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807

抑制剂 & 化合物

37

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T16834	S26131 N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide	MT Receptor	Neuroscience
	S26131 (N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide) 是一种选择性的褪黑激素配体 MT1 和 MT2 拮抗剂，对 MT1 和 MT2 的 Ki 值分别为 0.5 和 112 nM。
T8361	Tetraethylammonium bromide 四乙基溴化铵,TEAB,TEA bromide	Potassium Channel	Membrane transporter/Ion channel
	Tetraethylammonium bromide (TEA bromide) 可以选择性阻断钾通道。
T9604	beta-Estradiol 17-hemisuccinate	Estrogen Receptor/ERR	Endocrinology/Hormones
	beta-Estradiol 17-hemisuccinate 选择性染色富含雌激素受体 (ER) 的细胞。
T5536	SJA710-6	Others	Others
	SJA710-6 是一种能够特异性地分化 MSCs 为肝细胞样的小分子。
T77628	Bisindolylmaleimide III	PKC	Chromatin/Epigenetic; Cytoskeletal Signaling
	Bisindolylmaleimide III is a potent and selective inhibitor of protein kinase C (PKC).Bisindolylmaleimide III selectively interacts with PKCα or ribosomal S6 protein kinase 1 upon activation of these kinases.
T32108	HXJ42 HXJ-42,HXJ 42	Others	Others
	HXJ42 是一种 PP1 类似物，可选择性地有效作用于野生型 ZAP-70 (AS)。
T8819	SU-9516	CDK	Cell Cycle/Checkpoint
	SU-9516 是一种选择性有效的 ATP 竞争性 CDK 抑制剂。
T8745	PROTAC BRAF-V600E degrader-1 Compound 23	Raf	MAPK
	PROTAC BRAF-V600E degrader-1 (Compound 23) 选择性地诱导 BRAF-V600E 的降解，而不是野生型 BRAF。
T19319	Ethyl docosa-4,7,10,13,16,19-hexaenoate	Others	Others
	Ethyl cis-4,7,10,13,16,19-Docosahexaenoate, the ethyl ester of Docosahexaenoate (DHA), is selectively enriched in the ethyl ester fraction through the alcoholysis process involving fatty acid ethyl esters from tuna oil and lauryl alcohol.
T17266	Xipamide 希伯胺,Diurexan,Aquaphor	Others	Others
	Xipamide (Diurexan) 是一种磺胺类利尿剂，具有抗高血压特性。Xipamide 可选择性地抑制阴离子交换器。
T0333	Aniracetam Ro 13-5057,阿尼西坦,茴拉西坦	Dopamine Receptor; 5-HT Receptor; GluR; AChR; iGluR	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Aniracetam (Ro 13-5057) 是一种促智和神经保护药物，可选择性地调节 AMPA 受体和 nAChR。
T6801	CeMMEC13	Carboxypeptidase; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Proteases/Proteasome
	CeMMEC13 是一种异喹啉酮，可选择性抑制 TAF1 的第二个溴结构域，IC50为 2.1 μM。
T5097	Ezatiostat TER199(free base),TLK199	Apoptosis; Glutathione Peroxidase; GST	Apoptosis; Metabolism; oxidation-reduction
	Ezatiostat (TER199(free base)) 是一种谷胱甘肽的三肽类似物，也是一种选择性的口服活性的谷胱甘肽 S-转移酶 P1-1 (GSTP1) 抑制剂。它通过抑制GSTP1导致 JNK 激活，刺激淋巴细胞生成和骨髓祖细胞增殖，可研究骨髓增生异常综合症。
T6418	BMS-378806 BMS378806,BMS-806,1-[(2R)-4-苯甲酰基-2-甲基-1-哌嗪基]-2-(4-甲氧基-1H-吡咯并[2,3-B]吡啶-3-基)-1,2-乙二酮	gp120/CD4; HIV Protease	Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome
	BMS-378806 (BMS-806) 是一种 HIV-1 抑制剂，可选择性抑制 HIV-1 gp120 结合到 CD4 受体，EC50为 0.85-26.5 nM。
T7008	Vacquinol-1 Vacquinol 1	JNK	MAPK
	Vacquinol-1 能够激活 MAPK 通路，是MKK4特异性激活剂。它可以诱导肝细胞癌细胞凋亡，在多形性胶质母细胞瘤小鼠模型中特异性诱导人胶质母细胞瘤细胞死亡、减缓肿瘤进展并延长生存期。
T37596	Terevalefim	c-Met/HGFR	Tyrosine Kinase/Adaptors
