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50

抑制剂 & 化合物

11

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T60006	Aromatase inhibitor 23	Others	Others
	Aromatase inhibitor 23 是一种针对 RAD51 重组酶家族中蛋白质-蛋白质相互作用的抑制剂。
T60022	Aromatase-IN-2	Others	Others
	Aromatase-IN-2 具有抗炎、抗肿瘤和平喘作用。
T61444	Nonsteroidal aromatase inhibitor 1
	Nonsteroidal aromatase inhibitor 1 (Compound 13h) effectively inhibits the enzyme CYP19A1 with an IC50 value of 0.09 nM. Due to its potent inhibitory activity, Nonsteroidal aromatase inhibitor 1 holds promise for research in the field of breast cancer [1].
T7197	Fadrozole	Aromatase	Endocrinology/Hormones
	Fadrozole 是一种有效的、非甾体类的、选择性的芳香化酶抑制剂(IC50:6.4 nM)。
T61463	Monoamine oxidase/Aromatase-IN-1
	Monoamine oxidase/Aromatase-IN-1 (compound 2q) is a potent dual inhibitor of monoamine oxidase (MAO) and aromatase, with IC50 values of 39 nM and 31 nM for MAO-B and aromatase, respectively. It holds significant potential for research in neurological disorders and breast cancer [1].
T11991	Mefentrifluconazole	P450; Antifungal	Metabolism; Microbiology/Virology
	Mefentrifluconazole 是一种有效的、选择性的和具有口服活性的真菌 CYP51 (Kd= 0.5 nM) 抑制剂，但对人芳香酶的抑制活性较低，IC50值为0.92 μM。它是一种新型唑类衍生物，用作农用广谱抗真菌剂。
T0393	Anastrozole 阿那曲唑,ZD1033	Aromatase	Endocrinology/Hormones
	Anastrozole (ZD1033) 是芳香酶的选择性抑制剂，能够抑制胎盘芳香化酶(IC50:15 nM)。
T7556	Fadrozole hydrochloride CGS 16949A,盐酸法倔唑	Aromatase	Endocrinology/Hormones
	Fadrozole hydrochloride (CGS 16949A) 是一种选择性的、有效，和非甾体类的芳香化酶抑制剂(IC50:6.4 nM)。
T1103	Aminoglutethimide DL-Aminoglutethimide,氨鲁米特,BA-16038,NSC-330915	Aromatase	Endocrinology/Hormones
	Aminoglutethimide (BA-16038) 是一种芳香酶抑制剂，IC50=10 μM，用于治疗晚期 BREAST Y。
T20625	Prochloraz 咪鲜胺,Sporgon,Prelude	Estrogen Receptor/ERR; AhR; Androgen Receptor; Antifungal	Endocrinology/Hormones; Immunology/Inflammation; Metabolism; Microbiology/Virology
	Prochloraz (Prelude) 是咪唑类抗真菌剂。Prochloraz 抑制羊毛甾醇的细胞色素 P450 依赖性 14α-脱甲基作用，由此抑制麦角固醇的生物合成，从而导致真菌细胞膜破裂和细胞死亡。它也是雌激素受体和雄激素受体的拮抗剂，IC50分别为25 μM 和4 μM，并激活芳烃受体，EC50为1μM。
T1587	Exemestane EXE,依西美坦,FCE 24304,PNU155971	Aromatase	Endocrinology/Hormones
	Exemestane (EXE) 是一种选择性的、具有口服活性的、不可逆的甾体芳香酶抑制剂，能够作用于人胎盘芳香酶 (IC50:30 nM) 和大鼠卵巢芳香酶 (IC50:40 nM)，可用于研究激素依赖性乳腺癌。
T4281	Endoxifen (E/Z)-N-desmethyl-4-hydroxy Tamoxifen,N-去甲基-4-羟基-,(E/Z)-Endoxifen	Estrogen Receptor/ERR; Aromatase; Estrogen/progestogen Receptor; Parasite; Drug Metabolite	Endocrinology/Hormones; Metabolism; Microbiology/Virology
	Endoxifen ((E/Z)-Endoxifen) 是 Tamoxifen 的关键活性代谢物，能抑制芳香酶的活性，与雌激素受体有较高的亲和力和特异性。它有潜力研究乳腺癌。
T71708	Minamestane	Aromatase	Endocrinology/Hormones
	Minamestane 是一种新型不可逆芳香化酶抑制剂。Minamestane 引起人胎盘芳香化酶的时间依赖性抑制，半衰期为4分钟，K 为59nM。Minamestane 具有抗肿瘤活性。
T27320	Finrozole MPV 2213ad,MPV-2213ad,MPV 2213,MPV-2213,MPV2213ad	Aromatase	Endocrinology/Hormones
	Finrozole (MPV 2213ad) 是一种新型选择性芳香化酶抑制剂，对于乳房发育是部分可逆的。
T23549	YM 511	P450; Aromatase	Endocrinology/Hormones; Metabolism
	YM 511 是一种高度特异性的非甾体芳香酶 (aromatase) 抑制剂。YM 511 竞争性抑制大鼠卵巢和人胎盘微粒体中的芳香酶活性 (IC50 分别为 0.4 和 0.12 nM)。YM 511 轻微抑制其他类固醇激素的产生。YM 511 具有用于抑制雌激素依赖性作用研究，不会影响其他类固醇激素的血清水平的潜力。
T2280	Endoxifen (Z-isomer) Z-因多昔芬,Endoxifen Z-isomer,4-[(1E)-1-{4-[2-(甲基氨基)乙氧基]苯基}-2-苯基-1-丁烯-1-基]苯酚	Estrogen Receptor/ERR; EGFR; Potassium Channel; Estrogen/progestogen Receptor; HER	Angiogenesis; Endocrinology/Hormones; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
	Endoxifen Z-isomer (EDX)是 Tamoxifen 重要的代谢产物,在表达 ERα的乳腺癌细胞中发挥抗雌激素作用。它以浓度依赖的方式抑制 hERG, IC50值为1.6μM。
T72310	Antibacterial agent 132	Antifungal	Microbiology/Virology
