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Search Results for " autophosphorylation "

82

抑制剂 & 化合物

1

天然产物

11

重组蛋白

2

同位素标记化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T39185	pp60 (v-SRC) Autophosphorylation Site, Phosphorylated pp60 (v-SRC) Autophosphorylation Site, Phosphorylated
	pp60 (v-SRC) Autophosphorylation Site, Phosphorylated is a phosphorylated peptide derived from an EGFR substrate. It serves as a valuable tool for quantifying phosphorylated substrates in screening EGFR Kinase inhibitors.
T21761	HNMPA	IGF-1R	Tyrosine Kinase/Adaptors
	HNMPA 是膜不可渗透的胰岛素受体酪氨酸激酶 (insulin receptor tyrosine kinase) 抑制剂。HNMPA 可以抑制人胰岛素受体的酪氨酸和丝氨酸自磷酸化。HNMPA 对环 AMP 依赖性蛋白激酶或蛋白激酶 C 活性没有影响。
T36287	Pirtobrutinib	BTK	Angiogenesis; Tyrosine Kinase/Adaptors
	Pirtobrutinib (LOXO-305) is an advanced BTK inhibitor that displays high selectivity and operates through a non-covalent mechanism. This compound effectively inhibits various BTK C481 substitution mutations, leading to tumor regression in BTK-dependent lymphoma tumors in mouse xenograft models. Furthermore, Pirtobrutinib exhibits remarkable selectivity for BTK, with more than a 300-fold difference compared to 370 other kinases tested. Notably, at a concentration of 1 μM, Pirtobrutinib demonstrat...
T14765	BOS-172722	Kinesin	Cytoskeletal Signaling
	BOS-172722 是一种单极纺锤体 1 (MPS1) 检查点抑制剂，对MPS1 (1 mM ATP) 和P-MPS1 的IC50值分别为 11 nM 和 63 nM。它可研究多种乳腺癌。
T14137	AG 1295	PDGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	AG 1295 是选择性血小板衍生生长因子受体酪氨酸激酶抑制剂。它能抑制 PDGFR 的自磷酸化，对 EGF 受体的自磷酸化无影响。
T1770	GNE-9605	LRRK2	Autophagy
	GNE-9605 是一个高效，选择性和能脑渗透的LRRK2抑制剂，IC50为19 nM。
T22396	PF-6274484 PF 6274484	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	PF-6274484 是一种EGFR 抑制剂，对于 EGFR-L858R/T790M 和 WT-EGFR 的 Ki 值分别为 0.14 和 0.18 nM。它在 H1975 肿瘤细胞和 A549 肿瘤细胞中抑制EGFR-L858R/T790M 自身磷酸化和EGFR-WT，IC50分别为6.6和 5.8 nM。
T2694	KN-62	CaMK; P2X Receptor; Autophagy	Autophagy; Membrane transporter/Ion channel; Neuroscience
	KN-62 是一种选择性的、可逆的钙调蛋白依赖性蛋白激酶 II (CaMK-II) 抑制剂，直接与 CaMK-II 酶的钙调蛋白结合位点结合，对大鼠脑 CaMK-II 的IC50值为 0.9 μM。它是非竞争性的P2X7受体拮抗剂，IC50约为 15 nM。
T38562	AKN-028	FLT	Angiogenesis; Tyrosine Kinase/Adaptors
	AKN-028 是酪氨酸激酶 FLT3的抑制剂，可剂量依赖性的诱导 FLT3的自磷酸化。
T4014	CP-724714 CP724714,CP 724714	Apoptosis; EGFR	Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	CP-724714 (CP724714) 是一种高效、选择性口服活性的 ErbB2 (HER2)酪氨酸激酶抑制剂，IC50为 10 nM。它能抑制完整细胞中 ErbB2 受体的自磷酸化，具有抗肿瘤活性。它对 EGFR 激酶有明显的选择性，IC50值为6400 nM。
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。
T5168	EGFR-IN-12 EGFR Inhibitor	Apoptosis; EGFR	Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	EGFR-IN-12 (EGFR Inhibitor) 是一种 4,6-二取代的嘧啶，可诱导细胞凋亡，具有抗肿瘤活性。它是ATP 竞争性，不可逆且高度选择性的EGFR 抑制剂，IC50为 21 nM。它对EGFR 的选择性高于 HER4 和 55种其他激酶。它还抑制突变型EGFRL858R 和EGFRL861Q，IC50分别为 63 nM 和 4 nM。
