Stem Cell(干细胞)
- CK1(5)
- EZH2(10)
- GSK-3(68)
- HSC(6)
- iPSC(6)
- Hedgehog(43)
- Notch(37)
- Smoothened(35)
- Wnt/β-catenin(139)
- Hippo Signaling(6)
- Cancer stem cell(28)
- MST1/2(1)
- ESC(1)
- Oct3/4(5)
- Porcupine(6)
- YAP(34)
- Casein Kinase(47)
- Cat.No. 产品名称 Information
-
GC11045
HPI 1
A Hedgehog pathway inhibitor
-
GC11193
SANT-2
N-[3-(1H-苯并咪唑-2-基)-4-氯苯基]-3,4,5-三乙氧基苯甲酰胺
A Smoothened receptor antagonist -
GC15256
JK 184
N-(4-乙氧基苯基)-4-(2-甲基咪唑并[1,2-A]吡啶-3-基)噻唑-2-胺
An inhibitor of downstream hedgehog signaling -
GC15683
LY2940680
4-氟-N-甲基-N-[1-[4-(1-甲基-1H-吡唑-5-基)-1-酞嗪基]-4-哌啶基]-2-(三氟甲基)苯甲酰胺,LY2940680
A Smo antagonist -
GC11548
Tankyrase Inhibitors (TNKS) 49
TNKS 49;TNKS49;TNKS-49
Tankyrase inhibitor -
GC15041
Tankyrase Inhibitors (TNKS) 22
TNKS 22;TNKS22;TNKS-22
Tankyrase inhibitor -
GC17153
CHIR-99021 (CT99021) HCl
CHIR-99021 monohydrochloride; CT99021 monohydrochloride
A selective GSK3 inhibitor -
GC12176
CHIR-98014
A reversible, cell-permeable inhibitor of GSK3
-
GC13280
PF-5274857
PF-5274857 是一种有效的、选择性的、具有口服活性的脑渗透性 Smo 拮抗剂,IC50 为 5.8 nM,Ki 为 4.6 nM。 PF-5274857 具有研究肿瘤类型的潜力,包括由激活的 Hh 通路驱动的脑肿瘤和脑转移。
-
GC13441
Cyclopamine
环巴胺; 11-Deoxojervine
Cyclopamine是一种天然存在的Hedgehog (Hh)特异性小分子信号甾体生物碱抑制剂,对肿瘤生长具有深远的抑制作用,在人乳腺癌细胞中具有显著的抗侵袭、抗增殖和抗雌激素活性。 -
GC13037
CX-4945 (Silmitasertib)
CX 4945;CX4945
A potent, orally bioavailable CK2 inhibitor -
GC14482
Verteporfin
维替泊芬; CL 318952
维替泊芬是一种有效的 PD-L1 表达抑制剂,用于治疗年龄相关性黄斑变性、鲜红斑痣和癌症。 -
GC10359
GANT61
2,2'-[[二氢-2-(4-吡啶基)-1,3(2H,4H)-嘧啶二基]二(亚甲基)]二[N,N-二甲基苯胺],NSC 136476
GANT61 能够有效阻断 GLI1 和 GLI2 诱导的转录,IC50 为 5 μM。 -
GC12781
XAV-939
3,5,7,8-四氢-2-[4-(三氟甲基)苯基]-4H-噻喃并[4,3-D]嘧啶-4-酮
XAV-939 选择性抑制 β-连环蛋白介导的转录。 -
GC15548
Ellagic acid
鞣花酸
Polyphenolic antioxidant -
GC13028
SB 415286
3-[(3-氯-4-羟苯基)氨基]-4-(2-硝苯基)-1H-吡咯-2,5-二酮
A selective inhibitor of GSK-3 -
GC10463
SB 216763
SB 216763是一种强效、选择性且ATP竞争性的GSK-3抑制剂,显著作用于GSK-3α和GSK-3β,其IC50仅为34.3 nM。
-
GC15064
Purmorphamine
嘌呤胺
Purmorphamine是第一个针对Smoothened蛋白开发的小分子激动剂, 能够直接结合并激活Smo,阻断BODIPY-cyclopamine与Smo结合。 -
GC17043
StemRegenin 1 (SR1)
SR1
Antagonizes hematopoietic stem cell differentiation -
GC16893
ICG 001
ICG001 是一种靶向 Wnt/β-catenin 通路的小分子抑制剂。
-
GC14572
KY 02111
Induces stem cell differentiation
-
GC11674
WIKI4
Tankyrase 1/2 Inhibitor V
A potent TNKS1/2 inhibitor -
GC12869
JW 55
Tankyrase 1/2 Inhibitor IV
A TNKS1/2 inhibitor -
GC16584
TCS 21311
NIBR3049
A JAK3 inhibitor -
GC10649
TTP 22
TTP22;TTP-22
A CK2 inhibitor -
GC14037
Triptonide
雷公藤内酯酮; NSC 165677; PG 492
A diterpenoid with diverse biological activities -
GC12181
TBB