	Antibacterial agent 132 对 C. parapsilosis (ATCC 22019) 和 C. krusei (ATCC 6258) 实验中显示出抗菌作用，MIC90 值分别为 <0.06 μg/mL 和 62.50 μg/mL。Antibacterial agent 132 对芳香化酶 (aromatase enzyme)具有抑制作用，IC50 为 0.047μM。
T27918	LY 43578 LY-43578,LY43578	P450; Aromatase	Endocrinology/Hormones; Metabolism
	LY 43578 是一种具有口服活性的芳香酶 (aromatase) 抑制剂。LY 43578 对大鼠肝微粒体 P-450依赖的 p-nitroanisole 的 O -去甲基化和 ethylmorphine 的 N -去甲基化有抑制作用，IC50 分别为 0.3 和 5 μΜ。LY 43578 可用于研究神经系统疾病和心血管疾病。
T26322	Vorozole R83839,R 83839,R-83839,(+)-Vorozole,R83842	P450; Aromatase	Endocrinology/Hormones; Metabolism
	Vorozole (R83842) 是一种具有口服活性、有效性和选择性的非甾体芳香酶抑制剂。Vorozole 在体内表现出抗肿瘤活性，可用于研究乳腺癌。
T26322L	(-)-Vorozole (-)-Vorozole(Isomer-129731-10-8)	P450; Aromatase	Endocrinology/Hormones; Metabolism
	(-)-Vorozole 是一种具有口服活性的非甾体芳香酶抑制剂,具有有效性和选择性。(-)-Vorozole在体内实验中表现出抗肿瘤活性。(-)-Vorozole 可用于研究乳腺癌。
T6827L	Endoxifen hydrochloride
	Endoxifen hydrochloride，Tamoxifen的主要活性代谢产物，具备较高的对雌激素受体(estrogen receptor)的亲和力和特异性，并能抑制芳香酶活性。它在乳腺癌研究中表现出潜在应用价值。
T11847L	Liarozole R75251 dihydrochloride,利阿唑	P450; Retinoid Receptor	Metabolism
	Liarozole (R75251 dihydrochloride) 是一种咪唑衍生物，是一种具有口服活性的维甲酸 (RA) 代谢阻断剂(RAMBA)，具有抗肿瘤作用。它能够抑制维甲酸依赖的细胞色素P450(CYP26) 4- 羟基化 (IC50=7 μM)，导致组织维甲酸水平增加。
T70558	Org 33201
	Org 33201 is a potent aromatase inhibitor.
T27868	LY 113174 LY-113174,LY113174
	LY 113174, a novel nonsteroidal aromatase inhibitor, may prove useful in the treatment of estrogen-dependent diseases.
T71897	Vatalanib succinate
	Vatalanib succinate is a VEGFR, PDGFR-β, c-Kit, c-Fms, and aromatase inhibitor.
T27369	FR 901537 FR901537,FR-901537
	FR 901537 is a new aromatase inhibitor with antitumor effects.
T70404	MPV-2213AD
	MPV-2213AD is an aromatase inhibitor.
T20683	Letrozole related compound B Letrozole specified impurity A
	Letrozole related compound B is an impurity of aromatase inhibitor.
T71410	Cgs 18320B
	Cgs 18320B is a non-steroidal aromatase inhibitor
T7197L	Fadrozole HCl hydrate Fadrozole,CGS-16949A,Fadrozole hydrochloride hemihydrate,CGS16949A,CGS 16949A
	Fadrozole is a selective inhibitor of aromatase. It also effective in the treatment of estrogen-dependent diseases including breast cancer.
T27922	LY 56110 LY56110,LY-56110
	LY 56110 is a novel nonsteroidal aromatase inhibitor.
T25716	Liarozole fumarate Liazal,R85246,R-85246,R 85246
	Liarozole fumarate is used as a retinoic acid metabolism blocking agent (RAMBA) and an aromatase inhibitor.
T12319	Org30958	Aromatase	Endocrinology/Hormones
	Org30958 is a potent inhibitor of aromatase in vivo.
T30837	Cgp 47645 Leflutrozole,Cgp-47645,Cgp47645
	CGP 47645 (Leflurozole) is an oral active non-steroidal aromatase inhibitor and antitumor agent with anti-tumor and endocrine effects.
T30834	Cgp 45688 Cgp45688,Cgp-45688
	CGP 45688 is an oral active non-steroidal aromatase inhibitor with anti-tumor and endocrine effects on rat breast tumors.
T61787	SYN20028567
	SYN20028567, an aromatase (CYP19) inhibitor, exhibits an IC50 value of 9.4 nM. It has potential applications in breast cancer research [1].
T81012	Testololactone
	Testololactone，一种芳香酶抑制剂，常用于乳腺癌研究。
T71073	Tan 931
	Tan 931 is a nonsteroidal aromatase inhibitor that was first isolated from the culture filtrate of a soil isolate fungus, No. 8974
T6060L	Anabasine HCl BB-NC-0036,CCG-38440,H-8174,AR-1H7273,ZX-BK000320,ST-24041653
	Anabasine HCl is used as a clinical biomarker for tobacco smoke exposure and as an insecticide. It is also a depolarizing NMJ blocker, aromatase inhibitor, nAChr antagonist, and teratogen found in species of Nicotiana.
