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Search Results for " mcf-7 cells "

140

抑制剂 & 化合物

55

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T21806	HNHA	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	HNHA 是组蛋白去乙酰化酶抑制剂。它通过 p21诱导将细胞周期阻滞在 G1/S 期，抑制肿瘤生长及肿瘤新生血管形成。HNHA 可能是一种有效的抗乳腺癌药物。
T9244	σ1 Receptor antagonist-1	Sigma receptor	GPCR/G Protein
	σ1 Receptor antagonist-1 是高选择性的 sigma 1受体拮抗剂，pKi 为10.28。它抑制细胞生长，在 G0/G1 期阻滞细胞周期并诱导 MCF-7/ADR 细胞凋亡。
T6588	Mitoxantrone 米托蒽醌,mitozantrone	Topoisomerase; PKC	Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair
	Mitoxantrone (mitozantrone) 是一种拓扑异构酶 II 的抑制剂，也可抑制蛋白激酶C (PKC)，IC50值为8.5 μM。
T15249	Estrogen receptor modulator 1	Estrogen Receptor/ERR	Endocrinology/Hormones
	Estrogen receptor modulator 1 是一种有效的、具有口服活性的、选择性雌激素受体(estrogen receptor)调节剂 (SERM)，其 pIC50为 0.46。它能够诱导 Tamoxifen 耐药、激素非依赖性异种移植瘤的消退。
T2085	PQ401 IGF-1R Inhibitor II	Apoptosis; IGF-1R	Apoptosis; Tyrosine Kinase/Adaptors
	PQ401 (IGF-1R Inhibitor II) 是一种IGF-IR 抑制剂。在 MCF-7 细胞中，它抑制 IGF-I 刺激的 IGF-IR 自磷酸化，可有效抑制 IGF-I 刺激的 MCF-7 细胞生长。它诱导 caspase 介导的细胞凋亡，有用于乳腺癌和其他对 IGF-I 敏感的癌症的研究潜力。
T22288	(1E)-CFI-400437 dihydrochloride CFI-400437 dihydrochloride	PLK	Cell Cycle/Checkpoint
	(1E)-CFI-400437 dihydrochloride (CFI-400437 dihydrochloride) 是一种选择性和有效的 polo 样激酶 4 (PLK4) 抑制剂，IC50为 0.6 nM。它还抑制 Aurora A、 Aurora B、 KDR 和 FLT-3，IC50分别为 0.37、0.21、0.48 和 0.18 μM，具有抗增殖活性。
T5882	3-Bromopyruvic acid Hexokinase II Inhibitor II, 3-BP,3-溴丙酮酸,Bromopyruvic acid	Apoptosis; Hexokinase; Autophagy	Apoptosis; Autophagy; Metabolism
	3-Bromopyruvic acid (Hexokinase II Inhibitor II, 3-BP) 是己糖激酶 II 抑制剂，是针对肝癌细胞的一种抗肿瘤剂。
T0158	Mitoxantrone dihydrochloride 米托蒽醌二盐酸盐,盐酸米托蒽醌,Mitoxantrone 2HCl,Mitoxantrone hydrochloride,NSC-301739,mitozantrone dihydrochloride	Topoisomerase; PKC	Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair
	Mitoxantrone dihydrochloride (NSC-301739) 是一种拓扑异构酶 II 的抑制剂；也可抑制蛋白激酶C (PKC)，IC50值为8.5 μM。
T6010	Idarubicin hydrochloride 盐酸伊达比星,Idamycin,4-demethoxydaunorubicin (NSC256439, 4-DMDR) HCl,4-Demethoxydaunorubicin hydrochloride,Idarubicin HCl,伊达比星盐酸盐,Zavedos	Topoisomerase; Antibacterial; Autophagy; Antifungal	Autophagy; DNA Damage/DNA Repair; Microbiology/Virology
	Idarubicin hydrochloride (Zavedos) 是一种蒽环类抗白血病药物，能抑制细菌和酵母菌生长，还抑制拓扑异构酶 II，干扰 DNA 复制和 RNA 转录。
T72470	Estrone O-sulfamate Estrone 3-O-sulfamate	Others	Others
	Estrone O-sulfamate (Estrone 3-O-sulfamate) 是一种高效的的类固醇硫酸酯酶 (STS) 抑制剂。Estrone O-sulfamate 是一种胎盘微粒体抑制剂 (P.M.) ，IC50 值分别为 18 nM。Estrone O-sulfamate 在 MCF-7 细胞中对 STS 显示出抑制作用，IC50 值分别为 0.83 nM。Estrone O-sulfamate 可用于研究癌症。
T10325	ANI-7	Chk	Cell Cycle/Checkpoint
	ANI-7是芳香烃受体（AhR）途径的激活剂。ANI-7抑制多种癌症细胞的生长，并有效且选择性地抑制MCF-7乳腺癌症细胞的生长（GI50:0.56μM）。
T9541	CTB Cholera Toxin B subunit	Epigenetic Reader Domain	Chromatin/Epigenetic
	CTB (Cholera Toxin B subunit) 是一种 p300 组蛋白乙酰转移酶的激活剂，可诱导 MCF-7 细胞凋亡。
T64348	Antiproliferative agent-16 Antiproliferative agent-16	Others	Others
	Antiproliferative agent-16 (Antiproliferative agent-16)是一种具有抗癌活性的吲哚酰肼-腙化合物。 Antiproliferative agent-16 对乳腺癌细胞表现出特异性 (对 MCF-7 细胞的 IC50 为 6.94 μM)。
T36488	LYG-202 LYG202,LYG 202	Apoptosis; ROS	Apoptosis; Immunology/Inflammation
	LYG-202是一种具有哌嗪替代的新型类黄酮，在体内和体外都具有抗肿瘤作用。LYG-202 诱导 MCF-7、MDA-MB-231 和 MDA-MB-435 细胞凋亡，增加了细胞内 ROS 的产生。
T36970	STD1T	DUB	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
	STD1T 是一种具有选择性和有效性的脱泛素酶 USP2a 抑制剂，具有潜在的抗癌活性，可降低 HCT116 结肠和 MCF-7 乳腺癌细胞中的细胞周期蛋白 D1 蛋白水平。