T7673	ATH686 ATH 686	Apoptosis; FLT	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	ATH686 是一种选择性的，ATP 竞争性的FLT3抑制剂，具有抗白血病作用。它靶向突变 FLT3 蛋白激酶活性，并通过诱导凋亡和抑制细胞周期来抑制具有 FLT3 突变的细胞的增殖。
T3058	(Z)-SMI-4a TCS PIM-1 4a,SMI-4a	Pim	Chromatin/Epigenetic; JAK/STAT signaling
	(Z)-SMI-4a (TCS PIM-1 4a) 是一种选择性的，细胞可渗透的且具有 ATP 竞争性的 Pim-1抑制剂，IC50为 24 μM，Ki 为 0.6 μM。它还抑制 Pim-2，IC50为 100 μM，具有抗癌活性。
T9564	IRE1α kinase-IN-1	IRE1	Cell Cycle/Checkpoint
	IRE1α kinase-IN-1 是IRE1α 的选择性抑制剂(IC50为 77 nM)，对 IRE1α 的选择性高于 IRE1β 亚型 100 倍。它抑制内质网诱导的 IRE1α 寡聚和自磷酸化，并抑制 IRE1α RNase 活性 (IC50=80 nM)。
T8330	BIO-013077-01 6-(3-(6-甲基吡啶-2-基)-1H-吡唑-4-基)喹噁啉	TGF-beta/Smad	Stem Cells
	BIO-013077-01 是吡唑类TGF-β抑制剂。
T8976	PD-089828	EGFR; FGFR; PDGFR; Src	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	PD-089828 是受体酪氨酸激酶 FGFR1、PDGFRβ 和 EGFR 的竞争性抑制剂，IC50分别为0.15、1.76 和 5.47 µM。它也是非受体酪氨酸激酶 c-Src 的非竞争性抑制剂，IC50 为 0.18 µM。
T2655	CEP-37440 CEP37440	FAK; ALK	Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	CEP-37440 是一种新型的 FAK (IC50:2.3 nM) 和 ALK (IC50:120 nM) 双重抑制剂。
T4327	Prexasertib dihydrochloride LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368	Apoptosis; Chk; S6 Kinase	Apoptosis; Cell Cycle/Checkpoint; MAPK; PI3K/Akt/mTOR signaling
	Prexasertib dihydrochloride (LY2606368) 是一种选择性的，ATP 竞争性的细胞周期检测点激酶 1 抑制剂，Ki 为 0.9 nM，IC50为 <1 nM。它抑制 CHK2(IC50=8 nM) 和 RSK1 (IC50=9 nM)。它引起双链 DNA 断裂和复制突变，导致细胞凋亡，有抗肿瘤活性。
T4205	AG-494 Tyrphostin AG-494,AG 494,Tyrphostin B48	EGFR; CDK	Angiogenesis; Cell Cycle/Checkpoint; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	AG-494 (Tyrphostin B48) 是一种高效、选择性的 EGFR 酪氨酸激酶抑制剂，IC50为0.7 μM。它阻断 Cdk2 的激活并抑制 EGF 依赖的 DNA 合成。它抑制 EGFR、ErbB2、HER1-2 和 PDGF-R 的自磷酸化，IC50为 1.1、39、45 和 6 μM。
T23127	PD-161570 PD 161570	EGFR; FGFR; PDGFR; Src	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	PD-161570 是一种有效的 ATP 竞争性人 FGF-1 受体抑制剂，IC50 为 39.9 nM，Ki 为 42 nM。它还是骨形态发生蛋白 (BMPs) 和TGF-β信号抑制剂。它抑制PDGF 刺激的自磷酸化和FGF-1受体磷酸化，IC50分别为 450 和 622 nM。它抑制 PDGFR、EGFR 和 c-Src 酪氨酸激酶，IC50 值分别为 310、240 和 44 nM。
T4310	Prexasertib 5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368	Apoptosis; Chk	Apoptosis; Cell Cycle/Checkpoint
	Prexasertib (LY2606368) 是一种具有潜在抗肿瘤活性的检查点激酶 1 抑制剂。它可引起双链 DNA 断裂和复制突变，导致细胞凋亡。
T0373	Erlotinib OSI-744,NSC 718781,CP358774,埃罗替尼,R1415	EGFR; Autophagy	Angiogenesis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Erlotinib (CP358774) 是一种 EGFR 一代抑制剂，抑制 EGFR 19 Del 和 L858R 突变。Erlotinib 具有抗肿瘤活性，用于治疗 EGFR 突变的非小细胞肺癌。Erlotinib 用药会产生 EGFR C797S 耐药突变。
T1667	Tandutinib MLN518,CT53518,NSC726292,坦度替尼	Apoptosis; FLT; CSF-1R; PDGFR; Src; c-Kit	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	Tandutinib (CT53518) 是一种选择性 FLT3抑制剂，其 IC50为 0.22 μM。它还抑制c-Kit 和PDGFR，其IC50分别为 0.17 μM 和 0.20 μM。它可穿透血脑屏障，用于急性骨髓性白血病。