T38424	(R)-Fadrozole FAD286,(R)-CGS 16949A free base,(R)-Fadrozole
	(R)-Fadrozole ((R)-CGS 16949A; FAD286) is a potent nonsteroidal inhibitor. (R)-Fadrozole also inhibits human placental aromatase (pIC 50 = 6.17) and aldosterone biosynthesis. (R)-Fadrozole reverses cardiac fibrosis in spontaneously hypertensive heart failure rats..
T71010	Norendoxifen
	Norendoxifen, also known as 4-hydroxy-N, N-didesmethyltamoxifen, is a nonsteroidal aromatase inhibitor of the triphenylethylene group that was never marketed. It is an active metabolite of the selective estrogen receptor modulator tamoxifen.
T80057	Cytochrome P450 reductase
	Cytochrome P450reductase，一种NADPH-细胞色素还原酶，发挥作用于促进芳香酶构象，以最适合底物结合。
T61919	Anticancer agent 78
	Anticancer agent 78 具有抗芳香酶活性（IC50= 0.9 μM）。Anticancer agent 78 是一种有效的抗癌剂，显示细胞毒性。Anticancer agent 78 在乳腺癌中有研究潜力。
T35676	17β-hydroxy Exemestane
	17β-hydroxy Exemestane is the primary active metabolite of exemestane . It is formed by metabolism of exemestane by the cytochrome P450 (CYP) isoforms CYP1A and CYP4A11. 17β-hydroxy Exemestane is an aromatase inhibitor (IC50 = 69 nM using human placental microsomes) and an androgen receptor (AR) agonist (IC50 = 39.6 nM) that is selective for AR over estrogen receptor α (ERα; IC50 = 21.2 μM). It stimulates growth of AR- and ERα-positive MCF-7 (EC50 = 2.7 μM) and T47D breast cancer cells (EC50s = ...
T11847	Liarozole dihydrochloride R75251 dihydrochloride	Others	Others
	Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an imidazole derivative; it is being investigated as a non-hormonal agent in prostate cancer and in the treatment of various other cancers and skin disorders.
T37560	Nidulin
	Nidulin is a depsidone originally isolated from A. nidulans. It is active against the bacteria M. tuberculosis and M. ranoe, as well as the fungi T. tonsurans and M. audouini. It also inhibits the growth of methicillin-resistant S. aureus (MRSA; MIC = 4 μg/ml) and has larvicidal activity toward Artemia (LC50 = 2.8 μg/ml). Nidulin is cytotoxic to MOLT-3 cells (IC50 = 21.2 μM) but not HuCCA-1, HepG2, or A549 cells (IC50s = >112.7 μM). It inhibits aromatase with an IC50 value of 11.2 μM.
T25716L	Liarozole HCl R75251,Liarozole hydrochloride,R 75251,R-75251
	Liarozole HCl is a benzimidazole derivative with antineoplastic activity. As a retinoic acid metabolism blocking agent, liarozole inhibits CYP450-dependent all-trans-retinoic acid (ATRA)-4-hydroxylase, leading to an increase in endogenous ATRA production,
T83907	10-Chloroestra-1,4-diene-3,17-dione 10-chloro-1,4-Estradiene
	10-Chloroestra-1,4-diene-3,17-dione 是一个对雌性激素受体α (ERα) 具有激动作用的类固醇。它能增加在S. cerevisiae 中报告基因的表达（对人类受体的EC50 = 0.36 nM）。同时，它也是一种芳香化酶抑制剂（IC50 = 2.4 µM）。
T78590	Dibenzylfluorescein DBF
	Dibenzylfluorescein（DBF）是一款荧光探针，作为细胞色素P450（CYP）亚型，包括CYP3A4、CYP2C8、CYP2C9、CYP2C19和CYP19的特异性底物，常在Km值0.87-1.9 µM（Ex=485nm，Em=535nm）范围内应用。该探针主要用于监测药物或疾病导致的CYP催化活性变化。
T71578	Endoxifen mesylate
	Endoxifen, also known as N-desmethyl-4-hydroxytamoxifen, is a chemical that is under development for estrogen receptor-positive breast cancer. It is also being evaluated as an antipsychotic for treatment of mania and other psychotic disorders. Endoxifen is a nonsteroidal selective estrogen receptor modulator (SERM) of the triphenylethylene group. It is an active metabolite of tamoxifen and has been found to be effective in patients that have failed previous hormonal therapies (tamoxifen, aromat...

