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Search Results for " cell viability "

128

抑制剂 & 化合物

26

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T8308	NL-1	Mitochondrial Metabolism; Autophagy	Autophagy; Metabolism
	NL-1 是一种mitoNEET 抑制剂，具有抗白血病作用。它抑制 REH 和 REH/Ara-C 细胞生长，IC50分别为 47.35 µM 和 56.26 µM。
T9776	TRPM4 inhibitor 8	TRP/TRPV Channel	Membrane transporter/Ion channel
	TRPM4 inhibitor 8 是瞬态受体电位 melastatin 4 (TRPM4) 的抑制剂，它有助于活力、迁移、细胞周期转变和粘附。
T9662	SRI 37892	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	SRI 37892是一种 Fzd7抑制剂，对 Wnt/β-catenin 信号传导和癌症细胞活性具有强大的活性。
T5627	Methoxychlor	Others	Others
	Methoxychlor 是一种有机氯农药，被认为是一种内分泌干扰物，会影响不同细胞模型中的 Ca²⁺ 稳态和细胞活力。
T7366	NGI-1 ML414	Virus Protease	Microbiology/Virology
	NGI-1 (ML414) 是一种可渗透细胞的寡糖转移酶 (OST) 抑制剂，直接靶向和阻断 OST 催化亚基 STT3A 和 STT3B 的功能，可有效降低病毒感染性而不影响细胞活力。
T16040	Mepazine 甲哌啶嗪,Pecazine	Apoptosis; MALT	Apoptosis; Immunology/Inflammation
	Mepazine (Pecazine) 是一种有效的特异性 MALT1 抑制剂。 Mepazine 抑制 GSTMALT1 全长和 GSTMALT1 325-760，IC50 为 0.83 μM 和 0.42 μM。 Mepazine 增强细胞凋亡并影响细胞活力。
T12896L	Shepherdin 79-87 acetate Shepherdin 79-87 acetate (861224-28-4 free base)	HSP; Survivin	Apoptosis; Cytoskeletal Signaling; Metabolism
	Shepherdin 79-87 acetate 是 Hsp90 和 survivin 之间复合物的拟肽拮抗剂，survivin 是肿瘤细胞活力的另一个关键调节剂。
T68051	Delequamine RS 15385-197	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Delequamine (RS 15385-197) 是一种有效的选择性 α2-肾上腺素受体拮抗剂。
T6682	STF-118804 STF 118804,STF118804	Apoptosis; NAMPT	Apoptosis; Metabolism
	STF-118804是一种烟酰胺磷酸核糖基转移酶 Nampt 高选择性抑制剂，降低大多数 B-ALL 细胞系的活力，IC50 <10 nM。
T14017	2-NBDG 2-(N-7-硝基-2,1,3-苯并恶二唑-4-氨基)-2-脱氧-D-葡萄糖	Others	Others
	2-NBDG 是一种荧光指示剂 (λex=467 nm，λem=542 nm)，是一种荧光 D-葡萄糖类似物，可用于监测活细胞中的葡萄糖吸收。
T77660	TINK-IN-1	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	TINK-IN-1 是一种具有选择性和高效性的 TNIK 抑制剂(IC50：8 nM)。TINK-IN-1 抑制结直肠癌细胞活力，可用于研究智力发育障碍。
T11940	Malic enzyme inhibitor ME1 ME1	Others	Others
	Malic enzyme inhibitor ME1 (ME1) 是苹果酸酶的特异性抑制剂 (IC50 = 0.15 μM)。苹果酸酶抑制剂 ME1 降低细胞活力/代谢活性。
T72968	ZINC00640089	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	ZINC00640089 是一种选择性的脂质运载蛋白-2 (LCN2) 抑制剂。ZINC00640089 对细胞增殖、细胞活力有抑制作用，可减少 SUM149 细胞的 AKT 磷酸化水平。ZINC00640089 可用于研究炎症性乳腺癌 (IBC) 。
T83653	SACLAC	Apoptosis; Caspase	Apoptosis; Proteases/Proteasome
	SACLAC 是一种半胱天冬酶活化抑制剂，具有抗肿瘤活性，可降低AML细胞活力，抑制AML细胞增殖，增加AML细胞死亡，并诱导AML细胞凋亡，可用于研究急性髓系白血病和癌症。
T9955	EX-A5758	NOS	Immunology/Inflammation
	EX-A5758是一种新型推定的小分子 nNOS-NOS1 AP 抑制剂，可抑制炎症性伤害感受和化疗引起的神经性疼痛，并与紫杉醇协同降低肿瘤细胞活力
T28543	RK-9123016 RK9123016,RK 9123016	Sirtuin	Chromatin/Epigenetic; DNA Damage/DNA Repair
	RK-9123016是一种SIRT2抑制剂。RK-9123016增加真核翻译起始因子5A（eIF5A）（SIRT2的生理底物）的乙酰化水平，降低人乳腺癌细胞的细胞活力，同时降低c-Myc 表达。
T18894	5(6)-CFDA CFDA,5-(6)-Carboxyfluorescein diacetate,5(6)-羧基荧光素二乙酸酯	Others	Others
	5(6)-CFDA (5-(6)-Carboxyfluorescein diacetate) 是具有细胞渗透性的胺反应型绿色荧光探针(λex: 492 nm; λem: 517 nm)，可用于细胞染色分析。
T1642	Lenalidomide 来那度胺,CC-5013	Apoptosis; TNF; Ligand for E3 Ligase; Molecular Glues	Apoptosis; PROTAC
	Lenalidomide (CC-5013) 是 Thalidomide 的衍生物，也是具有口服活性免疫调节剂，以分子胶的方式作用。它是泛素 E3 连接酶 cereblon (CRBN) 的配体，可通过 CRBN-CRL4 泛素连接酶对两种淋巴转录因子 IKZF1 和 IKZF3 进行选择性泛素化和降解。
T5580	1-Naphthaleneacetic acid potassium salt α-萘醋酸钾,α-Naphthaleneacetic acid,Potassium alpha-naphthylacetate,Potassium 1-Naphthaleneacetate,1-NAA Potassium Salt	Phospholipase	Metabolism
	1-Naphthaleneacetic acid potassium salt (1-NAA Potassium Salt) 是一种合成的植物生长素，能够促进植物生长，也是一种PLA2抑制剂，IC50=13.16 μM。
T1937	Spautin-1 Spautin 1	Apoptosis; DUB; Autophagy	Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
	Spautin-1是一种特异性自噬抑制剂，可抑制泛素特异性肽酶 USP10和 USP13，IC50s 约为0.6到0.7 μM。
T22429	SR18662	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	SR18662 是 ML264 类似物，可抑制 Krüppel 样因子 5 (KLF5)，IC50 为 4.4 nM，降低多种结直肠癌细胞系的活力并诱导细胞凋亡。
