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Targets Recommended: mTOR

68

抑制剂 & 化合物

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Cat. No. Product Name
L2550 谷氨酰胺代谢化合物库

565 compounds
565 种谷氨酰胺代谢相关的分子,可以用于高通量和高内涵筛选;

化合物库

谷氨酰胺代谢化合物库
Cat.No: L2550
Compounds: 565
Cat. No. Product Name Target Signaling Pathways
T81743 mTORC1-IN-1

mTOR PI3K/Akt/mTOR signaling
mTORC1-IN-1(compound T1)为一种rapalog及选择性mTORC1抑制剂,调节细胞生长和代谢,与多种疾病如癌症相关。该化合物通过与FKBP12-FRB复合物结合(对接分数−11.6 kcal/mol)来靶向mTORC1
T16156 MT 63-78

Apoptosis; AMPK; mTOR Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
MT 63-78 是一种有效的直接AMPK 激活剂,EC50为 25 μM。它诱导细胞有丝分裂阻滞和细胞凋亡,通过抑制脂肪生成和mTORC1途径来阻止前列腺癌的生长,具有抗肿瘤作用。
T4215 TCS-PIM-1-4a

5-[[3-(三氟甲基)苯基]亚甲基]-2,4-噻唑烷二酮,SMI-4a

Apoptosis; Pim Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling
TCS-PIM-1-4a (SMI-4a) 是一种泛-Pim 激酶抑制剂,可通过激活 AMPK 来阻断 mTORC1的活性。它可杀死多种髓样和淋巴样细胞系,IC50值为 0.8 μM 至 40 μM。
T35343 MTI-31

MTI-31,LXI-15029

mTOR PI3K/Akt/mTOR signaling
MTI-31 (LXI-15029) 是口服有效的,高度选择性的mTORC1mTORC2抑制剂,对 mTOR 的Kd 为 0.20 nM,IC50为 39 nM。MTI-31可用于乳腺癌的研究。
T6543 Indoximod

NLG-8189,Indoximod (NLG-8189),1-Methyl-D-tryptophan,吲哚莫德

Indoleamine 2,3-Dioxygenase (IDO) Metabolism
Indoximod (Indoximod (NLG-8189)) 是一种具有口服具有活力的吲哚胺2,3-双加氧酶(IDO) 途径抑制剂。它在调节 mTOR 中充当 Trp 模拟物。它是一种可用于癌症研究的免疫代谢佐剂。
T2475 KU-0063794

mTOR PI3K/Akt/mTOR signaling
KU0063794 是一种特异性的,有效的 mTOR 抑制剂,能够抑制 mTORC1mTORC2,IC50值均约为 10 nM。
T6045 Torin 1

DNA-PK; PI3K; mTOR; Autophagy Autophagy; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
Torin 1 是一种 mTOR 抑制剂,可以抑制 mTORC1mTORC2 (IC50=2/10 nM),具有选择性和 ATP 竞争性。Torin 1 可以诱导细胞自噬,具有抗肿瘤、抗炎、抗衰老活性。
T10413 Autogramin-1

mTOR; Autophagy Autophagy; PI3K/Akt/mTOR signaling
Autogramin-1可以有效抑制由饥饿诱导和 Rapamycin (通过抑制 mTORC1) 诱导的自噬 ,IC50分别为 0.17 μM 和 0.44 μM。
T2414 Torkinib

PP 242

Apoptosis; Mitophagy; PI3K; mTOR; Autophagy Apoptosis; Autophagy; PI3K/Akt/mTOR signaling
Torkinib (PP 242) 是一种选择性,ATP 竞争型的mTOR 抑制剂,IC50为 8 nM。它也抑制mTORC1mTORC2,IC50分别为 30 nM 和 58 nM。
T6319 OSI-027

