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Search Results for " prostatic "

49

抑制剂 & 化合物

8

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T81550	PAP 248–286 Prostatic Acid Phosphatase(248-286)
	PAP 248–286是一种精液衍生的生物活性肽，也称为前列腺酸性磷酸酶 (248-286) 或PAP (248-286) 肽，属于精液中的精液衍生病毒感染增强子 (SEVI) 因子。该肽能显著增强HIV病毒颗粒与靶细胞间的附着，从而增加HIV感染率。
T0488	Finasteride 非那雄胺,MK-906	Reductase	Endocrinology/Hormones; Metabolism
	Finasteride (MK-906) 是 5α-还原酶的竞争性抑制剂，对 II 型 5α-还原酶的IC50为 4.2 nM，对 II 型 5α-还原酶的亲和力是 I 型酶的 100 倍。它可用于研究前列腺增生和雄激素性脱发。
T0696	Naftopidil KT-611,萘哌地尔,BM-15275	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Naftopidil (KT-611) 是一种选择性的 alpha1-肾上腺素受体 (α1-adrenoceptor) 拮抗剂，对克隆的人类 α1a、α1b 和 α1d 亚型肾上腺素受体的亲和力Ki 分别为 3.7 nM、20 nM 、1.2 nM。它具有抗增殖活性，可用于研究前列腺增生。
T0091	Alfuzosin hydrochloride SL 77499-10,Alfuzosin HCl,盐酸阿夫唑嗪	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Alfuzosin hydrochloride (Alfuzosin HCl) 是一种 α1 肾上腺素受体拮抗剂，可用于良性前列腺增生(BPH)的研究。
T1504	Silodosin 西洛多辛,KAD 3213,KMD 3213	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Silodosin (KAD 3213) 是有选择性的、强效的、口服活性的 α1A-adrenergic receptor 阻滞剂，是一种有效且耐受性良好的试剂，可用于研究 LUTS/BPH。它对 α1A-AR 表现出高度的亲和力，是 α1B-AR 和 α1D-AR 亲和力的 162 和 50 倍。
T0197	Terazosin hydrochloride 盐酸特拉唑嗪,Terazosin HCl,Terazosine,Blavin,Hytrin,Zayasel,Fosfomic	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Terazosin hydrochloride (Hytrin) 是一种竞争性和口服活性的 α1-肾上腺素受体拮抗剂，是一种喹唑啉衍生物。它通过舒张血管和打开膀胱来起作用。它可用于良性前列腺增生和高血压的研究。
T6600	Naftopidil dihydrochloride KT-611,KT-611 2HCl,盐酸萘哌地尔,Naftopidil DiHCl	5-HT Receptor; Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Naftopidil dihydrochloride (KT-611 2HCl) 是一种选择性的 alpha1-肾上腺素受体 (α1-adrenoceptor) 拮抗剂，对克隆的人类 α1a、α1b 和 α1d 亚型肾上腺素受体的亲和力Ki 分别为 3.7 nM、20 nM、1.2 nM。它具有抗增殖活性，可用于研究前列腺增生。
T6701	Terazosin hydrochloride dihydrate Flotrin dihydrate,Terazosin HCl Dihydrate,Dysalfa dihydrate,Heitrin dihydrate,盐酸特拉唑嗪(二水合物)	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Terazosin hydrochloride dihydrate (Heitrin dihydrate) 是一种竞争性和口服活性的 α1-肾上腺素受体(α1-adrenoceptor) 拮抗剂，是一种喹唑啉衍生物，通过舒张血管和打开膀胱的方式起作用。它可用于研究良性前列腺增生 (BPH) 和高血压。
T9220	Naftopidil hydrochloride 1-[4-(2-methoxyphenyl)piperazin-1-yl]-3-,萘哌地尔盐酸盐,KT-611 hydrochloride,BM-15275 hydrochloride	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Naftopidil hydrochloride (BM-15275 hydrochloride) 是一种选择性的 alpha1-肾上腺素受体 (α1-adrenoceptor) 拮抗剂，对克隆的人类 α1a、α1b 和 α1d 亚型肾上腺素受体的亲和力 Ki 分别为 3.7 nM、20 nM、1.2 nM。它具有抗增殖活性，可用于研究前列腺增生。
T14843	Bifluranol BX341	Androgen Receptor	Endocrinology/Hormones
	Bifluranol (BX341) 具有抗雄激素活性，在体内实验中显示出显著的抗前列腺活性，可用于治疗良性前列腺增生（BPH）。
T11220L	UK 227786 hydrochloride(150452-18-9 Free base),1-[4-(1,3-Benzodioxol-5a-ylmethylamino)-6-chloroquinazolin-2-yl]piperidine-4-carboxylic acid;hydrochloride(150452-18-9 Free base),1-[4-(1,3-Benzodioxol-5a-ylmethylamino)-6-chloroquinazolin-2-yl]piperidine-4-carboxylic acid	PDE	Metabolism
	UK 227786是磷酸二酯酶5（PDE5）抑制剂，可用于前列腺疾病治疗的研究。
T13703	Gestonorone Capronate	Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation
	Gestonorone Capronate 是一种孕激素，在良性前列腺肥大和子宫内膜癌领域有研究价值。
T35182	Xinidamine BRN 0891979,Xinidaminum,Xinidamino
	Xinidamine (BRN 0891979) 具有抗肿瘤活性，可用于研究良性前列腺增生、黄斑变性和前列腺上皮内瘤。Xinidamine 对PWR-1E 细胞的增殖具有抑制作用，IC50为4μM。
T22316	Doxazosin UK 33274,多沙唑嗪	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Doxazosin (UK 33274) 是选择性的拮抗突触后的α1肾上腺素受体。
T27798	Lapisteride CS891B,CS-891,CS-891B,CS891	Others	Others
	Lapisteride (CS-891) 一种类固醇5α-还原酶抑制剂，可用于治疗良性前列腺增生(BPH)和雄激素性脱发，可有效预防或治疗AGA 。
