AhR modulator-1

Modify Date: 2024-01-08 20:17:19

AhR modulator-1 Structure
AhR modulator-1 structure
Common Name AhR modulator-1
CAS Number 115039-00-4 Molecular Weight 285.55
Density N/A Boiling Point N/A
Molecular Formula C13H7Cl3O Melting Point N/A
MSDS N/A Flash Point N/A

 Use of AhR modulator-1


AhR modulator-1 (compound 6-MCDF) is a selective and orally active aryl hydrocarbon receptor (AhR) modulator. AhR modulator-1 inhibits metastasis, in part, by inhibiting prostatic VEGF production prior to tumor formation. AhR modulator-1 also possess anti-estrogenic properties in rat uterus[1].

 Names

Name AhR modulator-1

 AhR modulator-1 Biological Activity

Description AhR modulator-1 (compound 6-MCDF) is a selective and orally active aryl hydrocarbon receptor (AhR) modulator. AhR modulator-1 inhibits metastasis, in part, by inhibiting prostatic VEGF production prior to tumor formation. AhR modulator-1 also possess anti-estrogenic properties in rat uterus[1].
Related Catalog
Target

Aryl hydrocarbon receptor (AhR) [1][2] Prostatic VEGF[1] Estrogenic[1]

In Vitro AhR modulator-1 (6-MCDF; 0.1-10 μM; 48-96 hours; ASPC-1 cells) treatment exhibits dose-dependent growth inhibitory effects with growth inhibitory effects of 26, 43 and 99% at concentrations of 0.1, 1 and 10 μM, respectively[2]. Cell Proliferation Assay[2] Cell Line: ASPC-1 cells Concentration: 0.1 μM, 1 μM and 10 μM Incubation Time: 48 hours, 72 hours, 96 hours Result: Exhibited dose-dependent growth inhibitory effects.
In Vivo AhR modulator-1 (6-MCDF; 0-40 mg/kg; oral administration; daily; for 12 weeks; C57BL/6-Tg(TRAMP)8247Ng/J mice) treatment reduces the frequency of pelvic lymph node metastasis in mice fed the 40 mg/kg diet. And serum VEGF concentrations are also reduced. Prostate tumor incidence and size are not significantly reduced[1]. Animal Model: C57BL/6-Tg(TRAMP)8247Ng/J (TRAMP) mice (8-week-old)[1] Dosage: 0 mg/kg, 10 mg/kg, 40 mg/kg Administration: Oral administration; daily; for 12 weeks Result: The frequency of pelvic lymph node metastasis was reduced 5-fold in mice fed the 40 mg /kg diet.S erum VEGF concentrations were also reduced.
References

[1]. Fritz WA, et al. The selective aryl hydrocarbon receptor modulator 6-methyl-1,3,8-trichlorodibenzofuran inhibits prostate tumor metastasis in TRAMP mice. Biochem Pharmacol. 2009 Apr 1;77(7):1151-60.

[2]. Koliopanos A, et al. Increased arylhydrocarbon receptor expression offers a potential therapeutic target for pancreatic cancer. Oncogene. 2002 Sep 5;21(39):6059-70.

 Chemical & Physical Properties

Molecular Formula C13H7Cl3O
Molecular Weight 285.55
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