T6911	NSC-87877 disodium NSC87877	Apoptosis; Phosphatase	Apoptosis; Metabolism
	NSC-87877 disodium (NSC87877) 是一种有效的Shp2和Shp1蛋白质酪氨酸磷酸酶抑制剂，IC50值分别为0.318 μM 和0.355 μM。NSC-87877还抑制双特异性磷酸酶26。
T8421	TED-347	YAP	Stem Cells
	TED-347 是不可逆的、共价的 YAP-TEAD 蛋白质-蛋白质相互作用变构抑制剂，对 TEAD4•Yap1 蛋白质-蛋白质相互作用的 EC50为 5.9 μM。它与 TEAD4 中央口袋内的 Cys-367 特异性共价结合(Ki:10.3 μM)。它可以抑制 TEAD 的转录活性，并且具有抗肿瘤作用。
T37518	Diphenyl disulfide Phenyl disulfide	Apoptosis; BCL; Endogenous Metabolite	Apoptosis; Metabolism
	Diphenyl disulfide (Phenyl disulfide) 在乳腺癌细胞系中显示出抗癌活性。Diphenyl disulfide 通过Bax 蛋白水解活化和伴随的自噬来诱导并增强乳腺癌细胞的凋亡。Diphenyl disulfide 以剂量依赖性方式抑制细胞增殖和活力，并减少集落形成。Diphenyl disulfide 可用来治疗乳腺癌。
T13983	0990CL	cAMP; Others	GPCR/G Protein; Others
	0990CL 是一种有效的异三聚体Gαi subunit 特异性抑制剂，可与纯化的Go±在gdp 结合状态下相互作用，能够阻断α2AR 介导的cAMP 调控。在细胞模型中低浓度0990CL 能够部分恢复cAMP 水平，高浓度的0990CL (10 μM)下，开始对细胞活力产生负面影响。
T28773	SI-2 SI2,EPH 116,EPH116,EPH-116	Others	Others
	SI-2是类固醇受体辅激活因子-3（SRC-3或 AIB1）的抑制剂（SMI）。SI-2可选择性降低细胞中 SRC-3的转录活性和蛋白浓度，并选择性诱导低纳摩尔范围（3-20 nM）内的乳腺癌症细胞死亡，但不影响正常细胞存活率。
T2331	Solithromycin 索利霉素,OP-1068,CEM-101	Antibacterial; Antibiotic	Microbiology/Virology
	Solithromycin (OP-1068) 是口服可生物利用的抗菌剂，抑制肺炎链球菌、葡萄球菌、金黄色葡萄球菌和流感嗜血杆菌的细胞活力、蛋白质合成和生长速率， IC50 值分别为 7.5 ng/mL、40 ng/mL 和 125 ng/mL。它可与核糖体的大 50S 亚基结合抑制蛋白质生物合成。
T36493	CMLD-2	Apoptosis; HuR	Apoptosis; Chromatin/Epigenetic
	CMLD-2是一种 HuR-ARE 相互作用的抑制剂（Ki：350 nM），能竞争性地结合 HuR 蛋白并破坏其与富含腺嘌呤元素（ARE）的 mRNA 目标的相互作用。CMLD-2诱导细胞凋亡并通过 MAD2下调表现出抗肿瘤作用。CMLD-2 (1-75 μM ; 24-72 h) 对甲状腺癌细胞的活力具有抑制作用.CMLD-2 (20-30 μM ; 24-48 h) 激活 Caspases 并诱导H1299和A549细胞凋亡.CMLD-2 (30 μM ; 24-48 h) 诱导H1299和A549细胞的G1细胞周期停止和线粒体扰动。 CMLD-2（30μM；24-48小时）减少H1299细胞中HuR 和HuR 调节的mRNAs 和蛋白质的表达.CMLD-2（35μM；72小时）降低SW1736、8505C、BCPAP 和K1细胞的定向迁移能力。CMLD-2诱导SW1736、8505C、BCPAP 和K1细胞中的MAD2 mRNA 水平强烈下降。
T34695	Spiclomazine HCl APY-606,Diceplon,Disepron,APY606,Spiclomazine Hydrochloride
	Spiclomazine HCl induced apoptosis in pancreatic cancer cells, which was generally related to cell viability, migration, and invasion.
T24423	LY5 LY 5,LY-5
	LY5 is an inhibitor of STAT3 that acts by inhibiting cell viability, cell migration, and angiogenesis in medulloblastoma cells.
T36141	Boscalid	Mitochondrial Metabolism	Metabolism
	Boscalid 是一种广谱羧酰胺类杀菌剂，通过与线粒体复合物 II/琥珀酸脱氢酶的泛醌位点结合来抑制真菌呼吸。
T7650L	Resazurin Resazoin,Diazoresorcinol,Azoresorcin,Resazurine
	Resazurin is used as an oxidation-reduction indicator in cell viability.
T71413	U 26384
	U 26384 is a phospholipase A2 inhibitor reduces the severity of cell injury, but does not maintain cell viability in cultured human astroglial cell line UC-11MG during ATP depletion.
T19771	SXT1596 NSC-65667,SXT-1596,NSC 65667,SXT 1596,NSC65667
	SXT1596 is a novel SS18-SSX/TLE1 interaction inhibitor. SXT1596 reduces cell viability and reactivates EGR1 expression in synovial sarcoma.
T40143	PROTAC CBP/P300 Degrader-1 PROTAC CBP/P300 Degrader-1
	PROTAC CBP/P300 Degrader-1 is an effective compound that degrades CBP/P300 in a potent manner. It significantly reduces cell viability in various cancer cell lines.
T31696	EthD-1 EthD1,Ethidium Homodimer-1
	EthD-1 is a cell-impermeant viability indicator. It acts as a high-affinity nucleic acid stain.
T68773	NSC-311068
	NSC-311068 is a novel selective inhibitor of TET1 transcription and 5-hydroxymethylcytosine (5hmC) modification, effectively inhibiting cell viability in AML with high expression of TET1.
T71620	iBAP-II
	iBAP-II represses neuroendocrine lineage-specific ASCL1/MYCL/E2F signaling in SCLC cell lines, and dramatically inhibits SCLC cell viability and tumor growth in vivo.
T18932	Calcein tetraethyl ester 钙黄绿素四乙酯,Fluorexon tetraethyl ester	Others	Others