ASP4786,OSI027

DNA-PK; PI3K; mTOR; Autophagy Autophagy; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
OSI-027 (ASP4786) 是一种选择性、可口服和 ATP 竞争性的mTOR 激酶活性抑制剂,IC50为 4 nM。它抑制mTORC1mTORC2,IC50分别为 22 nM 和 65 nM。
T14886 Cbz-B3A

mTOR PI3K/Akt/mTOR signaling
Cbz-B3A 是一种具有现在性的 mTORC1 信号转导抑制剂,抑制 eIF4E 结合蛋白 1 (4EBP1) 的磷酸化并阻断 68% 的翻译。
T12123 mTOR inhibitor-3

mTOR PI3K/Akt/mTOR signaling
mTOR inhibitor-3 是有效的 mTOR 抑制剂(Ki= 1.5 nM)。在细胞实验及体内实验中,mTOR inhibitor-3 均抑制 mTORC1mTORC2。
T5472 PQR620

mTOR PI3K/Akt/mTOR signaling
PQR620 是一种可透过血脑屏障的,具有口服活性的mTORC1/2选择性抑制剂。
T9013 Autogramin-2

tert-butyl 2-(4-isopropoxybenzamido)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate

Autophagy Autophagy
Autogramin-2 (tert-butyl 2-(4-isopropoxybenzamido)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate) 有效抑制由饥饿诱导的自噬,IC50为 0.27 μM。它也抑制 Rapamycin,通过抑制 mTORC1 诱导的自噬,IC50为 0.14 μM。
T6730 WAY-600

6-(1H-吲哚-5-基)-4-(4-吗啉基)-1-[1-(3-吡啶基甲基)-4-哌啶基]-1H-吡唑并[3,4-D]嘧啶,WAY600

VEGFR; PI3K; Src; mTOR Angiogenesis; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
WAY-600 是一种有效的,选择性的,ATP 竞争型的mTOR 抑制剂,抑制重组 mTOR 酶,其 IC50=9 nM。它能够阻断 mTOR 复合物 1/2 (mTORC1/2) 组装和激活。
T14552 Dactolisib Tosylate

BEZ235 Tosylate,NVP-BEZ 235 Tosylate

PI3K; mTOR PI3K/Akt/mTOR signaling
Dactolisib Tosylate (BEZ235 Tosylate) 是一种双重激酶抑制剂,针对 PI3K 和mTOR。Dactolisib Tosylate 表现出对于PI3Kα, β, γ, δ的IC50值分别为4, 75, 7, 5 nM。Dactolisib Tosylate 抑制 mTORC1mTORC2。
T36200 AZD 3147

mTOR PI3K/Akt/mTOR signaling
AZD 3147 是一种 mTORC 抑制剂,对 mTORC1mTORC2 的 IC50 分别为 40.7 和 5.75 nM。 AZD 3147 对 PI3Kα、PI3Kβ、PI3Kδ 和 PI3Kγ 的 IC50 值分别为 912、5495、9333 和 6310 nM。
T16741 Rheb inhibitor NR1

mTOR PI3K/Akt/mTOR signaling
Rheb inhibitor NR1 是一种 Rheb 抑制剂和选择性 mTORC1 抑制剂。Rheb inhibitor NR1 可抑制 T389pS6K1 的磷酸化,促进S473pAKT 的磷酸化。
T12270 NV-5138

mTOR PI3K/Akt/mTOR signaling
NV-5138 是一种具有选择性的、口服活性的脑内mTORC1激动剂,能够与 Sestrin2 结合。它是一种亮氨酸类似物。它可用于抗抑郁的生物研究。
T6731 WYE-354

4-[6-[4-[(甲氧羰基)氨基]苯基]-4-(4-吗啉基)-1H-吡唑并[3,4-D]嘧啶-1-基]-1-哌啶羧酸甲酯

Apoptosis; PI3K; mTOR; Autophagy Apoptosis; Autophagy; PI3K/Akt/mTOR signaling
WYE-354 是一种 ATP 竞争性的mTOR 抑制剂,IC50为 5 nM。它抑制PI3Kα和PI3Kγ,IC50分别为 1.89 μM 和 7.37 μM,也抑制mTORC1mTORC2。它在体外能诱导自噬激活。
T6732 WYE-687

