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Targets Recommended: VEGFR

137

抑制剂 & 化合物

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同位素标记化合物

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Cat. No. Product Name
L2190 抗肺癌化合物库

1702 compounds
1702 种与肺癌相关的化合物,可以用于抗肺癌药物研发和药理研究;

化合物库

抗肺癌化合物库
Cat.No: L2190
Compounds: 1702
Cat. No. Product Name Target Signaling Pathways
T9929 Ramucirumab

VEGFR Angiogenesis; Tyrosine Kinase/Adaptors
Ramucirumab 是一种人 VEGFR-2 拮抗剂,具有抗实体瘤活性。它是人源化单克隆抗体,能够与 VEGFR-2 结合,阻碍 VEGFR 配体 VEGF-A,VEGF-C 和 VEGF-D 结合。
T10777 CG347B

HDAC Chromatin/Epigenetic; DNA Damage/DNA Repair
CG347B 是一种选择性HDAC6抑制剂。
T21588 Olomoucine

ERK; CDK Cell Cycle/Checkpoint; MAPK
Olomoucine 是 Cdk2/cyclin A、Cdc2/CyclinB、CDK2/CyclinE、CDK5/p35 和 ERK1/p44 MAP 激酶的 ATP 竞争性抑制剂,IC50 分别为 7、7、7、3 和 25 µM。 Olomoucine 调节细胞周期并表现出抗黑色素肿瘤活性。
T2325 Neratinib

HKI-272,来那替尼

EGFR; HER Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Neratinib (HKI-272) 是一种酪氨酸激酶受体抑制剂,可以抑制 HER2 和 EGFR (IC50=59/92 nM),具有不可逆性和口服活性。Neratinib 具有抗肿瘤活性,可以用于治疗乳腺癌。
T9865 Almonertinib mesylate

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Almonertinib mesylate 是一种不可逆的 EGFR 酪氨酸激酶抑制剂,对 EGFR 敏感突变和 T790M 耐药突变具有高选择性。 它可用于非小细胞肺癌研究。
T8756 KRAS inhibitor-9

DUN09716

Apoptosis; Ras Apoptosis; GPCR/G Protein; MAPK
KRAS inhibitor-9 (DUN09716) 是一种 KRAS 抑制剂,阻止 GTP-KRAS 的形成和 KRAS 下游激活。它以中等的结合亲和力与 KRAS G12D、KRAS G12C 和 KRAS Q61H 蛋白结合,选择性抑制具有 KRAS 突变的 NSC-LC 细胞的增殖。它可导致 G2/M 细胞周期停滞并诱导凋亡。
T60076 Oritinib

SH-1028

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Oritinib (SH-1028) 是一种 EGFR 抑制剂,对 EGFR (wt)、EGFR (L858R)、EGFR (L861Q)、EGFR (L858R/T790M)、EGFR (d746-750) 的 IC50 分别为 18、0.7、4、0.1、1.4 和 0.89 nM , EGFR (d746-750/T790M), 分别。奥瑞替尼可用于治疗非小细胞肺癌的研究。
T5462 Almonertinib

HS-10296,阿美替尼

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Almonertinib (HS-10296) 是EGFR 激活突变抑制剂和EGFR T790M 耐受突变抑制剂,对 EGFR 致敏和 T790M 耐药突变具有高选择性,用于非小细胞肺癌的研究。它对 T790M、T790M/L858R 和 T790M/Del19 表现出较强的抑制活性,对野生型的抑制作用较弱。
T8656 CAY10404

3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T

Apoptosis; Akt; COX Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; Neuroscience; PI3K/Akt/mTOR signaling
CAY10404 (3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T) 是一种有效且高度选择性的 COX-2 和 COX-1 抑制剂。 它还是 PKB/Akt 和 MAPK 信号通路的有效抑制剂,可诱导 NSC-LC 细胞凋亡,具有镇痛、抗炎和抗癌活性。
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。
T5675 Almonertinib hydrochloride

HS-10296 hydrochloride,盐酸阿美替尼

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Almonertinib hydrochloride (HS-10296 hydrochloride) 是一种 EGFR 激活突变和 T790M 耐药突变的小分子抑制剂,用于非小细胞肺癌的研究,对 T790M、T790M/L858R 和 T790M/Del19 表现出较强的抑制活性,对野生型的抑制作用较弱。
T1758 ABT-751

E7010

Microtubule Associated; Autophagy Autophagy; Cytoskeletal Signaling
ABT-751 (E7010) 是一种新型的生物相容性的微管蛋白结合剂,用于治疗肺癌、非小细胞肺癌和非小细胞肺癌。它是磺胺类抗有丝分裂抑制剂,对神经母细胞瘤细胞株和非神经母细胞瘤细胞株的IC50分别为1.5 和 3.4 μM。
T15390 Glufosfamide

D 19575,Glucosylifosfamide mustard

Others Others
Glufosfamide 是一种新型噁唑磷胺化合物,具有抗癌活性,可用于研究晚期非小细胞肺癌。
T36404L PRLX-93936 HCL

PRLX-93936 hcl(903499-49-0 Free base)

Ferroptosis; Reactive Oxygen Species Apoptosis; Immunology/Inflammation; Metabolism; NF-κB
PRLX-93936 HCL 是 erastin 的类似物,并显示出与顺铂对非小细胞肺癌 (NSCLC) 细胞的协同作用。
T39275 Befotertinib

D-0316,Befotertinib

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Befotertinib (D-0316) 是一种 EGFR 酪氨酸激酶抑制剂,可用于 EGFR T790M 阳性非小细胞肺癌的研究。
T30087 Antroquinonol