	Calcein tetraethyl ester, a fluorescent dye, is utilized in biological studies for its ability to penetrate cellular membranes into living cells. This property renders it valuable for assessing cell viability and short-term cell labeling.
T33219	MB725 MB 725,MB-725
	MB725 is a strong and selective inducer of viability reduction in several cancer cell lines containing the oncogenic p53-Y220C mutation.
T18931	Calcein-AM Calcein acetoxymethyl ester,钙黄绿素-AM	Others	Others
	Calcein-AM is a cell-permeable fluorescent dye used for the determination of cell viability.
T37602	GSK 143
	Spleen tyrosine kinase (Syk) inhibitor (pIC50 = 7.5). Also inhibits phosphorylated Erk (pIC50 = 7.1). Decreases cell number and viability in chronic lymphocytic leukemia (CCL) cell lines. Liddle et al (2011) Discovery of GSK143, a highly potent, selective and orally efficacious spleen tyrosine kinase inhibitor. Bioorg.Med.Chem.Lett. 21 6188 PMID:21903390 \|Varghese et al (2018) Highly selective SYK inhibitor, GSK143, abrogates survival signals in chronic lymphocytic leukaemia. Br.J.Haematol 182 9...
T36326	Calcein Orange™ Diacetate
	Calcein Orange Diacetate is a fluorogenic dye that is used to assess cell viability. It is hydrolyzed to the fluorescent probe Calcein Orange . Calcein Orange is retained by living cells and displays excitation/emission maxima of 525/550 nm, respectively. Calcein Orange Diacetate is an orange-emitting variant of the green fluorophore Calcein AM , which has been used to evaluate cell viability and cytotoxicity.
T11972	Mcl-1 inhibitor 3	BCL	Apoptosis
	Mcl-1 inhibitor 3 shows good pharmacokinetic properties and excellent in vivo efficacy without toxicity.Mcl-1 inhibitor 3 is a highly potent and orally activate macrocyclic Mcl-1 inhibitor (Ki= 0.061 nM; IC50=19 nM in an OPM-2 cell viability assay).
T35611	CytoCalcein™ Violet 450
	CytoCalcein Violet 450 is a fluorogenic dye used to assess cell viability. It is a cell-permeable dye that, upon entering cells, is cleaved by intracellular esterases. CytoCalcein Violet 450 is retained by living cells and displays excitation/emission maxima of 405/450 nm, respectively.
T16131	MPT0E028	Others	Others
	MPT0E028 is an orally active and selective inhibitor of HDAC (IC50s of 53.0 nM, 106.2 nM, 29.5 nM for HDAC1, HDAC2, and HDAC6, respectively). MPT0E028 has good anticancer activity. MPT0E028 decreases the viability of B-cell lymphomas by inducing apoptosis
T36327	Calcein Red™ AM
	Calcein Red AM is a fluorogenic dye that is used to assess cell viability. As the acetoxymethyl ester, Calcein Red AM is non-fluorescent but cell-permeant and is hydrolyzed to the fluorescent probe Calcein Red by intracellular esterases. Calcein Red is retained by living cells and displays excitation/emission maxima of 560/574 nm, respectively. Calcein Red AM is a red-emitting variant of the green fluorophore calcein AM , which has been used to evaluate cell viability and cytotoxicity.
T70291	PCC0208018
	PCC0208018 is a novel activator of effector T cells, enhancing T cell proliferation and activation to release interferon gamma (IFN-γ) and interleukin-2 (IL-2) without blocking the programmed cell death 1 (PD-1)/programmed cell death-ligand 1 (PD-L1) binding and not directly affecting tumor cell viability in vitro.
T70103	KSK213
	KSK213 is a potent inhibitor of Chlamydia trachomatis Infectivity (EC50 = 60 nM). KSK213 potently inhibited multiple serovars of C. trachomatis while not affecting the growth of key species from the commensal flora or host cell viability at 25 μM.
T71639	AUH-6-96
	AUH-6-96 is an inhibitor of JAK/STAT signaling, inhibiting both constitutive and interleukin-6-induced STAT3 phosphorylation, selectively affecting cell viability only of cancer cells harboring aberrant JAK/STAT signaling.

