5-Ph-IAA
CAS No. 168649-23-8
5-Ph-IAA( —— )
Catalog No. M23758 CAS No. 168649-23-8
5-Ph-IAA is a derivative of Indole-3-acetic acid (IAA), which is a plant hormone and acts as an enzyme or prodrug combination for cancer gene therapy.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 61 | In Stock |
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| 5MG | 55 | In Stock |
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| 10MG | 92 | In Stock |
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| 25MG | 187 | In Stock |
|
| 50MG | 306 | In Stock |
|
| 100MG | 519 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name5-Ph-IAA
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NoteResearch use only, not for human use.
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Brief Description5-Ph-IAA is a derivative of Indole-3-acetic acid (IAA), which is a plant hormone and acts as an enzyme or prodrug combination for cancer gene therapy.
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Description5-Ph-IAA is a derivative of Indole-3-acetic acid (IAA), which is a plant hormone and acts as an enzyme or prodrug combination for cancer gene therapy.
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In VitroWestern Blot Analysis Cell Line:HCT116 cells Concentration:1 μM Incubation Time:6 hours Result:Depleted DHC1-mAC efficiently in HCT116 cells constitutively expressing OsTIR1(F74G).
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In VivoAnimal Model:Balb/c-nu female mice (7 weeks old; 16–20?g ) bearing mAID-BRD4 and TOP2A-mAC xenograft tumours cells Dosage:0 mg/kg, 1 mg/kg, 3 mg/kg and 10?mg/kg Administration:Intraperitoneally injection; every day; 7 days Result:Displayed significant tumour suppression of mAID-BRD4 xenografts and TOP2A-mAC xenografts.
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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 Number168649-23-8
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Formula Weight251.28
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Molecular FormulaC16H13NO2
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Purity>98% (HPLC)
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SolubilityDMSO:125 mg/mL?(497.45 mM;?Need ultrasonic)
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SMILESC1=CC=C(C=C1)C2=CC3=C(C=C2)NC=C3CC(=O)O
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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.O Greco,et al. Horseradish peroxidase-mediated gene therapy: choice of prodrugs in oxic and anoxic tumor conditions. Mol Cancer Ther. 2001 Dec;1(2):151-60.
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