CDDO-2P-Im
CAS No. 1883650-96-1
CDDO-2P-Im( CDDO-2-P-Im )
Catalog No. M26555 CAS No. 1883650-96-1
CDDO-2P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can reduce the size and severity of the lung tumors in the mouse lung cancer model.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 297 | In Stock |
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| 5MG | 217 | In Stock |
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| 10MG | 353 | In Stock |
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| 25MG | 584 | In Stock |
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| 50MG | 808 | In Stock |
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| 100MG | 1088 | In Stock |
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| 200MG | 1460 | 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 NameCDDO-2P-Im
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NoteResearch use only, not for human use.
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Brief DescriptionCDDO-2P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can reduce the size and severity of the lung tumors in the mouse lung cancer model.
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DescriptionCDDO-2P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can reduce the size and severity of the lung tumors in the mouse lung cancer model.(In Vitro):In RAW264.7 cells, CDDO-2P-Im suppresses NO production (IC50: 5.8 nM). CDDO-2P-Im (100 nM) induces differentiation of U937 cells.(In Vivo):CDDO-2P-Im significantly elevates heme oxygenase-1 and quinone reductase mRNA and protein levels. In A/J mice, CDDO-2P-Im (50-200 mg/kg) decreases the number, size, and severity of tumors.
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In VitroCDDO-2P-Im (100 nM; 4 days) induces differentiation of U937 cells at 100 nM.CDDO-2P-Im suppresses NO production in RAW264.7 cells with an IC50 of 5.8 nM. Apoptosis Analysis Cell Line:U937 cells Concentration:30 nM, 100 nM Incubation Time:4 days Result:Induced differentiation of U937 cells at 100 nM.
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In VivoCDDO-2P-Im is more stable than CDDO-Im in pharmacokinetic studies.CDDO-2P-Im significantly elevates heme oxygenase-1 (HO-1) and quinone reductase (NQO1) mRNA and protein levels in various mouse tissues in vivo.CDDO-2P-Im (50-200 mg/kg; diet; for 16 weeks) decreases the number, the size and the severity of tumors in A/J mice. Animal Model:Seven week-old female A/J mice Dosage:50 mg/kg, 200 mg/kg Administration: Diet; for 16 weeks Result:Decreased the number, the size and the severity of tumors.
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SynonymsCDDO-2-P-Im
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number1883650-96-1
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Formula Weight618.822
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Molecular FormulaC39H46N4O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 200 mg/mL (323.20 mM)
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SMILES[H][C@@]12CC(C)(C)CC[C@@]1(CC[C@]1(C)[C@]2([H])C(=O)C=C2[C@@]3(C)C=C(C#N)C(=O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=O)n1cnc(c1)-c1ccccn1
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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
1.Zhang J, et al. Low dose of Bisphenol A enhance the susceptibility of thyroid carcinoma stimulated by DHPN and iodine excess in F344 rats. Oncotarget. 2017 Jul 22;8(41):69874-69887.
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