Reactive Oxygen Species; Nrf2 Immunology/Inflammation; Metabolism; NF-κB
Antroquinonol 是一种来源于 Antrodia camphorata 的泛醌衍生物,具有抗炎和抗癌活性。Antroquinonol 通过增强 Nrf2 信号通路降低氧化应激,抑制局灶节段性肾小球硬化小鼠的炎症和硬化。Antroquinonol 具有治疗非小细胞肺癌的潜力,可用于结肠癌的研究。
T67934 MRT-2359

Others Others
MRT-2359 是一种有效的且可口服的 GSPT1 降解剂,具有抗肿瘤活性。MRT-2359 对耐药非小细胞肺癌 (NSCLC) 和小细胞肺癌 (SCLC) 细胞的生长具有抑制作用。MRT-2359 在 MYC 驱动的细胞系中表现出优先活性。
T0373L Erlotinib hydrochloride

盐酸埃罗替尼,OSI-744,NSC 718781,Erlotinib HCl,CP-358774

EGFR; Autophagy Angiogenesis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Erlotinib hydrochloride (NSC 718781) 抑制EGFR 激酶的IC50为 2 nM,用于治疗非小细胞肺癌。
T9673 RET-IN-3

c-RET Apoptosis; Tyrosine Kinase/Adaptors
RET-IN-3 是一种具有选择性和高效性的 RETV804M 激酶抑制剂,具有潜在抗癌活性,可用于研究非小细胞肺癌。
T39764 KER047

ALK2-IN-4

ALK Angiogenesis; Tyrosine Kinase/Adaptors
KER047 (ALK2-IN-4) 是一种 ALK2 抑制剂,具有潜在 的抗癌活性,可用于研究非小细胞肺癌。
T13564L2 AZ7550 trimesylate salt

AZ7550 Mesylate,AZ7550 trimesylate salt (1421373-99-0 free base)

MLK MAPK
AZ7550 trimesylate salt (AZ7550 Mesylate) 是奥希替尼的活性代谢产物,AZ7550 trimesylate salt 抑制 IGF1R 活性,可用于研究非小细胞肺癌。
T6084 Rabusertib

LY2603618,IC-83

Chk; PDK; Autophagy Autophagy; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling
Rabusertib (IC-83) 是一种有效的选择性的Chk1抑制剂,IC50为 7 nM。它有潜在的化学增强活性,用于各种癌症和肿瘤治疗的试验。
T72043 SCFSkp2-IN-2

Apoptosis; E1/E2/E3 Enzyme Apoptosis; Ubiquitination
SCFSkp2-IN-2 是一种 Skp2抑制剂,其 KD 为 28.77 μM。AAA-237 诱导 NSCLC 细胞凋亡 (apoptosis),显示出抗肿瘤活性。
T76792 Sibrotuzumab

BIBH 1,Anti-Human FAP Recombinant Antibody

Others Others
Sibrotuzumab (BIBH 1) 是一种靶向成纤维细胞激活蛋白 (FAP)的人源化 IgG1 单克隆抗体。Sibrotuzumab 可用于研究结直肠癌和非小细胞肺癌。
T74982 Akt3 degrader 1

Akt Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
Akt3 degrader 1 是一种特异性 Akt3 降解剂,具有抗癌抗增殖活性,可抑制小鼠体内肿瘤的生长。Akt3 degrader 1 可用于研究非小细胞肺癌和胰腺癌。
T9901A-002 Enoblituzumab

MGA271,TJ-271

Others Others
Enoblituzumab 是一种人源化 IgG1κ 单克隆抗体,可以识别人 B7-H3 蛋白 ,可用于研究非小细胞肺癌 (NSCLC)等实体肿瘤。
T40292 Opnurasib

NVP-JDQ443,JDQ-443,Opnurasib

Ras GPCR/G Protein; MAPK
Opnurasib (JDQ-443) 是一种可口服且具有选择性和有效性的共价 KRAS G12C 抑制剂,具有抗肿瘤活性,可用于研究晚期非小细胞肺癌。
T35901 EGFR-IN-99

JBJ-03-142-02

EGFR; HER Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
EGFR-IN-99 (JBJ-03-142-02) 是一种 EGFR 和 HER2 Exon 20 插入突变抑制剂,具有抗增殖活性,可用于研究非小细胞肺癌 (NSCLC) 。
T78156 MC4033

Apoptosis; Histone Acetyltransferase Apoptosis; Chromatin/Epigenetic
MC4033 是一种选择性的赖氨酸乙酰转移酶8 (KAT8) 抑制剂(IC50:12.1 μM),具有抗癌作用,可诱导凋亡 ,可用于研究非小细胞肺癌。
T61016 EMI1

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
EMI1 是 EGFR 三重突变体 (EGFR ex19del/T790M/C797S, EGFR L858R/T790M/C797S) 的有效抑制剂。EMI1 可用于 EGFR 突变相关的耐药型非小细胞肺癌 (NSCLC) 的研究。
T64028 Iruplinalkib

WX-0593

ALK; ROS Kinase Angiogenesis; Tyrosine Kinase/Adaptors
Iruplinalkib (WX-0593) 是一种具有口服活性、选择性和高效性的 ALK 和 ROS1 酪氨酸激酶抑制剂,具有抗癌活性,可用于研究非小细胞肺癌。
T35391 Vibostolimab (anti-TIGIT)

Vibostolimab (anti-TIGIT)

Others Others
Vibostolimab 是一种抗 T 细胞免疫蛋白和 ITIM 域的单克隆抗体。Vibostolimab 在体外实验中显示出抗肿瘤活性,可用于研究非小细胞肺癌 (NSCLC) 和黑色素瘤。
T35916 Simotinib

