without a prefix generally implies the enantiomer L-theanine, which is the form found in tea leaves and as a dietary supplement.

An enantioselective reaction is one in which one enantiomer is formed in preference to the other, in a reaction that creates an optically.

double bond, it still has two enantiomers as the 9-methyl group can exist in an (R) or (S) conformation.

The (S) enantiomer has similar effects to Δ9-THC.

is, excluding the opposing enantiomer).

Diastereomers have different physical properties (unlike most aspects of enantiomers) and often different chemical.

compound by a method that favors the formation of a specific enantiomer or diastereomer.

Only the (S)-enantiomer is active as an agonist, with the (R)-enantiomer being a weak antagonist at D2 receptors.

chiral forms, so different enantiomers of a chiral drug molecule bind differently (or not at all) to target receptors.

One enantiomer of a drug may have a desired.

activity is specific to the R-(+) enantiomer, whereas the sedative and ataxic effects are specific to the S-(-) enantiomer.

enantiomer's Meaning':

either one of a pair of compounds (crystals or molecules

Synonyms:

chemical compound; compound; enantiomorph;

Antonyms:

smooth; rough; simple; decrease;