T40233	(Iso)-MS4322 (Iso)-YS43-22,MS4322 (isomer),YS43-22 (isomer)	Histone Methyltransferase	Chromatin/Epigenetic
	(Iso)-MS4322 ((Iso)-YS43-22) 是一种具有选择性和强效性的蛋白质精氨酸甲基转移酶 5 (PRMT5) 降解剂，具有潜在的抗癌活性，有效地降低 MCF-7 细胞中的 PRMT5 蛋白水平，可抑制多种癌细胞的生长。
T28589	Ro 41-5253 Ro-41-5253,Ro 415253	Apoptosis; Retinoid Receptor	Apoptosis; Metabolism
	Ro 41-5253 是一种具有口服活性的 RARα 拮抗剂，是过氧化物酶体增殖物激活受体（PPAR）-γ 的配体和部分激动剂，具有抗肿瘤活性，抑制 MCF-7 和 ZR-75.1 雌激素受体阳性乳腺癌细胞的增殖并诱导细胞凋亡。
T83627	Pim-1 kinase inhibitor 8	Pim; PKC	Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling
	Pim-1 kinase inhibitor 8 是一种高效的 Pim-1 kinase 抑制剂，具有抗癌活性，可有效抑制细胞迁移。Pim-1 kinase inhibitor 8 对 MCF-7 和 HepG2 细胞有细胞毒性，是研究乳腺癌的候选化合物。
T77575	P-gb-IN-1	P-gp	Membrane transporter/Ion channel; Neuroscience
	P-gb-IN-1 是一种有效的 P-糖蛋白 (P-gp) 抑制剂，通过抑制 P-gp 外流展现出逆转活性。P-gb-IN-1 通过与残基 Asn 721 和 Met 986 形成氢键相互作用从而显示出对 P-gp 的抑制作用。P-gb-IN-1 在 MCF-7/ADR 细胞中显示出低毒性。
T7057	Methylstat	Histone Demethylase; Others	Chromatin/Epigenetic; Others
	Methylstat 是一种含有 Jumonji C 结构域的组蛋白去甲基化酶 (JMJD) 抑制剂的甲酯前药，具有良好的细胞渗透性。在体外试验中，methylstat 的游离酸可抑制 JMJD2A、JMJD2C、JMJD2E、PHF8 和 JMJD3，IC50 值分别约为 4.3、3.4、5.9、10 和 43 µM。 Methylstat 抑制 JMJD2C 敏感的食管癌细胞系 KYSE150 的生长，GI50 为 5.1 µM，而 methylstat 的游离酸在高达 100 µM 时不抑制细胞生长。 Methylstat 以浓度依赖性方式在多个位点诱导组蛋白高甲基化（KYSE150 细胞中 H3K4me3 和 H3K9me3 的 EC50 = 10.3 和 8.6 µM，MCF-7 细胞中的 EC50 分别为 6.7 和 6.3 µM）。
T1960	YL-109	AhR; Aryl Hydrocarbon Receptor	Immunology/Inflammation; Metabolism
	YL-109是一种抗肿瘤剂，可以通过芳烃受体 AhR 信号传导诱导 Hsp70 相互作用蛋白 (CHIP) 表达，具有抑制乳腺癌细胞生长和侵袭性的能力。
T2283	PX-12 2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12	Thioredoxin	Metabolism
	PX-12 (PX12) 是一种可逆的硫氧还蛋白-1(Trx-1)抑制剂，能够抑制 MCF-7 细胞(IC50:1.9 μM)和HT-29 细胞(IC50:2.9 μM)的生长。
T18981	DMA	Others	Others
	DMA 是一种荧光试剂 (λex=340 nm, λem=478 nm)。
T68147	T-900607	Microtubule Associated	Cytoskeletal Signaling
	T-900607是一种新型微管蛋白活性剂，通过独特的作用机制破坏微管聚合。t-900607具有心脏毒性。
T36696	DMBA
	7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.1,2It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adductsin vivo, and it has been commonly used to induce tumor formation in various rodent models.2,3,1DMBA increase...
T61899	VEGFR2-IN-1	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR2-IN-1 是一种具有选择性和高效性的 VEGFR2 抑制剂，具有抗肿瘤活性，可抑制细胞的增殖和迁移，可用于研究乳腺癌。
T4464	Irosustat 667-Coumate,BN83495,STX64	Others	Others
	Irosustat (667-Coumate) 是类固醇硫酸酯酶抑制剂(IC50:8 nM)，具有抗乳腺癌作用。
T72076	H2-Gamendazole	HSP	Cytoskeletal Signaling; Metabolism
	H2-Gamendazole 是一种抑制精子发生和癌症治疗的新型化合物，可作为热休克蛋白和/或延伸因子1 α的抑制剂，是 Hsp90调节剂。
T73582	EB1	MNK	MAPK
	EB1 是一种具有有效性和选择性的 MNK 激酶抑制剂，对 MNK1和 MNK2 具有抑制作用 IC50 分别为 0.69 μM 和 9.4 μM。EB1 抑制癌细胞的生长，促进细胞凋亡，抑制 eIF4E 磷酸化。
T10133	3'-Azido-3'-deoxy-5-methylcytidine	Antiviral; HIV Protease	Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	3'-Azido-3'-deoxy-5-methylcytidine 抑制 HIV-1 逆转录酶 (EC50 = 0.06 μM)，是异嗜性鼠白血病相关逆转录病毒 (XMRV, CC50 = 43.5 μM) 的有效抑制剂。
T13685	ERD-308	Others	Others
	ERD-308 induces >95% of ER degradation at concentrations as low as 5 nM in both cell lines (DC50 (concentration causing 50% of protein degradation) of 0.17 nM and 0.43 nM in MCF-7 and T47D ER+ cells, respectively).ERD-308 is a highly potent PROTAC degrade
T13292	VDR agonist 1	Others	Others
	VDR agonist 1 (compound 28) 是一种非甾体类维生素 D 受体 (VDR)的激动剂，在MCF-7 细胞中测得其IC50值为 690 nM。VDR agonist 1 通过上调 p21 和 p27 的表达来抑制细胞周期，通过增加 BAX 的表达来促进细胞凋亡，降低 Bcl-2 的表达，具有治疗乳腺癌的潜力。
T16357	DA-3003-1 NSC 663284	Phosphatase	Metabolism