T15688	L-771688 SNAP 6383	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	L-771688（SNAP 6383）是一种新型有效和选择性的 α1A-肾上腺素受体拮抗剂， Ki 值为 0.43±0.02 nM。L-771688 KE 用于治疗良性前列腺增生。
T83965	Tamsolusin Hydrochloride YM 12617,LY-253352	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Tamsolusin Hydrochloride (YM 12617) 是一种高选择性α-1A肾上腺素受体拮抗剂，可用于治疗良性前列腺肥大。
T28922	Taprizosin Taprizosin Mesylate,UK-338003,UK-338,003,UK338003,UK 338003	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Taprizosin（UK-338003）是一种具有选择性和口服活性的 α1-肾上腺素受体 (α1-adrenoceptor) 拮抗剂，可用于舒张血管，用于治疗良性前列腺增生症。
T1499	Dutasteride GG 745,Avodart,度他雄胺,GI 198745	Apoptosis; Reductase	Apoptosis; Endocrinology/Hormones; Metabolism
	Dutasteride (GI 198745) 是一种 5α 还原酶同工酶抑制剂，还可能因其结构域 DHT 相似对雄激素受体产生脱靶效应。
T22232	Alfuzosin
	Alfuzosin 是选择性和竞争性的α1肾上腺素受体拮抗剂，可用于良性前列腺增生（BPH）的研究。
T11286	Fiduxosin A 185980.1,ABT 980	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Fiduxosin 是一种具有选择性和有效性的 α1-adrenoceptor 拮抗剂，对 α1a-adrenoceptor，α1b-adrenoceptor 和 α1d-adrenoceptor 有抑制作用，Ki 值分别为 0.160 nM，24.9 nM 和 0.920 nM。Fiduxosin 可用于治疗良性前列腺增生。
T0272	Nilutamide 尼鲁米特,RU23908	Androgen Receptor	Endocrinology/Hormones
	Nilutamide (RU23908) 是一种非甾体抗雄激素药物，有用于转移性前列腺癌的潜力。
T0210L	Tamsulosin LY253351 free base,HSDB7744,(R)-(-)-YM12617 free base,Harnal-D,Flowmax,HSDB 7744,HSDB-7744	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Tamsulosin ((R)-(-)-YM12617 free base) 是一种肾上腺素能受体α 1A 拮抗剂，用于良性前列腺增生(BPH)的治疗。Tansulosin 用于治疗排尿困难，这是前列腺肥大的一种常见症状。Tansulosin 和其他被称为α受体阻滞剂的药物通过放松膀胱颈部肌肉和前列腺本身的肌肉纤维来发挥作用，使其更容易排尿。
T20681	Estramustine NSC-89201,NSC 89201,LEO 275,LEO275,雌莫司汀,NSC89201,LEO-275	Microtubule Associated	Cytoskeletal Signaling
	Estramustine (LEO-275) 是一种与雌二醇相连的氮芥，通常为磷酸盐。它已被用于治疗前列腺肿瘤；还具有防辐射功能。它被前列腺细胞选择性吸收，并通过干扰微管动力学和降低血浆睾酮水平发挥抗肿瘤作用。
T1050	Prazosin hydrochloride Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress	Potassium Channel; MRP; Adrenergic Receptor; ABC; Autophagy	Autophagy; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience
	Prazosin hydrochloride (Vasoflex) 是一种选择性肾上腺素能 α-1 拮抗剂，可降低外周阻力并放松血管平滑肌。它可用于研究高血压和酒精使用障碍。它是一种合成哌嗪衍生物，具有降压抗肾上腺素能特性。它抑制有机阳离子转运蛋白 OCT-1 和 OCT-3，IC50分别为 1.8 和 13 μM 。
T70396	Fexapotide triflutate
	Fexapotide triflutate is a caspase and TNF signaling pathway activator used to treat benign prostatic hyperplasia (BPH).
T11220	ER21355	Others	Others
	ER21355, utilized for the treatment of prostatic diseases, acts as a phosphodiesterase 5 (PDE5) inhibitor.
T28956	TF-505 FR-146687,FK-687,TF 505,FK687
	TF-505, a steroid 5α-reductase inhibitor, is used potentially for the treatment of benign prostatic hyperplasia.
T32029	GYKI-16084 GYKI 16084
	GYKI-16084 is a postsynaptic alpha2 receptor blocker with potential efficacy in the treatment of benign prostatic hyperplasia.
T20024	Tadalafil, (6R ,12aS)- Tadalafil (6R ,12aS)- Lilly,Tadalafil specified impurity A,(-)-Tadalafil (6R ,12aS) diastereomer
	Tadalafil is a carboline derivative and Phosphodiesterase 5 Inhibitor. It is used primarily to treat Erectile dysfunction, Benign Prostatic Hyperplasia, and Primary Pulmonary Hypertension.
T33826	Osaterone
	Osaterone is effective against prostatic hyperplasia in dogs.
T31681	Estradiol undecylate AI352642,AI3-52642,AI3 52642
	Estradiol undecylate can be used in the treatment of prostatic cancer.
T4451L	Estramustine phosphate LS 299,NSC 89199,NSC-89199,LS-299,LS299
	Estramustine phosphate can be used to treat prostatic neoplasms; also has radiation protective properties.
T24378	L-771688 dihydrochloride L 771688 dihydrochloride
