「enantiomer S」の共起表現一覧(1語右で並び替え)
該当件数 : 55件
of pharmaceutical compounds, separation of | enantiomers, analysis of inorganic organometallics, and |
e pair of possible stereoisomers, which are | enantiomers and epimers. |
This method produces a mixture of both | enantiomers and requires similar knowledge to that requ |
Both | enantiomers are known in nature; 1S,5S- or (−)-α-pinene |
Both | enantiomers are active, with the levo- form acting mere |
cal activity profiles of the two losigamone | enantiomers are not identical and suggest further that |
metimes used to explicitly denote that both | enantiomers are applied. |
Two | enantiomers are possible, D-ribulose (D-erythro-pentulo |
Both | enantiomers, as well as the racemates are presented in |
ine racemates and predicted how mixtures of | enantiomers behave in a heterogeneous system of solid a |
it was found that not only the "normal" (-) | enantiomers, but also the "unnatural" (+) enantiomers o |
Panthenol comes in two | enantiomers, D and L. Only D-panthenol (dexpanthenol) i |
It consists of | enantiomers D- and L-valine (Val), D-hydroxyvaleric aci |
It is a chiral compound having two | enantiomers, D-3-hydroxybutyric acid and L-3-hydroxybut |
The molecule is chiral and the separate | enantiomers have been isolated. |
The (S) | enantiomers in this series are more active as opioid ag |
ral object (the enzyme) converts one of the | enantiomers into product at a greater reaction rate tha |
This means that the racemic mix of the two | enantiomers is a mixed agonist-antagonist, with relativ |
such but the preparation of the individual | enantiomers is. |
This compound may exist as one of two | enantiomers, named (+)-pentazocine and (-)-pentazocine. |
Both | enantiomers occur in nature. |
lyhedron compound is a composition of the 2 | enantiomers of the great inverted snub icosidodecahedro |
drugs dextromoramide and levomoramide, two | enantiomers of a chiral molecule. |
which catalyzes the interconversion of the | enantiomers of mandelate via an enol intermediate. |
ysis showed that both positive and negative | enantiomers of BCH-189 had in vitro activity against HI |
are very useful for differentiating between | enantiomers of chiral molecules. |
may be formed from Pirkle's alcohol and the | enantiomers of the analyte. |
Both "normal" and "unnatural" | enantiomers of various opioid analgesic drugs including |
The two | enantiomers of O-desmethyltramadol show quite distinct |
electivity of around 12x. Resolution of the | enantiomers of AM-4030 yields an even more potent compo |
The two | enantiomers of dichloroisoprenaline |
Fischer projections depicting of the two | enantiomers of threose |
"Synthesis and Biological Activity of | Enantiomers of Antitumor Irofulven". |
two naturally occurring stereoisomers, the | enantiomers of erythrose and threose having the D confi |
lyhedron compound is a composition of the 2 | enantiomers of the snub icosidodecadodecahedron. |
lyhedron compound is a composition of the 2 | enantiomers of the snub dodecadodecahedron. |
lyhedron compound is a composition of the 2 | enantiomers of the great snub icosidodecahedron. |
It results from composing the two | enantiomers of the compound of 3 square antiprisms. |
It also results from composing the two | enantiomers of the compound of 5 truncated tetrahedra. |
lyhedron compound is a composition of the 2 | enantiomers of the snub cube. |
l (PAC) is an organic compound that has two | enantiomers, one with R- and one with S-configuration. |
gous indamine class where both of the trans | enantiomers possessed significant TRI activity at all t |
The complex can be resolved into | enantiomers that are described as Δ and Λ. Usually the |
"2-deoxyribose" may refer to either of two | enantiomers: the biologically important D-2-deoxyribose |
It exists as two | enantiomers: the D and L forms. |
In a mixture of | enantiomers, these methods can help quantify the optica |
s largely controlled by the ratio of D to L | enantiomers used, and to a lesser extent on the type of |
ocyclohexane] can be separated into the two | enantiomers using enantiomerically pure tartaric acid a |
nti conformer has planar chirality and both | enantiomers were separated by chiral column chromatogra |
The 2S,3S and 2R,3R isomers are a pair of | enantiomers, whereas the 2R,3S isomer is a meso compoun |
This anion can be resolved into the | enantiomers, which are optically stable (the picture sh |
Enantiomorphic protons of the analyte | enantiomers, which without Pirkle's alcohol are indisti |
Methopholine has two | enantiomers, with the levo (R) enantiomer being the act |
Carvedilol has | enantiomers with distinct pharmacodynamics. |
Unifiram has two | enantiomers, with (R)-(+)-unifiram being the more activ |
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