Hedgehog
Hh (Hedgehog) signalling is a evolutionarily conserved pathway that is critical for embryonic development, tissue and organ morphogenesis. Mammalian Hh protein ligands include Sonic Hh, Desert Hh and Indian Hh. Dysfunctions of Hh singalling lead to developmental abnormalities and cancer.
Products for Hedgehog
- Cat.No. 产品名称 Information
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GC91424
S1PL-IN-31
Sphingosine-1-Phosphate Lyase Inhibitor 31; S1PL Inhibitor 31; S1P Lyase Inhibitor 31
S1PL-IN-31是一种抑制神经酰胺-1-磷酸(S1P)裂解酶的抑制剂(IC50 = 210 nM)。它也是平滑蛋白受体(Smo)的拮抗剂(IC50 = 440 nM)。 -
GC66390
3-epi-Vitamin D3
Epicholecalciferol
3-epi-Vitamin D3 (Epicholecalciferol) (Compound 4) 是维生素 D3 类似物,是一种 Hedgehog pathway 抑制剂,在U87MG 细胞中测定的 IC50 为 39.2 μM。
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GC64134
Hh-Ag1.5
SAg1.5
Hh-Ag1.5 (SAg1.5) 是一种有效的 Hedgehog (Hh) 激动剂,EC50 为 1 nM。Hh-Ag1.5 介导的重编程打破了非损伤肝脏干细胞的静止状态,从而挽救了肝衰竭。 -
GC49651
19-alkyne Cholesterol
19-ethynyl Cholesterol
An alkyne derivative of cholesterol for click chemistry - GC48062 RU-SKI 201 (hydrochloride) A neuropeptide with diverse biological activities
- GC47570 Lipoxygenin An inhibitor of 5-LO
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GC47474
Itraconazole-d5
R51211-d5
An internal standard for the quantification of itraconazole - GC47435 HPI-1 (hydrate) A Hedgehog pathway inhibitor
- GC39359 Ciliobrevin D Ciliobrevin D (compound 5) is a cell-permeable, reversible and specific antagonist of AAA+ (ATPases associated with diverse cellular activities) ATPase motor cytoplasmic dynein. Ciliobrevin D perturbs primary cilia formation and blocks Hedgehog (Hh) signaling.
- GC37573 RU-SKI 43 An inhibitor of hedgehog acyltransferase
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GC45090
Triparanol
曲帕拉醇,MER-29
An inhibitor of DHCR24 -
GC44855
RU-SKI 43 (hydrochloride)
RU-SKI 43(盐酸盐)
An inhibitor of hedgehog acyltransferase -
GC44458
N-Palmitoyl-L-Aspartate
BRN 2295471
A natural N-acylaspartate -
GC44321
Nat-20(S)-yne
Click Tag Nat-20(S)-yne
Nat-20(S)-OHC with a terminal alkyne group -
GC43809
Hedgehog Antagonist VIII
Hh Antagonist VIII
An inhibitor of hedgehog pathway signaling -
GC43346
Cyclopamine-KAAD
3-酮-N-氨基乙基-N'-氨基己酰二氢肉桂酰环杷明,Cyclopamine-KAAD
A potent inhibitor of hedgehog signaling - GC18475 Robotnikinin A direct inhibitor of sonic hedgehog
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GC11217
CUR 61414
G-856
A potent inhibitor of hedgehog-induced activity -
GC17713
Oxy-16
20(R),22(R)-dihydroxy Cholesterol
A synthetic oxysterol -
GC13630
MK-4101
5-(3,3-二氟环丁基)-3-[4-[4-甲基-5-[2-(三氟甲基)苯基]-4H-1,2,4-三唑-3-基]双环[2.2.2]辛烷-1-基]-1,2,4-恶二唑
A Smoothened receptor antagonist -
GC12068
SAG
Smoothened Agonist
An agonist of Smoothened -
GC15422
20(S)-Hydroxycholesterol
20Α-羟基胆固醇,20α-hydroxy Cholesterol
An allosteric Smo agonist - GC15284 U 18666A U18666A是一种具有细胞渗透性和两亲性的小分子,可以抑制3β羟基甾醇-Δ(24)还原酶 (DHCR24)活性, 从而阻止胆固醇从晚期核内体和溶酶体外流[2]。
- GC15889 SANT-1 An antagonist of Smoothened
- GC12429 AY 9944 dihydrochloride A cholesterol synthesis inhibitor
- GC14715 AZ 12080282 dihydrochloride 刺猬抑制剂
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GC11111
Jervine
蒜黎芦碱; 11-Ketocyclopamine
An inhibitor of the hedgehog signaling pathway -
GC11476
Ciliobrevin A
HPI-4
A hedgehog pathway inhibitor - GC11045 HPI 1 A Hedgehog pathway inhibitor
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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 -
GC17153
CHIR-99021 (CT99021) HCl
CHIR-99021 monohydrochloride; CT99021 monohydrochloride
A selective GSK3 inhibitor - 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。
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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。 -
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。 -
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。 -
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 -
GC10493
GDC-0449 (Vismodegib)
维莫德吉; GDC-0449
GDC-0449 (Vismodegib) (GDC-0449) 是一种具有口服活性的hedgehog 通路抑制剂,IC50 为3 nM。 GDC-0449 (Vismodegib) 还抑制 P-gp、ABCG2,IC50 值分别为 3.0 μM 和 1.4 μM。