N-[4-[4-(4-吗啉基)-1-[1-(3-吡啶甲基)-4-哌啶基]-1H-吡唑并[3,4-D]嘧啶-6-基]苯基]氨基甲酸甲酯

p38 MAPK; PI3K; Src; mTOR Angiogenesis; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
WYE-687 是 ATP 竞争性的 mTOR 抑制剂,其 IC50=7 nM。它能够抑制PI3Kα和PI3Kγ,IC50分别为 81 nM 和 3.11 μM。它能够抑制mTORC1mTORC2活化。
T16567 PQR530

PQR-530

PI3K; mTOR PI3K/Akt/mTOR signaling
PQR530 是一具有口服活性,种 ATP 竞争性的,可透过血脑屏障的 PI3K/mTORC1/2双重抑制剂,对于 PI3Kα 和 mTOR (分别为 0.84 和 0.33 nM) 的Kd 为亚摩尔。它具有抗肿瘤作用。
T61831 NS1-IN-1

Influenza Virus Microbiology/Virology
NS1-IN-1 是一种有效的NS1抑制剂。NS1-IN-1 通过以 TSC1-TSC2 依赖性方式抑制 mTORC1 的活性来显示抗病毒活性。NS1-IN-1 降低病毒蛋白水平,有助于减少病毒复制。
T3514 CZ415

mTOR PI3K/Akt/mTOR signaling
CZ415 是高选择性的mTOR 抑制剂,其 pIC50=8.07。它对mTORC1mTORC2复合体具有抑制作用。
T3541 CC-115

CC 115

DNA-PK; PI3K; mTOR DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
CC-115 是一种双重 mTOR/DNA-PK 的抑制剂,IC50分别为 21 nM 和 13 nM,可阻断mTORC1mTORC2信号通路。
T1961 Vistusertib

AZD2014

Apoptosis; Akt; PI3K; S6 Kinase; mTOR; Autophagy Apoptosis; Autophagy; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling
Vistusertib (AZD2014) 是一种ATP 竞争性的mTOR 抑制剂,IC50为 2.81 nM。它抑制mTORC1mTORC2复合物。
T6103 VS-5584

SB2343,VS 5584,VS5584

PI3K; mTOR PI3K/Akt/mTOR signaling
VS-5584 (SB2343) 是pan-PI3K/mTOR 激酶抑制剂。它能够阻断mTORC2和mTORC1。它能够抑制 PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ 和 mTOR,IC50分别为 16 nM, 68 nM, 42 nM, 25 nM 和 37 nM。
T11191 EN6

Proton pump; Autophagy Autophagy; Membrane transporter/Ion channel
EN6 是一种小分子体内自噬激活剂,其共价靶向溶酶体v-ATP 酶的 ATP6V1A 亚基中的半胱氨酸 277。它以溶酶体依赖性方式清除 TDP-43 聚集体,这是额颞叶痴呆的病原体。它介导的 ATP6V1A 修饰使 v-ATP 酶与 Rags 分离,从而抑制 mTORC1 信号传导、增加溶酶体酸化和激活自噬。
T1927 CCT007093

Apoptosis; Phosphatase; Autophagy Apoptosis; Autophagy; Metabolism
CCT007093 是蛋白磷酸酶 1D(PPM1D Wip1)的抑制剂,IC50值为8.4 μM。Wip1 抑制可激活 mTORC1 通路,增强肝切除手术后肝细胞的增殖。
T1861 Omipalisib

GSK458,GSK2126458

PI3K; mTOR; Autophagy Autophagy; PI3K/Akt/mTOR signaling
Omipalisib (GSK2126458) 是一种磷脂酰肌醇 3-激酶(PI3K) 的小分子吡啶磺酰胺抑制剂,具有抗肿瘤活性。它抑制 p110α/β/δ/γ,mTORC1/2 的活性,Ki 值分别为 0.019 nM/0.13 nM/0.024 nM/0.06 nM 和 0.18 nM/0.3 nM。
T1859 AZD-8055

Apoptosis; mTOR; Autophagy Apoptosis; Autophagy; PI3K/Akt/mTOR signaling
AZD-8055 是一种选择性、具有口服活性和 ATP 竞争性的 mTOR 抑制剂,IC50为 0.8 nM。AZD-8055 抑制 mTORC1mTORC2。
T2706 Palomid 529