T2610	BMS-599626 AC480	EGFR; MEK; HER; Src	Angiogenesis; JAK/STAT signaling; MAPK; Tyrosine Kinase/Adaptors
	BMS-599626 (AC480) 是可口服的选择性 HER1和HER2抑制剂，IC50分别为 20 和 30 nM。它对 HER4 的 IC50值为 190 nM，可抑制肿瘤细胞增殖，有治疗肿瘤的潜力。
T4324	PQ401 hydrochloride (196868-63-0(free base))	IGF-1R	Tyrosine Kinase/Adaptors
	PQ401 hydrochloride (196868-63-0(free base)) 抑制 IGF-1R 结构域的自磷酸化，IC50 <1 μM。
T62285	Enbezotinib	c-RET	Apoptosis; Tyrosine Kinase/Adaptors
	Enbezotinib 是一种能够抑制 RET 自磷酸化的抑制剂。Enbezotinib 能够用于研究癌症。
T3545	RG13022 RG 13022,Tyrphostin RG13022	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	RG13022 (Tyrphostin RG13022) 是一种酪氨酸激酶抑制剂，抑制EGF 受体自身磷酸化的IC50值为4 μM。
T3654	APY29	IRE1	Cell Cycle/Checkpoint
	APY29 是 IRE1α 的变构调节剂；抑制 IRE1α 自磷酸化，IC50值为 280 nM，并激活 IRE1α RNase 活性。
T16550	PKR-IN-C16	Others	Others
	PKR-IN-C16 是一种特异性蛋白激酶抑制剂。它能够抑制 PKR 的自磷酸化，解除 PKR 在原代神经元细胞培养中诱导的翻译阻断。
T3042	JAK2 Inhibitor V JAK2 Inhibitor V Z3,Z3,NSC42834	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	JAK2 Inhibitor V (JAK2 Inhibitor V Z3) 是一种新型的 Jak2 特异性抑制剂，以剂量依赖性方式抑制 Jak2-V617F 和 Jak2-WT 自磷酸化。
T67779	Compound TPX-0046	c-RET	Apoptosis; Tyrosine Kinase/Adaptors
	Compound TPX-0046 是有效的RET 的抑制剂。化合物TPX-046可以抑制RET 的自磷酸化。
T9650	AZ12672857	Src; Ephrin Receptor	Angiogenesis; Tyrosine Kinase/Adaptors
	AZ12672857 是一种 EphB4 抑制剂，IC50 为 1.3 nM。 AZ12672857 抑制 Src 转染 3T3 细胞的细胞增殖，IC50 为 2 nM，抑制转染 CHO-K1 细胞中 EphB4 的自磷酸化，IC50 为 9 nM。
T4053	AST 487 NVP-AST 487	VEGFR; FLT; c-RET; Bcr-Abl; c-Kit	Angiogenesis; Apoptosis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	AST 487 (NVP-AST 487) 是 RET 激酶抑制剂 (IC50:880 nM)，能够抑制 RET 自磷酸化，及下游效应器激活，也抑制 Flt-3 (IC50:520 nM)。
T7119	Y15 1,2,4,5-苯四胺四盐酸盐,1,2,4,5-Benzenetetramine tetrahydrochlor,FAK Inhibitor 14	FAK	Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	Y15 (1,2,4,5-Benzenetetramine tetrahydrochlor) 是一种特异性的粘着斑激酶抑制剂，能够降低其自身磷酸化活性，抑制癌细胞的活力，阻断肿瘤生长。
T6619	Desmethyl Erlotinib hydrochloride OSI420,OSI-420,DesMethyl Erlotinib (CP-473420) HCl,去甲厄洛替尼,CP-473420,Desmethyl Erlotinib,OSI 420	EGFR; Drug Metabolite	Angiogenesis; JAK/STAT signaling; Metabolism; Tyrosine Kinase/Adaptors
	Desmethyl Erlotinib hydrochloride (OSI 420) 是 Erlotinib 的活性代谢物。Erlotinib 是 EGFR 酪氨酸激酶抑制剂。
T11569	HKI-357	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	HKI-357 是一种不可逆的 EGFR 和ERBB2双重抑制剂，IC50分别为 34 nM 和 33 nM。HKI-357 抑制 EGFR 自磷酸化 (Y1068位点)，及 MAPK 和AKT 磷酸化。
T2693	AG1024 Tyrphostin AG 1024,Tyrphostin,AGS 200	Apoptosis; IGF-1R	Apoptosis; Tyrosine Kinase/Adaptors
	AG1024 (Tyrphostin) 是一种可逆的，竞争性和选择性的胰岛素样生长因子-1 受体抑制剂，IC50为 7 μM。它抑制胰岛素受体的磷酸化，IC50值为 57 μM。它诱导细胞凋亡并具有抗癌活性。
