TGF-β / Smad Signaling
Transforming growth factor-beta (TGF-beta) is a multifunctional cytokine that regulates proliferation, migration, differentiation, and survival of many different cell types. Deletion or mutation of different members of the TGF-β family have been shown to cause vascular remodeling defect and absence of mural cell formation, leading to embryonic lethality or severe vascular disorders. TGF-β induces smooth muscle differentiation via Notch or SMAD2 and SMAD3 signaling in ES cells or in a neural crest stem cell line. TGF-β binds to TGF-βRI and to induce phosphorylation of SMAD2/3, thereby inhibiting proliferation, tube formation, and migration of endothelial cells (ECs).
TGF-β is a pluripotent cytokine with dual tumour-suppressive and tumour-promoting effects. TGF-β induces the epithelial-to-mesenchymal transition (EMT) leading to increased cell plasticity at the onset of cancer cell invasion and metastasis.
Products for TGF-β / Smad Signaling
- Cat.No. Product Name Information
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GC62478
Ζ-Stat
ζ-Stat (NSC37044) 是一种特异且非典型的 PKC-ζ 的抑制剂,IC50 值为 5 μM。ζ-Stat 可以减少黑色素瘤细胞系的增殖并诱导细胞凋亡,在体外具有抗肿瘤活性。
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GC13890
(±)-Palmitoylcarnitine chloride
intermediate in mitochondrial fatty acid oxidation
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GC16081
(-)-epicatechin
inducer of pancreatic β-cell regeneration
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GC10603
(-)-epicatechin gallate
major catechin in green tea
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GC17242
(-)-epigallocatechin
green tea epicatechin
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GC14049
(-)-Epigallocatechin gallate (EGCG)
Antioxidant, antiangiogenic and antitumor agent
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GC14012
(-)-Indolactam V
A protein kinase C activator
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GC41737
(S)-Glycyl-H-1152 (hydrochloride)
Two Rho-associated kinases (ROCK), ROCK-I and ROCK-II, act downstream of the G protein Rho to regulate cytoskeletal stability.
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GC18062
1,2-Dilauroyl-sn-glycerol
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GC14134
1,2-Dimyristoyl-sn-glycerol
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GC13877
1,2-Dipalmitoyl-sn-glycerol
weak activator of PKC
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GC12662
1,2-Distearoyl-sn-glycerol
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GC12172
1-Naphthyl PP1
Src family kinases inhibitor
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GC41863
10,11-dehydro Curvularin
A natural mycotoxin
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GN10444
12-O-tetradecanoyl phorbol-13-acetate
An activator of ERK/MAPK
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GC13927
A 77-01
Potent ALK5 inhibitor
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GC10166
A 83-01
ALK-5 inhibitor
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GC63829
A 83-01 sodium
A 83-01 sodium 是一种有效的 TGF-β I 型受体 ALK5,ALK4 和 ALK7 的抑制剂,能够抑制 ALK5,ALK4 和 ALK7 诱导的转录,IC50 值分别为 12 nM,45 nM 和 7.5 nM。
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GC35210
A 83-01 sodium salt
A potent inhibitor of TGF-β type I receptor ALK5 kinase
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GC60037
A-3 hydrochloride
A-3 hydrochloride 是靶向多种激酶 (kinase) 的强效、细胞渗透的、可逆的、ATP 竞争性的非选择性拮抗剂。A-3 hydrochloride 是针对 PKA (Ki=4.3 µM),酪蛋白激酶 II (Ki=5.1 µM) 和肌球蛋白轻链激酶 (MLCK) (Ki=7.4 µM) 的抑制剂。A-3 hydrochloride 还抑制 PKC 和酪蛋白激酶 I 的活性,Ki 分别为 47 µM 和 80 µM。
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GC15579
Adaphostin
P210bcr/abl tyrosine kinase inhibitor
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GC16475
Afuresertib
pan-AKT inhibitor
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GC42747
Afuresertib (hydrochloride)
Afuresertib is a selective, orally bioavailable inhibitor of Akt1, 2, and 3 with Ki values of 0.08, 2, and 2.6 nM, respectively.