化合物

Aromatase inhibitor 23

Cat.No: T60006

Target: Others

Aromatase-IN-2

Cat.No: T60022

Target: Others

Nonsteroidal aromatase inhibitor 1

Cat.No: T61444

Cat.No: T7197

Target: Aromatase

Monoamine oxidase/Aromatase-IN-1

Cat.No: T61463

Mefentrifluconazole

Cat.No: T11991

Target: P450, Antifungal

Cat.No: T0393

Synonym: 阿那曲唑,ZD1033

Target: Aromatase

Fadrozole hydrochloride

Cat.No: T7556

Synonym: CGS 16949A,盐酸法倔唑

Target: Aromatase

Aminoglutethimide

Cat.No: T1103

Synonym: DL-Aminoglutethimide,氨鲁米特,BA-16038,NSC-330915

Target: Aromatase

Cat.No: T20625

Synonym: 咪鲜胺,Sporgon,Prelude

Target: Estrogen Receptor/ERR, AhR, Androgen Receptor, Antifungal

Cat.No: T1587

Synonym: EXE,依西美坦,FCE 24304,PNU155971

Target: Aromatase

Cat.No: T4281

Synonym: (E/Z)-N-desmethyl-4-hydroxy Tamoxifen,N-去甲基-4-羟基-,(E/Z)-Endoxifen

Target: Estrogen Receptor/ERR, Aromatase, Estrogen/progestogen Receptor, Parasite, Drug Metabolite

Cat.No: T71708

Target: Aromatase

Cat.No: T27320

Synonym: MPV 2213ad,MPV-2213ad,MPV 2213,MPV-2213,MPV2213ad

Target: Aromatase

Cat.No: T23549

Target: P450, Aromatase

Endoxifen (Z-isomer)