	Terevalefim 是干细胞生长因子的一种类似物，对c-Met 受体有选择性激活作用。
T7830	Windorphen	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	Windorphen 是一种 Wnt 抑制剂，可选择性地消除 Wnt 信号传导。
T10276	AKT Kinase Inhibitor	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	AKT Kinase Inhibitor 是一种具有抗肿瘤活性的 Akt 抑制剂，以剂量依赖的方式选择性抑制细胞增殖。
T5345	V-9302	Others	Others
	V-9302 是一种跨膜谷氨酰胺通量的竞争性拮抗剂。它选择性的靶向氨基酸转运体 ASCT2 (SLC1A5)，不影响 ASCT1。它能够阻碍 HEK-293 细胞中由 ASCT2 介导的谷氨酰胺摄取 (IC50=9.6 μM)。
T11234	ESI-08	cAMP	GPCR/G Protein
	ESI-08 是 EPAC2 的有效拮抗剂，IC50 为 8.4 μM。 ESI-08 特异性阻断 cAMP 诱导的 EPAC 活化，但不阻断 cAMP 介导的 PKA 活化。
T28895	T-0509 T 0509,T0509	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	T-0509 是一种选择性 beta 1 受体激动剂，可增加犬心室肌的肌力，选择性下调大鼠心脏 β 1-肾上腺素受体。
T10459	Banoxantrone dihydrochloride AQ4N dihydrochloride,AZD1689 2HCl	NOS	Immunology/Inflammation
	Banoxantrone dihydrochloride (AQ4N dihydrochloride) 是一种新型缺氧细胞毒素，通过 iNOS 依赖机制选择性地杀死缺氧细胞。
T11533	Z-HA155 CS-963	PDE	Metabolism
	Z-HA155 (CS-963) 是一种高效的 ATX 选择性抑制剂，其 IC50=5.7 nM。
T9587	CCTA-1523	Others; ABC	Membrane transporter/Ion channel; Others
	CCTA-1523 是 ABCG2 抑制剂的外排功能。它选择性地逆转癌细胞中 ABCG2 介导的 MDR。
T11142	EACC	Autophagy	Autophagy
	EACC 是自噬的可逆抑制剂，可阻断自噬通量。它对自噬体特异性的 SNARE Stx17 易位具有选择性抑制作用，从而阻止自噬体与溶酶体的融合。
T11153	EG00229	Others	Others
	EG00229 selectively inhibits VEGF-A binding to NRP1 b1 domain with an IC50 of 3 μM, but has no effect on VEGFA binding to VEGFR-1 and VEGFR-2. EG00229 is a neuropilin 1 (NRP1) receptor antagonist.
T5170	KHS101 hydrochloride 盐酸KHS101	FGFR; Microtubule Associated	Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	KHS101 hydrochloride 能够选择性的诱导神经元分化表型，能够与转化酸性含螺旋蛋白发生相互作用。
T24159	IHR-1 IHR 1	Smo	Stem Cells
	IHR-1 是一种Smo 拮抗剂，不能透过细胞膜。
T6388	Amprenavir 141W94,安普那韦,Prozei,KVX-478,VX-478,安瑞那韦	SARS-CoV; HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Amprenavir (KVX-478) 是一种 HIV 蛋白酶抑制剂，Ki 为0.6 nM。它也是 SARS-CoV 3CLpro 抑制剂，IC50为 1.09 μM。
TP1015	NFAT Inhibitor VIVIT peptide	Others	Others
	NFAT Inhibitor (VIVIT peptide) 是NFAT 的细胞渗透性肽抑制剂，能够选择性抑制钙调磷酸酶介导的NFAT 脱磷酸作用。
T19518L	Physalaemin acetate	Neurokinin receptor	GPCR/G Protein; Neuroscience
	Physalaemin acetate 是一种非哺乳动物速激肽，在选择性结合神经激肽 1 (NK1) 受体时具有高亲和力。
T1801	SR9243	Liver X Receptor	Metabolism
	SR9243 是一种 liver-X-receptor 的反向激动剂，可诱导 LXR-辅阻遏物相互作用。
T4348	Syk Inhibitor II	5-HT Receptor; Syk	Angiogenesis; GPCR/G Protein; Neuroscience; Tyrosine Kinase/Adaptors
	Syk Inhibitor II 是一种可渗透细胞、具有 ATP 竞争性的嘧啶-甲酰胺化合物，可选择性且可逆地抑制 Syk，IC50为 41 nM。
T24542	NP-313 NP 313,NSC 4264,NSC-4264,NSC4264
	NP-313 (NSC-4264) 是一种有效的抗血栓剂，对血栓素 A 2 合成和选择性抑制由 SOCC 介导的 Ca 2+ 内流有抑制作用，可以抑制血小板的聚集和活化。
T15019	CUR61414	Hedgehog/Smoothened	GPCR/G Protein; Stem Cells
	CUR61414 是 Hedgehog 信号通路的细胞渗透性抑制剂 (IC50 = 100-200 nM)，并选择性地结合 smoothened (Ki = 44 nM)。
T7175	Alflutinib mesylate 甲磺酸伏美替尼,AST2818 mesylate	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Alflutinib mesylate (AST2818 mesylate) 是一种不可逆的酪氨酸激酶抑制剂，可选择性抑制 EGFR 突变。
