Eubulus-A80
CAS No. 2703776-20-7
Eubulus-A80( —— )
Catalog No. M35360 CAS No. 2703776-20-7
Eubulus-A80 is a anti-tumor agent (WO2021/183702, Compound A80).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 472 | In Stock |
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| 2MG | 278 | In Stock |
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| 5MG | 426 | In Stock |
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| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameEubulus-A80
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NoteResearch use only, not for human use.
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Brief DescriptionEubulus-A80 is a anti-tumor agent (WO2021/183702, Compound A80).
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DescriptionGPX4-IN-8 (compound A80) is a potent GPX4 inhibitor. GPX4-IN-8 shows antiproliferative activity.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number2703776-20-7
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Formula Weight396.87
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Molecular FormulaC22H21ClN2O3
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Purity>98% (HPLC)
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Solubility——
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SMILESN(C(C#C)=O)(C1(C(NCC2=CC=CC=C2)=O)CCOCC1)C3=CC(Cl)=CC=C3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Egg yolk phosphatidy...
Lecithins, egg can be used as an excipient. Pharmaceutical excipients, or pharmaceutical auxiliaries, refer to other chemical substances used in the pharmaceutical process other than pharmaceutical ingredients. Pharmaceutical excipients generally refer to inactive ingredients in pharmaceutical preparations, which can improve the stability, solubility and processability of pharmaceutical preparations. Pharmaceutical excipients also affect the absorption, distribution, metabolism, and elimination (ADME) processes of co-administered drugs.
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BCPA
BCPA is a non-cytotoxic Pin1 modulator.BCPA modulates osteoclast activation and attenuates the reduction of Pin1 protein, thereby inhibiting RANKL-induced receptor activators of osteoclastogenesis.BCPA is used in the study of osteoporosis.
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VU 0357017 hydrochlo...
VU 0357017 hydrochloride is highly selective M1 agonists act at an allosteric site to activate the receptor (EC50: 477 ± 172 nM; Pec50: 6.37 ± 0.15).
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