化合物

Cat.No: T8308

Target: Mitochondrial Metabolism, Autophagy

TRPM4 inhibitor 8

Cat.No: T9776

Target: TRP/TRPV Channel

Cat.No: T9662

Target: Wnt/beta-catenin

Cat.No: T5627

Target: Others

Cat.No: T7366

Synonym: ML414

Target: Virus Protease

Cat.No: T16040

Synonym: 甲哌啶嗪,Pecazine

Target: Apoptosis, MALT

Shepherdin 79-87 acetate

Cat.No: T12896L

Synonym: Shepherdin 79-87 acetate (861224-28-4 free base)

Target: HSP, Survivin

Cat.No: T68051

Synonym: RS 15385-197

Target: Adrenergic Receptor

Cat.No: T6682

Synonym: STF 118804,STF118804

Target: Apoptosis, NAMPT

Cat.No: T14017

Synonym: 2-(N-7-硝基-2,1,3-苯并恶二唑-4-氨基)-2-脱氧-D-葡萄糖

Target: Others

Cat.No: T77660

Target: Wnt/beta-catenin

Malic enzyme inhibitor ME1

Cat.No: T11940

Synonym: ME1

Target: Others

Cat.No: T72968

Target: Akt

Cat.No: T83653

Target: Apoptosis, Caspase

Cat.No: T9955

Target: NOS

Cat.No: T28543

Synonym: RK9123016,RK 9123016

Target: Sirtuin

Cat.No: T18894

Synonym: CFDA,5-(6)-Carboxyfluorescein diacetate,5(6)-羧基荧光素二乙酸酯

Target: Others

Cat.No: T1642

Synonym: 来那度胺,CC-5013

Target: Apoptosis, TNF, Ligand for E3 Ligase, Molecular Glues

1-Naphthaleneacetic acid potassium salt

Cat.No: T5580

Synonym: α-萘醋酸钾,α-Naphthaleneacetic acid,Potassium alpha-naphthylacetate,Potassium 1-Naphthaleneacetate,1-NAA Potassium Salt