	L-771688 is an α1A-adrenoceptor antagonist potentially for the treatment of benign prostatic hyperplasia.
T10780	CGP-53153	Others	Others
	CGP-53153 is a steroidal inhibitor of 5 alpha-reductase (IC50s: 36 and 262 nM in rat and human prostatic tissue).
T3290L	Pikamilone Sodium GABA-NG,Nicotinoyl-GABA sodium salt,GABA NG,GABANG,Pikamilone Na
	Pikamilone Sodium is a prodrug of GABA used for therapy of neurogenic bladder in spinal and benign prostatic hyperplasia.
T69927	Fiduxosin hydrochloride
	Fiduxosin hydrochloride is an alpha 1a-adrenoceptor antagonist that may be useful in the treatment of Benign Prostatic Hyperplasia.
T21016	Cyproterone BAY 94-8367,Ciproterone,Androcur,SH 80881
	Cyproterone, an anti-androgen, is used in combination with estrogen for the therapy of hirsutism and severe acne in females and as a palliative in prostatic carcinoma.
T10273	AhR modulator-1	Others	Others
	AhR modulator-1 is a selective and orally active aryl hydrocarbon receptor (AhR) modulator. It inhibits metastasis, in part, by inhibiting prostatic VEGF production prior to tumor formation. It also possesses anti-estrogenic properties in rat uterus.
T61729	Terazosin
	Terazosin, a quinazoline derivative, is an orally active and competitive antagonist of α1-adrenoceptors. Its mechanism of action involves relaxing blood vessels and promoting bladder opening. Terazosin exhibits therapeutic potential for treating benign prostatic hyperplasia (BPH) and high blood pressure [1][2][3].
T78945	WCA-814	Androgen Receptor	Endocrinology/Hormones
	WCA-814是雄激素受体(AR)拮抗剂与Hsp90抑制剂的融合化合物，能够诱导全长AR及AR-V7降解，并展现出对前列腺癌细胞的细胞毒性(IC50: LNCaP细胞为171.2 nM，22Rv1细胞为26.5 nM)。
TP1094	TAK-448 MVT-602
	TAK-448 (MVT-602) is a potent and full KISS1R agonist with an IC50 of 460 pM and an EC50 of 632 pM.TAK-448 has been used in trials studying the treatment of Prostate Cancer, Low Testosterone, Prostatic Neoplasms, and Hypogonadotropic Hypogonadism.
T28245	ONO-0300302 ONO 0300302
	ONO-0300302 is a slow tight binding LPA1 antagonist (IC50: 0.16 nM) used to treat Benign Prostatic Hyperplasia. ONO-0300302 inhibits significantly an LPA-induced increase of intraurethral pressure (IUP) in rat (3 mg/kg, p.o.) and dog (1 mg/kg, p.o.) over
T76430	GR 87389
	GR 87389 是一种有效的NK2受体拮抗剂。GR 87389 以竞争性方式拮抗 GA 64349 诱导的人类逼尿肌、前列腺和前列腺尿道平滑肌条收缩。
T9660	Bexlosteride
	Bexlosteride (LY300502) 是一种苯并喹啉酮类人 I 型 5α-还原酶抑制剂。Bexlosteride 在 LNCaP 细胞培养物中显示出代谢抑制、抗增殖和抗分泌作用。Bexlosteride 可用于前列腺癌的研究。
T76275	Fexapotide
	Fexapotide (NX-1207 free acid) 在细胞水平上通过选择性诱导细胞凋亡，降低前列腺体积。它主要用于研究下尿路症状(LUTS)与良性前列腺增生(BPH)。
T75377	Thymolphthalein monophosphate disodium hydrate
	Thymolphthalein monophosphate disodium hydrate 是用于测定酸性及碱性磷酸酶显色底物。反应过程中释放的百里酚酞可增加介质pH，促使颜色产生并终止水解作用，特别适合于血清中前列腺磷酸酶的特异性检测。
T69618	XR3054
	XR3054 is a novel inhibitor of farnesyl protein transferase (FPTase). XR3054 inhibited the proliferation of the prostatic cancer cell lines LnCAP and PC3 and the colon carcinoma SW480 and HT1080 (IC50 values of 12.4, 12.2, 21.4 and 8.8 microM, respectively) but was relatively inactive when tested against a panel of breast carcinoma cell lines. The activity did not relate to the presence of mutant or wild-type ras in the cell lines tested. In conclusion XR3054 inhibits ras farnesylation, MAP kina...
T21668	Finasteride acetate
	Finasteride (MK-906) acetate 是一种高效的5α-还原酶 (5α-reductase) 竞争性抑制剂，其对 II 型 5α-还原酶的IC50值仅为 4.2 nM，其对该型酶的亲和力是对 I 型酶亲和力的约100倍。因此，Finasteride acetate 主要在良性前列腺增生症 (BPH) 和雄激素性脱发研究领域中应用。