AL-6802,SIM-6802

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Simotinib (AL-6802) 是一种具有选择性和口服生物活性的 EGFR 酪氨酸激酶抑制剂( IC50 :19.9 nM),具有抗肿瘤活性,可用于研究非小细胞性肺癌。
T9460 iMDK

PI3K PI3K/Akt/mTOR signaling
iMDK 是PI3K 抑制剂,能够抑制生长因子MDK。它能够与 MEK 抑制剂协同抑制非小细胞肺癌,而不会伤害正常细胞和小鼠。
T36316 mTOR inhibitor-8

mTOR-IN-8

mTOR; Autophagy Autophagy; PI3K/Akt/mTOR signaling
mTOR inhibitor-8 是一种有效的 mTOR 抑制剂和自噬诱导剂,具有抗病毒和抗肿瘤活性。mTOR inhibitor-8 抑制A549细胞的生长,可用于研究非小细胞肺癌。
T35394 Sintilimab (anti-PD-1)

IBI308,Sintilimab (anti-PD-1)

PD-1/PD-L1 Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation
Sintilimab (IBI308) 是一种人源化的 IgG4 单克隆抗体,具有显著的抗肿瘤活性,通过与 PD-1 结合从而阻断 PD-1 与其配体 (PD-L1 和 PL-L2) 的相互作用,进而恢复内源性抗肿瘤 T 细胞反应。Sintilimab 联合其他化合物来治疗经典霍奇金淋巴瘤、非小细胞肺癌和食管癌。
T9754 BLU-945

BLU945,BLU 945

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
BLU-945 是一种强效的、高选择性的、口服有效的、可逆的表皮生长因子受体酪氨酸激酶抑制剂 (TKIs)。BLU-945 可有效抑制具有 L858R 和/或外显子 19 缺失突变、T790M 突变和 C797S 突变的 EGFR。BLU-945 可用于肺癌包括非小细胞肺癌(NSCLC)的研究。
T60039 KSQ-4279

USP1-IN-1

PARP; DUB Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Ubiquitination
KSQ-4279 (USP1-IN-1)是 USP1 和 PARP 的抑制剂。KSQ-4279 具有抗癌活性,可用于研究非小细胞肺癌、骨肉瘤、卵巢癌、乳腺癌、胶质母细胞瘤、膀胱癌、子宫癌和胰腺癌。
T76796 Patritumab

U3-1287,AMG-888

ERK; EGFR; Akt; HER Angiogenesis; Cytoskeletal Signaling; JAK/STAT signaling; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
Patritumab(U3-1287)是抗 HER3 单克隆抗体,具有潜在的抗肿瘤活性,对 EGFR,HER2,HER3,ERK 和 AKT 的磷酸化有抑制作用和。Patritumab 促使细胞凋亡 (apoptosis),抑制非小细胞肺癌的增殖。
T35392 Tiragolumab

RO 7092284,RG6058-10,MTIG-7192A,RG6058-11,RG-6058

Others Others
Tiragolumab(MTIG-7192A) 是一种靶向 T 细胞免疫球蛋白和 ITIM 结构域 (TIGIT) 的单克隆抗体。Tiragolumab (anti-TIGIT) 常与 PD-L1 抑制剂 Atezolizumab 联合使用用来治疗像非小细胞肺癌类的实体恶性肿瘤。
T14997 Conteltinib

SY-707,CT-707

FAK; PYK2; ALK Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
Conteltinib (CT-707) 是一种靶向FAK、ALK 和 Pyk2 的酶抑制剂,具有抗肿瘤活性。Conteltinib 对 FAK 有明显的抑制作用,通过抑制 YAP 信号传导来克服肝细胞癌中缺氧介导的索拉非尼耐药性,可用于晚期 ALK 阳性非小细胞肺癌和淋巴癌。
T72784 OTUB1/USP8-IN-1

DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
OTUB1/USP8-IN-1 是一种高效的 OTUB1/USP8 抑制剂,具有潜在的抗癌活性,对 OTUB1 和 USP8 的 IC50 值分别为 0.17 和 0.28 nM。OTUB1/USP8-IN-1 可用于研究非小细胞肺癌。
T22443 Triglycidyl isocyanurate

Tris(2,3-epoxypropyl) Isocyanurate,Teroxirone,TGIC,1,3,5-三缩水甘油-S-三嗪三酮,TGI

Apoptosis Apoptosis
Triglycidyl isocyanurate (Teroxirone) 是一种三氮烯三环氧化合物,可通过 p53的激活抑制非小细胞肺癌细胞的生长。它诱导细胞凋亡,具有抗血管生成和抗肿瘤活性,用于癌症研究。
T2490 Osimertinib

AZD-9291,Mereletinib,奥希替尼

EGFR Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Osimertinib (AZD-9291) 是一种 EGFR 三代抑制剂,抑制二代 EGFR 抑制剂产生的 T790M 耐药突变,具有不可逆性和口服活性。Osimertinib 具有抗肿瘤活性,用于治疗 EGFR 突变的非小细胞肺癌。
T76703 Tislelizumab

VDT-482,BGB-A317

PD-1/PD-L1 Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation
Tislelizumab (BGB-A317) 是一种靶向人程序性死亡受体-1(PD-1)IgG4类单克隆抗体,具有抗肿瘤活性,抑制 Fcγ 受体与巨噬细胞的结合,可用于研究晚期鳞状非小细胞肺癌。
T72953 Zidesamtinib