T21674L	PKA inhibitor fragment (6-22) amide Acetate PKA inhibitor fragment (6-22) amide Acetate(121932-06-7 Free base)	PKA	Tyrosine Kinase/Adaptors
	PKA inhibitor fragment (6-22) amide Acetate 是一种通过结合底物位点选择性抑制PKA 活性的合成肽(IC50 < 2 nM)。
T6180	INH6	Apoptosis; Microtubule Associated	Apoptosis; Cytoskeletal Signaling
	INH6 是一种有效的 Hec1 抑制剂，可选择性地破坏 Hec1/Nek2 相互作用并诱导染色体错位。它抑制HeLa 细胞生长的IC50值为2.4 μM。
T60150	(1S,2R)-Alicapistat	Cysteine Protease	Proteases/Proteasome
	(1S,2R)-Alicapistat ((1S,2R)-ABT-957) is a highly efficient, orally active compound that selectively inhibits human calpains 1 and 2, with promising implications for Alzheimer's disease (AD) therapy [1]. This compound effectively addresses the metabolic liability associated with carbonyl reduction, while demonstrating potent inhibition of calpain 1 with an IC50 value of 395 nM [2].
T0101	Doxazosin mesylate UK 33274 mesylate,甲磺酸多沙唑嗪	Mitophagy; Adrenergic Receptor; Autophagy	Autophagy; GPCR/G Protein; Neuroscience
	Doxazosin mesylate (UK 33274 mesylate) 是一种喹唑啉衍生物。它是一种选择性拮抗突触后α1-肾上腺素能受体。
T9575	MRTX9768	Histone Methyltransferase	Chromatin/Epigenetic
	MRTX-9768 是一种有效的、选择性的、具有口服活性的 PRMT5-MTA 复合体抑制剂，可选择性靶向 MTAP/CDKN2A 缺失的肿瘤。
T37562	C16 Ceramide N-acylsphingosine,C16 Ceramide (d18:1/16:0),Palmitoyl Ceramide,N-Palmitoylsphingosine	p53	Apoptosis
	C16 Ceramide (Palmitoyl Ceramide) 是一种天然小分子，通过直接选择性结合激活 p53。
T15769	LMT-28	IL Receptor	Immunology/Inflammation
	LMT-28 是一种 IL-6 抑制剂，选择性抑制 IL-6 诱导的 gp130、STAT3 和 JAK2 磷酸化。
T8234	ML401	EBI2/GPR183	GPCR/G Protein
	ML401 是EBI2(也称为GPR183)的选择性拮抗剂(IC50:1.03 nM)。它在趋化性分析中显示活性 (IC50:6.24 nM)。它表现出良好的稳定性，且无细胞毒性。可用作化学探针。
T5313	Sobetirome IACS-010759,QRX-431	Thyroid hormone receptor(THR)	Endocrinology/Hormones
	Sobetirome (IACS-010759) 是一种甲状腺激素受体 β (TRβ) 激动剂，能够选择性的结合到TRβ-1(EC50:0.16 μM)。
T1519	Rimonabant hydrochloride 盐酸利莫那班,SR 151716A,SR 141716A	Cannabinoid Receptor; Antibacterial	GPCR/G Protein; Microbiology/Virology
	Rimonabant hydrochloride (SR 141716A) 是中心大麻素受体 1 的高效选择性反向激动剂， Ki 值为1.8 nM。它也能够抑制分枝杆菌膜蛋白3。
T22086	HA 155 Autotaxin Inhibitor IV	PDE	Metabolism
	HA 155 (Autotaxin Inhibitor IV) 是一种基于硼酸的化合物，通过选择性结合其催化苏氨酸来抑制 ATX，IC50 为 5.7 nM。
T37170	N1-Acetylspermidine hydrochloride N1-Acetylspermidine (hydrochloride)	Endogenous Metabolite	Metabolism
	N1-Acetylspermidine hydrochloride 是亚精胺的乙酰基衍生物。 N1-Acetylspermidine hydrochloride 是多胺氧化酶的底物，可选择性地提高其在人结直肠腺癌中的水平。
T5330	Fluralaner AH252723,氟雷拉纳,A1443	GABA Receptor; Parasite	Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience
	Fluralaner (A1443) 是一种异恶唑啉杀外寄生虫剂。它有效且选择性地抑制 GABA 受体通道阻滞剂 EBOB 与家蝇头膜的结合，IC50值为 455 pM。
T2037	TH588	DNA/RNA Synthesis; MTH1	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	TH588 是 nudix 水解酶家族抑制剂，可有效和选择性地参与和抑制细胞中的 MTH1，IC50值 5 nM。