化合物

Cat.No: T81550

Synonym: Prostatic Acid Phosphatase(248-286)

Cat.No: T0488

Synonym: 非那雄胺,MK-906

Target: Reductase

Cat.No: T0696

Synonym: KT-611,萘哌地尔,BM-15275

Target: Adrenergic Receptor

Alfuzosin hydrochloride

Cat.No: T0091

Synonym: SL 77499-10,Alfuzosin HCl,盐酸阿夫唑嗪

Target: Adrenergic Receptor

Cat.No: T1504

Synonym: 西洛多辛,KAD 3213,KMD 3213

Target: Adrenergic Receptor

Terazosin hydrochloride

Cat.No: T0197

Synonym: 盐酸特拉唑嗪,Terazosin HCl,Terazosine,Blavin,Hytrin,Zayasel,Fosfomic

Target: Adrenergic Receptor

Naftopidil dihydrochloride

Cat.No: T6600

Synonym: KT-611,KT-611 2HCl,盐酸萘哌地尔,Naftopidil DiHCl

Target: 5-HT Receptor, Adrenergic Receptor

Terazosin hydrochloride dihydrate

Cat.No: T6701

Synonym: Flotrin dihydrate,Terazosin HCl Dihydrate,Dysalfa dihydrate,Heitrin dihydrate,盐酸特拉唑嗪(二水合物)