NVL-520

ROS Kinase Tyrosine Kinase/Adaptors
Zidesamtinib (NVL-520)是一种具有口服活性、选择性、高效性和可透过血脑屏障的 ROS1 融合和抗性突变抑制剂,抑制 ROS1 和 ROS1 G2032R ,可用于研究非小细胞肺癌和实体瘤。
T63343 ULK1-IN-2

Apoptosis; Autophagy Apoptosis; Autophagy
ULK1-IN-2 是一种有效的 ULK1 抑制剂,具有潜在的抗癌活性,可诱导细胞凋亡同时阻断自噬。ULK1-IN-2 对癌细胞具有较高的细胞毒作用,对 A549 细胞的 IC50 值为 1.94 μM。ULK1-IN-2 可用于研究非小细胞肺癌。
T77401 Bavituximab

Anti-PS MAb 3G4

Others Others
Bavituximab (Anti-Human Phosphatidylserine Recombinant Antibody) 是一种针对磷脂酰丝氨酸 (PS) 的单克隆抗体,具有血管靶向和免疫调节特性,能够重新激活抗肿瘤免疫来抑制肿瘤生长。Bavituximab 具有抗癌活性,常联合Paclitaxel 和 Carboplatin 来研究非小细胞肺癌。
T61575 USP15-IN-1

DUB Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
USP15-IN-1 是一种有效的 USP15 抑制剂(IC50 为 3.76 μM)。USP15-IN-1对非小细胞肺癌和白血病细胞具有高度的抗增殖活性 。USP15是 cGAS 的互作蛋白,并且 USP15可以促进 cGAS 识别DNA 激活下游信号通路。
T83626 YS-67

Apoptosis; EGFR; Akt Angiogenesis; Apoptosis; Cytoskeletal Signaling; JAK/STAT signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
YS-67 是一种可口服且具有选择性和高效性的 EGFR 抑制剂,具有抗肿瘤活性,抑制 p-EGFR 和 p-AKT,抑制 A549、PC-9 和 A431 细胞的增殖。YS-67在 G0/G1 期阻止细胞周期进程并诱导细胞凋亡,可用于研究非小细胞肺癌。

化合物

Ramucirumab
Cat.No: T9929
Synonym:
Target: VEGFR
CG347B
Cat.No: T10777
Synonym:
Target: HDAC
Olomoucine
Cat.No: T21588
Synonym:
Target: ERK, CDK
Neratinib
Cat.No: T2325
Synonym: HKI-272,来那替尼
Target: EGFR, HER
Almonertinib mesylate
Cat.No: T9865
Synonym:
Target: EGFR
KRAS inhibitor-9
Cat.No: T8756
Synonym: DUN09716
Target: Apoptosis, Ras
Oritinib
Cat.No: T60076
Synonym: SH-1028
Target: EGFR
Almonertinib
Cat.No: T5462
Synonym: HS-10296,阿美替尼
Target: EGFR
CAY10404
Cat.No: T8656
Synonym: 3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T
Target: Apoptosis, Akt, COX
Erlotinib
Cat.No: T0373
Synonym: OSI-744,NSC 718781,CP358774,埃罗替尼,R1415
Target: EGFR, Autophagy
Almonertinib hydrochloride
Cat.No: T5675
Synonym: HS-10296 hydrochloride,盐酸阿美替尼
Target: EGFR
ABT-751
Cat.No: T1758
Synonym: E7010
Target: Microtubule Associated, Autophagy
Glufosfamide
Cat.No: T15390
Synonym: D 19575,Glucosylifosfamide mustard
Target: Others
PRLX-93936 HCL
Cat.No: T36404L
Synonym: PRLX-93936 hcl(903499-49-0 Free base)
Target: Ferroptosis, Reactive Oxygen Species
Befotertinib
Cat.No: T39275
Synonym: D-0316,Befotertinib
Target: EGFR
Antroquinonol
Cat.No: T30087
Synonym:
Target: Reactive Oxygen Species, Nrf2
MRT-2359
Cat.No: T67934
Synonym:
Target: Others
Erlotinib hydrochloride
Cat.No: T0373L
Synonym: 盐酸埃罗替尼,OSI-744,NSC 718781,Erlotinib HCl,CP-358774
Target: EGFR, Autophagy
RET-IN-3
Cat.No: T9673
Synonym:
Target: c-RET
KER047
Cat.No: T39764
Synonym: ALK2-IN-4
Target: ALK
AZ7550 trimesylate salt
Cat.No: T13564L2
Synonym: AZ7550 Mesylate,AZ7550 trimesylate salt (1421373-99-0 free base)
Target: MLK
Rabusertib
Cat.No: T6084
Synonym: LY2603618,IC-83
Target: Chk, PDK, Autophagy
SCFSkp2-IN-2
Cat.No: T72043
Synonym:
Target: Apoptosis, E1/E2/E3 Enzyme
Sibrotuzumab
Cat.No: T76792
Synonym: BIBH 1,Anti-Human FAP Recombinant Antibody
Target: Others
Akt3 degrader 1
Cat.No: T74982
Synonym:
Target: Akt
Enoblituzumab
Cat.No: T9901A-002
Synonym: MGA271,TJ-271
Target: Others
Opnurasib
Cat.No: T40292
Synonym: NVP-JDQ443,JDQ-443,Opnurasib
Target: Ras
EGFR-IN-99
Cat.No: T35901
Synonym: JBJ-03-142-02
Target: EGFR, HER
MC4033
Cat.No: T78156
Synonym:
Target: Apoptosis, Histone Acetyltransferase
EMI1
Cat.No: T61016
Synonym:
Target: EGFR
Iruplinalkib
Cat.No: T64028
Synonym: WX-0593
Target: ALK, ROS Kinase
Vibostolimab (anti-TIGIT)
Cat.No: T35391
Synonym: Vibostolimab (anti-TIGIT)
Target: Others
Simotinib
Cat.No: T35916
Synonym: AL-6802,SIM-6802
Target: EGFR
iMDK
Cat.No: T9460
Synonym:
Target: PI3K
mTOR inhibitor-8
Cat.No: T36316
Synonym: mTOR-IN-8
Target: mTOR, Autophagy
Sintilimab (anti-PD-1)
Cat.No: T35394
Synonym: IBI308,Sintilimab (anti-PD-1)
Target: PD-1/PD-L1
BLU-945
Cat.No: T9754
Synonym: BLU945,BLU 945
Target: EGFR
KSQ-4279
Cat.No: T60039
Synonym: USP1-IN-1
Target: PARP, DUB
Patritumab
Cat.No: T76796
Synonym: U3-1287,AMG-888
Target: ERK, EGFR, Akt, HER
Tiragolumab
Cat.No: T35392
Synonym: RO 7092284,RG6058-10,MTIG-7192A,RG6058-11,RG-6058
Target: Others
Conteltinib
Cat.No: T14997
Synonym: SY-707,CT-707
Target: FAK, PYK2, ALK
OTUB1/USP8-IN-1
Cat.No: T72784
Synonym:
Target: DUB
Triglycidyl isocyanurate
Cat.No: T22443
Synonym: Tris(2,3-epoxypropyl) Isocyanurate,Teroxirone,TGIC,1,3,5-三缩水甘油-S-三嗪三酮,TGI
Target: Apoptosis
Osimertinib
Cat.No: T2490
Synonym: AZD-9291,Mereletinib,奥希替尼
Target: EGFR
Tislelizumab
Cat.No: T76703
Synonym: VDT-482,BGB-A317
Target: PD-1/PD-L1
Zidesamtinib
Cat.No: T72953
Synonym: NVL-520
Target: ROS Kinase
ULK1-IN-2
Cat.No: T63343
Synonym:
Target: Apoptosis, Autophagy
Bavituximab
Cat.No: T77401
Synonym: Anti-PS MAb 3G4
Target: Others
USP15-IN-1
Cat.No: T61575
Synonym:
Target: DUB
YS-67
Cat.No: T83626
Synonym:
Target: Apoptosis, EGFR, Akt
Cat. No. Product Name Target Signaling Pathways
T2870 Matrine

