>>Signaling Pathways>> Endocrinology and Hormones>> Androgen Receptor>>HE-3235

HE-3235 (Synonyms: Apoptone,17α-Ethynyl-5α-androstane-3α,17ß-diol)

Catalog No.GC14221

HE-3235, 3β-androstanediol의 합성 유사체는 경구 생체이용 가능한 항암제입니다. HE-3235는 전립선 및 유방암의 설치류 모델에서 활성입니다.

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HE-3235 Chemical Structure

Cas No.: 183387-50-0

Size 가격 재고 수량
1mg
US$44.00
재고 있음
5mg
US$195.00
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10mg
US$342.00
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25mg
US$752.00
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

HE-3235 is a novel antagonist of androgen receptor.

Androgen receptor (AR) is an adrenal hormone belongs to the steroid hormone receptor family of molecules. AR is responsible for mediating the physiologic effects of androgens by binding to specific DNA sequences that influence transcription of androgen-responsive genes. Variations in the AR gene may lead to genetic predisposition to prostate cancer development and severity [2].

In vitro: In LNCaP cells expressing a mutated androgen receptor, HE3235 significantly inhibited activity for AED-stimulated LNCaP proliferation. This inhibitory activity is accompanied by an increase in the number of apoptotic cells [1].

In vivo: Animal studies have confirmed the cytoreductive activity of HE3235 on LNCaP tumours. The results suggest that this compound may be of clinical use in castration-resistant prostate cancer. In castrated male mice implanted subcutaneously with LuCaP35V CaP xenografts, treatment with HE3235 significantly prolonged the tumor doubling time of LuCaP35V, decreased androgen receptor expression, and lowered levels of intratumoral testosterone by 89% and dihydrotestosterone by 63% in both the presence and the absence of AED. HE3235 inhibited tumor growth in the bone environment. HE3235 inhibited the growth of subcutaneous CRPC as well as CRPC in the bone environment. HE3235 exhibited a wide range of effects, including alteration of androgen receptor signaling and reductions in levels of intratumoral androgens. Weights of tumored tibiae of HE3235-treated animals were lower than those of control [3].

References:
[1] Trauger R, Corey E, Bell D, et al.  Inhibition of androstenediol-dependent LNCaP tumour growth by 17α-ethynyl-5α-androstane-3α, 17β-diol (HE3235)[J]. British journal of cancer, 2009, 100(7): 1068-1072.
[2] Gelmann E P.  Molecular biology of the androgen receptor[J]. Journal of Clinical Oncology, 2002, 20(13): 3001-3015.
[3 Gelmann E P.  Molecular biology of the androgen receptor[J]. Journal of Clinical Oncology, 2002, 20(13): 3001-3015.] Koreckij T D, Trauger R J, Montgomery R B, et al. HE3235 inhibits growth of castration-resistant prostate cancer[J]. Neoplasia, 2009, 11(11): 1216IN22-1225IN23.

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