	DA-3003-1 (DA-3003-1) 是一种可渗透进细胞膜且具有有效性和选择性的 Cdc25 dual specificity phosphatase 抑制剂，具有抗肿瘤活性，对 Cdc25B2、Cdc25A、Cdc25B2 和 Cdc25C具有抑制作用。
T27078	CPUY201112 CPUY 201112,CPUY-201112
	CPUY201112, a novel inhibitor of heat shock protein Hsp90, induces p53-mediated apoptosis in MCF-7 cells.
T62905	GLS-1-IN-1
	GLS-1-IN-1 (compound 1d) 是一种 GLS-1 抑制剂，能够抑制 Hep G2、MCF 7 和 MCF 10A 细胞。
T63676	Bcl-2-IN-6
	Bcl-2-IN-6 是 Bcl-2 (b 细胞淋巴瘤-2) 的有效抑制剂，可下调 Bcl-2 的表达，并提高 p53、Bax、caspase-7 mRNA 的表达。Bcl-2-IN-7 能够诱导乳腺癌 MCF-7 细胞周期阻滞和凋亡。Bcl-2-IN-7 能够作用于 MCF-7 细胞 (IC50: 20.91 μM)、LoVo 细胞 (IC50: 22.30 μM)、HepG2 细胞 (IC50: 42.29 μM) 和 A549 细胞 (IC50: 48.00 μM) 均显示出良好的抗肿瘤效果。
T31936	GLL398 GLL 398,GLL-398
	GLL398 is an oral selective estrogen receptor down-regulating agent that strongly binds to ERα (IC50 =1.14 nM) and effectively degrades ERα in MCF-7 breast cancer cells (IC50 = 0.21 μM).
T79109	Estrogen receptor modulator 8	Estrogen Receptor/ERR	Endocrinology/Hormones
	Estrogen receptor modulator8 (compound 4) 为一口服活性化合物，作用为抑制雌激素受体/ERR α（IC50=0.437 nM，MCF-7 细胞）。此化合物能有效抑制MCF-7细胞的增殖，其IC50值仅为0.1 nM。
T60555	Antiproliferative agent-3
	Antiproliferative agent-3 (comp 4) 对 MCF-7 癌细胞表现出良好的活性，IC50值为 0.19 nM。
T82715	Cisplatin-resistant cells-IN-1
	Cisplatin-resistant cells-IN-1（化合物8）对顽固的铂类药物抗性细胞具有较高的细胞毒性。在低纳摩尔浓度范围内（IC50：0.14–1.79 μM in A549/A549-R, K562/K562-R, and MCF-7/MCF-7TamR cells），该化合物能有效降低代谢活性。
T63521	Bcl-2-IN-7
	Bcl-2-IN-7 是 Bcl-2(b 细胞淋巴瘤 -2) 的有效抑制剂，能够下调 Bcl-2 的表达，提高 p53、Bax、caspase-7 mRNA 的表达，能够诱导乳腺癌 MCF-7 细胞周期阻滞和凋亡。Bcl-2-IN-7 对 MCF-7 细胞 (IC50: 20.17 μM)、LoVo 细胞 (IC50: 22.64 μM)、HepG2 细胞 (IC50:45.57 μM) 和 A549 细胞 (IC50: 51.50 μM)均表现出良好的抗肿瘤活性。
T63455	PI3K/Akt/mTOR-IN-3
	PI3K/Akt/mTOR-IN-3 是 PI3K/Akt/mTOR 的有效抑制剂。PI3K/Akt/mTOR-IN-3 能够抑制 MCF-7 细胞 (IC50: 0.77 μM)、HeLa 细胞 (IC50: 1.23 μM) 和 HepG2 细胞(IC50: 4.57 μM)。PI3K/Akt/mTOR-IN-3 在 4 μM 浓度下可抑制 MCF-7 和 HeLa 细胞的迁移。PI3K/Akt/mTOR-IN-3 能够将细胞周期阻滞在 S 期，并诱导细胞凋亡 (apoptosis)。
T39203	Raloxifene 6-Monomethyl Ether
	Compound 7, or Raloxifene 6-Monomethyl Ether, is a derivative of Raloxifene that effectively inhibits estrogen receptor α. It also displays the inhibitory effects on MCF-7 cells, with an IC50 of 250 nM and a pIC50 of 6.6.
T79727	EGFR/CDK2-IN-2	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	EGFR/CDK2-IN-2（compound 6a）是一种针对EGFR和CDK-2的双重抑制剂，具有19.6 nM和87.9 nM的IC50s。该化合物能在MCF-7细胞内诱导凋亡，并在S期引发细胞周期停滞。此外，EGFR/CDK2-IN-2展现出IC50为0.39 μM的显著抗癌活性，对MCF-7细胞具有强效的细胞毒性。
T22159	TCS HDAC6 20b
	TCS HDAC6 20b 是一种HDAC6选择性抑制剂，可阻断雌激素受体 α 阳性乳腺癌 MCF-7 细胞的生长。
T83017	Antiproliferative agent-40
	抗增殖剂-40（化合物9）对HT1080和MCF-7细胞系展示了明显的抑制效果，其IC50值分别为52 μM和8.2 μM。
T83874	S-72
	S-72是一种微管聚合抑制剂，以1, 3, 10 µM的浓度在无细胞测定中抑制微管聚合，并在MCF-7和耐紫杉醇的MCF-7/T乳腺癌细胞中降低细胞活性（IC50分别为15.64和26.32 nM）。50 nM浓度的S-72能抑制MCF-7和MCF-7/T细胞的迁移和侵袭，并减少划痕实验中的伤口闭合百分比。100 nM的S-72在MCF-7/T细胞中诱导G2/M期的细胞周期阻滞以及凋亡，并在同一浓度下抑制这些细胞中干扰素基因激活剂（STING）的激活。以每天15 mg/kg的剂量，S-72抑制了耐紫杉醇的MCF-7/T和MX-1/T小鼠异种移植模型中的肿瘤生长。
T72523	Antitumor agent-46
	Antitumor agent-46 是一种抗肿瘤剂。Antitumor agent-46 对 MCF-7 细胞具有明显更高的抗增殖活性，IC50值为 2.08 µM。
T80537	Ac-AAVALLPAVLLALLAP-LEHD-CHO	Caspase	Apoptosis; Proteases/Proteasome
	Ac-AAVALLPAVLLALLAP-LEHD-CHO 是半胱天冬酶4、5和9的抑制剂，能够对Neocarzinostatin处理的MCF-7细胞展现保护效果。
T79729	EGFR/CDK2-IN-4	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	EGFR/CDK2-IN-4（化合物4c）是一种EGFR与CDK-2的双重抑制剂，其IC50值分别为89.6 nM和165.4 nM。该化合物在MCF-7细胞中能诱导(apoptosis)凋亡，并导致细胞周期在S期停滞。EGFR/CDK2-IN-4显示出显著的抗癌细胞毒性，对MCF-7细胞的IC50为2.74 μM。