Vegard,苦参碱,Matridin-15-one,Matrinium,α-Matrine,(+)-Matrine

Mitophagy; Ferroptosis; Opioid Receptor; Autophagy Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Neuroscience
Matrine (Vegard) 是一种从槐属植物中分离出来的生物碱,可作为一种κ阿片受体激动剂,有抗肿瘤活性。
T25192 Butyrolactone I

Olomoucin,丁酸内酯I

CDK Cell Cycle/Checkpoint
Butyrolactone I (Olomoucin) 是 CDK 和 cdc2 激酶家族的 ATP 竞争性抑制剂。 Butyrolactone I 在非小细胞肺、小细胞肺和前列腺癌细胞系中显示出抗肿瘤作用。
T7849 Norspermine

Others Others
Norspermine 是一种多胺类似物,用于治疗非小细胞肺癌和乳腺癌。
TN5254 Wighteone

Erythrinin B,6-Isopentenylgenistein

Antifungal Microbiology/Virology
Wighteone (Erythrinin B) 是一种从 Genista ephedroides 中提取出来的小分子化合物,具有潜在的抗真菌和抗癌活性,对 EGFR L858R/T790M 突变非小细胞肺癌具有抗肿瘤作用。。
TN1721 Gypenoside L

ERK; p38 MAPK; Calcium Channel; NF-κB; ROS Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Metabolism; NF-κB
Gypenoside L 是存在于绞股蓝中的一种皂苷,可增加 SA-β-半乳糖苷酶活性,促进衰老相关分泌细胞因子的产生。它还可以激活p38和ERK MAPK 通路和NF-κB 通路以诱导衰老,具有抗肿瘤和抗炎活性。
TN3972 Epimedokoreanin B

Apoptosis; Others; Antibacterial Apoptosis; Microbiology/Virology; Others
Epimedokoreanin B (EKB) 是一种从韩国淫羊藿中分离出的异戊烯化类黄酮,在人非小细胞肺癌(NSCLC)A549和NCI-H292细胞中展现出抗癌活性。Epimedokoreanin B 还具有抗炎和抗菌活性,可有清除 DPPH 自由基的活性,能以剂量依赖的方式抑制 MCF-7 和 HepG2 的增殖。Epimedokoreanin B 能显著抑制 N (δ) -(羧甲基)赖氨酸(CML)和 N (Ï) -(羧甲基)精氨酸(CMA)的形成,可通过抑制高级糖化终产物(AGEs)预防糖尿病的临床并发症。
TN3355 Agatharesinol acetonide

Antifection Microbiology/Virology
Agatharesinol acetonide shows anticancer activity towards the A549 non-small-cell lung-cancer cell line (IC50 = 27.1 microM).
TN4355 Jolkinol A

Others Others
Jolkinol A can inhibit both MCF-7 (breast adenocarcinoma), NCI-H460 (non-small cell lung cancer) cell lines, with GI50 values ranging between 40.9 microM and 95.3 microM.
TN1642 Ferruginol

铁锈罗汉柏醇

BCL; PARP; Caspase Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome
Ferruginol has anti-plasmodial, leishmanicidal, anti-ulcerogenic, cardioprotective, anticancer, anti-oxidative and anti-inflammatory activities, it can induce apoptosis in non-small cell lung cancer (NSCLC) cells.
TN4166 Griffipavixanthone

