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Targets Recommended: PI3K

24

抑制剂 & 化合物

2

重组蛋白

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Cat. No. Product Name Target Signaling Pathways
T6704 TG 100713

TG100713

PI3K PI3K/Akt/mTOR signaling
TG 100713 是一种PI3K 的抑制剂,抑制PI3Kδ,γ,α和β的IC50值分别为24、50、165 和 215 nM。
T3065 TG101209

Apoptosis; FLT; c-RET; JAK; Autophagy Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
TG101209 是一种选择性有效的 JAK2抑制剂,IC50值为 6 nM。它能抑制 Flt3和RET 的活性,IC50值分别为 25 nM 和 17 nM。
T13157 TG 100801

TG100801,TG 100572

VEGFR; Src Angiogenesis; Tyrosine Kinase/Adaptors
TG 100801 是 VEGFr2 和 Src 家族(Src 和 YES)激酶的双重抑制剂,是治疗年龄相关性黄斑变性(AMD)的候选化合物。
T20743 TG-46

TG46,TG 46

FLT; JAK Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
TG-46 (TG46) 对 JAK2, FLT3, RET, JAK3 具有抑制作用,可用于研究青光眼。
T2428 TG6-10-1

5-HT Receptor; Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
TG6-10-1 是一种 EP2 拮抗剂。
T1901 (E/Z)-TG003

TG003

BCL; CDK Apoptosis; Cell Cycle/Checkpoint
(E/Z)-TG003 是一种有效的 ATP 竞争性 Cdc2 样激酶 (Clk) 抑制剂,抑制 Clk1 和 Clk4 的 IC50值分别为 20 和 15 nM。它是 (Z)-TG003 和 (E)-TG003的消旋体。
T20742 TG-89

FLT; c-RET; JAK Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
TG-89是 JAK2、JAK3、RET 和 FLT3的抑制剂,对 JAK2的 IC50值为11.2 μM,在卵巢癌和宫颈癌的治疗中显示出抗癌活性。
T13156L TG 100572 Hydrochloride

VEGFR; FGFR; PDGFR; Src Angiogenesis; Tyrosine Kinase/Adaptors
TG 100572 Hydrochloride 是一种多靶点激酶抑制剂,能够抑制受体酪氨酸激酶和Src 激酶。
T5482 TG4-155

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
TG4-155 是一种脑渗透性 EP2 拮抗剂,对 EP2 和 DP1 具有低纳摩尔的拮抗活性。它作用于 EP2 的 KB 为 2.4 nM,比对 DP1 受体的选择性高 14 倍,比对 EP1、EP3、EP4 和 IP 的选择性比高 550-4750 倍。
T2672 TG100-115

PI3K PI3K/Akt/mTOR signaling
TG100-115 是 PI3Kγ/PI3Kδ 的选择性抑制剂,IC50分别为 83 和 235 nM。
T28958 TG6-129

TG6 129

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
TG6-129 是有效的EP2受体选择性拮抗剂,可降低 butaprost 诱导的 P388D1 巨噬细胞中炎症因子的表达。
T74800 HAT-SIL-TG-1&AT

HAT-SIL-TG-1&AT 是一种 Janus 酪氨酸激酶 (JAK) 抑制剂,具有抗肿瘤作用。HAT-SIL-TG-1&AT 是缺氧激活的前药,可抑制肿瘤组织中的JAK-STAT 信号传导。HAT-SIL-TG-1&AT 在低氧条件下抑制 HEL 细胞增殖并下调磷酸化的STAT3/5。
T60274 TG-2-IN-1

TG-2-IN-1 (Compound D003) 是一种转谷氨酰胺酶-2 (TGM-2) 抑制剂,可用于近视研究。
T60367 TG003

TG003 是一种有效的 Clk1/Sty 抑制剂,抑制 Clk1 和 Clk4 的 IC50值分别为 20 和 15 nM。
T66481 TG-693

TG693, an orally available inhibitor of CLK1, promotes the skipping of the endogenous mutated exon 31 in Duchenne muscular dystrophy (DMD) patient-derived cells and increased the production of the functional exon 31-skipped dystrophin protein.
T71652 TG100948

TG100948 is a novel dual VEGFR/Src kinase inhibitor.
T83855 TG2-179-1

TG2-179-1是BRCA1相关蛋白1(BAP1)的抑制剂。它在25 µM至1.5 mM的浓度范围内,通过无细胞测定法抑制BAP1的去泛素化活性。TG2-179-1对八种结肠癌细胞系表现出细胞毒性(IC50s = 4.48-7.52 µM)。在体内,TG2-179-1(10和30 mg/kg)能够减少HCT116结肠癌小鼠异种移植模型中的肿瘤体积。
T69608 TG11-77 HCl