P529,SG 00529

Apoptosis; mTOR Apoptosis; PI3K/Akt/mTOR signaling
Palomid 529 (SG 00529) 是一种mTORC1mTORC2复合体抑制剂,已用于研究治疗年龄相关性黄斑变性的试验。
T1970 Gedatolisib

PF-05212384,PKI-587

PI3K; mTOR PI3K/Akt/mTOR signaling
Gedatolisib (PF-05212384) 是一种高效的双重 PI3Kα (IC50:0.4 nM),PI3Kγ (IC50:5.4 nM) 和 mTOR (IC50:1.6 nM)抑制剂。它在 mTOR 复合物mTORC1mTORC2中同样有效。
T6030 XL388

P450; PI3K; mTOR Metabolism; PI3K/Akt/mTOR signaling
XL388 是高效的、 ATP 竞争性的 mTOR 抑制剂,其 IC50=9.9 nM。它能够抑制 mTORC1mTORC2。
T7014 Voxtalisib

XL765,SAR245409

DNA-PK; PI3K; mTOR DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
Voxtalisib (XL765) 是一种PI3K 抑制剂,抑制p110α,p110β,p110γ和p110δ。它抑制mTORC1mTORC2,IC50s 分别为 160 和 910 nM。它也抑制 DNA-PK (其 IC50=150 nM) 和 mTOR (其 IC50=157 nM)。
T2235 Dactolisib

2-甲基-2-[4-[3-甲基-2-氧代-8-(喹啉-3-基)-2,3-二氢咪唑并[4,5-c]喹啉-1-基]苯基]丙腈,BEZ235,NVP-BEZ235

ATM/ATR; PI3K; mTOR; Autophagy Autophagy; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
Dactolisib (BEZ235) 是一种可口服的 pan-class IPI3K 和 mTOR 抑制剂,抑制 mTORC1mTORC2,作用于 p110α/γ/δ/β和 mTOR,IC50分别为 4 nM/5 nM/7 nM/75 nM 和 20.7 nM。
T6510 GDC-0349

RG-7603

PI3K; mTOR; Autophagy Autophagy; PI3K/Akt/mTOR signaling
GDC-0349 (RG-7603) 是一种ATP 竞争性的选择性mTOR 抑制剂,Ki 值为 3.8 nM。它对 PI3Kα 和其他 266 种激酶的抑制作用是 790 倍,可抑制mTORC1mTORC2复合体。
T6143 PI-103

PI103,PI 103

Apoptosis; DNA-PK; PI3K; mTOR; Autophagy Apoptosis; Autophagy; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
PI-103 是一种 PI3K 和 mTOR 抑制剂,抑制 p110α、p110β、p110δ、p110γ、mTORC1mTORC2,IC50分别为 8 nM、88 nM、48 nM、150 nM、20 nM 和 83 nM。它可诱导自噬,还抑制 DNA-PK,IC50为 2 nM。
T6346 WYE-132

WYE 125132,WYE125132,WYE-125132

Apoptosis; mTOR Apoptosis; PI3K/Akt/mTOR signaling
WYE-132 (WYE-125132) 是一种高度有效的 ATP 竞争性和特异性 mTOR 激酶抑制剂,IC50为 0.19±0.07 nM。它抑制 mTORC1mTORC2。
T3351 Onatasertib

CC223,CC 223,CC-223

Apoptosis; c-Fms; DNA-PK; FLT; PI3K; mTOR Angiogenesis; Apoptosis; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
Onatasertib (CC223) 是一种口服有效的mTOR 激酶抑制剂,抑制mTOR 激酶,IC50为 16 nM。它抑制mTORC1mTORC2。
T9533 BC-LI-0186

4-(2,3-dimethyl-5-oxo-4-propan-2-ylpyrazol-1-yl)-N-(2-phenoxyethyl)benzenesulfonamide

Others Others
BC-LI-0186 (4-(2,3-dimethyl-5-oxo-4-propan-2-ylpyrazol-1-yl)-N-(2-phenoxyethyl)benzenesulfonamide) 是选择性抑制亮氨酸 tRNA 合成酶与 Ras 相关的 GTP 结合蛋白 D 相互作用(IC50=46.11 nM)。BC-LI-0186能有效抑制肿瘤相关 MTOR 突变体的特性和雷帕霉素耐药癌细胞的生长,能够用于肺癌的相关研究。
T6883 Samotolisib