ERK; Raf; ROS; MEK; Caspase Apoptosis; Immunology/Inflammation; MAPK; Proteases/Proteasome
Griffipavixanthone inhibits the growth of human Non-small-cell lung cancer H520 cells in dose- and time-dependent manners, it induces cell apoptosis through mitochondrial apoptotic pathway accompanying with ROS production. It can inhibit tumor metastasis
TN6062 1,3,9-Trimethyluric acid

1,3,9-Trimethyluric acid exhibits in vitro cytotoxic activity against breast cancer (MCF-7), human neuroblastoma (SHSY5Y), human non-small cell lung cancer (A549) and human liver cancer (HEPG2) with IC50 value in the range of 1-3 uM. 1,3,9-Trimethyluric a
TN5440 Catechin-7-O-xyloside

Catechin 7-O-β-D-xylopyranoside

Others Others
Catechin-7-O-xyloside(C7Ox)具有抗癌活性,它通过内质网应激和线粒体功能障碍诱导人非小细胞肺癌H1299细胞凋亡。
TN4774 Physalin A

ERK; BCL; p38 MAPK; NF-κB; Androgen Receptor; ROS; JAK; JNK; STAT; p53; Autophagy Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Endocrinology/Hormones; Immunology/Inflammation; JAK/STAT signaling; MAPK; NF-κB; Stem Cells
Physalin A exerts anti-tumor activity in non-small cell lung cancer cell lines by suppressing JAK/STAT3 signaling, it inhibits androgen-independent prostate cancer cell growth through activation of cell apoptosis and downregulation of androgen receptor ex
T11009 Destruxin B

Others Others
Destruxin B is a cyclic peptide with insecticidal and anticancer activity isolated from the insect pathogenic fungus Metarhizium isopliae. Destruxin B induces apoptosis of human non-small cell lung cancer cells through the Bcl-2 family-dependent mitochond
T81132 Soladulcoside A

Others Others
Soladulcoside A,一种甾体糖苷及抗肿瘤剂,源自龙葵全株。该化合物可抑制A549细胞,并展示对治疗非小细胞肺癌(NSCLC)等癌症的潜在应用。
T81201 Sartorypyrone B

Sartorypyrone B为Chevalone C的2β-乙酰氧基衍生物,由海绵源真菌Neosartorya tsunodae(KUFC 9213)的培养物中乙酸乙酯提取得到。该化合物对MCF-7、NCI-H460和A375-C5细胞系展示出较强的生长抑制活性,GI50s值分别为17.8、20.5和25.0 μM,显示其在乳腺癌、非小细胞肺癌和黑色素瘤研究中的应用潜力。
TN7505 Thujopsene

NSC 44707

Others Others
Thujopsene, a sesquiterpene found in T. dolabrata, exhibits a wide range of biological activities. It inhibits Na+/K+-ATPase and cytochrome P450 (CYP) isoform CYP2B6 with IC50 values of 25.9 µg/ml and Ki of 0.8 µM, respectively. Additionally, thujopsene demonstrates antimicrobial efficacy against both Gram-positive and Gram-negative bacteria, such as S. aureus, M. luteus, and S. typhimurium, with MICs ranging from 25-50 µg/ml. It also suppresses antigen-induced β-hexosaminidase release in IgE-se...

天然产物

Matrine
Cat.No: T2870
Synonym: Vegard,苦参碱,Matridin-15-one,Matrinium,α-Matrine,(+)-Matrine
Target: Mitophagy, Ferroptosis, Opioid Receptor, Autophagy
Butyrolactone I
Cat.No: T25192
Synonym: Olomoucin,丁酸内酯I
Target: CDK
Norspermine
Cat.No: T7849
Synonym:
Target: Others
Wighteone
Cat.No: TN5254
Synonym: Erythrinin B,6-Isopentenylgenistein
Target: Antifungal
Gypenoside L
Cat.No: TN1721
Synonym:
Target: ERK, p38 MAPK, Calcium Channel, NF-κB, ROS
Epimedokoreanin B
Cat.No: TN3972
Synonym:
Target: Apoptosis, Others, Antibacterial
Agatharesinol acetonide
Cat.No: TN3355
Synonym:
Target: Antifection
Jolkinol A
Cat.No: TN4355
Synonym:
Target: Others
Ferruginol
Cat.No: TN1642
Synonym: 铁锈罗汉柏醇
Target: BCL, PARP, Caspase
Griffipavixanthone
Cat.No: TN4166
Synonym:
Target: ERK, Raf, ROS, MEK, Caspase
1,3,9-Trimethyluric acid
Cat.No: TN6062
Synonym:
Target:
Catechin-7-O-xyloside
Cat.No: TN5440
Synonym: Catechin 7-O-β-D-xylopyranoside
Target: Others
Physalin A
Cat.No: TN4774
Synonym:
Target: ERK, BCL, p38 MAPK, NF-κB, Androgen Receptor, ROS, JAK, JNK, STAT, p53, Autophagy
Destruxin B
Cat.No: T11009
Synonym:
Target: Others
Soladulcoside A
Cat.No: T81132
Synonym:
Target: Others
Sartorypyrone B
Cat.No: T81201
Synonym:
Target:
Thujopsene
Cat.No: TN7505
Synonym: NSC 44707
Target: Others
Cat. No. Product Name Species Expression System
TMPY-03958 TGF alpha Protein, Human, Recombinant

transforming growth factor α,转化生长因子,transforming growth fact...