化合物

Cat.No: T16834

Synonym: N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide

Target: MT Receptor

Tetraethylammonium bromide

Cat.No: T8361

Synonym: 四乙基溴化铵,TEAB,TEA bromide

Target: Potassium Channel

beta-Estradiol 17-hemisuccinate

Cat.No: T9604

Target: Estrogen Receptor/ERR

Cat.No: T5536

Target: Others

Bisindolylmaleimide III

Cat.No: T77628

Target: PKC

Cat.No: T32108

Synonym: HXJ-42,HXJ 42

Target: Others

Cat.No: T8819

Target: CDK

PROTAC BRAF-V600E degrader-1

Cat.No: T8745

Synonym: Compound 23

Target: Raf

Ethyl docosa-4,7,10,13,16,19-hexaenoate

Cat.No: T19319

Target: Others

Cat.No: T17266

Synonym: 希伯胺,Diurexan,Aquaphor

Target: Others

Cat.No: T0333

Synonym: Ro 13-5057,阿尼西坦,茴拉西坦

Target: Dopamine Receptor, 5-HT Receptor, GluR, AChR, iGluR

Cat.No: T6801

Target: Carboxypeptidase, DNA/RNA Synthesis

Cat.No: T5097

Synonym: TER199(free base),TLK199

Target: Apoptosis, Glutathione Peroxidase, GST

Cat.No: T6418

Synonym: BMS378806,BMS-806,1-[(2R)-4-苯甲酰基-2-甲基-1-哌嗪基]-2-(4-甲氧基-1H-吡咯并[2,3-B]吡啶-3-基)-1,2-乙二酮

Target: gp120/CD4, HIV Protease

Cat.No: T7008

Synonym: Vacquinol 1

Target: JNK

Cat.No: T37596

Target: c-Met/HGFR

Cat.No: T7830

Target: Wnt/beta-catenin

AKT Kinase Inhibitor

Cat.No: T10276

Target: Akt

Cat.No: T5345

Target: Others

Cat.No: T11234

Target: cAMP

Cat.No: T28895

Synonym: T 0509,T0509

Target: Adrenergic Receptor

Banoxantrone dihydrochloride

Cat.No: T10459

Synonym: AQ4N dihydrochloride,AZD1689 2HCl

Target: NOS

Cat.No: T11533

Synonym: CS-963

Target: PDE

Cat.No: T9587

Target: Others, ABC

Cat.No: T11142

Target: Autophagy

Cat.No: T11153

Target: Others

KHS101 hydrochloride

Cat.No: T5170

Synonym: 盐酸KHS101

Target: FGFR, Microtubule Associated

Cat.No: T24159

Synonym: IHR 1

Target: Smo

Cat.No: T6388

Synonym: 141W94,安普那韦,Prozei,KVX-478,VX-478,安瑞那韦

Target: SARS-CoV, HIV Protease

Cat.No: TP1015

Synonym: VIVIT peptide

Target: Others

Physalaemin acetate

Cat.No: T19518L

Target: Neurokinin receptor

Cat.No: T1801

Target: Liver X Receptor

Syk Inhibitor II

Cat.No: T4348

Target: 5-HT Receptor, Syk

Cat.No: T24542

Synonym: NP 313,NSC 4264,NSC-4264,NSC4264

Cat.No: T15019

Target: Hedgehog/Smoothened

Alflutinib mesylate

Cat.No: T7175

Synonym: 甲磺酸伏美替尼,AST2818 mesylate

Target: EGFR

PKA inhibitor fragment (6-22) amide Acetate

Cat.No: T21674L

Synonym: PKA inhibitor fragment (6-22) amide Acetate(121932-06-7 Free base)

Target: PKA

Cat.No: T6180

Target: Apoptosis, Microtubule Associated

(1S,2R)-Alicapistat

Cat.No: T60150

Target: Cysteine Protease

Doxazosin mesylate

Cat.No: T0101

Synonym: UK 33274 mesylate,甲磺酸多沙唑嗪

Target: Mitophagy, Adrenergic Receptor, Autophagy

Cat.No: T9575

Target: Histone Methyltransferase

Cat.No: T37562

Synonym: N-acylsphingosine,C16 Ceramide (d18:1/16:0),Palmitoyl Ceramide,N-Palmitoylsphingosine

Target: p53

Cat.No: T15769

Target: IL Receptor

Cat.No: T8234

Target: EBI2/GPR183

Cat.No: T5313

Synonym: IACS-010759,QRX-431

Target: Thyroid hormone receptor(THR)