化合物

Cat.No: T21806

Target: HDAC

σ1 Receptor antagonist-1

Cat.No: T9244

Target: Sigma receptor

Cat.No: T6588

Synonym: 米托蒽醌,mitozantrone

Target: Topoisomerase, PKC

Estrogen receptor modulator 1

Cat.No: T15249

Target: Estrogen Receptor/ERR

Cat.No: T2085

Synonym: IGF-1R Inhibitor II

Target: Apoptosis, IGF-1R

(1E)-CFI-400437 dihydrochloride

Cat.No: T22288

Synonym: CFI-400437 dihydrochloride

Target: PLK

3-Bromopyruvic acid

Cat.No: T5882

Synonym: Hexokinase II Inhibitor II, 3-BP,3-溴丙酮酸,Bromopyruvic acid

Target: Apoptosis, Hexokinase, Autophagy

Mitoxantrone dihydrochloride

Cat.No: T0158

Synonym: 米托蒽醌二盐酸盐,盐酸米托蒽醌,Mitoxantrone 2HCl,Mitoxantrone hydrochloride,NSC-301739,mitozantrone dihydrochloride

Target: Topoisomerase, PKC

Idarubicin hydrochloride

Cat.No: T6010

Synonym: 盐酸伊达比星,Idamycin,4-demethoxydaunorubicin (NSC256439, 4-DMDR) HCl,4-Demethoxydaunorubicin hydrochloride,Idarubicin HCl,伊达比星盐酸盐,Zavedos

Target: Topoisomerase, Antibacterial, Autophagy, Antifungal

Estrone O-sulfamate

Cat.No: T72470

Synonym: Estrone 3-O-sulfamate

Target: Others

Cat.No: T10325

Target: Chk

Cat.No: T9541

Synonym: Cholera Toxin B subunit

Target: Epigenetic Reader Domain

Antiproliferative agent-16

Cat.No: T64348

Synonym: Antiproliferative agent-16

Target: Others

Cat.No: T36488

Synonym: LYG202,LYG 202

Target: Apoptosis, ROS

Cat.No: T36970

Target: DUB

Cat.No: T40233

Synonym: (Iso)-YS43-22,MS4322 (isomer),YS43-22 (isomer)