Target: Phospholipase

Cat.No: T1937

Synonym: Spautin 1

Target: Apoptosis, DUB, Autophagy

Cat.No: T22429

Target: DNA/RNA Synthesis

NSC-87877 disodium

Cat.No: T6911

Synonym: NSC87877

Target: Apoptosis, Phosphatase

Cat.No: T8421

Target: YAP

Diphenyl disulfide

Cat.No: T37518

Synonym: Phenyl disulfide

Target: Apoptosis, BCL, Endogenous Metabolite

Cat.No: T13983

Target: cAMP, Others

Cat.No: T28773

Synonym: SI2,EPH 116,EPH116,EPH-116

Target: Others

Cat.No: T2331

Synonym: 索利霉素,OP-1068,CEM-101

Target: Antibacterial, Antibiotic

Cat.No: T36493

Target: Apoptosis, HuR

Spiclomazine HCl

Cat.No: T34695

Synonym: APY-606,Diceplon,Disepron,APY606,Spiclomazine Hydrochloride

Cat.No: T24423

Synonym: LY 5,LY-5

Cat.No: T36141

Target: Mitochondrial Metabolism

Cat.No: T7650L

Synonym: Resazoin,Diazoresorcinol,Azoresorcin,Resazurine

Cat.No: T71413

Cat.No: T19771

Synonym: NSC-65667,SXT-1596,NSC 65667,SXT 1596,NSC65667

PROTAC CBP/P300 Degrader-1

Cat.No: T40143

Synonym: PROTAC CBP/P300 Degrader-1

Cat.No: T31696

Synonym: EthD1,Ethidium Homodimer-1

Cat.No: T68773

Cat.No: T71620

Calcein tetraethyl ester

Cat.No: T18932

Synonym: 钙黄绿素四乙酯,Fluorexon tetraethyl ester

Target: Others

Cat.No: T33219

Synonym: MB 725,MB-725

Cat.No: T18931

Synonym: Calcein acetoxymethyl ester,钙黄绿素-AM

Target: Others

Cat.No: T37602

Calcein Orange™ Diacetate

Cat.No: T36326

Mcl-1 inhibitor 3

Cat.No: T11972

Target: BCL

CytoCalcein™ Violet 450

Cat.No: T35611

Cat.No: T16131

Target: Others

Calcein Red™ AM

Cat.No: T36327

Cat.No: T70291

Cat.No: T70103

Cat.No: T71639

Cat. No.	Product Name	Target	Signaling Pathways
T7982	3,6-Dihydroxyflavone	Others	Others
	3,6-Dihydroxyflavone 是一种抗癌剂。它能够提高细胞内氧化应激和脂质过氧化。它是能够根据剂量和时间依赖性地降低细胞活力，并活化半胱天冬酶级联、切割聚 (ADP-核糖) 聚合酶 (PARP) 诱导细胞凋亡。
T2S1396	3-O-Acetyloleanolic acid 齐墩果酸3-乙酸酯,齐墩果酸 3-乙酸酯	Apoptosis	Apoptosis
	3-O-Acetyloleanolic acid 是从 Vigna sinensisK. 种子中提取得到的一种齐墩果醇酸，可诱导癌细胞凋亡并拥有抗血管生成作用。
TN1425	Bacoside A3 苦艾素A3,白花猪母菜甙 A3	ATPase; ROS; P-gp	Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience
	Bacoside A3 是一种天然的三萜皂苷，是Bacopa monnieri 的主要活性成分之一，显示出神经保护活性。
T6S1780	Protosappanin B 原苏木素B,Q-100961,FT-0689654	Apoptosis	Apoptosis
	Protosappanin B (Q-100961) 是从苏木中提取的一种多酚类天然产物，具有抗肿瘤作用。它通过激活 MDM2 依赖性泛素化过程诱导 p53 蛋白降解。它显著提高细胞活力，抑制细胞凋亡并上调生长相关蛋白 43 的表达。
T5S0636	Citric acid 柠檬酸,Citro,Citretten	Apoptosis; Others; Endogenous Metabolite; Antibacterial; Antibiotic	Apoptosis; Metabolism; Microbiology/Virology; Others
	Citric acid (Citro) 是柑橘类水果中发现的弱有机三羧酸。柠檬酸是食品添加剂和天然防腐剂。
TN1405	Arnicolide D 山金车内酯 D,山金车内酯D	Akt; Caspase; PI3K; STAT; mTOR	Apoptosis; Cytoskeletal Signaling; JAK/STAT signaling; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells
	Arnicolide D 是从石胡荽中分离出的一种倍半萜内酯，以浓度和时间依赖性方式抑制鼻咽癌细胞活力。它调节细胞周期，激活 caspase 信号通路并抑制 PI3K/AKT/mTOR 和 STAT3 信号通路。
T3S1873	Talatisamine 塔拉乌头胺,塔拉萨敏	Potassium Channel	Membrane transporter/Ion channel
	Talatisamine 是一种乌头生物碱，对K+通道有特异性阻滞作用。它能减弱 beta- 淀粉样低聚物对培养的皮层神经元的毒性。
T6S1653	Albiflorin Alibiflorin,芍药内酯苷	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	Albiflorin (Alibiflorin) 是一种牡丹根中的主要成分，是一种单萜糖苷。它具有神经保护、抗炎、抗氧化和缓解疼痛作用。
T2897	(Rac)-Shikonin (±)-Shikonin,Alkanet extract,Anchusin,紫草素,Anchusa acid	Others	Others
	(Rac)-Shikonin (Anchusin) 具有抗肿瘤作用。它能够诱导坏死死亡来绕过癌症耐药性。
T4S1615	Sanggenon C 桑根酮C,桑根酮 C,Sanggenone C	NF-κB	NF-κB
	Sanggenon C (Sanggenone C) 是一种从桑属的根皮中分离得到的黄烷酮 Diels-Alder 加合物化合物。它可抑制NF-κB 活性，抑制 RAW264.7 细胞中诱导型一氧化氮合酶的表达，以及肿瘤坏死因子-α 刺激的细胞粘附和血管细胞粘附分子-1 的表达。它具有抗氧化和抗炎作用，也有抑制胰脂肪酶作用。
T6S2391	L-Chicoric Acid (-)-Chicoric acid,trans-Caffeoyltartaric acid,Chicoric acid,L-菊苣酸,dicaffeoyltartaric acid,菊苣酸	Others; HIV Protease	Microbiology/Virology; Others; Proteases/Proteasome
	L-Chicoric Acid (trans-Caffeoyltartaric acid) 是一种二咖啡酰酒石酸，是一种选择性可逆的 HIV-1 整合酶抑制剂，IC50约为 100 nM。它还可抑制 HIV-1 复制。
T40834	5-Hydroxymethyl-2'-deoxycytidine 5hmdC,2'-脱氧-5-(羟甲基)胞啶	PARP	Chromatin/Epigenetic; DNA Damage/DNA Repair
	5-Hydroxymethyl-2'-deoxycytidine 是 DNA 中 5-methyl-2'-deoxycytidine (5-mdC) 的氧化衍生物，引起DNA损伤反应，染色体畸变，复制叉损伤和细胞活力丧失。5-Hydroxymethyl-2’-deoxycytidine 复制叉不稳定性与染色质上聚（ADP-核糖）聚合酶1（PARP1）的存在有关。
T4958	(-)-Alkannin Alkannin,左旋紫草素,紫草素,Shikonin	Apoptosis; PI3K	Apoptosis; PI3K/Akt/mTOR signaling
	(-)-Alkannin (Shikonin) 是从紫朱草中发现的一种天然产物，具有抗癌活性，可抑制细胞周期，诱导细胞凋亡，用作食品着色剂，在 Rho 激酶途径中可改善肝脏炎症。
T2860	Vanillyl Alcohol 4-Hydroxy-3-methoxybenzenemethanol,3-Methoxy-4-hydroxybenzyl alcohol,4-Hydroxy-3-methoxybenzyl alcohol,香兰醇,Vanillin alcohol,Vanillic alcohol	Apoptosis; Others	Apoptosis; Others
	Vanillyl Alcohol (3-Methoxy-4-hydroxybenzyl alcohol) 是一种酚类醇，具有抗血管生成、抗惊厥、抗炎、抗氧化、神经保护和抗伤害活性。它由香兰素衍生而来，在食品和饮料中用作调味剂。
T5S0053	Coptisine 黄连碱,Coptisin	Indoleamine 2,3-Dioxygenase (IDO)	Metabolism
	Coptisine (Coptisin) 是一种从黄连中分离到的生物碱，是非竞争性的IDO 抑制剂，Ki=为 5.8 μM，IC50=6.3 μM。
T3826	Polygalasaponin F 异牡荆苷,瓜子金皂苷己	NF-κB; TLR; Akt; PI3K	Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; PI3K/Akt/mTOR signaling
	Polygalasaponin F 是从瓜子金中提取的齐墩果烷型三萜皂苷，可通过调节TLR4-PI3K/AKT-NF-kB 信号通路减少神经炎症细胞因子的分泌，能降低炎性细胞因子肿瘤坏死因子 α 的释放。
T38495	Gypenoside LXXV
	Gypenoside LXXV, derived from Gynostemma pentaphyllum, is a deglycosylated form of ginsenoside Rb1. This compound effectively decreases cancer cell viability and exhibits potent anti-cancer properties.
TN3737	Cycloartane-3,24,25-triol	ATPase	Membrane transporter/Ion channel
	Cycloartane-3,24,25-triol has potential for development as an anti-cancer agent against prostate cancer. It reduces the viability of PC-3 and DU145 cell lines with IC50 values of 2.226 ± 0.28 μM and 1.67 ± 0.18 μM respectively.