Rimonabant hydrochloride

Cat.No: T1519

Synonym: 盐酸利莫那班,SR 151716A,SR 141716A

Target: Cannabinoid Receptor, Antibacterial

Cat.No: T22086

Synonym: Autotaxin Inhibitor IV

Target: PDE

N1-Acetylspermidine hydrochloride

Cat.No: T37170

Synonym: N1-Acetylspermidine (hydrochloride)

Target: Endogenous Metabolite

Cat.No: T5330

Synonym: AH252723,氟雷拉纳,A1443

Target: GABA Receptor, Parasite

Cat.No: T2037

Target: DNA/RNA Synthesis, MTH1

Cat. No.	Product Name	Target	Signaling Pathways
T3719	Daminozide Succinic Acid,DMASA,Aminozide,丁酰肼	Histone Demethylase	Chromatin/Epigenetic
	Daminozide (Succinic Acid) 是一种植物生长调节剂，选择性地抑制 KDM2/7 JmjC 亚家族，对PHF8、KDM2A 和KIAA1718的IC50值分别为 0.55、1.5 和 2.1 μM。
TN3575	(±)-Cannabichromene Cannabichromene,大麻色原烯,Cannabichrome	Cannabinoid Receptor	GPCR/G Protein
	(±)-Cannabichromene 是一种发现于大麻的 2,2-dimethyl-2H-chromene 衍生物。
T0344L	Miconazole nitrate NSC 169434 Nitrate,硝酸咪康唑,R18134 nitrate	Antibacterial; Antibiotic; Antifungal	Microbiology/Virology
	Miconazole nitrate (R18134 nitrate) 是咪唑类可抗菌的抗真菌剂。
T8165	Erythrodiol	Endogenous Metabolite; ABC	Membrane transporter/Ion channel; Metabolism
	Erythrodiol 是一种橄榄油的成分，能够选择性抑制ABCA1蛋白的降解来促进胆固醇外流，有用于动脉粥样硬化的研究潜力。
TN1560	Dehydroeffusol 去氢厄弗酚,5-Ethenyl-1-Methylphenanthrene-2,7-Diol,Dehydro Effusol	MMP; ERK; GPR; Others	Endocrinology/Hormones; GPCR/G Protein; MAPK; Others; Proteases/Proteasome
	Dehydroeffusol (Dehydro Effusol) 通过选择性诱导肿瘤抑制性内质网应激和中度细胞凋亡来抑制胃癌细胞生长和致瘤性，具有抗癌、抗焦虑和镇静作用。
T6290	Tanespimycin 坦螺旋霉素,17-AAG,CP 127374,NSC 330507,KOS 953	Apoptosis; Mitophagy; HSP; Antibacterial; Antibiotic; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling; Metabolism; Microbiology/Virology
	Tanespimycin (KOS 953) 是一种 Hsp90 抑制剂，可选择性抑制 BT474 肿瘤细胞 Hsp90，IC50为 5 nM。它消耗细胞内 STK38/NDR1，并降低 STK38 激酶活性，还能下调stk38基因表达。
TJS1183	Cyclen 轮环藤宁,1,4,7,10-tetraazacyclododecane	Others	Others
	Cyclen (1,4,7,10-tetraazacyclododecane) 是一种氮杂冠醚的类似物，是制备有效的大环螯合物的中间体，是制备磁共振造影剂的前体物质。
T1879	3-Methyladenine 3-MA,3-甲基腺嘌呤,NSC 66389	Mitophagy; PI3K; Endogenous Metabolite; Autophagy	Autophagy; Metabolism; PI3K/Akt/mTOR signaling
	3-Methyladenine (3-MA) 是一种 PI3K 抑制剂，选择性抑制 IB 类 PI3Kγ (IC50=60 μM) 和 III 类 VPS34 (IC50=25 μM)。3-Methyladenine 具有自噬抑制活性。
TN6848	Piperonylic acid 胡椒酸,2H-1,3-benzodioxole-5-carboxylic acid	P450	Metabolism
	Piperonylic acid (2H-1,3-benzodioxole-5-carboxylic acid) 是一种具有亚甲二氧基活性的天然分子，与反式肉桂酸结构相似，可作为选择性反式肉桂酸 4-羟化酶的灭活剂。
T8641	Vancomycin	Antibacterial; Antibiotic; Autophagy	Autophagy; Microbiology/Virology
	Vancomycin 是一种糖肽类抗生素，可以通过改变细胞膜的渗透性并选择性地抑制核糖核酸的合成以发挥抗菌活性。Vancomycin 可以用于治疗所有抗生素均无效的严重感染。
T3030	L-Sophoridine L-槐定碱,Sophoridine,Matridin-15-one	Others	Others
	L-Sophoridine (Matridin-15-one) 一种从药用植物中提取的天然产物，具有多种药理作用，包括抗Y 作用，可在体外和体内选择性诱导多种人体Y 细胞凋亡；然而，其作用机制需要进一步阐述。
T2996	Tetrandrine NSC-77037,d-Tetrandrine,Hanfangchin A,粉防己碱,Fanchinine,Sinomenine A,汉防己甲素	Potassium Channel; Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Tetrandrine (Sinomenine A) 是来自粉防己的一种双苯基异喹啉生物碱，可抑制电压门控钙离子通道 (ICa) 和 Ca2+激活的钾离子通道。