GTPL8918,LY3023414

DNA-PK; PI3K; mTOR; Autophagy Autophagy; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
Samotolisib (LY3023414) 在低纳摩尔浓度下,有效抑制mTORC1/2。它选择性地有效抑制PI3Kα、PI3Kβ、PI3Kδ、PI3Kγ、DNA-PK 和mTOR,IC50分别为 6.07 nM、77.6 nM、38 nM、23.8 nM、4.24 nM 和 165 nM。它可用于多种肿瘤和癌症的试验。
T2265 Bimiralisib

5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine,PQR309,PI3K-IN-2

Others; PI3K; S6 Kinase; mTOR MAPK; Others; PI3K/Akt/mTOR signaling
Bimiralisib (PI3K-IN-2) 是一种有效的,可渗透脑的 mTOR/PI3K 抑制剂,是一种 mTORC1mTORC2抑制剂。它能够抑制 PI3Kα,PI3Kδ,PI3Kβ,PI3Kγ和 mTOR,IC50分别为 33 nM,451 nM,661 nM,708 nM 和 89 nM。
T39959 RMC-6272

RM-006,RMC-6272

Others Others
RMC-6272 (RM-006) is a bi-steric inhibitor that selectively targets mTORC1, displaying potent and selective (> 10-fold) inhibition over mTORC2. Compared to Rapamycin, RMC-6272 demonstrates enhanced inhibition of mTORC1 and induces increased cell death in TSC2 null tumors.
T36089 RMC-5552

Others Others
RMC-5552 is a potent and selective inhibitor of mTORC1. RMC-5552 inhibits phosphorylation of mTORC1 pS6K and p4EBP1 with IC50s of 0.14 nM and 0.48 nM, respectively. RMC-5552 has anti-cancer activity.
T30441 BI-860585

BI860585

Others Others
BI-860585 is an inhibitor of Raptor-Mammalian Target of Rapamycin (mTOR) Complex 1 (mTOR Complex 1; mTORC1) and rictor-mTOR Complex 2 (mTOR Complex 2; mTORC2), with potential Anti-tumor activity.
T28439 PP30

PP 30,PP-30

Others Others
PP30 is an inhibitor of mTORC1 and mTORC2. It is selective within the PI3K family, inhibiting other PI3Ks only at high concentrations.
T11328 FT-1518

mTOR PI3K/Akt/mTOR signaling
FT-1518 ,exhibits antitumor activity, is a new generation selective, potent and oral bioavailable mTORC1 and mTORC2 inhibitor.
T74283 RMC-4627

Others Others
RMC-4627是一种选择性的mTORC1抑制剂,可激活4EBP1并抑制肿瘤生长。
T69864 CIDD-0067106

Others Others
CIDD-0067106 is a novel potent and selective antiproliferative agent, inhibiting the activity of the mtorc1 pathway

