L685818

Catalog No.: A28078
Antifungal Reagent
L685818 is a specific immunophilin ligand that exhibits antifungal activity against Cryptococcus neoformans. In addition to its antifungal properties, L685818 demonstrates neuroregenerative effects by safeguarding dopaminergic neurons from toxicity associated with MPP+ and 6-OHDA. The compound effectively reduces the loss of tyrosine hydroxylase (TH) and promotes neuronal process regeneration, making it a valuable tool for research in neurodegenerative disease models and fungal infections.
Grouped product items
Size Price Stock Qty
25mg
$1,275.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionL685818 is a specific immunophilin ligand that exhibits antifungal activity against Cryptococcus neoformans. In addition to its antifungal properties, L685818 demonstrates neuroregenerative effects by safeguarding dopaminergic neurons from toxicity associated with MPP+ and 6-OHDA. The compound effectively reduces the loss of tyrosine hydroxylase (TH) and promotes neuronal process regeneration, making it a valuable tool for research in neurodegenerative disease models and fungal infections.
Product Information
Catalog NumA28078
FormulaC43H69NO13
Molecular Weight808.01
CAS Number143839-74-1
SMILESO=C([C@@](CCCC1)([H])N1C(C([C@@]2(O)[C@H](C)C[C@H](OC)[C@@](O2)([H])[C@@H](OC)C[C@@H](C)[C@H](O)/C(C)=C/[C@H]3CC)=O)=O)O[C@H](/C(C)=C/[C@H]4C[C@@H](OC)[C@H](O)CC4)[C@H](C)[C@@H](O)CC3=O
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