Allithiamine/ja: Difference between revisions

From Azupedia
Allithiamine/ja
Jump to navigation Jump to search
Created page with "<!--Pharmacokinetic data--> | bioavailability = | metabolism = | elimination_half-life = | excretion ="
Tags: Mobile edit Mobile web edit
 
Created page with "<!--Chemical data--> | C=15 | H=22 | N=4 | O=2 | S=2 | smiles = O=CN(/C(=C(\SSC\C=C)CCO)C)Cc1cnc(nc1N)C | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C15H22N4O2S2/c1-4-7-22-23-14(5-6-20)11(2)19(10-21)9-13-8-17-12(3)18-15(13)16/h4,8,10,20H,1,5-7,9H2,2-3H3,(H2,16,17,18)/b14-11- | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = WNCAVNGLACHSRZ-KAMYIIQDSA-N }}"
Tags: Mobile edit Mobile web edit
Line 21: Line 21:
| excretion =
| excretion =


<div lang="en" dir="ltr" class="mw-content-ltr">
<!--Identifiers-->
<!--Identifiers-->
| CAS_number_Ref = {{cascite|changed|??}}
| CAS_number_Ref = {{cascite|changed|??}}
Line 32: Line 31:
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 2301021
| ChemSpiderID = 2301021
</div>


<div lang="en" dir="ltr" class="mw-content-ltr">
<!--Chemical data-->
<!--Chemical data-->
| C=15 | H=22 | N=4 | O=2 | S=2  
| C=15 | H=22 | N=4 | O=2 | S=2  
Line 43: Line 40:
| StdInChIKey = WNCAVNGLACHSRZ-KAMYIIQDSA-N
| StdInChIKey = WNCAVNGLACHSRZ-KAMYIIQDSA-N
}}
}}
</div>


<div lang="en" dir="ltr" class="mw-content-ltr">
<div lang="en" dir="ltr" class="mw-content-ltr">

Revision as of 08:32, 3 April 2024

Allithiamine/ja
アリチアミンの骨格式
アリチアミン分子のボール&スティックモデル
Clinical data
ATC code
  • None
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC15H22N4O2S2
Molar mass354.49 g·mol−1
3D model (JSmol)
 ☒NcheckY (what is this?)  (verify)

Allithiamine (thiamine allyl disulfide or TAD) is a lipid-soluble form of vitamin B1 which was discovered in garlic (Allium sativum) in the 1950s along with its homolog prosultiamine. They were both investigated for their ability to treat Wernicke–Korsakoff syndrome and beriberi better than thiamine.