Human E. coli
The miR-137 served as a tumor suppressor in non-small cell lung cancer (NSCLC) and its suppressive effect is mediated by repressing TGFA expression. TGFA gene expression was significantly higher in tumor tissues compared to adjacent normal tissue and high TGFA gene expression strongly correlated with poor survival in patients with lung adenocarcinoma, and miR-374a suppresses lung adenocarcinoma cell proliferation and invasion via targeting TGFA gene expression. Transforming growth factor alpha (...
TMPK-01034 SEMA4B Protein, Mouse, Recombinant (His)

SEMA4B,SemC,Semaphorin-C,MGC131831,Semaphorin-4B,KIAA1745,SE...

Mouse HEK293 Cells
Semaphorin 4B (SEMA4B) inhibits the invasion of non-small cell lung cancer (NSCLC) through PI3K-dependent suppression of MMP9 activation. SEMA4B may induce FoxO1 nuclear retention through suppressing PI3K/Akt signaling pathway, which subsequently inhibited cell growth through the direct nuclear target of FoxO1, p21. A role of SEMA4B in suppressing NSCLC growth, besides its role in inhibiting cell metastasis, and highlights SEMA4B as a promising therapeutic target for NSCLC.
TMPK-00906 PSCA Protein, Mouse, Recombinant (hFc)

UNQ206,PSCA,PRO232

Mouse HEK293 Cells
Gastric cancer is a deadly malignancy and is a prognostically unfavorable entity with restricted therapeutic strategies available. Prostate stem cell antigen (PSCA) is a glycosylphosphatidylinositol (GPI)-anchored cell surface protein widely expressed in bladder, prostate, and pancreatic cancers. Existing studies have thoroughly recognized the availability of utilizing anti-PSCA CAR-T cells in the treatment of metastatic prostate cancer and non-small-cell lung cancer. PSCA Protein, Mouse, Recomb...
TMPK-00728 PSCA Protein, Human, Recombinant (hFc)

UNQ206,PRO232,PSCA

Human HEK293 Cells
Gastric cancer is a deadly malignancy and is a prognostically unfavorable entity with restricted therapeutic strategies available. Prostate stem cell antigen (PSCA) is a glycosylphosphatidylinositol (GPI)-anchored cell surface protein widely expressed in bladder, prostate, and pancreatic cancers. Existing studies have thoroughly recognized the availability of utilizing anti-PSCA CAR-T cells in the treatment of metastatic prostate cancer and non-small-cell lung cancer. PSCA Protein, Human, Recomb...
TMPK-00341 ALCAM Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated

ALCAM,KG-CAM,MEMD,CD166,CD6L

Human HEK293 Cells
Brain metastasis (BM) in non-small-cell lung cancer (NSCLC) has a very poor prognosis. Recent studies have demonstrated the importance of cell adhesion molecules in tumor metastasis.Elevated levels of ALCAM expression promote BM formation in NSCLC through increased tumor cell dissemination and interaction with the brain endothelial cells. Therefore, ALCAM could be targeted to reduce the occurrence of BM. ALCAM Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated is expressed ...
TMPK-00339 ALCAM Protein, Mouse, Recombinant (His & Avi), Biotinylated

CD6L,ALCAM,MEMD,KG-CAM,CD166

Mouse HEK293 Cells
Brain metastasis (BM) in non-small-cell lung cancer (NSCLC) has a very poor prognosis. Recent studies have demonstrated the importance of cell adhesion molecules in tumor metastasis.Elevated levels of ALCAM expression promote BM formation in NSCLC through increased tumor cell dissemination and interaction with the brain endothelial cells. Therefore, ALCAM could be targeted to reduce the occurrence of BM. ALCAM Protein, Mouse, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian...
TMPK-00340 ALCAM Protein, Human, Recombinant (His & Avi), Biotinylated

CD166,CD6L,KG-CAM,ALCAM,MEMD

Human HEK293 Cells
Brain metastasis (BM) in non-small-cell lung cancer (NSCLC) has a very poor prognosis. Recent studies have demonstrated the importance of cell adhesion molecules in tumor metastasis.Elevated levels of ALCAM expression promote BM formation in NSCLC through increased tumor cell dissemination and interaction with the brain endothelial cells. Therefore, ALCAM could be targeted to reduce the occurrence of BM. ALCAM Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian...
TMPY-04375 Casein Kinase 1 alpha Protein, Human, Recombinant (GST)

CKIa,casein kinase 1, alpha 1,casein kinase 1, α1,CK1a,Casei...

Human Baculovirus Insect Cells
Casein kinase I isoform alpha, also known as CKI-alpha, CK1 and CSNK1A1, is a cytoplasm protein which belongs to theprotein kinase superfamily, CK1 Ser/Thr protein kinase family and casein kinase I subfamily. Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates. High expression of CSNK2A1, or concomitantly high expression of CSNK2A1, are independent prognostic factors of poor survival in NSCLC patients. CSNK2A1 are use...
TMPY-02399 TRF1 Protein, Human, Recombinant (His)

TRF,telomeric repeat binding factor (NIMA-interacting) 1,hTR...