TG11-77 HCl is a novel, Potent, Selective, Water Soluble, Brain-Permeable EP2 Receptor Antagonist. TG11-77 HCl has a Schild KB of 9.7 nM on EP2, a water solubility of 2.5 mM, a brain-to-plasma ratio of 0.4, and a plasma half-life of 2.4 h in mice. TG11-77 HCl are representative second generation EP2 antagonists with improved pharmacodynamic and pharmacokinetic properties.
T69609 TG11-77 free base

TG11-77 free base is a novel, Potent, Selective, Water Soluble, Brain-Permeable EP2 Receptor Antagonist. TG11-77 free base has a Schild KB of 9.7 nM on EP2, a water solubility of 2.5 mM, a brain-to-plasma ratio of 0.4, and a plasma half-life of 2.4 h in mice. TG11-77 free base are representative second generation EP2 antagonists with improved pharmacodynamic and pharmacokinetic properties.
T69878 AA9 TG2 inhibitor

AA9 is a novel transglutaminase (TG2) inhibitor.
T70413 TG2-IN-3h

TG2-IN-3h is a highly selective, potent, cell-permeable fluorescent irreversible tissue transglutaminase (tg2) inhibitor
T79505 PROTAC TG2 degrader-1

PROTACs PROTAC
PROTACTG2 degrader-1(化合物 11)是一种靶向组织转谷氨酰胺酶 (TG2) 的VHL基PROTAC,具有68.9 μM的KD值。该化合物通过蛋白酶体途径降低卵巢癌细胞中TG2的水平。
T69933 VA4 TG2 inhibitor

VA4 is a novel irreversible TG2 transamidase site-specific inhibitor.
T79315 PROTAC TG2 degrader-2

PROTACs PROTAC
PROTACTG2 degrader-2(compound 7)是一种针对Transglutaminase 2(TG2)的选择性竞争性降解剂,其Kd值大于100 μM。该化合物能有效抑制卵巢癌细胞的迁移,并降低其TG2表达水平,因此可作为卵巢癌研究的工具。

化合物

TG 100713
Cat.No: T6704
Synonym: TG100713
Target: PI3K
TG101209
Cat.No: T3065
Synonym:
Target: Apoptosis, FLT, c-RET, JAK, Autophagy
TG 100801
Cat.No: T13157
Synonym: TG100801,TG 100572
Target: VEGFR, Src
TG-46
Cat.No: T20743
Synonym: TG46,TG 46
Target: FLT, JAK
TG6-10-1
Cat.No: T2428
Synonym:
Target: 5-HT Receptor, Prostaglandin Receptor
(E/Z)-TG003
Cat.No: T1901
Synonym: TG003
Target: BCL, CDK
TG-89
Cat.No: T20742
Synonym:
Target: FLT, c-RET, JAK
TG 100572 Hydrochloride
Cat.No: T13156L
Synonym:
Target: VEGFR, FGFR, PDGFR, Src
TG4-155
Cat.No: T5482
Synonym:
Target: Prostaglandin Receptor
TG100-115
Cat.No: T2672
Synonym:
Target: PI3K
TG6-129
Cat.No: T28958
Synonym: TG6 129
Target: Prostaglandin Receptor
HAT-SIL-TG-1&AT
Cat.No: T74800
Synonym:
Target:
TG-2-IN-1
Cat.No: T60274
Synonym:
Target:
TG003
Cat.No: T60367
Synonym:
Target:
TG-693
Cat.No: T66481
Synonym:
Target:
TG100948
Cat.No: T71652
Synonym:
Target:
TG2-179-1
Cat.No: T83855
Synonym:
Target:
TG11-77 HCl
Cat.No: T69608
Synonym:
Target:
TG11-77 free base
Cat.No: T69609
Synonym:
Target:
AA9 TG2 inhibitor
Cat.No: T69878
Synonym:
Target:
TG2-IN-3h
Cat.No: T70413
Synonym:
Target:
PROTAC TG2 degrader-1
Cat.No: T79505
Synonym:
Target: PROTACs
VA4 TG2 inhibitor
Cat.No: T69933
Synonym:
Target:
PROTAC TG2 degrader-2
Cat.No: T79315
Synonym:
Target: PROTACs
Cat. No. Product Name Species Expression System
TMPY-00218 CXCL7 Protein, Mouse, Recombinant (aa 40-113, His)

b-TG1,pro-platelet basic protein (chemokine (C-X-C ...

Mouse E. coli
CXCL7 Protein, Mouse, Recombinant (aa 40-113, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 10.4 kDa and the accession number is Q9EQI5.
TMPY-00469 CXCL7 Protein, Human, Recombinant (His)

LA-PF4,TC1,LDGF,NAP-2,TGB,CTAP-III,PBP,Beta-TG<...

Human E. coli
CXCL7 Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 9.9 kDa and the accession number is P02775.

重组蛋白

CXCL7 Protein, Mouse, Recombinant (aa 40-113, His)
Cat.No: TMPY-00218
Species: Mouse
Expression System: E. coli
CXCL7 Protein, Human, Recombinant (His)
Cat.No: TMPY-00469
Species: Human
Expression System: E. coli
TargetMol Loading
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