==作用機序{{Anchor|Mechanism of action}}==
==化学{{Anchor|Chemistry}}==
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{{Short description|Database of chemicals owned by the Royal Society of Chemistry}}
{{Self reference|For the use of ChemSpider on Wikipedia, see [[Wikipedia:ChemSpider]].}}
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| products = Ansys suite of engineering simulation software
==Corporate history==
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..., Massachusetts|マサチューセッツ州ボストン]]に本社を置く、アメリカのバイオ医薬品企業である。[[:en:combinatorial chemistry|コンビナトリアルケミストリー]]ではなく、[[:en:Drug design|合理的な薬剤設計]]という明確な戦略を採用した最初のバイオテック企業の一
==History==
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...atic access to chemical annotations integrated in PubChem |journal=Journal of Cheminformatics |date=9 August 2019 |volume=11 |issue=1 |page=56 |doi=10.11
...ubChem can be accessed for free through a [[web user interface]]. Millions of compound structures and descriptive datasets can be freely downloaded via [
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| ImageName = Skeletal formula of biguanide
| ImageName1 = Ball and stick model of biguanide
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...of Lebanon]] cone showing flecks of resin as used in the [[mummification]] of [[Pharaoh|Egyptian Pharaohs]].]]
...iupac.org|doi=10.1351/goldbook.RT07166}}</ref> Resins are usually mixtures of [[organic compound]]s. This article focuses on naturally occurring resins.
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| Image = X-ray by Wilhelm Röntgen of Albert von Kölliker's hand - 18960123-02.jpg
...ja|医療処置]]のことである。人間ドックや視力検査、[[diagnostic imaging/ja|画像診断]]、遺伝子検査、[[clinical chemistry/ja|臨床化学]]や[[molecular diagnostics/ja|分子診断学]]に関連する化学・細胞分析などの医学検査は、一般的に[[medi
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| ImageName = Skeletal formula of biguanide
| ImageName1 = Ball and stick model of biguanide
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...ide''' ('''NR''', '''SR647''') is a [[pyridine]]-[[nucleoside]] and a form of [[Vitamin B3|vitamin B<sub>3</sub>]]. It functions as a precursor to [[nico
==Chemistry==
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| alt = Skeletal formula of sulbutiamine
| alt2 = Space-filling model of the sulbutiamine molecule
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...ide''' ('''NR''', '''SR647''') is a [[pyridine]]-[[nucleoside]] and a form of [[Vitamin B3|vitamin B<sub>3</sub>]]. It functions as a precursor to [[nico
==Chemistry== <!--T:3-->
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| alt = Skeletal formula of sulbutiamine
| alt2 = Space-filling model of the sulbutiamine molecule
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<!-- History and culture -->
ナイアシンアミドは1935年から1937年にかけて発見された。[[WHO Model List of Essential Medicines/ja|世界保健機関の必須医薬品リスト]]に掲載されている。ナイアシンアミドは[[generic medicat
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ビグアニジンのさまざまな[[derivative (chemistry)/ja|誘導体]]が薬物として使用されている。
{{details/ja|metformin/ja#History}}
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== History ==
...受賞しました。ギルバートは1980年に「[[:en:NA sequencing|DNA塩基配列]]の解明」で[[:en:Nobel Prize in Chemistry|ノーベル化学賞]]を、Sharpは1993年に「[[:en:split gene|分裂遺伝子]]の発見」で[[:en:Nobel Prize in P
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...t common side effects are musculoskeletal pain, peripheral edema (swelling of legs and hands), atrial fibrillation, and arthralgia (joint pain). Other co
...(EPA). The US [[Food and Drug Administration]] (FDA) granted the approval of icosapent ethyl in 2012 to Amarin Corporation, and it became the second [[f
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...t common side effects are musculoskeletal pain, peripheral edema (swelling of legs and hands), atrial fibrillation, and arthralgia (joint pain). Other co
...(EPA). The US [[Food and Drug Administration]] (FDA) granted the approval of icosapent ethyl in 2012 to Amarin Corporation, and it became the second [[f
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{{Anchor|Use in biosynthesis of coenzyme A}}
...（または''パンテノール''）を使用する。[[Shelf-stable food/ja|常温可能な可能な]][[Functional analog (chemistry)/ja|アナログ]]を使用するのが一般的であり、消費されるとパントテン酸に変換される。パントテン酸カルシウムは、酸、[[alkali/ja|アルカリ]
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{{Short description|Substance composed of multiple elements that are chemically bonded}}
...The [[ball-and-stick model]] of the molecule shows the spatial association of two parts [[hydrogen]] (white) and one part [[oxygen]] (red)
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