Human Baculovirus Insect Cells
Telomeric repeat binding factor 1 (TRF1), also known as TERF1, the shelterin complex, which modulates the telomere structures. TRF1 protein structure contains a C-terminal Myb motif, a dimerization domain near its N-terminus and an acidic N-terminus. Pin2/TRF1 was originally identified as a protein bound to telomeric DNA (TRF1) and as a protein involved in mitotic regulation (Pin2). Pin2/TRF1 negatively regulates telomere length and importantly, its function is tightly regulated during the cell ...
TMPY-04417 DAPK1 Protein, Human, Recombinant (aa 1-363, His & GST)

DAPK,death-associated protein kinase 1,ROCO3

Human Baculovirus Insect Cells
Death-associated protein kinase 1, also known as DAP kinase 1, DAPK1 and DAPK, is a cytoplasm protein which belongs to theprotein kinase superfamily, CAMK Ser / Thr protein kinase family and DAP kinase subfamily. DAPK1 contains tenANK repeats, onedeath domain and oneprotein kinase domain. DAPK1 is a calcium / calmodulin-dependent serine/threonine kinase which acts as a positive regulator of apoptosis. DAPK1 gene is a candidate tumor suppressor (TSG) and the abnormal methylation of DAPK1 g...
TMPY-02796 KIAA0101 Protein, Human, Recombinant (His)

L5,NS5ATP9,p15PAF,OEATC1,p15(PAF),OEATC,PAF,p15/PAF,OEATC-1,...

Human E. coli
KIAA11, also known as p15(PAF), is a proliferating cell nuclear antigen-associated factor that interacts with proliferating cell nuclear antigen(PCNA). It was initially isolated in a yeast two-hybrid screen for PCNA binding partners and was shown to bind PCNA competitively with the cell cycle regulator p21(WAF). KIAA11 is localized primarily in the nucleus. It shares the conserved PCNA binding motif with several other PCNA binding proteins including CDK inhibitor p21. KIAA11 is involved in cell ...
TMPJ-00281 CADM1 Protein, Mouse, Recombinant (hFc)

IgSF4,NECL-2,Nectin-like protein 2,Immunoglobulin superfamil...

Mouse HEK293 Cells
Cell adhesion molecule 1(CADM1) is a single-pass type I membrane protein and belongs to the nectin family. It contains 2 Ig-like C2-type (immunoglobulin-like) domains and 1 Ig-like V-type (immunoglobulin-like) domain. CADM1 acts as a tumor suppressor in non-small-cell lung cancer (NSCLC) cells. Interaction with CRTAM promotes natural killer (NK) cell cytotoxicity and interferon-gamma (IFN-gamma) secretion by CD8+ cells in vitro as well as NK cell-mediated rejection of tumors expressing CADM3 in...

重组蛋白

TGF alpha Protein, Human, Recombinant
Cat.No: TMPY-03958
Species: Human
Expression System: E. coli
SEMA4B Protein, Mouse, Recombinant (His)
Cat.No: TMPK-01034
Species: Mouse
Expression System: HEK293 Cells
PSCA Protein, Mouse, Recombinant (hFc)
Cat.No: TMPK-00906
Species: Mouse
Expression System: HEK293 Cells
PSCA Protein, Human, Recombinant (hFc)
Cat.No: TMPK-00728
Species: Human
Expression System: HEK293 Cells
ALCAM Protein (Primary Amine Labeling), Human, Recombinant (His), Biotinylated
Cat.No: TMPK-00341
Species: Human
Expression System: HEK293 Cells
ALCAM Protein, Mouse, Recombinant (His & Avi), Biotinylated
Cat.No: TMPK-00339
Species: Mouse
Expression System: HEK293 Cells
ALCAM Protein, Human, Recombinant (His & Avi), Biotinylated
Cat.No: TMPK-00340
Species: Human
Expression System: HEK293 Cells
Casein Kinase 1 alpha Protein, Human, Recombinant (GST)
Cat.No: TMPY-04375
Species: Human
Expression System: Baculovirus Insect Cells
TRF1 Protein, Human, Recombinant (His)
Cat.No: TMPY-02399
Species: Human
Expression System: Baculovirus Insect Cells
DAPK1 Protein, Human, Recombinant (aa 1-363, His & GST)
Cat.No: TMPY-04417
Species: Human
Expression System: Baculovirus Insect Cells
KIAA0101 Protein, Human, Recombinant (His)
Cat.No: TMPY-02796
Species: Human
Expression System: E. coli
CADM1 Protein, Mouse, Recombinant (hFc)
Cat.No: TMPJ-00281
Species: Mouse
Expression System: HEK293 Cells
Cat. No. Product Name Target Signaling Pathways
T11067 VX-984

M9831

DNA-PK DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
VX-984 (M9831) 是一种可口服的、具有选择性的的、可透过血脑屏障的 DNA-PK 抑制剂。VX-984 对非同源性末端 NHEJ 的接合具有抑制作用,可作用于 DSBs 使 DNA 双链断裂。VX-984常见于对胶质母细胞瘤 (GBM) 和非小细胞肺癌 (NSC-LC) 的研究。
TMIH-0413 Osimertinib-d6

Osimertinib-d6 是 Osimertinib 的氘代化合物。Osimertinib 的 CAS 号为 1421373-65-0。Osimtinib 是一种小分子酪氨酸激酶受体抑制剂和抗肿瘤剂,用于治疗选定形式的晚期非小细胞肺癌,其有效抑制 L858R 和 L858R/T790M EGFR,IC50 为 12 和 1 nM。
T72818 Dosimertinib-d3

Dosimertinib-d3是一种有效的口服活性EGFR 抑制剂。Dosimertinib-d3降低 p-EGFR 和 p-ERK 蛋白水平的表达。Dosimertinib-d3显示出抗增殖和抗肿瘤活性。Dosimertinib-d3具有非小细胞肺癌 (NSCLC) 研究的潜力。
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

VX-984
Cat.No: T11067
Synonym: M9831
Target: DNA-PK
Osimertinib-d6
Cat.No: TMIH-0413
Synonym:
Target:
Dosimertinib-d3
Cat.No: T72818
Synonym:
Target:
Erlotinib-13C6
Cat.No: T35915
Synonym: Erlotinib-13C6
Target:
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