T6947	Piperlongumine PPLGM,荜茇酰胺,Piplartine	Apoptosis; ERK; Ferroptosis; Reactive Oxygen Species; ROS; Antibacterial; Autophagy	Apoptosis; Autophagy; Immunology/Inflammation; MAPK; Metabolism; Microbiology/Virology; NF-κB
	Piperlongumine (Piplartine) 是一种来自 Piper longum L. 的天然生物碱，具有抗炎、抗菌、抗血管生成、抗氧化、抗肿瘤和抗糖尿病等活性。它选择性地杀死癌细胞并增强活性氧的水平。它具有抗心肌纤维化的作用，通过抑制 ERK1/2 信号通路抑制肌成纤维细胞的转化。
TN1037	Groenlandicine	Topoisomerase	DNA Damage/DNA Repair
	Groenlandicine 是来自黄连的一种原小檗碱生物碱，能诱导拓扑异构酶 I 介导的 DNA 裂解。它对人类重组醛糖还原酶(HRAR)具有中度的抑制作用，IC50值为 154.2 μM。
T3862	Irigenin	NF-κB; Integrin	Cytoskeletal Signaling; NF-κB
	Irigenin 可通过特异性和选择性地阻断 Extra Domain A 域的 C-C 环上α9β1和α4β1整合素结合位点，介导其抗转移作用。可通过增强胃癌细胞中促凋亡分子的表达来敏化 TRAIL 诱导的凋亡，具有抗癌作用。
T4900	(±)-Methyl Jasmonate (±)-茉莉酸甲酯,甲基茉莉酮酸酯,(±)-Jasmonic Acid methyl ester,Methyl 2-(3-oxo-2-(pent-2-en-1-yl)cyclopentyl)acetate	Others; Endogenous Metabolite	Metabolism; Others
	Methyl 2-(3-oxo-2-(pent-2-en-1-yl)cyclopentyl)acetate ((±)-Jasmonic Acid methyl ester) 是内源性代谢产物的一种。
T13752	L-(+)-Arabinose	Endogenous Metabolite	Metabolism
	L-(+)-Arabinose 能够选择性抑制肠道蔗糖酶，并抑制因蔗糖摄入而导致的血浆葡萄糖提高。
TQ0163	Sagittatoside A Icariin-A,箭藿苷 A	Estrogen/progestogen Receptor	Endocrinology/Hormones
	Sagittatoside A selectively activates estrogen response element (ERE)-luciferase activity via ERα.
T11274	Ferulenol	Others	Others
	Ferulenol, a sesquiterpene prenylated coumarin derivative, exhibits potent antimycobacterial activity and haemorrhagic action. This compound selectively targets succinate ubiquinone reductase within the ubiquinone cycle as its specific mode of inhibition.
T78477	Drupanin
	Drupanin是从绿色蜂胶中分离出的一种化合物，能选择性抑制AKR1C3酶，并具有研究乳腺癌的潜力。
T35605	Apoptolidin
	Apoptolidin is an apoptosis inducer originally isolated from Nocardiopsis bacteria. It inhibits the mitochondrial F1FO ATPase (Ki = 4-5 μM). Apoptolidin selectively kills transformed glial cells without significantly affecting untransformed cells. It also has antibiotic and antifungal actions.
T78491	Phytohemagglutinin P PHA-P
	Phytohemagglutinin P（PHA-P）是一类植物凝集素，以选择性方式激活血源性或淋巴样单核细胞的有丝分裂。
T19886	Cirsilineol Fastigenin,SPM 927,Eupatrin	Apoptosis; COX; STAT	Apoptosis; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells
	Cirsilineol (Eupatrin) 是从 Artemisia vestita Wall 的草本植物中分离出来的，具有免疫抑制、抗增殖和抗肿瘤特性。 Cirsilineol 通过线粒体途径选择性诱导细胞凋亡。
T37055	Cytostatin
	Cytostatin is a natural antitumor inhibitor of cell adhesion to extracellular matrix, blocking adhesion of B16 melanoma cells to laminin and collagen type IV in vitro (IC50s = 1.3 and 1.4 μg/ml, respectively) and B16 cells metastatic activity in mice. It induces apoptosis of FS3 mouse fibrosarcoma cells (IC50 = 3.1 μg/ml). Cytostatin potently and selectively inhibits protein phosphatase 2A (PP2A; IC50 = 29 nM against the catalytic subunit), while having no effect against PP1, PP2B, or PP5.
TN2681	Elasticamide 2-(2'-Hydroxytetracosanoylamino)-octadecane-1,3,4-triol	Others	Others
	(2S,3S,4R,2'R)-2-(2'-hydroxytetracosanoylamino)octadecane-1,3,4-triol shows selectively inhibitory activity against phospholipase A 2 (PLA 2) secreted from Crotalus adamenteus venom at concentration of 100 ug/mL.