4,5,6,7-四溴-1H-苯并三唑,NSC 231634; TBB (enzyme inhibitor);1H-Benzotriazole, 4,5,6,7-tetrabromo-
An inhibitor of CK2 -
GC18107
Salinomycin sodium salt
盐霉素钠; Salinomycin sodium; Sodium salinomycin
A selective cancer stem cell inhibitor -
GC14882
Salinomycin
盐霉素; Procoxacin
A selective cancer stem cell inhibitor -
GC10556
PF-670462
4-[1-环己基-4-(4-氟苯基)-1H-咪唑-5-基]-2-嘧啶胺盐酸盐,PF 670462;PF670462
An inhibitor of the CK1 isoforms CK1ε and CK1δ -
GC17187
LY2090314
LY 2090314;LY-2090314
A potent and selective inhibitor of GSK3 -
GC14169
LDE225 Diphosphate
LDE 225 Diphosphate;NVP-LDE 225 Diphosphate;Erismodegib Diphosphate;LDE-225 Diphosphate
A Smo antagonist -
GC16454
IWP-2
IWP 2
IWP-2 是Wnt信号通路中Porcupine 酶的特异性抑制剂,IC50值为 27 nM。 -
GC12951
HhAntag
N-[4-氯-3-[5-(二甲基氨基)-1H-苯并咪唑-2-基]苯基]-3,5-二甲氧基苯甲酰胺
A hedgehog pathway inhibitor -
GC17534
GSK343
GSK-343;GSK 343
A selective, cell-permeable EZH2 inhibitor -
GC15783
GSK126
EZH2 inhibitor;GSK-126;GSK 126
GSK126(GSK2816126A, GSK2816126)是一种高选择性EZH2甲基转移酶抑制剂,在体外的IC50为12.6~17.4nM;在体内的IC50为9.9nM。 -
GC16789
GANT 58
4,44乔,4乔(2,3,4,5-Thiophentetrayl)tetrakis-pyridine,NSC 75503;GANT58;GANT-58;NSC-75503
An inhibitor of Gli transcription -
GC12134
FH535
2,5-二氯-N-(2-甲基-4-硝基苯基)苯磺酰胺,FH 535;FH-535
An inhibitor of β-catenin signaling -
GC16044
Emodin
大黄素; Frangula emodin
Natural CK2 inhibitor and ER agonist -
GC17837
DMAT
2-二甲基氨基-4,5,6,7-四溴苯并咪唑,Casein kinase II Inhibitor;CK2 Inhibitor
A cell-permeable inhibitor of CK2 -
GC13202
D4476
4-[4-(2,3-二氢-1,4-苯并二氧杂环己-6-基)-5-(2-吡啶基)-1H-咪唑-2-基]苯甲酰胺,Casein Kinase I Inhibitor;D 4476;D-4476
Inhibitor of CK1 and ALK5 -
GC13628
BMS-833923
BMS 833923;BMS833923;XL-139;XL139;XL 139
An orally bioavailable Smo inhibitor -
GC15425
AR-A014418
AR-AO 14418;AR 0133418;AR 014418;GSK 3β inhibitor
A selective inhibitor of GSK3β -
GC17107
PluriSIn #1 (NSC 14613)
NSC 14613
A selective inhibitor of stearoyl-CoA desaturase -
GC12653
LY3039478
LY3039478
A Notch inhibitor -
GC15794
Valproic acid sodium salt (Sodium valproate)
丙戊酸钠; Sodium Valproate sodium
Valproic acid sodium salt (Sodium valproate)(VPA)是一种具有口服活性的组蛋白脱乙酰酶 (HDAC)抑制剂,IC50 值为1.5mM,抑制HDAC1的IC50值为400μM,同时可诱导HDAC2的降解。 -
GC13878
EPZ005687
EPZ 005687,EPZ-005687
A potent, selective inhibitor of EZH2 -
GC13673
BMS-708163 (Avagacestat)
BMS-708163
A potent inhibitor of γ-secretase -
GC12191
LY-411575
(AS)-N-[(1S)-2-[[(7S)-6,7-二氢-5-甲基-6-氧代-5H-二苯并[B,D]氮杂卓-7-基]氨基]-1-甲基-2-氧代乙基]-3,5-二氟-ALPHA-羟基苯乙酰胺
A γ-secretase inhibitor -
GC17671
YO-01027 (Dibenzazepine, DBZ)
二苯并氮卓,gamma-Secretase Inhibitor XX,YO01027
An inhibitor of γ-secretase