TGF-β / Smad Signaling(TGF-β / Smad 信号转导)
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. 产品名称 Information
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GC43286
CMPD101
A GRK2 and GRK3 inhibitor
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GC43184
CAY10622
A ROCK1 and ROCK2 inhibitor
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GC43105
C8 Ceramide (d18:1.8:0)
N-辛酰基-D-神经鞘氨醇; N-Octanoyl-D-erythro-sphingosine
A cell-permeable ceramide analog -
GC42747
Afuresertib (hydrochloride)
GSK2110183 hydrochloride
A pan-Akt inhibitor -
GC41863
10,11-dehydro Curvularin
α,β-dehydro Curvularin
A natural mycotoxin -
GC41737
(S)-Glycyl-H-1152 (hydrochloride)
Rho Kinase Inhibitor IV
A ROCK inhibitor -
GC40928
Trimethylamine N-oxide
三甲胺N-氧化物
A metabolite of choline, phosphatidylcholine, and L-carnitine
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GC40770
L-erythro Sphingosine (d18:1)
双琥珀酰亚胺辛二酸酯
A bioactive sphingolipid -
GC34493
BIBF0775
BIBF-0775 is a selective inhibitor of transforming growth factor β Receptor I (TGFβRI,Alk5) with an IC50 of 34nM.
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GC40197
Pirfenidone-d5
5-甲基-1-(苯基-2,3,4,5,6-D5)-2(1H)-吡啶酮,AMR69-d5
An internal standard for the quantification of pirfenidone -
GC40080
Bosutinib-d8
SKI-606 D8
An internal standard for the quantification of bosutinib -
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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GC34060
Disitertide (P144)
地司特泰,P144
Disitertide (P144) (P144) 是一种肽类转化生长因子-β 1 (TGF-β1) 抑制剂,专门设计用于阻断与其受体的相互作用。 Disitertide (P144) (P144) 也是一种 PI3K 抑制剂和凋亡诱导剂。 -
GC33901
Pentanoic acid
Pentanoicacid是一种短链脂肪酸,是细菌代谢产物,与过敏性皮肤病有关系。Pentanoicacid能够激活ROCK信号通路。
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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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GC33351
CZC-8004 (CZC-00008004)
N2-(4-(氨甲基)苯)-5-氟-N4-苯基嘧啶-2,4-二胺,CZC-00008004
A tyrosine kinase inhibitor -
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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GC33310
Rho-Kinase-IN-1
Rho-Kinase-IN-1是一个rho激酶抑制剂,来自专利US20090325960A1,化合物1.008。
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GC33201
GZD856
GZD856是一种新型,有口服活性的PDGFRα/β抑制剂,IC50分别为68.6和136.6nM。具有抗肺癌活性。也是Bcr-AblT315I的抑制剂,对Bcr-Abl和T315I突变型的IC50分别为19.9和15.4 nM。
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GC33120
ZINC00881524
A ROCK inhibitor
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GC32914
EMT inhibitor-1
EMTinhibitor-1是Hippo,TGF-β和Wnt信号通路的抑制剂,并拥有抗肿瘤活性。
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GC32870
Ingenol ((-)-Ingenol)
巨大戟醇; (-)-Ingenol
A PKC activator -
GC32868
BDP5290
BDP5290对MRCKβ、ROCK1、ROCK2的IC50值分别为17nM、230nM、123nM和100nM,是ROCK和MRCK的有效抑制剂。
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GC32867
Flumatinib (HHGV678)
4-[(4-甲基-1-哌嗪基)甲基]-N-[6-甲基-5-[[4-(3-吡啶基)-2-嘧啶基]氨基]-3-吡啶基]-3-(三氟甲基)苯甲酰胺,HHGV678
A Bcr-Abl inhibitor -
GC32840
R-268712
R-268712 is a potent and selective inhibitor of ALK5 with an IC50 of 2.5 nM.