T23128	PD180970 PD 180970	Bcr-Abl; Src; c-Kit	Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	PD180970 是一种 Bcr-Abl 抑制剂，对于 p210Bcr-Abl、Src 和 Kit 的自磷酸化，IC50 分别为 5 nM、0.8 nM 和 50 nM。 PD180970 可用于慢性粒细胞白血病的研究。
T3599	BFH772 BFH-722	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	BFH772 是 VEGFR2抑制剂(IC50:3 nM)，具有口服活性。
T6337	RepSox ALK5 Inhibitor II,SJN 2511,E-616452	ALK; TGF-beta/Smad	Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors
	RepSox (ALK5 Inhibitor II) 是一种 TGFβR-1/ALK5 的抑制剂，可以抑制 ATP 与 ALK5 结合以及 ALK5 自磷酸化 (IC50=23/4 nM)，具有选择性。RepSox 可以诱导 MEFs 细胞的脂肪生成。
T6184	Orantinib SU6668,TSU-68,NSC 702827	Apoptosis; VEGFR; FGFR; PDGFR	Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors
	Orantinib (NSC 702827) 是一种多靶点受体酪氨酸激酶抑制剂，对 Flt-1、PDGFRβ和FGFR1的Ki 值分别为 2.1 μM、8 nM 和 1.2 μM。
T30855	CGP77675 CGP-77675,1-(4-(4-amino-5-(3-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)phenethyl)piperidin-4-ol,ZINC1488120,CGP 77675	EGFR; VEGFR; Bcr-Abl; Src	Angiogenesis; Cytoskeletal Signaling; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	CGP77675 (ZINC1488120) 是一种有效的选择性 Src 家族激酶抑制剂，IC50 为 5-20 和 40 nM，用于肽底物的磷酸化和纯化的 Src 的自磷酸化。 CGP77675 具有抗癌活性。
T3691	(Rac)-SAR131675 SAR131675	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	(Rac)-SAR131675 是一种有效的、选择性的VEGFR3抑制剂，其IC50=23 nM。
T2066	Quizartinib AC220,奎扎替尼	Apoptosis; FLT; Autophagy; Ligands for Target Protein for PROTAC	Angiogenesis; Apoptosis; Autophagy; PROTAC; Tyrosine Kinase/Adaptors
	Quizartinib (AC220) 是一种第二代 Ⅱ 型 FLT3 酪氨酸激酶抑制剂，具有口服活性和高选择性，抑制 FLT3-WT 和 FLT3-ITD 自磷酸化 (IC50=4.1/1.1 nM)。Quizartinib 可以诱导肿瘤细胞凋亡。
T70568	H-1356	Others	Others
	H-1356 is an insulin-like growth factor 1(IGF-I) analog that inhibits autophosphorylation of IGF-I receptor.
T22462	1,2,3,4,5,6-Hexabromocyclohexane	Others	Others
	The compound effectively and directly inhibits JAK2 tyrosine kinase autophosphorylation and specifically inhibits ligand-dependent JAK2 activation. It has no cytotoxicity at 100 μM. A 16-hour treatment with compound (1 μM) decreases JAK2 tyrosine autophos
T69863	Dihydrogenistein	Others	Others
	Dihydrogenistein is a derivative of Genistein -- a compound that exhibits specific inhibitory activity against tyrosine kinases including autophosphorylation of epidermal growth factor receptor kinase.
T69260	Genistein Diglucuronide	Others	Others
	Genistein Diglucuronide is a metabolite of Genistein which exhibits specific inhibitory activity against tyrosine kinases including autophosphorylation of epidermal growth factor receptor kinase.
T68360	HKI-357 dimaleate	Others	Others
	HKI-357 dimaleate is an irreversible dual inhibitor of EGFR and ERBB2. HKI-357 suppresses EGFR autophosphorylation (at Y1068), and AKT and MAPK phosphorylation.