Cat.No: T2280

Synonym: Z-因多昔芬,Endoxifen Z-isomer,4-[(1E)-1-{4-[2-(甲基氨基)乙氧基]苯基}-2-苯基-1-丁烯-1-基]苯酚

Target: Estrogen Receptor/ERR, EGFR, Potassium Channel, Estrogen/progestogen Receptor, HER

Antibacterial agent 132

Cat.No: T72310

Target: Antifungal

Cat.No: T27918

Synonym: LY-43578,LY43578

Target: P450, Aromatase

Cat.No: T26322

Synonym: R83839,R 83839,R-83839,(+)-Vorozole,R83842

Target: P450, Aromatase

Cat.No: T26322L

Synonym: (-)-Vorozole(Isomer-129731-10-8)

Target: P450, Aromatase

Endoxifen hydrochloride

Cat.No: T6827L

Cat.No: T11847L

Synonym: R75251 dihydrochloride,利阿唑

Target: P450, Retinoid Receptor

Cat.No: T70558

Cat.No: T27868

Synonym: LY-113174,LY113174

Vatalanib succinate

Cat.No: T71897

Cat.No: T27369

Synonym: FR901537,FR-901537

Cat.No: T70404

Letrozole related compound B

Cat.No: T20683

Synonym: Letrozole specified impurity A

Cat.No: T71410

Fadrozole HCl hydrate

Cat.No: T7197L

Synonym: Fadrozole,CGS-16949A,Fadrozole hydrochloride hemihydrate,CGS16949A,CGS 16949A