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GC11050
ALK5 Inhibitor II (hydrochloride)
ALK5 inhibitor
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GC34300
AR-13324 analog mesylate
AR-13324类似物甲磺酸盐是AR-13324的类似物。
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GC19034
AR-13324 mesylate
AR-13324 is a small-molecule inhibitor of Rho kinase and a norepinephrine transporter; reduces intraocular pressure (IOP) in normotensive monkey eyes.
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GC31959
AS2521780
AS2521780是新颖的PKCθ选择性抑制剂,IC50值为0.48nM。
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GC32703
Asciminib (ABL001)
Asciminib(ABL001)是一种有效和选择性的变构Bcr-Abl抑制剂;抑制Ba/F3细胞生长的IC50值为0.25nM。
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GN10534
Asiaticoside
Asiaticoside (Madecassol) is the active chemical component of the plant Centella asiatica. Asiaticoside is used to study potential treatments for wounds and burns.
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GC10914
AST 487
RET kinase inhibitor
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GC17712
AT13148
Multi-AGC kinase inhibitor,ATP-competitive
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GC10638
AT9283
Aurora kinase/JAK inhibitor
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GC50589
AZ 12799734
Potent TGF-βRI inhibitor
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GC35442
Azaindole 1
Azaindole 1是有口服活性,ATP-竞争型的 ROCK 抑制剂,对ROCK-1 和 ROCK-2 的 IC50 值分别为0.6 和 1.1 nM。
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GC35462
Bafetinib
Bcr-Abl/Lyn tyrosine kinase inhibitor
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GC33343
BCR-ABL-IN-1
BCR-ABL-IN-1是一种BCR-ABL酪氨酸激酶抑制剂,pIC50值为6.46,可能用于慢性髓细胞白血病的研究。
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GC33368
BCR-ABL-IN-2
BCR-ABL-IN-2是BCR-ABL1激酶的抑制剂,其对ABL1native和ABL1T315I的IC50值分别为57nM,773nM。
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GC32868
BDP5290
BDP5290是ROCK和MRCK的有效抑制剂,对于ROCK1,ROCK2,MRCKα和MRCKβ的IC50值分别为5nM,50nM,10nM和100nM。
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GC34493
BIBF0775
BIBF0775是有效,选择性的TGFβI型受体(Alk5)的抑制剂,IC50为34nM。
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GC62868
BIO-013077-01
BIO-013077-01 是一种吡唑类的 TGF-β 抑制剂。
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GC12135
Bisindolylmaleimide II
protein kinase C (PKC) inhibitor
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GC14716
Bisindolylmaleimide IV
protein kinase C (PKC) inhibitor
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GC17239
Bisindolylmaleimide V
negative control for protein kinase C (PKC)-inhibitory activity
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GC13226
Bisindolylmaleimide VIII (acetate)
A protein kinase C (PKC) inhibitor
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GC18354
Bisindolylmaleimide X (hydrochloride)
Bisindolylmaleimide X is a cell-permeable, reversible, ATP-competitive protein kinase C (PKC) inhibitor (IC50 = 15 nM, rat brain PKC).
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GC35530
BJE6-106
BJE6-106 (B106) 是一种有效的选择性 PKCδ 抑制剂,IC50 值为 0.05 μM,BJE6-106 (B106) 靶向 PKCδ 的选择性是 PKC 同工酶 PKCα 的 1000倍 (IC50=50 μM)。BJE6-106 (B106) 可以诱导 caspase 依耐性细胞凋亡 (apoptosis)。BJE6-106 (B106) 具有肿瘤特异性作用。
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GC50593
BMP signaling agonist sb4
Potent BMP4 agonist
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GC13343
Bosutinib (SKI-606)
A potent inhibitor of Src and Abl kinases
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GC40080
Bosutinib-d8
Bosutinib-d8 is intended for use as an internal standard for the quantification of bosutinib by GC- or LC-MS.
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GC17670
Bryostatin 1
PKC activator