T62625	11-O-Methylpseurotin A
	11-O-Methylpseurotin A为一种(PKS/NRPS)混合聚酮合成酶-非核糖体肽合成酶化合物，其特性为选择性抑制Hof1缺失菌株。
T27564	Hymenidin	5-HT Receptor	GPCR/G Protein; Neuroscience
	Hymenidin是一种从冲绳海绵Hymeniacidon sp。中分离出的生物碱，是一种5-羟色胺能受体拮抗剂和电压门控钾通道抑制剂，具有潜在的抗原生动物作用，可选择性结合 FOXO1 DNA ，可降低去极化诱导的细胞钙升高。
TN3655	Cimiside E	ERK; TNF; ROS; Akt; PI3K; PKC; PPAR	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; Metabolism; PI3K/Akt/mTOR signaling
	Cimiside E has anti-inflammatory activity, it selectively inhibits TNF-α-induced expression of VCAM-1 at least by upregulation of PPAR-γ, and signals for ERK1/2, PI3K, and PKC are involved in this effect.Cimiside E may be an effective chemopreventive agen
TN2147	Retrorsine	P450; OCT	Membrane transporter/Ion channel; Metabolism
	Retrorsine 特异性地抑制肝细胞增殖，并在肝损伤后唤起小肝细胞样祖细胞。逆转录酶可用于肝细胞损伤的研究。
TN2682	2-2'-(Hydroxytetracosanoylamino)-octadecane-1,3,4-triol tetraacetate	Others	Others
	(2S,3S,4R,2'R )-2-(2'-Hydroxytetracosanoylamino) octadecane-1,3,4-triol at concentration of 100 ug/mL shows selectively inhibitory activity against phospholipase A 2 (PLA 2) secreted from Crotalus adamenteus venom, but inactive against PLA 2 of bee venom
T1521	(±)-10-Hydroxycamptothecin Hydroxy Camptothecine,10-羟基喜树碱,10-Hydroxycamptothecin	Topoisomerase	DNA Damage/DNA Repair
	(±)-10-Hydroxycamptothecin (Hydroxy Camptothecine) 是一种从喜树茎木中分离出来的生物碱，抑制拓扑异构酶 I 活性，具有广谱抗肿瘤活性。
T75630	Ganoderic acid Mf
	Ganoderic acid Mf为具有抗肿瘤活性的三萜类化合物，能导致细胞周期在G1期停滞，并在正常细胞与癌细胞中显示高度选择性，通过线粒体介导途径促进细胞凋亡(apoptosis)。
T75686	Enfumafungin
	Enfumafungin，一种从Hormonema carpetanum菌提取的三萜糖苷，具有抗真菌特性，主要通过作为(1,3)-beta-D-葡聚糖合酶抑制剂影响真菌细胞壁发挥作用。其对酵母和多数真菌（除隐球菌外）有效，但不会抑制枯草芽孢杆菌的生长。
TN5033	Skullcapflavone I	IL Receptor; Caspase; Prostaglandin Receptor	Apoptosis; GPCR/G Protein; Immunology/Inflammation; Proteases/Proteasome
	Skullcapflavone I has anti-inflammatory and anti-allergic potential, it can significantly inhibit LPS stimulated NO and PGE(2) release in J774A.1 macrophages and inhibit LPS induced IL-6 production in a concentration dependent manner. Skullcapflavone I se
T69254	Ajmalicine hydrochloride Raubasine hydrochloride
	Ajmalicine (Raubasine) hydrochloride 是一种有效的抗肾上腺素 (adrenolytic) 剂，优先阻断 α1-肾上腺素受体 (α1-adrenoceptor)。Ajmalicine hydrochloride 是一种可逆性但非竞争性尼古丁受体 (nicotine receptor) 完全抑制剂，其 IC50为 72.3 μM。Ajmalicine hydrochloride 还可用于降压、蛇毒，具有镇静活性。
T36417	Nargenicin Antibiotic 47444
	Nargenicin is a macrolide antibiotic that selectively inhibits the growth of S. aureus, methicilin resistant S. aureus (MRSA), and M. luteus (MICs = 0.6, 0.3, and 2.5 μg/ml, respectively) over a panel of 11 Gram-positive and Gram-negative bacteria (MICs = >80 μg/ml). [1] It dose-dependently inhibits S. aureus DnaE in the presence of DNase I-activated DNA and E. coli DnaE when used at concentrations of 0.00001-0.1 and 0.01-100 μg/mL, respectively. [2] In murine BV-2 microglial cells, nargenicin (...
T37609	(rel)-Asperparaline A
	Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces...