化合物

pp60 (v-SRC) Autophosphorylation Site, Phosphorylated

Cat.No: T39185

Synonym: pp60 (v-SRC) Autophosphorylation Site, Phosphorylated

Cat.No: T21761

Target: IGF-1R

Cat.No: T36287

Target: BTK

Cat.No: T14765

Target: Kinesin

Cat.No: T14137

Target: PDGFR

Cat.No: T1770

Target: LRRK2

Cat.No: T22396

Synonym: PF 6274484

Target: EGFR

Cat.No: T2694

Target: CaMK, P2X Receptor, Autophagy

Cat.No: T38562

Target: FLT

Cat.No: T4014

Synonym: CP724714,CP 724714

Target: Apoptosis, EGFR

Cat.No: T2085

Synonym: IGF-1R Inhibitor II

Target: Apoptosis, IGF-1R

Cat.No: T5168

Synonym: EGFR Inhibitor

Target: Apoptosis, EGFR

Cat.No: T7673

Synonym: ATH 686

Target: Apoptosis, FLT

Cat.No: T3058

Synonym: TCS PIM-1 4a,SMI-4a

Target: Pim

IRE1α kinase-IN-1

Cat.No: T9564

Target: IRE1

Cat.No: T8330

Synonym: 6-(3-(6-甲基吡啶-2-基)-1H-吡唑-4-基)喹噁啉

Target: TGF-beta/Smad

Cat.No: T8976

Target: EGFR, FGFR, PDGFR, Src

Cat.No: T2655

Synonym: CEP37440

Target: FAK, ALK

Prexasertib dihydrochloride

Cat.No: T4327

Synonym: LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368

Target: Apoptosis, Chk, S6 Kinase

Cat.No: T4205

Synonym: Tyrphostin AG-494,AG 494,Tyrphostin B48

Target: EGFR, CDK

Cat.No: T23127

Synonym: PD 161570

Target: EGFR, FGFR, PDGFR, Src

Cat.No: T4310

Synonym: 5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368

Target: Apoptosis, Chk

Cat.No: T0373

Synonym: OSI-744,NSC 718781,CP358774,埃罗替尼,R1415

Target: EGFR, Autophagy

Cat.No: T1667

Synonym: MLN518,CT53518,NSC726292,坦度替尼

Target: Apoptosis, FLT, CSF-1R, PDGFR, Src, c-Kit

Cat.No: T2610

Synonym: AC480

Target: EGFR, MEK, HER, Src

PQ401 hydrochloride (196868-63-0(free base))

Cat.No: T4324

Target: IGF-1R

Cat.No: T62285

Target: c-RET

Cat.No: T3545

Synonym: RG 13022,Tyrphostin RG13022

Target: EGFR

Cat.No: T3654

Target: IRE1

Cat.No: T16550

Target: Others

JAK2 Inhibitor V

Cat.No: T3042

Synonym: JAK2 Inhibitor V Z3,Z3,NSC42834

Target: JAK

Compound TPX-0046

Cat.No: T67779

Target: c-RET

Cat.No: T9650

Target: Src, Ephrin Receptor

Cat.No: T4053

Synonym: NVP-AST 487

Target: VEGFR, FLT, c-RET, Bcr-Abl, c-Kit

Cat.No: T7119

Synonym: 1,2,4,5-苯四胺四盐酸盐,1,2,4,5-Benzenetetramine tetrahydrochlor,FAK Inhibitor 14