TN3742	Cycloeucalenol	Others	Others
	Cycloeucalenol produces mild cardiotonic effects. Cycloeucalenol and its regio-isomer were present in a ratio of 1.04:1, a dose-dependent decrease in cell viability was observed.
TN4699	Ohchinin	Others	Others
	Ohchinin exhibits potent inhibitory activities with 26 - 66% reduction of melanin content at 100 μm concentration with almost no or low toxicity to the B16 melanoma cells (70 - 99% cell viability at 100 μm).
T13922	Thevetiaflavone 2-Genistein-5-methyl ether,Apigenin-5-methyl ether	BCL; Caspase	Apoptosis; Proteases/Proteasome
	Thevetiaflavone (2-Genistein-5-methyl ether) 是一种来自 Wikstroemia indica 的天然类黄酮，可抑制乳酸脱氢酶从细胞质中泄漏并提高细胞活力。
T79982	2'-epi-2'-O-Acetylthevetin B GHSC-74	Apoptosis	Apoptosis
	2'-epi-2'-O-Acetylthevetin B (GHSC-74) 为源自Cerbera manghas L种子的强心苷，其抑制HepG2细胞增殖并诱导细胞凋亡(apoptosis)及线粒体膜电位降低。
TN1440	Beta-Hydroxyisovalerylshikonin	EGFR; Tyrosine Kinases; Prostaglandin Receptor; Src; AMPK; Fatty Acid Synthase	Angiogenesis; Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; Metabolism; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Beta-hydroxyisovalerylshikonin 是分离自Lithospermium radix 的天然产物，具有抑制PTK 的作用，对 EGFR 和 v-Src 受体作用的IC50分别为 0.7 μM 和 1 μM。它对多种肿瘤细胞系均有抑制作用，可以高效诱导 NCI-H522 和 DMS114 细胞的死亡。
T35770	Cylindrospermopsin
	Cylindrospermopsin, a tricyclic uracil derivative, is a cyanobacterial toxin that was first discovered in an algal bloom contaminating a local drinking supply on Palm Island in Queensland, Australia after an outbreak of a mysterious disease. Cylindrospermopsin targets protein and glutathione synthesis in hepatocytes (IC50s = 1.3 and 2.4 &#181M, respectively), leading to cell death. [1] It has been shown to inhibit the activity of the uridine monophosphate synthase complex with a Ki value of 10 &...
TN4592	Murrangatin	IL Receptor; TNF; COX; Prostaglandin Receptor	Apoptosis; GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Murrangatin may be a valuable anti-tumor-promoting agent, it can significantly inhibit Epstein-Barr virus early antigen (EBV-EA) activation, and preserve the high viability of Raji cells, it also exhibits cytotoxicity against cholangiocarcinoma cell line,
TN3323	Monomethyl lithospermate Lithospermic acid monomethyl ester	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Monomethyl lithospermate (Lithospermic acid monomethyl ester) 具有潜在的抗病毒活性，通过激活PI5K/Akt信号传导，减轻体内大脑中动脉闭塞小鼠缺血性中风损伤，并在体外保护氧葡萄糖剥夺/复氧诱导的SHSY-3Y细胞。Monomethyl lithospermate 能提高 SHSY-5Y 细胞的生存能力，抑制线粒体膜电位 (MMOP) 崩溃，抑制细胞凋亡。Monomethyl lithospermate 还降低中动脉闭塞 (MCAO) 大鼠脑组织中的氧化应激水平，改善缺血性中风 (IS) 大鼠神经损伤。