化合物

mTORC1-IN-1
Cat.No: T81743
Synonym:
Target: mTOR
MT 63-78
Cat.No: T16156
Synonym:
Target: Apoptosis, AMPK, mTOR
TCS-PIM-1-4a
Cat.No: T4215
Synonym: 5-[[3-(三氟甲基)苯基]亚甲基]-2,4-噻唑烷二酮,SMI-4a
Target: Apoptosis, Pim
MTI-31
Cat.No: T35343
Synonym: MTI-31,LXI-15029
Target: mTOR
Indoximod
Cat.No: T6543
Synonym: NLG-8189,Indoximod (NLG-8189),1-Methyl-D-tryptophan,吲哚莫德
Target: Indoleamine 2,3-Dioxygenase (IDO)
KU-0063794
Cat.No: T2475
Synonym:
Target: mTOR
Torin 1
Cat.No: T6045
Synonym:
Target: DNA-PK, PI3K, mTOR, Autophagy
Autogramin-1
Cat.No: T10413
Synonym:
Target: mTOR, Autophagy
Torkinib
Cat.No: T2414
Synonym: PP 242
Target: Apoptosis, Mitophagy, PI3K, mTOR, Autophagy
OSI-027
Cat.No: T6319
Synonym: ASP4786,OSI027
Target: DNA-PK, PI3K, mTOR, Autophagy
Cbz-B3A
Cat.No: T14886
Synonym:
Target: mTOR
mTOR inhibitor-3
Cat.No: T12123
Synonym:
Target: mTOR
PQR620
Cat.No: T5472
Synonym:
Target: mTOR
Autogramin-2
Cat.No: T9013
Synonym: tert-butyl 2-(4-isopropoxybenzamido)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate
Target: Autophagy
WAY-600
Cat.No: T6730
Synonym: 6-(1H-吲哚-5-基)-4-(4-吗啉基)-1-[1-(3-吡啶基甲基)-4-哌啶基]-1H-吡唑并[3,4-D]嘧啶,WAY600
Target: VEGFR, PI3K, Src, mTOR
Dactolisib Tosylate
Cat.No: T14552
Synonym: BEZ235 Tosylate,NVP-BEZ 235 Tosylate
Target: PI3K, mTOR
AZD 3147
Cat.No: T36200
Synonym:
Target: mTOR
Rheb inhibitor NR1
Cat.No: T16741
Synonym:
Target: mTOR
NV-5138
Cat.No: T12270
Synonym:
Target: mTOR
WYE-354
Cat.No: T6731
Synonym: 4-[6-[4-[(甲氧羰基)氨基]苯基]-4-(4-吗啉基)-1H-吡唑并[3,4-D]嘧啶-1-基]-1-哌啶羧酸甲酯
Target: Apoptosis, PI3K, mTOR, Autophagy
WYE-687
Cat.No: T6732
Synonym: N-[4-[4-(4-吗啉基)-1-[1-(3-吡啶甲基)-4-哌啶基]-1H-吡唑并[3,4-D]嘧啶-6-基]苯基]氨基甲酸甲酯
Target: p38 MAPK, PI3K, Src, mTOR
PQR530
Cat.No: T16567
Synonym: PQR-530
Target: PI3K, mTOR
NS1-IN-1
Cat.No: T61831
Synonym:
Target: Influenza Virus
CZ415
Cat.No: T3514
Synonym:
Target: mTOR
CC-115
Cat.No: T3541
Synonym: CC 115
Target: DNA-PK, PI3K, mTOR
Vistusertib
Cat.No: T1961
Synonym: AZD2014
Target: Apoptosis, Akt, PI3K, S6 Kinase, mTOR, Autophagy
VS-5584
Cat.No: T6103
Synonym: SB2343,VS 5584,VS5584
Target: PI3K, mTOR
EN6
Cat.No: T11191
Synonym:
Target: Proton pump, Autophagy
CCT007093
Cat.No: T1927
Synonym:
Target: Apoptosis, Phosphatase, Autophagy
Omipalisib
Cat.No: T1861
Synonym: GSK458,GSK2126458
Target: PI3K, mTOR, Autophagy
AZD-8055
Cat.No: T1859
Synonym:
Target: Apoptosis, mTOR, Autophagy
Palomid 529
Cat.No: T2706
Synonym: P529,SG 00529
Target: Apoptosis, mTOR
Gedatolisib
Cat.No: T1970
Synonym: PF-05212384,PKI-587
Target: PI3K, mTOR
XL388
Cat.No: T6030
Synonym:
Target: P450, PI3K, mTOR
Voxtalisib
Cat.No: T7014
Synonym: XL765,SAR245409
Target: DNA-PK, PI3K, mTOR
Dactolisib
Cat.No: T2235
Synonym: 2-甲基-2-[4-[3-甲基-2-氧代-8-(喹啉-3-基)-2,3-二氢咪唑并[4,5-c]喹啉-1-基]苯基]丙腈,BEZ235,NVP-BEZ235
Target: ATM/ATR, PI3K, mTOR, Autophagy
GDC-0349
Cat.No: T6510
Synonym: RG-7603
Target: PI3K, mTOR, Autophagy
PI-103
Cat.No: T6143
Synonym: PI103,PI 103
Target: Apoptosis, DNA-PK, PI3K, mTOR, Autophagy
WYE-132
Cat.No: T6346
Synonym: WYE 125132,WYE125132,WYE-125132
Target: Apoptosis, mTOR
Onatasertib
Cat.No: T3351
Synonym: CC223,CC 223,CC-223
Target: Apoptosis, c-Fms, DNA-PK, FLT, PI3K, mTOR
BC-LI-0186
Cat.No: T9533
Synonym: 4-(2,3-dimethyl-5-oxo-4-propan-2-ylpyrazol-1-yl)-N-(2-phenoxyethyl)benzenesulfonamide
Target: Others
Samotolisib
Cat.No: T6883
Synonym: GTPL8918,LY3023414
Target: DNA-PK, PI3K, mTOR, Autophagy
Bimiralisib
Cat.No: T2265
Synonym: 5-(4,6-dimorpholino-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine,PQR309,PI3K-IN-2
Target: Others, PI3K, S6 Kinase, mTOR
RMC-6272
Cat.No: T39959
Synonym: RM-006,RMC-6272
Target: Others
RMC-5552
Cat.No: T36089
Synonym:
Target: Others
BI-860585
Cat.No: T30441
Synonym: BI860585
Target: Others
PP30
Cat.No: T28439
Synonym: PP 30,PP-30
Target: Others
FT-1518
Cat.No: T11328
Synonym:
Target: mTOR
RMC-4627
Cat.No: T74283
Synonym:
Target: Others
CIDD-0067106
Cat.No: T69864
Synonym:
Target: Others
Cat. No. Product Name Target Signaling Pathways
T1537 Rapamycin