Target: Histone Methyltransferase

Cat.No: T28589

Synonym: Ro-41-5253,Ro 415253

Target: Apoptosis, Retinoid Receptor

Pim-1 kinase inhibitor 8

Cat.No: T83627

Target: Pim, PKC

Cat.No: T77575

Target: P-gp

Cat.No: T7057

Target: Histone Demethylase, Others

Cat.No: T1960

Target: AhR, Aryl Hydrocarbon Receptor

Cat.No: T2283

Synonym: 2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12

Target: Thioredoxin

Cat.No: T18981

Target: Others

Cat.No: T68147

Target: Microtubule Associated

Cat.No: T36696

Cat.No: T61899

Target: VEGFR

Cat.No: T4464

Synonym: 667-Coumate,BN83495,STX64

Target: Others

Cat.No: T72076

Target: HSP

Cat.No: T73582

Target: MNK

3'-Azido-3'-deoxy-5-methylcytidine

Cat.No: T10133

Target: Antiviral, HIV Protease

Cat.No: T13685

Target: Others

Cat.No: T13292

Target: Others

Cat.No: T16357

Synonym: NSC 663284

Target: Phosphatase

Cat.No: T27078

Synonym: CPUY 201112,CPUY-201112

Cat.No: T62905

Cat.No: T63676

Cat.No: T31936

Synonym: GLL 398,GLL-398

Estrogen receptor modulator 8

Cat.No: T79109

Target: Estrogen Receptor/ERR

Antiproliferative agent-3

Cat.No: T60555

Cisplatin-resistant cells-IN-1

Cat.No: T82715

Cat.No: T63521

PI3K/Akt/mTOR-IN-3

Cat.No: T63455

Raloxifene 6-Monomethyl Ether

Cat.No: T39203

Cat.No: T79727

Target: EGFR

Cat.No: T22159

Antiproliferative agent-40

Cat.No: T83017

Cat.No: T83874

Antitumor agent-46

Cat.No: T72523

Ac-AAVALLPAVLLALLAP-LEHD-CHO

Cat.No: T80537

Target: Caspase

Cat.No: T79729

Target: EGFR

Cat. No.	Product Name	Target	Signaling Pathways
TN1768	Iriflophenone	Estrogen Receptor/ERR; Estrogen/progestogen Receptor	Endocrinology/Hormones
	Iriflophenone 是从 Aquilaria sinensis 中分离得到，能诱导 MCF-7 和 T-47D 人乳腺癌细胞增殖。
T5724	Neogambogic acid neo-gambogic acid,新藤黄酸	Apoptosis; Others; Antibacterial	Apoptosis; Microbiology/Virology; Others
	Neogambogic acid 是藤黄的有效成分，可诱导细胞凋亡并具有抗癌作用。它有效抑制耐甲氧西林的金黄色葡萄球菌。
T2882	Genistin 染料木甙,Genistoside,Genistein glucoside,Genistein 7-glucoside,Genistine,Genistein 7-O-β-D-glucopyranoside,染料木苷	Apoptosis; Estrogen Receptor/ERR; Others	Apoptosis; Endocrinology/Hormones; Others
	Genistin (Genistoside) 是一种植物雌激素家族的异黄酮，是一种抗脂肪生成剂。它通过调节ERalpha 信号通路抑制乳腺癌细胞生长和促进凋亡细胞死亡。
T7786	Tryptanthrin	DNA gyrase	DNA Damage/DNA Repair
	Tryptanthrin 是一种口服具有活性的细胞内Leukotriene (LT) biosynthesis 抑制剂。它能够降低大鼠胸膜炎模型中的 LTB4 水平，并抑制人全血中Leukotriene 的形成 (IC50= 10 µM)。
T19768	γ-Tocotrienol gamma Tocotrienol,gammaTocotrienol,gamma-Tocotrienol,D-gamma-Tocotrienol,Plastochromanol,γ-生育三烯酚	Others	Others
	γ-Tocotrienol (Plastochromanol) 是一种维生素 E 的活性形式。
TN7041	(-)-Epipodophyllotoxin	Apoptosis	Apoptosis
	(-)-Epipodophyllotoxin 是一种从八角莲中分离的癌细胞抗增殖剂，在 HeLa 细胞和 MCF-7 细胞中的GI50值分别为 0.36 和 0.24 μM。它可在体外抑制有丝分裂纺锤体组装。
T12581	Puerarin-4'-O-β-D-glucopyranoside Puerarin4'-O-glucoside,葛根素-4'-Β-D-葡萄糖苷	Others	Others
	Puerarin-4'-O-β-D-glucopyranoside (Puerarin4'-O-glucoside) 是一种从葛根 (PLR) 中提取的异黄酮。它具有雌激素活性和抗 MCF-7 人乳腺癌细胞增殖作用。
T83321	4-Demethyldeoxypodophyllotoxin	Chk	Cell Cycle/Checkpoint
	4-Demethyldeoxypodophyllotoxin 是一种来自 Podophyllum peltatum 根部的芳基四氢萘木酚素类化合物，具有抗癌活性，可调节 MCF-7乳腺癌细胞中的Chk-2信号通路。
TMA2270	Alisol F 24-acetate	P-gp	Membrane transporter/Ion channel; Neuroscience
	Alisol F 24-acetate 是一种从 Alisma plantago-aquatica Linn [1] 中分离出来的天然产物。 Alisol F 24 Acetate 通过抑制 P-糖蛋白介导的药物流出来增强 MCF-7/DOX 细胞的化学敏感性和凋亡。
T4S0544	Furanodienone 呋喃二烯酮,莪术呋喃二烯酮	Apoptosis; HER	Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Furanodienone 是来源于姜黄根茎的一种主要生物活性成分，可诱导细胞凋亡。
T4519	Alisol A Alisol-A,泽泻醇 A	Autophagy	Autophagy
	Alisol A (Alisol-A) 是泽泻中的一种三萜类天然产物，可能是一种自噬诱导剂，具有抗癌活性。
T3411	Curdione 莪术二酮,(+)-Curdione	P450	Metabolism
	Curdione ((+)-Curdione) 是一种具有高生物活性的倍半萜类物质，从莪术中分离获得，具有抑制血小板聚集、抵抗血栓形成的作用。
TJS0387	Desoxyrhaponticin 去氧土大黄苷,Deoxyrhapontin,脱氧土大黄苷,Deoxyrhaponticin	Apoptosis; Fatty Acid Synthase	Apoptosis; Metabolism
	Desoxyrhaponticin (Deoxyrhaponticin) 是来自西藏营养食品唐古特大黄中的一种二苯乙烯苷。它是脂肪酸合成酶抑制剂，抑制细胞内 FAS 活性，下调人乳腺癌 MCF-7细胞中 FAS 的表达。它是控制糖尿病餐后高血糖的潜在药物。
T3S1416	Decursin Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素	Apoptosis; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling
	Decursin (Decursinol angelate) 是一种细胞毒性剂，是一种来自朝鲜当归根的有效蛋白激酶 C 激活剂。它通过 Hippo/YAP 信号通路抑制 HepG2 细胞的生长。它通过下调 CXCR7 表达来抑制胃癌中的肿瘤生长，迁移和侵袭。
T5S2358	Dehydrocorydaline Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine	BCL; PARP; p38 MAPK; Caspase; Parasite; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Proteases/Proteasome
	Dehydrocorydaline (13-Methylpalmatine) 是一种生物碱。它调节Bax，Bcl-2蛋白表达，激活caspase-7，caspase-8，并使PARP 失活。它能增强p38 MAPK 活化，具有抗炎、抗癌等功效。它具有强大的抗疟疾作用，并具低细胞毒性。
T3S2344	β,β-Dimethylacrylshikonin β,β-二甲基丙烯酰紫草素,Dimethylacrylshikonin,β, β-Dimethylacrylshikonin	ERK; HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; MAPK; Metabolism
