
Zotarolimus
CAS No. 221877-54-9
Zotarolimus( ABT-578 | A-179578 | ABT578 | A179578 | ABT 578 | A 179578 )
Catalog No. M13536 CAS No. 221877-54-9
Zotarolimus (ABT-578, A 179578) is a semi-synthetic analogue of rapamycin, inhibits FKBP-12.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 79 | In Stock |
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5MG | 132 | In Stock |
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10MG | 213 | In Stock |
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25MG | 372 | In Stock |
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50MG | 536 | In Stock |
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100MG | 776 | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameZotarolimus
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NoteResearch use only, not for human use.
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Brief DescriptionZotarolimus (ABT-578, A 179578) is a semi-synthetic analogue of rapamycin, inhibits FKBP-12.
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DescriptionZotarolimus (ABT-578, A 179578) is a semi-synthetic analogue of rapamycin, inhibits FKBP-12 binding with IC50 of 2.8 nM and shows less potent systemic immunosuppression than rapamycin; effectively inhibits both smooth muscle cell and endothelial cell proliferation, with IC50 values of 2.9 nM and 2.6 nM, respectively; exhibits high-affinity binding to the immunophilin FKBP12, inhibiting in vitro proliferation of both human and rat T cells; inhibits Con A-induced human T cells with IC50 of 7.0 nM; reduce early complications and improve late clinical outcomes in patients needing interventional cardiology.
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In Vitro——
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In Vivo——
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SynonymsABT-578 | A-179578 | ABT578 | A179578 | ABT 578 | A 179578
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PathwayPI3K/Akt/mTOR signaling
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TargetmTOR
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RecptorFKBP-12
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number221877-54-9
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Formula Weight966.21
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Molecular FormulaC52H79N5O12
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 33 mg/mL
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SMILESO=C([C@@](CCCC1)([H])N1C(C([C@@]2(O)[C@H](C)CC[C@@](O2)([H])C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C([C@H](OC)[C@H](O)/C(C)=C/[C@H]3C)=O)=O)=O)O[C@H]([C@H](C)C[C@H]4C[C@@H](OC)[C@@H](N5N=NN=C5)CC4)CC3=O
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Chemical NameRapamycin, 42-deoxy-42-(1H-tetrazol-1-yl)-, (42S)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Garcia-Touchard A, et al. Eur Heart J. 2006 Apr;27(8):988-93.
2. Chen YW, et al. J Cardiovasc Pharmacol. 2007 Apr;49(4):228-35.
3. Abizaid A, et al. Am J Cardiol. 2007 May 15;99(10):1403-8.
4. Wagner R, et al. Bioorg Med Chem Lett. 2005 Dec 1;15(23):5340-3.
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