Cat.No: T27922

Synonym: LY56110,LY-56110

Liarozole fumarate

Cat.No: T25716

Synonym: Liazal,R85246,R-85246,R 85246

Cat.No: T12319

Target: Aromatase

Cat.No: T30837

Synonym: Leflutrozole,Cgp-47645,Cgp47645

Cat.No: T30834

Synonym: Cgp45688,Cgp-45688

Cat.No: T61787

Cat.No: T81012

Cat.No: T71073

Cat.No: T6060L

Synonym: BB-NC-0036,CCG-38440,H-8174,AR-1H7273,ZX-BK000320,ST-24041653

Cat.No: T38424

Synonym: FAD286,(R)-CGS 16949A free base,(R)-Fadrozole

Cat.No: T71010

Cytochrome P450 reductase

Cat.No: T80057

Anticancer agent 78

Cat.No: T61919

17β-hydroxy Exemestane

Cat.No: T35676

Liarozole dihydrochloride

Cat.No: T11847

Synonym: R75251 dihydrochloride

Target: Others

Cat.No: T37560

Cat.No: T25716L

Synonym: R75251,Liarozole hydrochloride,R 75251,R-75251

10-Chloroestra-1,4-diene-3,17-dione

Cat.No: T83907

Synonym: 10-chloro-1,4-Estradiene

Dibenzylfluorescein

Cat.No: T78590

Synonym: DBF

Endoxifen mesylate

Cat.No: T71578

Cat. No.	Product Name	Target	Signaling Pathways
T7999	7-Hydroxyflavanone	Anti-infection	Microbiology/Virology
	7-Hydroxyflavanone 对肺炎链球菌临床分离株显示出抗菌活性。
T1590	Letrozole CGS 20267,来曲唑	Aromatase; Autophagy	Autophagy; Endocrinology/Hormones
	Letrozole (CGS 20267) 是一种可口服的，选择性可逆的非甾体类芳香化酶抑制剂，IC50值为 11.5 nM。它选择性抑制雌激素的生物合成，可研究乳腺癌。
T6917	Oleuropein 洋橄榄苦甙,橄榄苦苷	Apoptosis; Aromatase; ROS; PPAR	Apoptosis; DNA Damage/DNA Repair; Endocrinology/Hormones; Immunology/Inflammation; Metabolism
	Oleuropein 在橄榄叶和油中发现的天然产物，通过 p53 依赖性途径以及 Bax 和 Bcl2基因的调控来诱导乳腺癌细胞凋亡，还抑制芳香化酶。它可通过直接抑制 PPARγ转录活性来发挥抗氧化，抗炎和抗动脉粥样硬化作用。
T2O2744	alpha-Naphthoflavone 苯并黄素；α-萘黄酮；7,8-苯并黄酮,7,8-benzoflavone,α-萘黄酮	Aromatase	Endocrinology/Hormones
	alpha-Naphthoflavone (7,8-benzoflavone) 是合成的黄酮类化合物，是一种竞争性芳香酶抑制剂，其IC50=0.5 μM，Ki=0.2 μM。
TN3987	Eriodictyol chalcone	Anti-infection; Aromatase	Endocrinology/Hormones; Microbiology/Virology
	Eriodictyol chalcone 具有抗芳香化酶和抗 17β-HSD 的活性。它对恶性疟原虫的生长具有抗疟原虫作用。
T0530	Flavanone 2-Phenyl-4-chromanone,4-Flavanone,2,3-Dihydroflavone,黄烷酮,2-Phenylchroman-4-one	Others; Aromatase	Endocrinology/Hormones; Others
	Flavanone (2-Phenylchroman-4-one) 是天然的黄酮类化合物，对人类雌激素合成酶芳香化酶具有抑制作用。
T3390	Obacunone	Apoptosis; Aromatase; p38 MAPK	Apoptosis; Endocrinology/Hormones; MAPK
	Obacunone 是从沼泽白葡萄柚种子中分离得到的，通过诱导凋亡发挥抗癌作用。它在雄激素依赖性人前列腺 Y 细胞中具有细胞毒性。它对鼠伤寒沙门氏菌具有抗毒作用，可作为开发鼠伤寒沙门氏菌抗毒策略的先导化合物。
T3899	Calceolarioside B Desrhamnosyl isoacteoside,木通苯乙醇苷 B,Nuomioside A,木通苯乙醇苷B	Aromatase	Endocrinology/Hormones
	Calceolarioside B (Desrhamnosyl isoacteoside) 是一种分离自Stauntonia hexaphylla 叶片中的天然产物。它抑制 DPPH 自由基清除活性(IC50:94.60 μM)。它显著抑制大鼠晶状体醛糖还原酶(RLAR)活性(C50:23.99 μM。
TN1674	Garcinone D 伽升沃 D	Reactive Oxygen Species; Nrf2; STAT	Immunology/Inflammation; JAK/STAT signaling; Metabolism; NF-κB; Stem Cells
	Garcinone D 是来自山竹的一种呫吨酮，可促进 C17.2 神经干细胞的增殖。它以浓度和时间依赖的方式增加磷酸化信号转导和转录激活因子 3 (p-STAT3)、Cyclin D1 和核因子红细胞 2 相关因子 (Nrf2)、以及血红素加氧酶-1 (HO-1) 的蛋白质水平。
TN4605	Myriceric acid B	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Myriceric acid B is a potent HIV-1 entry inhibitor targeting gp41 and can serve as a lead compound for developing novel anti-HIV-1 drug. Myriceric acid B scavenges DPPH free radicals with IC50 value of 21.8 uM, it inhibits aromatase activity with IC50 val
TN4307	Isolimonexic acid	BCL; Caspase; COX; p53	Apoptosis; Immunology/Inflammation; Neuroscience; Proteases/Proteasome
	Isolimonexic acid exhibits cytotoxicity on MCF-7 cell lines, it also inhibits Panc-28 cancer cell growth.

天然产物

7-Hydroxyflavanone

Cat.No: T7999

Target: Anti-infection

Cat.No: T1590

Synonym: CGS 20267,来曲唑

Target: Aromatase, Autophagy

Cat.No: T6917

Synonym: 洋橄榄苦甙,橄榄苦苷

Target: Apoptosis, Aromatase, ROS, PPAR

alpha-Naphthoflavone

Cat.No: T2O2744

Synonym: 苯并黄素；α-萘黄酮；7,8-苯并黄酮,7,8-benzoflavone,α-萘黄酮

Target: Aromatase

Eriodictyol chalcone

Cat.No: TN3987

Target: Anti-infection, Aromatase

Cat.No: T0530

Synonym: 2-Phenyl-4-chromanone,4-Flavanone,2,3-Dihydroflavone,黄烷酮,2-Phenylchroman-4-one

Target: Others, Aromatase

Cat.No: T3390

Target: Apoptosis, Aromatase, p38 MAPK

Calceolarioside B

Cat.No: T3899

Synonym: Desrhamnosyl isoacteoside,木通苯乙醇苷 B,Nuomioside A,木通苯乙醇苷B

Target: Aromatase

Cat.No: TN1674

Synonym: 伽升沃 D

Target: Reactive Oxygen Species, Nrf2, STAT

Myriceric acid B

Cat.No: TN4605

Target: HIV Protease

Isolimonexic acid

Cat.No: TN4307

Target: BCL, Caspase, COX, p53

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