天然产物

Cat.No: T3719

Synonym: Succinic Acid,DMASA,Aminozide,丁酰肼

Target: Histone Demethylase

(±)-Cannabichromene

Cat.No: TN3575

Synonym: Cannabichromene,大麻色原烯,Cannabichrome

Target: Cannabinoid Receptor

Miconazole nitrate

Cat.No: T0344L

Synonym: NSC 169434 Nitrate,硝酸咪康唑,R18134 nitrate

Target: Antibacterial, Antibiotic, Antifungal

Cat.No: T8165

Target: Endogenous Metabolite, ABC

Cat.No: TN1560

Synonym: 去氢厄弗酚,5-Ethenyl-1-Methylphenanthrene-2,7-Diol,Dehydro Effusol

Target: MMP, ERK, GPR, Others

Cat.No: T6290

Synonym: 坦螺旋霉素,17-AAG,CP 127374,NSC 330507,KOS 953

Target: Apoptosis, Mitophagy, HSP, Antibacterial, Antibiotic, Autophagy

Cat.No: TJS1183

Synonym: 轮环藤宁,1,4,7,10-tetraazacyclododecane

Target: Others

3-Methyladenine

Cat.No: T1879

Synonym: 3-MA,3-甲基腺嘌呤,NSC 66389

Target: Mitophagy, PI3K, Endogenous Metabolite, Autophagy

Piperonylic acid

Cat.No: TN6848

Synonym: 胡椒酸,2H-1,3-benzodioxole-5-carboxylic acid

Target: P450

Cat.No: T8641

Target: Antibacterial, Antibiotic, Autophagy

Cat.No: T3030

Synonym: L-槐定碱,Sophoridine,Matridin-15-one

Target: Others

Cat.No: T2996

Synonym: NSC-77037,d-Tetrandrine,Hanfangchin A,粉防己碱,Fanchinine,Sinomenine A,汉防己甲素

Target: Potassium Channel, Calcium Channel

Cat.No: T6947

Synonym: PPLGM,荜茇酰胺,Piplartine

Target: Apoptosis, ERK, Ferroptosis, Reactive Oxygen Species, ROS, Antibacterial, Autophagy

Cat.No: TN1037

Target: Topoisomerase

Cat.No: T3862

Target: NF-κB, Integrin

(±)-Methyl Jasmonate

Cat.No: T4900

Synonym: (±)-茉莉酸甲酯,甲基茉莉酮酸酯,(±)-Jasmonic Acid methyl ester,Methyl 2-(3-oxo-2-(pent-2-en-1-yl)cyclopentyl)acetate

Target: Others, Endogenous Metabolite

L-(+)-Arabinose

Cat.No: T13752

Target: Endogenous Metabolite

Sagittatoside A

Cat.No: TQ0163

Synonym: Icariin-A,箭藿苷 A

Target: Estrogen/progestogen Receptor

Cat.No: T11274

Target: Others

Cat.No: T78477

Cat.No: T35605

Phytohemagglutinin P

Cat.No: T78491

Synonym: PHA-P

Cat.No: T19886

Synonym: Fastigenin,SPM 927,Eupatrin

Target: Apoptosis, COX, STAT

Cat.No: T37055

Cat.No: TN2681

Synonym: 2-(2'-Hydroxytetracosanoylamino)-octadecane-1,3,4-triol

Target: Others

11-O-Methylpseurotin A

Cat.No: T62625

Cat.No: T27564

Target: 5-HT Receptor

Cat.No: TN3655

Target: ERK, TNF, ROS, Akt, PI3K, PKC, PPAR

Cat.No: TN2147

Target: P450, OCT

2-2'-(Hydroxytetracosanoylamino)-octadecane-1,3,4-triol tetraacetate

Cat.No: TN2682

Target: Others

(±)-10-Hydroxycamptothecin

Cat.No: T1521

Synonym: Hydroxy Camptothecine,10-羟基喜树碱,10-Hydroxycamptothecin

Target: Topoisomerase

Ganoderic acid Mf

Cat.No: T75630

Cat.No: T75686

Skullcapflavone I

Cat.No: TN5033

Target: IL Receptor, Caspase, Prostaglandin Receptor

Ajmalicine hydrochloride

Cat.No: T69254

Synonym: Raubasine hydrochloride

Cat.No: T36417

Synonym: Antibiotic 47444

(rel)-Asperparaline A

Cat.No: T37609

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