Target: FAK

Desmethyl Erlotinib hydrochloride

Cat.No: T6619

Synonym: OSI420,OSI-420,DesMethyl Erlotinib (CP-473420) HCl,去甲厄洛替尼,CP-473420,Desmethyl Erlotinib,OSI 420

Target: EGFR, Drug Metabolite

Cat.No: T11569

Target: EGFR

Cat.No: T2693

Synonym: Tyrphostin AG 1024,Tyrphostin,AGS 200

Target: Apoptosis, IGF-1R

Cat.No: T23128

Synonym: PD 180970

Target: Bcr-Abl, Src, c-Kit

Cat.No: T3599

Synonym: BFH-722

Target: VEGFR

Cat.No: T6337

Synonym: ALK5 Inhibitor II,SJN 2511,E-616452

Target: ALK, TGF-beta/Smad

Cat.No: T6184

Synonym: SU6668,TSU-68,NSC 702827

Target: Apoptosis, VEGFR, FGFR, PDGFR

Cat.No: T30855

Synonym: CGP-77675,1-(4-(4-amino-5-(3-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)phenethyl)piperidin-4-ol,ZINC1488120,CGP 77675

Target: EGFR, VEGFR, Bcr-Abl, Src

(Rac)-SAR131675

Cat.No: T3691

Synonym: SAR131675

Target: VEGFR

Cat.No: T2066

Synonym: AC220,奎扎替尼

Target: Apoptosis, FLT, Autophagy, Ligands for Target Protein for PROTAC

Cat.No: T70568

Target: Others

1,2,3,4,5,6-Hexabromocyclohexane

Cat.No: T22462

Target: Others

Dihydrogenistein

Cat.No: T69863

Target: Others

Genistein Diglucuronide

Cat.No: T69260

Target: Others

HKI-357 dimaleate

Cat.No: T68360

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
TN1549	Damnacanthal 丹宁卡	IL Receptor; Akt; Syk	Angiogenesis; Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Damnacanthal possesses anti-cancer, immunomodulatory, antinociceptive and anti-inflammatory actions, it can treat or prevent hepatocellular carcinoma through its inhibitory effects on the HGF/c-Met axis.