Sirolimus,AY 22989,雷帕霉素,NSC-2260804

Others; Endogenous Metabolite; Antibiotic; mTOR; Autophagy; Antifungal Autophagy; Metabolism; Microbiology/Virology; Others; PI3K/Akt/mTOR signaling
Rapamycin (AY 22989) 属于大环内酯类天然产物,是一种 mTOR 抑制剂,具有特异性(HEK293 细胞:IC50=0.1 nM)。Rapamycin 具有免疫抑制活性,并能诱导自噬。
T3395 Timosaponin AIII

Filiferin B,知母皂苷 A-III,AneMarsaponin A3,Timosaponin A3

AChE; mTOR Neuroscience; PI3K/Akt/mTOR signaling
Timosaponin AIII (Timosaponin A3) 是一种乙酰胆碱酯酶活性抑制剂,其IC50=35.4 μM。
T6354 (+)-Usnic acid

D-Usnic Acid,松萝酸,(+)-Usniacin,(+)-地衣酸

Antiviral; Antibacterial; mTOR Immunology/Inflammation; Microbiology/Virology; PI3K/Akt/mTOR signaling
(+)-Usnic acid (D-Usnic Acid) 是地衣中的二苯并呋喃衍生物,可结合 mTOR 的 ATP 结合口袋,抑制 mTORC1/2的活性。它诱导自噬,有抗菌和抗肿瘤活性。

天然产物

Rapamycin
Cat.No: T1537
Synonym: Sirolimus,AY 22989,雷帕霉素,NSC-2260804
Target: Others, Endogenous Metabolite, Antibiotic, mTOR, Autophagy, Antifungal
Timosaponin AIII
Cat.No: T3395
Synonym: Filiferin B,知母皂苷 A-III,AneMarsaponin A3,Timosaponin A3
Target: AChE, mTOR
(+)-Usnic acid
Cat.No: T6354
Synonym: D-Usnic Acid,松萝酸,(+)-Usniacin,(+)-地衣酸
Target: Antiviral, Antibacterial, mTOR
Cat. No. Product Name Species Expression System
TMPJ-01126 RheB Protein, Human, Recombinant (GST)

RHEB,Ras Homolog Enriched in Brain,GTP-Binding Protein Rheb,...

