#1
レンダリング結果


TeXソース
TeXソース
入力コード
\documentclass[b4j]{tetsujsarticle}
\usepackage{tetsuchem}
\def\title#1{\br2\小見出し{#1}\br{.5}}
\begin{document}
\nousece
\setcrambond{2pt}{}{}
\setatomsep{2em}
\title{サリチル酸の二量体}
\chemfig{%
[:30]*6(-(-OH)=(-C(=[1]O%
-[,,,,dash pattern=on 1pt off 0.8pt]HO-[7]C(-(*6(=-=-=(-HO)-)))
(=[5]O-[4,,,,dash pattern=on 1pt off 0.8pt]\phantom{H})
)(-[7]OH))-=-=)
}
\title{フグ毒の成分 テトロドトキシン}
\setatomsep{3em}
\newlength{\bond}
\newlength{\bondw}
\setlength{\bond}{1.5pt}
\setlength{\bondw}{3\bond}
\def\bgcolor{white}
\setcrambond{\bond}{}{}
\chemfig{%
?[a]
(-[:60]-[0]OH)
(-[6]OH)
-[:170]?[b]-[:230]?[c]-[:10]
%
(<[:230]\chembelow{N}{H}-[:170,,,,line width=\bond]
(=[:230]HN)
>[:190]HN-[:50]?[c]
(-[:190]HO))
%
(-[:-10,,,,\bgcolor,line width=\bondw])-[:-10]
(<[:5]OH)-[:50]?[a]
(-[2,,,,\bgcolor,line width=\bondw]\phantom{O})
(-[2]O-[:170]
(-[2]OH)
(-[:190]O?[b])
(<[:230]
(-[:170,,,,\bgcolor,line width=\bondw])
(-[:170]HO)
(-[6,,,,\bgcolor,line width=\bondw])
(-[6,,,,line width=\bond])
(>[:50])%redraw
))}
\title{シアノコバラミン(ビタミンB12)}
\setatomsep{2.5em}
\chemfig{Co\rlap{${}^+$}(?[f])(-[2]CN)
%
(-[7,,,,<-]N*5(=(?[d])-(<:-[::60]-[::-60](=[::-60]O)-[::60]NH_2)
-(<[::-39]CH_3)(<:[::-69]CH_3)-?[a]-))
%
(-[1,,,,<-]N*5(=(-[,0.6]?[a,{=}])
-(<:-[::-60]-[::60](=[::60]O)-[::-60]NH_2)
-(<[::-84]-[::60](=[::60]O)
-[::-60]NH_2)(<:[::-24]CH_3)-?[b]-))
%
(-[3,,,,<-]N*5(=(-[,0.6]?[b,{=}](-[::60]CH_3))
-(<:-[::-60]-[::60](-[::60]H_2N)=[::-60]O)
-(<[::-84]-[::-60](-[::60]H_2N)=[::-60]O)(<:[::-24]H_3C)
-?[c](<:[::-90]H_3C)
-))
%
-[5]N*5(-(?[c])(<[::0]H)
-(<-[::-60](-[::60]H_2N)=[::-60]O)
-(<[::-24]CH_3)
(<:[::-84]
-[::60]-[::-60](=[::-60]O)-[::60]NH-[::-60]-[::60]
(<:[::60,0.7]CH_3)-[::-60]O
-[::60]P(=[::90]O)(-[::-90]HO)-[::0]O
-[6]*5([::36]-(-[6]-[::-60]HO)<O>
(-[2,4.7]N*5([::-18]-(*6(=-(-CH_3)=(-CH_3)-=-))
--N(?[f,,{dash pattern=on 1pt off 0.8pt}]\phantom{N})=-))
-(-[2,,,2]HO)-))
%
-(=[,0.6](?[d])-[::-60]CH_3)-)}
\title{イベルメクチン(ノーベル医学生理学賞2015)}
\setatomsep{1.75em}
\chemfig{H -[2]?[a](-[2,,,2]HO) <[7](-[2,0.5]H)(-[6]OCH_3)-[,1.2,,,line width=2pt]>[1](-[6]H)(-[3] O -[4,1.2]?[a](-[2]H)(-[6,0.4]CH_3)) -[2,1.3] O -[2] ?[b](-[2,,,2]HO) <[7](-[2,0.5]CH_3)(-[6]H)-[,1.2,,,line width=2pt]O>[1](-[2]H)(-[3] -[4,1.2]?[b](-[6,0.4]H)(-[2]OCH_3)) -[6] O>:[7]?[c](<[2]H) -[6,1.3] (<[6]H)(<:[5,,,2]H_3C) -[:-30,1.2]=[6]-[:-30,1.2]=[6]([:-72]*5(--O-(<:[6,0.9]H)(*6(-(<[:-60,0.9]OH)(<:[:-120,0.9]H)-(-CH_3)=-(-[2,1.2](=[:150]O)-[:30]O -[2] (<:[:-30]H) *6(--
(<[:-30]-[:30]-[2]?[d](<[7]CH_3)(<:[1]H))(<:[2]O-[:30]?[d](<[1]H)-[2,1.2](<:[1]CH_3)(<[2]H)-[:150]-[:-150,,,2]H_3C)
-O-(-[,1.1]-[:-150,1.2]=[:150,1.2]?[c]-[2]CH_3)--))(<[:30]H)-))--))}
\end{document}