Doramapimod
CAS No. 285983-48-4
Doramapimod( BIRB 796 | BIRB-796 | BIRB796 )
Catalog No. M13869 CAS No. 285983-48-4
A highly potent p38 MAPK inhibitor with Kd of 0.1 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 35 | In Stock |
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| 5MG | 29 | In Stock |
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| 10MG | 48 | In Stock |
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| 25MG | 68 | In Stock |
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| 50MG | 86 | In Stock |
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| 100MG | 120 | In Stock |
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| 200MG | 220 | In Stock |
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| 500MG | 370 | In Stock |
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| 1G | 551 | In Stock |
|
Biological Information
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Product NameDoramapimod
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NoteResearch use only, not for human use.
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Brief DescriptionA highly potent p38 MAPK inhibitor with Kd of 0.1 nM.
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DescriptionA highly potent p38 MAPK inhibitor with Kd of 0.1 nM; displays no activity on ERK1, IKK2b, ZAP-70, EGFR, PKA, PKC, etc.; shows inhibition of TNFα inTHP.1 with IC50 of 18 nM; orally active.
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In Vitro——
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In Vivo——
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SynonymsBIRB 796 | BIRB-796 | BIRB796
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PathwayMAPK/ERK Signaling
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Targetp38 MAPK
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Recptorp38α
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number285983-48-4
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Formula Weight527.6572
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Molecular FormulaC31H37N5O3
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C(NC1=C2C=CC=CC2=C(OCCN3CCOCC3)C=C1)NC4=CC(C(C)(C)C)=NN4C5=CC=C(C)C=C5
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Chemical NameUrea, N-[3-(1,1-dimethylethyl)-1-(4-methylphenyl)-1H-pyrazol-5-yl]-N'-[4-[2-(4-morpholinyl)ethoxy]-1-naphthalenyl]-
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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PAF (C16)
PAF (C16) is a potent MAPK and MEK/ERK activator that induces increased vascular permeability. PAF (C16) (PAF (C16)) is a platelet-activating factor, a phospholipid-derived mediator and a ligand for PAF G protein-coupled receptor (PAFR). PAF (C16) has shown anti-apoptotic and anti-inflammatory activity in vitro, inhibiting Caspase-dependent apoptosis by interacting with its receptor (PAF-R) to perform cell signaling.
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DAMGO
DAMGO is an opioid receptor agonist with the ability to affect the locomotive activity in rodents. Possible analgesic agent due to μ-opiod receptor interaction.
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AZD-7624
AZD-7624 is a potent, selective, inhaled p38α MAPK inhibitor with pIC50 of 10.0.
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