Pregnenolone Carbonitrile
CAS No. 1434-54-4
Pregnenolone Carbonitrile( 5-Pregnen-3β-ol-20-one-16α-carbonitrile | Pregnenolone 16α-carbonitrile? )
Catalog No. M27472 CAS No. 1434-54-4
Pregnenolone Carbonitrile is an activator of rodent-PXR and induces the expression of CYP3A.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 35 | Get Quote |
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| 5MG | 58 | Get Quote |
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| 10MG | 87 | Get Quote |
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| 25MG | 152 | Get Quote |
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| 50MG | 224 | Get Quote |
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| 100MG | 336 | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NamePregnenolone Carbonitrile
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NoteResearch use only, not for human use.
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Brief DescriptionPregnenolone Carbonitrile is an activator of rodent-PXR and induces the expression of CYP3A.
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DescriptionPregnenolone Carbonitrile is an activator of rodent-PXR and induces the expression of CYP3A.(In Vitro):Pregnenolone Carbonitrile is hepatoprotective by increasing resistance to subsequent stressful insults.(In Vivo):In WT mice, Pregnenolone Carbonitrile (40 mg/kg/day; i.p.) induces the expression of CYP3A11 and CYP2B10 at the mRNA, protein, and enzymatic levels. In adult female Sprague-Dawley rats, Pregnenolone Carbonitrile (100 mg/kg; i.p.) induces the expression of CYP3A mRNA. In male Sprague-Dawley rats, Pregnenolone Carbonitrile (35 mg/kg; gavage) increase in Pgp expression.
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In Vitro——
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In VivoAnimal Model:WT and Pxr-/- mice Dosage:40 mg/kg Administration:IP; per day for two days Result:Induced the expression of Cyp3a11 and Cyp2b10 at the mRNA, protein, and enzymatic levels in WT mice.Had little effect on the expression of Cyp3a11 in Pxr-/- mice
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Synonyms5-Pregnen-3β-ol-20-one-16α-carbonitrile | Pregnenolone 16α-carbonitrile?
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PathwayMetabolic Enzyme/Protease
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TargetP450
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Recptorenoyl-acyl carrier protein reductase (FabI)|S. aureus
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Research Area——
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Indication——
Chemical Information
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CAS Number1434-54-4
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Formula Weight341.49
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Molecular FormulaC22H31NO2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 20 mg/mL (58.57 mM)
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SMILESC[C@@]12[C@]([C@]3([C@](CC1)([C@]4(C)C(=CC3)C[C@@H](O)CC4)[H])[H])(C[C@@H](C#N)[C@@H]2C(C)=O)[H]
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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.Kim BY, Sohn YT. Solid state of CG-400549, a novel FabI inhibitor: characterization, dissolution, transformation. Arch Pharm Res. 2011 May;34(5):775-9.
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