3-Phenylpropyl isothiocyanate
CAS No. 2627-27-2
3-Phenylpropyl isothiocyanate( —— )
Catalog No. M28287 CAS No. 2627-27-2
3-Phenylpropyl isothiocyanate has a stronger inhibitory effect on N-nitrosomethyl-benzylamine (NMBA) tumorigenesis. 3-Phenylpropyl isothiocyanate has chemopreventive effects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 195 | In Stock |
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| 5MG | 249 | In Stock |
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| 10MG | 369 | In Stock |
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| 25MG | 562 | In Stock |
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| 50MG | 770 | In Stock |
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| 100MG | 1032 | In Stock |
|
| 200MG | 1376 | In Stock |
|
| 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 Name3-Phenylpropyl isothiocyanate
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NoteResearch use only, not for human use.
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Brief Description3-Phenylpropyl isothiocyanate has a stronger inhibitory effect on N-nitrosomethyl-benzylamine (NMBA) tumorigenesis. 3-Phenylpropyl isothiocyanate has chemopreventive effects.
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Description3-Phenylpropyl isothiocyanate has a stronger inhibitory effect on N-nitrosomethyl-benzylamine (NMBA) tumorigenesis. 3-Phenylpropyl isothiocyanate has chemopreventive effects.(In Vivo):3-Phenylpropyl isothiocyanate (5, 1, or 0.2 μmol; gavage; A/J mice; daily for 4 consecutive days prior to administration of 10 μmol of NNK by i.p. injection) effectively inhibited NNK-induced lung tumors. In vivo, 3-Phenylpropyl isothiocyanate decreases lung tumor formation induced by benzo[a]pyrene and NNK .
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In Vitro——
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In Vivo3-Phenylpropyl isothiocyanate (5, 1, or 0.2 μmol; gavage; A/J mice; daily for 4 consecutive days prior to administration of 10 μmol of NNK by i.p. injection) effectively inhibited NNK-induced lung tumors.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptortau|Tubulin
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Research Area——
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Indication——
Chemical Information
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CAS Number2627-27-2
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Formula Weight177.27
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Molecular FormulaC10H11NS
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Purity>98% (HPLC)
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Solubility——
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SMILESS=C=NCCCC1=CC=CC=C1
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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.Nozal V, et al. TDP-43 Modulation by Tau-Tubulin Kinase 1 Inhibitors: A New Avenue for Future Amyotrophic Lateral Sclerosis Therapy. J Med Chem. 2022;65(2):1585-1607.
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