Home >> Signaling Pathways >> TGF-β / Smad Signaling

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

  1. Cat.No. 产品名称 Information
  2. GC43286 CMPD101 A GRK2 and GRK3 inhibitor
  3. GC43184 CAY10622 A ROCK1 and ROCK2 inhibitor
  4. 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
  5. GC42747 Afuresertib (hydrochloride)

    GSK2110183 hydrochloride

    A pan-Akt inhibitor
  6. GC41863 10,11-dehydro Curvularin

    α,β-dehydro Curvularin

    A natural mycotoxin
  7. GC41737 (S)-Glycyl-H-1152 (hydrochloride)

    Rho Kinase Inhibitor IV

    A ROCK inhibitor
  8. GC40928 Trimethylamine N-oxide

    三甲胺N-氧化物

    A metabolite of choline, phosphatidylcholine, and L-carnitine

  9. GC40770 L-erythro Sphingosine (d18:1)

    双琥珀酰亚胺辛二酸酯

    A bioactive sphingolipid
  10. GC34493 BIBF0775 BIBF-0775 is a selective inhibitor of transforming growth factor β Receptor I (TGFβRI,Alk5) with an IC50 of 34nM.
  11. 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
  12. GC40080 Bosutinib-d8

    SKI-606 D8

    An internal standard for the quantification of bosutinib
  13. GC34300 AR-13324 analog mesylate AR-13324类似物甲磺酸盐是AR-13324的类似物。
  14. 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。
  15. 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。
  16. 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。
  17. 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
  18. 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。
  19. 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。
  20. 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。
  21. GC33120 ZINC00881524 A ROCK inhibitor
  22. 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。
  23. GC32870 Ingenol ((-)-Ingenol)

    巨大戟醇; (-)-Ingenol

    A PKC activator
  24. 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。
  25. 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
  26. GC32840 R-268712 R-268712 is a potent and selective inhibitor of ALK5 with an IC50 of 2.5 nM.
  27. GC32811 LXS196

    LXS196; IDE196

    A PKC inhibitor
  28. GC32788 SJ000291942 A BMP signaling activator
  29. 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。

  30. 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。
  31. GC32703 Asciminib (ABL001)

    ABL001

    An allosteric inhibitor of Abl1
  32. GC32250 Chebulinic acid

    诃子林鞣酸

    An ellagitannin with diverse biological activities
  33. GC31959 AS2521780 AS2521780是新颖的PKCθ选择性抑制剂,IC50值为0.48nM。
  34. 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。

  35. 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。
  36. GC31912 VTX-27 A PKCθ inhibitor
  37. GC31892 Decursin ((+)-Decursin)

    紫花前胡素; (+)-Decursin

    A phytochemical with diverse biological activities
  38. 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。
  39. 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。
  40. 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
  41. 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.
  42. 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。
  43. GC30200 PKC-theta inhibitor PKC-theta inhibitor (compound 20) inhibits PKC-θ with an IC50 of 18 nM.
  44. GC19447 SM 16 An inhibitor of ALK5
  45. GC19338 SRI-011381 hydrochloride A TGF-β signaling activator
  46. GC19234 LY3200882 An inhibitor of TGF-βRI
  47. GC19177 GSK180736A A ROCK1 and GRK2 inhibitor
  48. 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。
  49. GC18521 Cercosporin

    尾孢菌素

    A cytotoxic phytotoxin
  50. GC18354 Bisindolylmaleimide X (hydrochloride)

    BIM-X hydrochloride; Ro31-8425 hydrochloride

    A PKC inhibitor
  51. GC18246 R-59-949

    Diacylglycerol Kinase Inhibitor II, DKGI-II

    A DGK-α inhibitor

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