天然产物

3,6-Dihydroxyflavone

Cat.No: T7982

Target: Others

3-O-Acetyloleanolic acid

Cat.No: T2S1396

Synonym: 齐墩果酸3-乙酸酯,齐墩果酸 3-乙酸酯

Target: Apoptosis

Cat.No: TN1425

Synonym: 苦艾素A3,白花猪母菜甙 A3

Target: ATPase, ROS, P-gp

Protosappanin B

Cat.No: T6S1780

Synonym: 原苏木素B,Q-100961,FT-0689654

Target: Apoptosis

Cat.No: T5S0636

Synonym: 柠檬酸,Citro,Citretten

Target: Apoptosis, Others, Endogenous Metabolite, Antibacterial, Antibiotic

Cat.No: TN1405

Synonym: 山金车内酯 D,山金车内酯D

Target: Akt, Caspase, PI3K, STAT, mTOR

Cat.No: T3S1873

Synonym: 塔拉乌头胺,塔拉萨敏

Target: Potassium Channel

Cat.No: T6S1653

Synonym: Alibiflorin,芍药内酯苷

Target: Reactive Oxygen Species

Cat.No: T2897

Synonym: (±)-Shikonin,Alkanet extract,Anchusin,紫草素,Anchusa acid

Target: Others

Cat.No: T4S1615

Synonym: 桑根酮C,桑根酮 C,Sanggenone C

Target: NF-κB

L-Chicoric Acid

Cat.No: T6S2391

Synonym: (-)-Chicoric acid,trans-Caffeoyltartaric acid,Chicoric acid,L-菊苣酸,dicaffeoyltartaric acid,菊苣酸

Target: Others, HIV Protease

5-Hydroxymethyl-2'-deoxycytidine

Cat.No: T40834

Synonym: 5hmdC,2'-脱氧-5-(羟甲基)胞啶

Target: PARP

Cat.No: T4958

Synonym: Alkannin,左旋紫草素,紫草素,Shikonin

Target: Apoptosis, PI3K

Vanillyl Alcohol

Cat.No: T2860

Synonym: 4-Hydroxy-3-methoxybenzenemethanol,3-Methoxy-4-hydroxybenzyl alcohol,4-Hydroxy-3-methoxybenzyl alcohol,香兰醇,Vanillin alcohol,Vanillic alcohol

Target: Apoptosis, Others

Cat.No: T5S0053

Synonym: 黄连碱,Coptisin

Target: Indoleamine 2,3-Dioxygenase (IDO)

Polygalasaponin F

Cat.No: T3826

Synonym: 异牡荆苷,瓜子金皂苷己

Target: NF-κB, TLR, Akt, PI3K

Gypenoside LXXV

Cat.No: T38495

Cycloartane-3,24,25-triol

Cat.No: TN3737

Target: ATPase

Cat.No: TN3742

Target: Others

Cat.No: TN4699

Target: Others

Thevetiaflavone

Cat.No: T13922

Synonym: 2-Genistein-5-methyl ether,Apigenin-5-methyl ether

Target: BCL, Caspase

2'-epi-2'-O-Acetylthevetin B

Cat.No: T79982

Synonym: GHSC-74

Target: Apoptosis

Beta-Hydroxyisovalerylshikonin

Cat.No: TN1440

Target: EGFR, Tyrosine Kinases, Prostaglandin Receptor, Src, AMPK, Fatty Acid Synthase

Cylindrospermopsin

Cat.No: T35770

Cat.No: TN4592

Target: IL Receptor, TNF, COX, Prostaglandin Receptor

Monomethyl lithospermate

Cat.No: TN3323

Synonym: Lithospermic acid monomethyl ester

Target: Akt, PI3K

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