>>Signaling Pathways>> Chromatin/Epigenetics>> Epigenetic Reader Domain>>666-15

666-15 (Synonyms: Compound 3i)

Catalog No.GC32689

666-15는 IC50이 81nM인 강력하고 선택적인 CREB 억제제입니다. 666-15는 유방암 이종이식 모델에서 종양 성장을 억제합니다.

Products are for research use only. Not for human use. We do not sell to patients.

666-15 Chemical Structure

Cas No.: 1433286-70-4

Size 가격 재고 수량
10mM (in 1mL DMSO)
US$141.00
재고 있음
5mg
US$104.00
재고 있음
10mg
US$167.00
재고 있음
25mg
US$351.00
재고 있음
50mg
US$585.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Product has been cited by 2 publications

Description Protocol Chemical Properties Product Documents Related Products

666-15 is a potent and selective CREB inhibitor with an IC50 of 81 nM.

666-15 potently inhibits cancer cell growth. In MDA-MB-231 and MDA-MB-468 cells, the GI50 for 666-15 is 73 and 46 nM, respectively. In A549 and MCF-7 cells, it exhibits robust activity as well with GI50 of 0.47 and 0.31 μM. 666-15 is also found to be a rather weak inhibitor of CREB-CBP interaction with IC50 of 18.27 μM. 666-15 inhibits CREB's transcription activity in living cells independent of direct CREB or CBP binding interaction. 666-15 is very potent in inhibiting CREB's transcription activity. 666-15 also inhibits endogenous CREB target gene expression, the transcript level of nuclear receptor related 1 protein (Nurr1/NR4A2)[1].

Preliminary toxicity studies show that intraperitoneal (ip) injection of 10 mg/kg of 666-15 is well tolerated in mice. The tumor growth in the mice treated with 666-15 is efficaciously inhibited with complete tumor stasis. During the same period, the tumor volume in the vehicle-treated group is more than tripled. The body weights of 666-15-treated animals and vehicle-treated ones are indistinguishable from each other during the entire treatment period[1].

[1]. Xie F, et al. Identification of a Potent Inhibitor of CREB-Mediated Gene Transcription with Efficacious in Vivo Anticancer Activity. J Med Chem. 2015 Jun 25;58(12):5075-87.

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Average Rating: 5 ★★★★★ (Based on Reviews and 11 reference(s) in Google Scholar.)

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