Target: Adrenergic Receptor

Naftopidil hydrochloride

Cat.No: T9220

Synonym: 1-[4-(2-methoxyphenyl)piperazin-1-yl]-3-,萘哌地尔盐酸盐,KT-611 hydrochloride,BM-15275 hydrochloride

Target: Adrenergic Receptor

Cat.No: T14843

Synonym: BX341

Target: Androgen Receptor

Cat.No: T11220L

Synonym: hydrochloride(150452-18-9 Free base),1-[4-(1,3-Benzodioxol-5a-ylmethylamino)-6-chloroquinazolin-2-yl]piperidine-4-carboxylic acid;hydrochloride(150452-18-9 Free base),1-[4-(1,3-Benzodioxol-5a-ylmethylamino)-6-chloroquinazolin-2-yl]piperidine-4-carboxylic acid

Target: PDE

Gestonorone Capronate

Cat.No: T13703

Target: Prostaglandin Receptor

Cat.No: T35182

Synonym: BRN 0891979,Xinidaminum,Xinidamino

Cat.No: T22316

Synonym: UK 33274,多沙唑嗪

Target: Adrenergic Receptor

Cat.No: T27798

Synonym: CS891B,CS-891,CS-891B,CS891

Target: Others

Cat.No: T15688

Synonym: SNAP 6383

Target: Adrenergic Receptor

Tamsolusin Hydrochloride

Cat.No: T83965

Synonym: YM 12617,LY-253352

Target: Adrenergic Receptor

Cat.No: T28922

Synonym: Taprizosin Mesylate,UK-338003,UK-338,003,UK338003,UK 338003

Target: Adrenergic Receptor

Cat.No: T1499

Synonym: GG 745,Avodart,度他雄胺,GI 198745

Target: Apoptosis, Reductase

Cat.No: T22232

Cat.No: T11286

Synonym: A 185980.1,ABT 980

Target: Adrenergic Receptor

Cat.No: T0272

Synonym: 尼鲁米特,RU23908

Target: Androgen Receptor

Cat.No: T0210L

Synonym: LY253351 free base,HSDB7744,(R)-(-)-YM12617 free base,Harnal-D,Flowmax,HSDB 7744,HSDB-7744

Target: Adrenergic Receptor

Cat.No: T20681

Synonym: NSC-89201,NSC 89201,LEO 275,LEO275,雌莫司汀,NSC89201,LEO-275

Target: Microtubule Associated

Prazosin hydrochloride

Cat.No: T1050

Synonym: Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress

Target: Potassium Channel, MRP, Adrenergic Receptor, ABC, Autophagy

Fexapotide triflutate

Cat.No: T70396

Cat.No: T11220

Target: Others

Cat.No: T28956

Synonym: FR-146687,FK-687,TF 505,FK687

Cat.No: T32029

Synonym: GYKI 16084

Tadalafil, (6R ,12aS)-

Cat.No: T20024

Synonym: Tadalafil (6R ,12aS)- Lilly,Tadalafil specified impurity A,(-)-Tadalafil (6R ,12aS) diastereomer