	β,β-Dimethylacrylshikonin (Dimethylacrylshikonin) 是一种萘醌衍生物，从 Arnebia nobilis 中提取得到。它利用 PI3K 通路诱导 eNOS、VEGF 和 HIF-1α 的表达，促进血管生成，具有抗肿瘤活性。
T6S1315	Oroxylin A 千层纸素A,6-Methoxybaicalein,Baicalein 6-methyl ether	Virus Protease; HIF/HIF Prolyl-Hydroxylase; Autophagy	Autophagy; Chromatin/Epigenetic; Metabolism; Microbiology/Virology
	Oroxylin A (Baicalein 6-methyl ether) 是一种有活性的黄酮，具有较强的抗癌作用。
T3729	Ethyl gallate Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯	MMP; NF-κB; Akt; Antibacterial	Cytoskeletal Signaling; Microbiology/Virology; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome
	Ethyl gallate (gallic acid ethyl ester) 是一种非类黄酮酚过氧化氢清除剂。
T2S1865	Octyl gallate Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯	Antioxidant; Influenza Virus; Reactive Oxygen Species; Antibacterial; Antifungal; HSV	Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction
	Octyl gallate (Octyl 3,4,5-trihydroxybenzoate) 具有抗菌、抗氧化作用，有选择性和敏感性的荧光特性，广泛用作食品添加剂。它对 HSV-1，水泡性口炎病毒和脊髓灰质炎病毒有显著的抗病毒作用。
T17155	Trabectedin Ecteinascidin 743,曲贝替定,ET-743	Apoptosis; Reactive Oxygen Species	Apoptosis; Immunology/Inflammation; Metabolism; NF-κB
	Trabectedin (Ecteinascidin 743) 是一种四氢异喹啉生物碱，有抗肿瘤的活性，通过与 DNA 的小沟结合，阻断应激诱导的蛋白质的转录，诱导 DNA 骨架裂解和癌细胞凋亡，并增加 MCF-7 和 MDA-MB-453 细胞中 ROS 的生成。Trabectedin 在软组织肉瘤和卵巢癌中具有的研究价值。
TN5538	6-Methoxykaempferol	Others	Others
	6-Methoxykaempferol 是一种存在于 brazilian propolis 中的黄酮。6-Methoxykaempferol 对癌细胞具有抗增殖活性，对离体大鼠脑突触体的神经保护作用，可降低的谷胱甘肽水平。6-Methoxykaempferol 表现出一定的脂肪酶活性，可用于恶病质的治疗。
T8724	6-Methoxydihydrosanguinarine	Others	Others
	6-Methoxydihydrosanguinarine 是一种从M. cordata 果实中分离出的生物碱，它对 MCF-7 细胞系(IC50:0.61 μM)和 SF-268 细胞系(IC50:0.54 μM)具有强的细胞毒性。
T2902	Costunolide Costus lactone,NSC 106404,Costunolid,(+)-Costunolide,木香烃内酯	Apoptosis; Endogenous Metabolite; Telomerase	Apoptosis; DNA Damage/DNA Repair; Metabolism
	Costunolide (Costus lactone) 是一种天然的倍半萜内酯，具有抗氧化、抗炎、抗过敏、骨重塑、神经保护、促进毛发生长、抗癌和抗糖尿病的特性，可诱导乳腺癌细胞周期阻滞和凋亡。
T1174	Topotecan hydrochloride SKF 104864A,SKFS 104864A,NSC609699,Nogitecan HCl,NSC 609669,盐酸拓扑替康,Topotecan HCl	Apoptosis; Topoisomerase; Autophagy	Apoptosis; Autophagy; DNA Damage/DNA Repair
	Topotecan hydrochloride (NSC609699) 是一种具有抗癌活性的拓扑异构酶I 抑制剂。
TN2249	(+)-Syringaresinol	Sirtuin; Antifection	Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology
	(+)-Syringaresinol shows antioxidant potential, it exhibits cytoprotective activity in cultured MCF-7 cells stressed by H2O2.
T40940	7,3′,5′-Trihydroxyflavanone
	7,3′,5′-Trihydroxyflavanone, a flavanoid derivative, promotes apoptotic cell death in MCF-7 cells by augmenting Bax expression. Additionally, this compound demonstrates antioxidant properties.
T83301	5,7-Dimethoxy-2,3-phenanthrenediol
	5,7-Dimethoxy-2,3-phenanthrenediol 表现出雌激素活性，能够促进MCF-7细胞的增殖，并增强ERβ在MCF-7细胞系中的表达。
TN1578	Dihydroconiferyl alcohol	Others	Others
	Dihydroconiferyl alcohol exhibits cytoprotective activity in cultured MCF-7 cells stressed by H2O2.
T83089	Anticancer agent 149
	Anticanceragent 149 (compound 3) 是一种从薯蓣 (DM) 根茎中分离出的抗癌剂，其对MCF-7 细胞呈现选择性细胞毒活性，特有IC50值为31.41 μM。
T75484	Clionamine B
	Clionamine B, 一种海绵 Cliona celata 分离出来的刺激自噬的氨基类固醇，强烈刺激人乳腺癌 MCF-7 细胞的自噬。
T81529	Peganumine A
	Peganumine A，一种天然产物，源自Peganum harmala，具备对HL-60、MCF-7、PC-3、HepG2细胞线显示出细胞毒性作用，其IC50值依次为5.8、38.5、40.2、55.4 µM[1]< /sup>。
TN4903	Regiolone	Caspase	Apoptosis; Proteases/Proteasome
	Regiolone demonstrates phytotoxicity. Regiolone also has anti-proliferative and apoptotic activities, it can induce apoptosis in MCF-7 cells through the caspase-3 independent pathway.
T69368	GKK1032B
	GKK1032B is a fungal metabolite that has antiproliferative and antibacterial activities. GKK1032B inhibits the growth of HeLa S3 cervical and MCF-7 breast cancer cells and Vero cells. It also inhibits the growth of B. subtilis and M. tuberculosis.
TN3429	Aphagranin A	Others	Others
	Aphagranin A exhibits strong antiproliferative activity against the growth of six lines of human cancer cells (MCF-7, A549, HepG2, Bel-7402, SGC-7901, and BGC-823.
T75490	27-O-(tert-Butyldimethylsilyl)withaferin A
	27-O-(tert-Butyldimethylsilyl)withaferin A (compound 9a) 为一种天然茄内酯类化合物，具备诱导细胞凋亡 (apoptosis) 的能力。该化合物对人类癌细胞系HeLa、A-549、MCF-7以及正常Vero细胞展现出抗增殖活性。
TN2288	Uralenol 乌拉尔醇	Others; Estrogen/progestogen Receptor; Tyrosinase	Endocrinology/Hormones; Others; Proteases/Proteasome
	Uralenol significantly shows the inhibitory activities against the PTP1B enzyme; it also shows inhibitory activities on mushroom tyrosinase using l-tyrosine as substrate( IC50 =49.5 μM). Uralenol shows potent anti-proliferation effects on ER-positive breast cancer MCF-7 cells in vitro.
T73403	Aviculin
