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)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 79 | In Stock |
|
| 5MG | 132 | In Stock |
|
| 10MG | 213 | In Stock |
|
| 25MG | 372 | In Stock |
|
| 50MG | 536 | In Stock |
|
| 100MG | 776 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameZotarolimus
-
NoteResearch use only, not for human use.
-
Brief DescriptionZotarolimus (ABT-578, A 179578) is a semi-synthetic analogue of rapamycin, inhibits FKBP-12.
-
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.
-
In Vitro——
-
In Vivo——
-
SynonymsABT-578 | A-179578 | ABT578 | A179578 | ABT 578 | A 179578
-
PathwayPI3K/Akt/mTOR signaling
-
TargetmTOR
-
RecptorFKBP-12
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number221877-54-9
-
Formula Weight966.21
-
Molecular FormulaC52H79N5O12
-
Purity>98% (HPLC)
-
SolubilityDMSO: ≥ 33 mg/mL
-
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
-
Chemical NameRapamycin, 42-deoxy-42-(1H-tetrazol-1-yl)-, (42S)-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
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.
molnova catalog
related products
-
mTOR inhibitor 9b
mTOR inhibitor 9b is an enzyme inhibitor of protein kinase mTOR he phosphatidylinositol 3-kinase PIK3CA with IC50s of 0.76 nm and 1.262 μM, respectively.
-
Seco Rapamycin
Seco-rapamycin is the first in vivo open-ring metabolite of rapamycin that does not affect mTOR.
-
ElteN378
ElteN378 is a highly potent synthetic inhibitor of FKBP12 with Ki of 0.5 nM, a low atomic weight ligand with affinity comparable to that of the macrolide Rapamycin.
Cart
sales@molnova.com