Human E. coli
GTP-Binding Protein Rheb (RHEB) is a member of the small GTPase superfamily and encodes a lipid-anchored, cell membrane protein with five repeats of the RAS-related GTP-binding region. Highest levels of RHEB can be found in the skeletal and cardiac muscle, and it is vital in the regulation of growth and cell cycle progression due to its role in the Insulin/TOR/S6K signaling pathway. RHEB stimulates the phosphorylation of S6K1 and EIF4EBP1 through activation of mTORC1 signaling, and it activates...
TMPY-00473 NRBF2 Protein, Human, Recombinant (His & GST)

NRBF-2,nuclear receptor binding factor 2,COPR2,COPR1

Human Baculovirus Insect Cells
NRBF2 (Nuclear Receptor Binding Factor 2) is a Protein Coding gene. The encoded protein may modulate transcriptional activation by target nuclear receptors. It is widely expressed in the appendix, placenta, and other tissues. NRBF2/Atg38 has been identified as the fifth subunit of the macroautophagy/autophagy class III phosphatidylinositol 3-kinase (PtdIns3K) complex, along with ATG14/Barkor, BECN1/Vps30, PIK3R4/p150/Vps15, and PIK3C3/Vps34. NRBF2 is a critical molecular switch of PtdIns3K and a...
TMPY-04540 S6K1/RPS6KB1 Protein, Human, Recombinant (GST)

p70(S6K)-alpha,PS6K,p70-alpha,p70(S6K)-α,p70-α,p70 S6KA,S6K-...

Human Baculovirus Insect Cells
PS6K, also known as RPS6KB1, is a serine/threonine-protein kinase. It belongs to the RSK (ribosomal s6 kinase) family. Members of this family function in signal transduction. PS6K is an isoform of p70 ribosomal S6 kinase (S6K). S6K can be activated by mitogenic stimuli such as growth factors, insulin and cytokines. It phosphorylates the ribosomal protein S6. PS6K also phosphorylates other proteins such as elF4B, eEF2K and SKAR. It is a crucial effector of mTOR(rapamycin) signaling. PS6K is disso...
TMPY-02252 LAMTOR2 Protein, Human, Recombinant (His)

Ragulator2,p14,MAPBPIP,MAPKSP1AP,RP1

Human E. coli
Ragulator complex protein LAMTOR2, also known as Endosomal adaptor protein p14, Late endosomal/lysosomal Mp1-interacting protein, Late endosomal/lysosomal adaptor and MAPK and MTOR activator 2, Mitogen-activated protein-binding protein-interacting protein, Roadblock domain-containing protein 3, LAMTOR2, MAPBPIP, and ROBLD3, is a protein which belongs to the GAMAD family. LAMTOR2 / ROBLD3 is a regulator of the TOR pathway, a signaling cascade that promotes cell growth in response to growth factor...
TMPY-01769 4EBP1 Protein, Human, Recombinant (His)

4E-BP1,eukaryotic translation initiation factor 4E ...

Human E. coli
The translational suppressor eIF4E binding protein-1, 4E-BP1 functions as a key regulator in cellular growth, differentiation, apoptosis and survival. The Eif4ebp1 gene, encoding 4E-BP1, is a direct target of a transcription factor activating transcription factor-4 (ATF4), a master regulator of gene expression in stress responses. 4E-BP1 is characterized by its capacity to bind specifically to eIF4E and inhibit its interaction with eIF4G. Phosphorylation of 4E-BP1 regulates eIF4E availability, a...

重组蛋白

RheB Protein, Human, Recombinant (GST)
Cat.No: TMPJ-01126
Species: Human
Expression System: E. coli
NRBF2 Protein, Human, Recombinant (His & GST)
Cat.No: TMPY-00473
Species: Human
Expression System: Baculovirus Insect Cells
S6K1/RPS6KB1 Protein, Human, Recombinant (GST)
Cat.No: TMPY-04540
Species: Human
Expression System: Baculovirus Insect Cells
LAMTOR2 Protein, Human, Recombinant (His)
Cat.No: TMPY-02252
Species: Human
Expression System: E. coli
4EBP1 Protein, Human, Recombinant (His)
Cat.No: TMPY-01769
Species: Human
Expression System: E. coli
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