天然产物

Cat.No: TN1549

Synonym: 丹宁卡

Target: IL Receptor, Akt, Syk

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPK-00774	TrkA Protein, Human, Recombinant (aa 33-417, His) TrkAI,TrkA I,Trk-A,TRKA,NTRK1,MTC,TRK,TrkA-I	Human	HEK293 Cells
	TrkA, a tyrosine kinase receptor, is an essential component of the nerve growth factor (NGF) response pathway. The binding of NGF to the receptor induces receptor autophosphorylation and activation of intracellular signaling pathways, resulting in diverse biological effects.
TMPJ-00290	GFR Alpha-2/GFRA2 Protein, Human, Recombinant (hFc & His) TRNR2,GDNFR-beta,TGF-β-related neurotrophic factor receptor ...	Human	HEK293 Cells
	GDNF family receptor alpha-2 is a glycosylphosphatidylinosito l (GPI)-linked cell surface receptor. It is part of the GDNF receptor family. Glial cell line-derived neurotrophic factor (GDNF) and neurturin (NTN) are two structurally related, potent neurotrophic factors that play key roles in the control of neuron survival and differentiation. GFRA2 mediates the NRTN-induced autophosphorylation and activation of the RET receptor. It also able to mediate GDNF signaling through the RET tyrosine kina...
TMPH-02194	TAB2 Protein, Human, Recombinant (His & Myc) Mitogen-activated protein kinase kinase kinase 7-interacting...	Human	Baculovirus Insect Cells
	Adapter required to activate the JNK and NF-kappa-B signaling pathways through the specific recognition of 'Lys-63'-linked polyubiquitin chains by its RanBP2-type zinc finger (NZF). Acts as an adapter linking MAP3K7/TAK1 and TRAF6 to 'Lys-63'-linked polyubiquitin chains. The RanBP2-type zinc finger (NZF) specifically recognizes Lys-63'-linked polyubiquitin chains unanchored or anchored to the substrate proteins such as RIPK1/RIP1: this acts as a scaffold to organize a large signaling complex to ...
TMPY-03456	SRFBP1 Protein, Human, Recombinant (His & GST) STRAP,BUD22,P49,serum response factor binding protein 1,p49/...	Human	Baculovirus Insect Cells
	SRFBP1 contains 7 WD repeats and belongs to the WD repeat STRAP family. SRFBP1 may play a role in the cellular distribution of the SMN complex. The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing in the nucleus. SRFBP1 negatively regulates TGF-beta signaling but positively regulates the PDPK1 kinase activity by enhancing its autophosphorylation and by significantly reducing the association of PDPK1 with 14-3-3 protein. SRF...
TMPY-04406	Protein Kinase D2/PRKD2 Protein, Human, Recombinant (His & GST) protein kinase D2,nPKC-D2,PKD2,HSPC187	Human	Baculovirus Insect Cells
	Serine/threonine-protein kinase D2, also known as PRKD2 and PKD2, is a cytoplasm and membrane protein that belongs to the protein kinase superfamily, CAMK Ser/Thr protein kinase family and PKD subfamily. PRKD2 / PKD2 is widely expressed. It contains one PH domain, two phorbol-ester/DAG-type zinc fingers and one protein kinase domain. PRKD2 / PKD2 is activated by DAG and phorbol esters. Phorbol-ester/DAG-type domains bind DAG, mediating translocation to membranes. Autophosphorylation of Ser-71 an...
TMPY-04403	NLK/Nemo Like Kinase Protein, Human, Recombinant (His & GST) nemo-like kinase,LAK1	Human	Baculovirus Insect Cells
	Nemo-like kinase contains 1 protein kinase domain and belongs to the protein kinase superfamily, CMGC Ser/Thr protein kinase family, and MAP kinase subfamily. It also contains a TQE activation loop motif in which autophosphorylation of the threonine residue (Thr-298) is sufficient for kinase activation. As a serine/threonine-protein kinase, Nemo-like kinase regulates some transcription factors with key roles in cell fate determination. It is a positive effector of the non-canonical Wnt signaling...
TMPY-04412	Germinal Center Kinase/MAP4K2 Protein, Human, Recombinant (His & GST) mitogen-activated protein kinase kinase kinase kinase 2,GCK,...	Human	Baculovirus Insect Cells
	Mitogen-activated protein kinase kinase kinase kinase 2, also known as B lymphocyte serine/threonine-protein kinase, Germinal center kinase, MAPK/ERK kinase kinase kinase 2, MEK kinase kinase 2, Rab8-interacting protein, and MAP4K2, is cytoplasm and peripheral membrane protein that belongs to the protein kinase superfamily, STE Ser/Thr protein kinase family and STE2 subfamily. MAP4K2 contains one CNH domain and one protein kinase domain. Although this kinase is found in many tissues, its express...
TMPY-04555	GRK5 Protein, Human, Recombinant (His) G protein-coupled receptor kinase 5,GPRK5	Human	Baculovirus Insect Cells
	G protein-coupled receptor kinase 5, also known as G protein-coupled receptor kinase GRK5 and GRK5, is a member of the protein kinase superfamily, AGC Ser/Thr protein kinase family, and GPRK subfamily. GRKs specifically phosphorylate agonist-occupied G protein-coupled receptors at the inner surface of the plasma membrane (PM), leading to receptor desensitization. GRKs utilize a variety of mechanisms to bind tightly, and sometimes reversibly, to cellular membranes. GRKs play an important role in ...
TMPY-04260	p38 Protein, Human, Recombinant (His) mitogen-activated protein kinase 14,CSPB1,PRKM14,RK,p38α,CSB...	Human	Baculovirus Insect Cells
	MAPK14 contains 1 protein kinase domain and belongs to the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation, and development. MAPK14 can be detected in the brain, heart, placenta, pancreas, and skeletal muscle and it is expressed to a lesser extent in the lung, liver, and kidney. MAPK14 is activated by various environmental stresses ...
TMPY-04456	PKC nu Protein, Human, Recombinant (GST) PRKCN,nPKC-NU,PKC-NU,PKD3,EPK2,protein kinase D3	Human	Baculovirus Insect Cells
	Serine/threonine-protein kinase D3, also known as Protein kinase C nu type, Protein kinase EPK2, PRKD3, EPK2 and PRKCN, is a cytoplasm and membrane protein that belongs to the protein kinase superfamily, CAMK Ser/Thr protein kinase family and PKD subfamily. PRKD3 / PRKCN contains one PH domain, two phorbol-ester/DAG-type zinc fingers and one protein kinase domain. Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second ...
TMPH-02274	JAK2 Protein, Human, Recombinant (His) JAK2,Janus kinase 2,Tyrosine-protein kinase JAK2	Human	E. coli
	Non-receptor tyrosine kinase involved in various processes such as cell growth, development, differentiation or histone modifications. Mediates essential signaling events in both innate and adaptive immunity. In the cytoplasm, plays a pivotal role in signal transduction via its association with type I receptors such as growth hormone (GHR), prolactin (PRLR), leptin (LEPR), erythropoietin (EPOR), thrombopoietin (THPO); or type II receptors including IFN-alpha, IFN-beta, IFN-gamma and multiple int...