	Aviculin 是一种木聚糖苷，是一种有效的抗癌剂 (anticanceragent)。Aviculin 可降低 MCF-7 细胞代谢活性到 50% 以下，IC50为 75.47 μM。Aviculin 通过内在凋亡途径诱导乳腺癌细胞凋亡 (apoptosis)。Aviculin 增加了 caspase-9、caspase-7和 PARP 的表达。Aviculin 使 Bax/Bcl-2 的比值升高。
TN3049	4-Methoxycinnamyl alcohol	Others	Others
	4-Methoxycinnamyl alcohol 对MCF-7、HeLa 和DU145癌症细胞系显示出毒性，IC50值分别为14.24、7.82和22.10μg/mL。4-methoxycinnamyl alcohol 是从Foeniculum vulgare 中分离出来的。4-Methoxycinnamyl alcohol 没有显示出凋亡作用，却在10μg/mL DNA 碎片研究显示48小时后发生了坏死。
TN3084	5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone	Estrogen Receptor/ERR; Others	Endocrinology/Hormones; Others
	5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone 具有抗癌活性，体外对 ER 阳性乳腺癌MCF-7细胞表现出较强的抗增殖作用，对MCF-7细胞的IC50值为4.41 uM。5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone 能显著下调雌激素受体-α (ER-α)的表达浓度，并能抑制人乳腺癌细胞系BCAP-37异种移植模型体内的肿瘤生长。
TN5657	Goniotriol
	Goniotriol shows antimycobacterial activity against Mycobacterium tuberculosis (MIC =100 microg/mL). It exhibits antiplasmodial activity against Plasmodium falciparum (IC50=2.6 microg/mL). Goniotriol shows cytotoxicity against cancer cells, KB, BC1, NCI-H
TN5647	Confluentin
	Confluentin has antimicrobial activity against the gram-positive bacteria.Confluentin significantly inhibits compound 48/80-induced histamine release from rat peritoneal mast cells. Confluentin also shows weak cytotoxicity against four human tumor cell li
T1166	Ellipticine 玫瑰树碱,NSC 71795,Elliptisine	Topoisomerase	DNA Damage/DNA Repair
	Ellipticine (Elliptisine) 是一种有效的抗肿瘤剂，抑制 DNA 拓扑异构酶 II 活性，对白血病、神经母细胞瘤和胶质母细胞瘤有部分活性。
TN2767	2'-Hydroxygenistein 鲁冰花	Antifection	Microbiology/Virology
	2'-Hydroxygenistein has antifungal activity, dimerization of it causes a remarkable increase of antifungal activity. It shows significant concentration-dependent inhibitory effects on the release of beta-glucuronidase and lysozyme from rat neutrophils in response to formyl-Met-Leu-Phe/cytochalasin B. 2'-Hydroxygenistein of genistein can enhance its antioxidant activity and cell cytotoxicity in MCF-7 human breast cancer cells.
TN4552	Methyl p-hydroxyphenyllactate	Others	Others
	Methyl para-hydroxyphenyllactate(MeHPLA) can suppress the cellular proliferation of estrogen-sensitive MCF-7 breast cancer cells in vitro and to suppress the growth of rat uteri in vivo, high affinity of MeHPLA for the type II estrogen binding site (EBS)
TN5930	Ocotillone
	Ocotillone has potent antibacterial activity against Gram-negative bacteria, P. aeruginosa and S. typhimurium, that are without hemolytic activity, whereas it has weak antimicrobial activity against Gram-positive bacteria and fungi. Ocotillone shows only
T3P2855	Chamigrenal	EGFR; NOS; PAFR; COX; Prostaglandin Receptor	Angiogenesis; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Tyrosine Kinase/Adaptors
	β-Chamigrenal has anti-inflammatory activity, it has inhibitory effects on lipopolysaccharide-induced nitric oxide and prostaglandin E2 production in RAW 264.7 macrophages. Chamigrenal shows platelet-activating factor antagonistic activity and the IC(50)
T83597	(+)-Menthyl acetate
	(+)-Menthyl acetate是一种从Cunila angustifolia Benth精油中分离得到的化学化合物。它对MCF-7细胞株具有较高的选择性，其半抑制浓度（IC50）为34.0 μg/mL，而对SK-Mel-28细胞株的选择性较低，IC50为279.9 μg/mL，并且对A549细胞没有致死作用。
TN3870	Iriflophenone 2-O-Rhamnoside Dimethylmatairesinol	Others	Others
	Dimethylmatairesinol can reduce the amount of Immunoglobulin E (IgE) secreted by human myeloma U266 cells, it has potential as an anti-allergic agent. Dimethylmatairesinol also exhibits significant cytotoxicity against three human tumor cells(A-549 lung c
T37452	Stephacidin B
	Stephacidin B is a fungal metabolite that has been found inA. ochraceus.1Dimeric stephacidin B is rapidly converted to a monomer, avrainvillamide ,in vitro.2Stephacidin B is cytotoxic to a variety of cancer cells, including testosterone-independent PC3 and -sensitive LNCaP prostate cancer cells (IC50s = 0.37 and 0.06 μM, respectively) and estradiol-independent SK-BR-3 and -sensitive MCF-7 breast cancer cells (IC50s = 0.32 and 0.27 μM, respectively).1It induces apoptosis in HepG2 and Huh7 hepatoc...
T35754	Aszonapyrone A
	Aszonapyrone A is a meroditerpene fungal metabolite that has been found in Neosartorya and has diverse biological activities.1,2,3 It inhibits the growth of MCF-7, NCI H460, and A375-C5 cancer cells (GI50s = 13.6, 11.6, and 10.2 μM, respectively).1 Aszonapyrone A is active against multidrug-resistant isolates of S. aureus, E. faecalis, and E. faecium (MICs = 8, 16, and 16 μg/ml, respectively) and inhibits S. aureus biofilm formation.2 It is also active against P. falciparum in vitro (IC50 = 1.34...
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天然产物

