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 | 8 unreviewed articles as of 29 June 2025
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| Created | Article | Extract | Class | Creator (# edits) | Notes |
|---|---|---|---|---|---|
| 2024-12-17 | Aminopentamide (Antispasmodic drug) | Aminopentamide is an anticholinergic antispasmodic and antidiarrheal drug and also a bird and rodent repellent. It is structurally related to Darifenacin. | C | Mo18ekula (260) | |
| 2025-06-19 | ACEA-1328 (NMDA receptor antagonist at the glycine site) | ACEA-1328 is an NMDA receptor antagonist. | Stub | Themonkey942 (399) | |
| 2025-06-24 | Silyl protecting groups | In organic chemistry, various triorganosilyl compounds are used as protecting groups. The simplest is the trimethylsilyl group, but others are known. | Start | Bernanke's Crossbow (9112) | |
| 2025-06-25 | .yokohama (generic top-level Internet domain) | .yokohama is the Internet Generic top-level domain for Yokohama, Japan. It was introduced on 5 June 2014 when ICANN and GMO Internet signed the registry agreement for GMO Registry (which also operates the .tokyo and .nagoya domains) to operate the domain. | Stub | DimensionalFusion (5679) | |
| 2025-05-23 | Cefepime/sulbactam (Combination antibiotic consisting of the IV generation) | Cefepime/sulbactam is a 1:1 fixed-dose combination of cefepime (a fourth-generation cephalosporin) and sulbactam (a β-lactamase inhibitor). The combination exerts a bactericidal effect by disrupting bacterial cell wall synthesis through transpeptidase inhibition, thereby impairing peptidoglycan cross-linking. | C | Хокус Покус 333 (31) | |
| 2025-06-25 | Tosifen (Possible heart rhythm drug) | Tosifen is a drug candidate for use as an antiarrhythmic agent. Tosifen was synthesized originally in a series of compounds whose basic structural moiety, the sulfonylurea nucleus, was of interest for potential hypoglycemic action. But tosifen is only a weak hypoglycemic agent. | Start | 92.31.192.97 | |
| 2025-06-27 | Lupane (compound) (Organic compound (C₃₀H₅₂); pentacyclic triterpene hydrocarbon) | Lupane is a pentacyclic triterpene hydrocarbon with the molecular formula C₃₀H₅₂. It serves as the core skeleton for various bioactive compounds, including lupeol and betulinic acid, which are prevalent in numerous plant species. It actually features a structure composed of five fused rings––four cyclohexane rings and one cyclopentane––and is one of the major triterpene skeletons alongside hopane, oleanane, and ursane types. | Start | G-Lignum (1051) | |
| 2025-05-19 | Transition metal catalytic asymmetric dearomatization reactions (Category of organic chemical reactions) | Catalyzed asymmetric dearomatization reactions (CADA reactions) are a category of asymmetric dearomatization reactions that catalytically transform aromatic compounds into enantioenriched polycycles and heterocyclic skeletons. The term was coined in 2012 by You et al. | FA | PchemExtraordinaire (38) |
Last updated by SDZeroBot operator / talk at 13:38, 29 June 2025 (UTC)
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