Cat.No: T33826

Estradiol undecylate

Cat.No: T31681

Synonym: AI352642,AI3-52642,AI3 52642

Estramustine phosphate

Cat.No: T4451L

Synonym: LS 299,NSC 89199,NSC-89199,LS-299,LS299

L-771688 dihydrochloride

Cat.No: T24378

Synonym: L 771688 dihydrochloride

Cat.No: T10780

Target: Others

Pikamilone Sodium

Cat.No: T3290L

Synonym: GABA-NG,Nicotinoyl-GABA sodium salt,GABA NG,GABANG,Pikamilone Na

Fiduxosin hydrochloride

Cat.No: T69927

Cat.No: T21016

Synonym: BAY 94-8367,Ciproterone,Androcur,SH 80881

AhR modulator-1

Cat.No: T10273

Target: Others

Cat.No: T61729

Cat.No: T78945

Target: Androgen Receptor

Cat.No: TP1094

Synonym: MVT-602

Cat.No: T28245

Synonym: ONO 0300302

Cat.No: T76430

Cat.No: T9660

Cat.No: T76275

Thymolphthalein monophosphate disodium hydrate

Cat.No: T75377

Cat.No: T69618

Finasteride acetate

Cat.No: T21668

Cat. No.	Product Name	Target	Signaling Pathways
T41288	Myristoleic acid cis-9-tetradecenoic acid,肉豆蔻酸,9-Tetradecenoic acid,(Z)-Tetradec-9-enoic acid	Apoptosis	Apoptosis
	Myristoleic acid (9-Tetradecenoic acid) 是 Serenoa repens 提取物中的一种细胞毒性成分。Myristoleic acid 诱导人前列腺 LNCaP 细胞凋亡和坏死。
TN5031	Sitostenone 豆甾-4-烯-3-酮	Others	Others
	Sitostenone 具有抗氧化活性。 Stigmasta-4-en-3-one(Sitostenone)可用于治疗雄激素依赖性疾病，尤其是治疗良性前列腺增生。
T19687	Phenylethyl isothiocyanate JC 5411,2-苯基乙基异硫代氰酸酯,JC5411,JC-5411	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	Phenylethyl isothiocyanate (JC5411) 是一种 HDAC 抑制剂。它有可能用于治疗良性前列腺肥大。
TCS1372	Atraric acid	Phosphatase; Androgen Receptor	Endocrinology/Hormones; Metabolism
	Atraric acid 衍生物作为一种新的化学先导结构，用于作为 AR 拮抗剂的新型治疗化合物，可用于预防或治疗前列腺疾病。它以剂量依赖性方式抑制 PTP1B 活性，IC50 值为 51.5 uM，表明阿特拉酸具有治疗糖尿病的潜力。
T0256	Citric acid trilithium salt tetrahydrate Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate	Dehydrogenase; GSK-3; HIF/HIF Prolyl-Hydroxylase; Antibacterial; GluR	Chromatin/Epigenetic; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells
	Citric acid trilithium salt tetrahydrate (Lithium citrate tribasic tetrahydrate) 是一种用于治疗精神疾病的药物。它也是一种医药和建筑材料, 可用于氨基酸定量分析时的梯度洗脱。
TN1061	Ganoderol B	Androgen Receptor	Endocrinology/Hormones
	Ganoderol B is a potent β ±-glucosidase and angiotensin-converting enzyme inhibitor, with an IC(50) of β ±-glucosidase is 119.8 uM. It may be useful in prostate cancer and benign prostatic hyperplasia (BPH) therapy through suppressing the function of andr
TN4164	Grandifloroside	TNF	Apoptosis
	Grandifloroside shows good antioxidative and potent anti-inflammatory activities, it also exhibits potent inhibitory activity against TNF-α and 5α-reductase, suggests that it might be developed as a source of potent anti-oxidative and anti-inflammatory ag
TN6198	Mahanine
	Mahanine has effects on the activation of the apoptotic pathway in human leukemia U937 cells, causes the mitochondrial membranes to lose their permeability, resulting in caspase-3 activation and apoptosis. Mahanine can reverse an epigenetically silenced g

天然产物

Myristoleic acid

Cat.No: T41288

Synonym: cis-9-tetradecenoic acid,肉豆蔻酸,9-Tetradecenoic acid,(Z)-Tetradec-9-enoic acid

Target: Apoptosis

Cat.No: TN5031

Synonym: 豆甾-4-烯-3-酮

Target: Others

Phenylethyl isothiocyanate

Cat.No: T19687

Synonym: JC 5411,2-苯基乙基异硫代氰酸酯,JC5411,JC-5411

Target: HDAC

Cat.No: TCS1372

Target: Phosphatase, Androgen Receptor

Citric acid trilithium salt tetrahydrate

Cat.No: T0256

Synonym: Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate

Target: Dehydrogenase, GSK-3, HIF/HIF Prolyl-Hydroxylase, Antibacterial, GluR

Cat.No: TN1061

Target: Androgen Receptor

Grandifloroside

Cat.No: TN4164

Target: TNF

Cat.No: TN6198

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