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GC32811
LXS196
LXS196; IDE196
A PKC inhibitor -
GC32788
SJ000291942
A BMP signaling activator
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GC32728
LSKL, Inhibitor of Thrombospondin TSP-1
LSKL, 血小板反应蛋白抑制剂 (TSP-1)
LSKL,InhibitorofThrombospondin(TSP-1)是一种四肽,源于潜在联系多肽,能够抑制TSP-1的活性,来降低TGF-β的活性,能够阻止肝损伤和肝纤维化。
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GC32714
Mitoxantrone (mitozantrone)
米托蒽醌; Mitozantrone; NSC 301739
米托蒽醌Mitoxantrone是一种抗肿瘤的蒽醌衍生物。 -
GC32703
Asciminib (ABL001)
ABL001
An allosteric inhibitor of Abl1 -
GC32250
Chebulinic acid
诃子林鞣酸
An ellagitannin with diverse biological activities -
GC31959
AS2521780
AS2521780是新颖的PKCθ选择性抑制剂,IC50值为0.48nM。
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GC31952
ROCK-IN-1
ROCK-IN-1是一种有效的ROCK抑制剂,能够抑制ROCK2的活性,IC50值为1.2nM。
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GC31950
Halofuginone hydrobromide (RU-19110 (hydrobromide))
常山酮溴酸盐; RU-19110 hydrobromide
Halofuginone (RU-19110) hydrobromid 是一种Ferifugine 衍生物,是一种竞争性脯氨酰-tRNA 合成酶抑制剂,Ki 为 18.3 nM。 -
GC31912
VTX-27
A PKCθ inhibitor
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GC31892
Decursin ((+)-Decursin)
紫花前胡素; (+)-Decursin
A phytochemical with diverse biological activities -
GC31883
ROCK2-IN-2
ROCK2-IN-2是一种选择性ROCK2抑制剂,IC50<1μM。详细信息请参考专利文献US20180093978A1中的化合物A-30。
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GC31711
PKC-IN-1
[(2S,5R)-2,5-二甲基-4-[(四氢-2H-吡喃-4-基)甲基]-1-哌嗪基][3-[(5-氟-2-甲基-4-嘧啶基)氨基]-4,6-二氢-6,6-二甲基吡咯并[3,4-C]吡唑-5(1H)-基]甲酮
PKC-IN-1是一种有效的,ATP-竞争性的,可逆的PKC抑制剂,对人PKCβ和PKCα的Ki值分别为5.3和10.4nM,对人PKCα,PKCβI,PKCβII,PKCθ,PKCγ,PKCmu和PKCε的IC50值分别为2.3,8.1,7.6,25.6,57.5,314,808nM。 -
GC31656
Ingenol Mebutate (Ingenol 3-angelate)
巨大戟醇甲基丁烯酸酯; Ingenol 3-angelate; PEP005
A natural cytotoxic diterpene ester -
GC31650
Halofuginone (RU-19110)
常山酮; RU-19110
Halofuginone (RU-19110) is the competitively inhibitor of prolyl-tRNA synthetase with Ki of 18.3 nM.It could also down-regulate Smad3 and blocked TGF-β signaling at 10 ng/ml in mammal. -
GC30545
Malantide
Malantide是一种十二肽,能够被PKA磷酸化,并且能够增强PKA的活性。
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GC30200
PKC-theta inhibitor
PKC-theta inhibitor (compound 20) inhibits PKC-θ with an IC50 of 18 nM.
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GC19447
SM 16
An inhibitor of ALK5
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GC19338
SRI-011381 hydrochloride
A TGF-β signaling activator
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GC19234
LY3200882
An inhibitor of TGF-βRI
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GC19177
GSK180736A
A ROCK1 and GRK2 inhibitor
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GC19034
AR-13324 mesylate
奈他地尔二甲磺酸盐
AR-13324 是一种有效的 ROCK I 和 ROCK II 抑制剂,已被证明可在低浓度下诱导培养的人和猪 TM 细胞发生形态学变化。 -
GC18521
Cercosporin
尾孢菌素
A cytotoxic phytotoxin -
GC18354
Bisindolylmaleimide X (hydrochloride)
BIM-X hydrochloride; Ro31-8425 hydrochloride
A PKC inhibitor -
GC18246
R-59-949
Diacylglycerol Kinase Inhibitor II, DKGI-II
A DGK-α inhibitor