重组蛋白

TrkA Protein, Human, Recombinant (aa 33-417, His)

Cat.No: TMPK-00774

Species: Human

Expression System: HEK293 Cells

GFR Alpha-2/GFRA2 Protein, Human, Recombinant (hFc & His)

Cat.No: TMPJ-00290

Species: Human

Expression System: HEK293 Cells

TAB2 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-02194

Species: Human

Expression System: Baculovirus Insect Cells

SRFBP1 Protein, Human, Recombinant (His & GST)

Cat.No: TMPY-03456

Species: Human

Expression System: Baculovirus Insect Cells

Protein Kinase D2/PRKD2 Protein, Human, Recombinant (His & GST)

Cat.No: TMPY-04406

Species: Human

Expression System: Baculovirus Insect Cells

NLK/Nemo Like Kinase Protein, Human, Recombinant (His & GST)

Cat.No: TMPY-04403

Species: Human

Expression System: Baculovirus Insect Cells

Germinal Center Kinase/MAP4K2 Protein, Human, Recombinant (His & GST)

Cat.No: TMPY-04412

Species: Human

Expression System: Baculovirus Insect Cells

GRK5 Protein, Human, Recombinant (His)

Cat.No: TMPY-04555

Species: Human

Expression System: Baculovirus Insect Cells

p38 Protein, Human, Recombinant (His)

Cat.No: TMPY-04260

Species: Human

Expression System: Baculovirus Insect Cells

PKC nu Protein, Human, Recombinant (GST)

Cat.No: TMPY-04456

Species: Human

Expression System: Baculovirus Insect Cells

JAK2 Protein, Human, Recombinant (His)

Cat.No: TMPH-02274

Species: Human

Expression System: E. coli

Cat. No.	Product Name	Target	Signaling Pathways
T19119	3-Hydroxy Midostaurin-D5 CGP52421-D5	Others	Others
	3-Hydroxy Midostaurin-D5 (CGP52421-D5) is a deuterium-labeled 3-Hydroxy Midostaurin which is a metabolite of PKC412. PKC412 effectively inhibits FMS-like tyrosine kinase-3 (FLT3) autophosphorylation (IC50s: 132 nM and 9.8 μM in culture medium and plasma).
T35915	Erlotinib-13C6 Erlotinib-13C6
	Erlotinib-13C6 (CP-358774-13C6) is a 13C-labeled Erlotinib. Erlotinib is a directly acting EGFR tyrosine kinase inhibitor, with an IC50 of 2 nM for human EGFR[1]. Erlotinib reduces EGFR autophosphorylation in intact tumor cells with an IC50 of 20 nM. Erlotinib is used for the treatment of non-small cell lung cancer[1].Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process[2]...

同位素标记化合物

3-Hydroxy Midostaurin-D5

Cat.No: T19119

Synonym: CGP52421-D5

Target: Others

Cat.No: T35915

Synonym: Erlotinib-13C6

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