Cat.No: TN1768

Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor

Neogambogic acid

Cat.No: T5724

Synonym: neo-gambogic acid,新藤黄酸

Target: Apoptosis, Others, Antibacterial

Cat.No: T2882

Synonym: 染料木甙,Genistoside,Genistein glucoside,Genistein 7-glucoside,Genistine,Genistein 7-O-β-D-glucopyranoside,染料木苷

Target: Apoptosis, Estrogen Receptor/ERR, Others

Cat.No: T7786

Target: DNA gyrase

Cat.No: T19768

Synonym: gamma Tocotrienol,gammaTocotrienol,gamma-Tocotrienol,D-gamma-Tocotrienol,Plastochromanol,γ-生育三烯酚

Target: Others

(-)-Epipodophyllotoxin

Cat.No: TN7041

Target: Apoptosis

Puerarin-4'-O-β-D-glucopyranoside

Cat.No: T12581

Synonym: Puerarin4'-O-glucoside,葛根素-4'-Β-D-葡萄糖苷

Target: Others

4-Demethyldeoxypodophyllotoxin

Cat.No: T83321

Target: Chk

Alisol F 24-acetate

Cat.No: TMA2270

Target: P-gp

Cat.No: T4S0544

Synonym: 呋喃二烯酮,莪术呋喃二烯酮

Target: Apoptosis, HER

Cat.No: T4519

Synonym: Alisol-A,泽泻醇 A

Target: Autophagy

Cat.No: T3411

Synonym: 莪术二酮,(+)-Curdione

Target: P450

Desoxyrhaponticin

Cat.No: TJS0387

Synonym: 去氧土大黄苷,Deoxyrhapontin,脱氧土大黄苷,Deoxyrhaponticin

Target: Apoptosis, Fatty Acid Synthase

Cat.No: T3S1416

Synonym: Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素

Target: Apoptosis, PKC

Dehydrocorydaline

Cat.No: T5S2358

Synonym: Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine

Target: BCL, PARP, p38 MAPK, Caspase, Parasite, Autophagy

β,β-Dimethylacrylshikonin

Cat.No: T3S2344

Synonym: β,β-二甲基丙烯酰紫草素,Dimethylacrylshikonin,β, β-Dimethylacrylshikonin

Target: ERK, HIF/HIF Prolyl-Hydroxylase

Cat.No: T6S1315

Synonym: 千层纸素A,6-Methoxybaicalein,Baicalein 6-methyl ether

Target: Virus Protease, HIF/HIF Prolyl-Hydroxylase, Autophagy

Cat.No: T3729

Synonym: Nipagallin A,Phyllemblin,gallic acid ethyl ester,没食子酸乙酯

Target: MMP, NF-κB, Akt, Antibacterial

Cat.No: T2S1865

Synonym: Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯

Target: Antioxidant, Influenza Virus, Reactive Oxygen Species, Antibacterial, Antifungal, HSV

Cat.No: T17155

Synonym: Ecteinascidin 743,曲贝替定,ET-743

Target: Apoptosis, Reactive Oxygen Species

6-Methoxykaempferol

Cat.No: TN5538

Target: Others

6-Methoxydihydrosanguinarine

Cat.No: T8724

Target: Others

Cat.No: T2902

Synonym: Costus lactone,NSC 106404,Costunolid,(+)-Costunolide,木香烃内酯

Target: Apoptosis, Endogenous Metabolite, Telomerase

Topotecan hydrochloride

Cat.No: T1174

Synonym: SKF 104864A,SKFS 104864A,NSC609699,Nogitecan HCl,NSC 609669,盐酸拓扑替康,Topotecan HCl

Target: Apoptosis, Topoisomerase, Autophagy

(+)-Syringaresinol

Cat.No: TN2249

Target: Sirtuin, Antifection

7,3′,5′-Trihydroxyflavanone

Cat.No: T40940

5,7-Dimethoxy-2,3-phenanthrenediol

Cat.No: T83301

Dihydroconiferyl alcohol

Cat.No: TN1578

Target: Others

Anticancer agent 149

Cat.No: T83089

Cat.No: T75484

Cat.No: T81529

Cat.No: TN4903

Target: Caspase

Cat.No: T69368

Cat.No: TN3429

Target: Others

27-O-(tert-Butyldimethylsilyl)withaferin A

Cat.No: T75490

Cat.No: TN2288

Synonym: 乌拉尔醇

Target: Others, Estrogen/progestogen Receptor, Tyrosinase

Cat.No: T73403

4-Methoxycinnamyl alcohol

Cat.No: TN3049

Target: Others

5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone

Cat.No: TN3084

Target: Estrogen Receptor/ERR, Others

Cat.No: TN5657

Cat.No: TN5647

Cat.No: T1166

Synonym: 玫瑰树碱,NSC 71795,Elliptisine

Target: Topoisomerase

2'-Hydroxygenistein

Cat.No: TN2767

Synonym: 鲁冰花

Target: Antifection

Methyl p-hydroxyphenyllactate

Cat.No: TN4552

Target: Others

Cat.No: TN5930

Cat.No: T3P2855

Target: EGFR, NOS, PAFR, COX, Prostaglandin Receptor

(+)-Menthyl acetate

Cat.No: T83597

Iriflophenone 2-O-Rhamnoside

Cat.No: TN3870

Synonym: Dimethylmatairesinol

Target: Others

Cat.No: T37452

Cat.No: T35754

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