Angiogenesis(血管生成)
- Cat.No. 产品名称 Information
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GC37034
PT2977
PT2977; MK-6482
PT2977 (Belzutifan, MK-6482), an orally active and selective HIF-2α inhibitor, increases potency and improves pharmacokinetic profile, providing a potential treatment for clear cell renal cell carcinoma (ccRCC). -
GC36861
PCI 29732
4-氨基-1-环戊基-3-(4-苯氧基苯基)-1H-吡唑并[3,4-D]嘧啶
A multi-kinase inhibitor - GC36821 OSU-T315 OSU-T315 (ILK-IN-2) is a potent Integrin-Linked Kinase (ILK) inhibitor with IC50 of 0.6 μM. OSU-T315 induces autophagy and apoptosis, both of which are integral to its antiproliferative activity. OSU-T315 exhibits anti-tumor activity.
- GC36661 MT-802 MT-802 is a potent PROTAC that induces Bruton's tyrosine kinase (BTK) knockdown. MT-802 recruits BTK to the cereblon E3 ubiquitin ligase complex to trigger BTK ubiquitination and degradation via the proteasome. MT-802 has potential for treatment of C481S mutant chronic lymphocytic leukemia (CLL).
- GC36500 LXW7 LXW7 是一种八聚二硫环肽,为整合素 αvβ3 的配体,能够有效、特异性地靶作用于内皮祖细胞 (EPCs) 和内皮细胞 (ECs)。在 ECs 细胞中,LXW7 可增强 VEGFR-2 的磷酸化和 ERK1/2 的活化。
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GC36289
Ibrutinib-biotin
依鲁替尼-生物素
Ibrutinib-biotin 是一种由 Ibrutinib 通过长链接头连接到生物素上组成的探针,具体可参考 WO2014059368A1 中 Compound 1-5,抑制 BTK,IC50 值为 0.755-1.02 nM。 -
GC36127
GDC-0834 Racemate
N-[3-[6-[[4-(1,4-二甲基-3-氧代-2-哌嗪基)苯基]氨基]-4,5-二氢-4-甲基-5-氧代-2-吡嗪基]-2-甲基苯基]-4,5,6,7-四氢苯并[B]噻吩-2-甲酰胺
GDC-0834 Racemate 是 GDC-0834 的外消旋体形式,它是一种有效的选择性 BTK 抑制剂,在生化和细胞试验中的体外 IC50 分别为 5.9 和 6.4 nM。 - GC36125 GB-110 GB-110 是一种有效的,具有口服活性的,非肽类的 protease activated receptor 2 (PAR2) 激动剂,选择性诱导 PAR2 介导的 HT29 细胞内 Ca2+ 释放,EC50 值为 0.28 μM。
- GC35684 CHMFL-EGFR-202 CHMFL-EGFR-202 是一种有效、不可逆的表皮生长因子受体 (EGFR) 突变型激酶抑制剂, 对 耐药突变型 EGFR T790M 和 WT EGFR 激酶作用的 IC50 值分别为 5.3 nM 和 8.3 nM。在细胞中,CHMFL-EGFR-202 对 EGFR L858R/T790M 的选择性是 EGFR 野生型的 10 倍。CHMFL-EGFR-202 以 “DFG-in-C-helix-out” 的不活跃结合构象形式共价结合 EGFR,对 EGFR 突变体驱动的非小细胞肺癌 (NSCLC) 细胞株具有较强的抗增殖作用。
- GC35683 CHMFL-BTK-01 CHMFL-BTK-01 (compound 9) 高度选择性的、不可逆的 BTK 抑制剂,IC50 值为 7 nM。CHMFL-BTK-01 (compound 9) 可有效抑制BTK Y223 的自磷酸化。
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GC35563
Btk inhibitor 1 R enantiomer hydrochloride
3-(4-苯氧基苯基)-1-(3R)-3-哌啶基-1H-吡唑并[3,4-D]嘧啶-4-胺盐酸盐(1:1)
Btk inhibitor 1 R enantiomer hydrochloride 是依鲁替尼的杂质。 IBT6A 可用于 IBT6A 依鲁替尼二聚体和 IBT6A 加合物的合成。 Ibrutinib 是一种选择性、不可逆的 Btk 抑制剂,IC50 为 0.5 nM。 - GC35562 Btk inhibitor 1 hydrochloride Btk inhibitor 1 hydrochloride 是 Btk inhibitor 1 R enantiomer 的消旋体. Btk inhibitor 1 R enantiomer (参考文献中的化合物14) 可用于合成 Ibrutinib 和基于 Ibrutinib 的活性探针 (ABP)。Ibrutinib 是一种共价且不可逆的 BTK 抑制剂。
- GC35561 Btk inhibitor 1 (Rac)-IBT6A (BTK inhibitor 1) is a racemate of IBT6A and an impurity of Ibrutinib, which is a Btk inhibitor (IC50=0.5 nM), and can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct.
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GC35230
Acetylarenobufagin
乙酰沙蟾毒精
Acetylarenobufagin 是一种类固醇缺氧诱导因子-1 (HIF-I) 调节剂。 -
GC45269
(±)10(11)-DiHDPA
(±)10,11-DiHDPE
An epoxygenase metabolite of DHA - GC45054 Tie2 Inhibitor 7 Blocks Tie2 kinase activity
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GC44966
Sucrose octasulfate (potassium salt)
蔗糖八硫酸酯钾
An alkaline aluminum?sucrose complex -
GC44956
Streptochlorin
3-(4-氯-5-恶唑基)-1H-吲哚
A bacterial metabolite with diverse biological activities - GC44800 Quininib A CysLT1 and CysLT2 receptor antagonist
- GC44584 PD 168368 An antagonist of NMB receptors
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GC44475
NVP-BEZ235 (hydrochloride)
Dactolisib
Dual inhibitor of PI3K and mTOR -
GC44465
NSC 12
NSC 172285
An FGF inhibitor - GC44358 Nebivolol O-β-D-Glucuronide An active metabolite of nebivolol
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GC44290
NAADP (sodium salt)
Nicotinic acid adenine dinucleotide phosphate
A secondary messenger that induces calcium mobilization
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GC43803
HA-1077 (hydrochloride)
盐酸法舒地尔,HA-1077 dihydrochloride; AT-877 dihydrochloride
A ROCK inhibitor -
GC43732
Ganglioside GM3 Mixture (sodium salt)
单唾液神经节苷酯GM3; Hematoside; Sialosyllactosylceramide
A mixture of ganglioside GM3 -
GC43727
Ganglioside GD1a mixture (sodium salt)
双唾液酸神经节苷酯GD1A,Ganglioside B1
A mixture of ganglioside GD1a -
GC43515
D-myo-Inositol-1,3,4,5,6-pentaphosphate (sodium salt)
Ins(1,3,4,5,6)P5, 1,3,4,5,6IP5
An anticancer inositol phosphate -
GC43514
D-myo-Inositol-1,3,4,5,6-pentaphosphate (ammonium salt)
Ins(1,3,4,5,6)P5, 1,3,4,5,6IP5 (sodium salt)
An anticancer inositol phosphate - GC43198 CAY10717 A multi-targeted kinase inhibitor
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GC42887
Axitinib Sulfoxide
阿西替尼杂质A
A major inactive metabolite of axitinib - GC42409 4-hydroxy Nebivolol (hydrochloride) A major metabolite of nebivolol
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GC41655
(±)19(20)-EDP Ethanolamide
19,20-DHEA epoxide, 19,20-epoxy Docosapentaenoic Acid Ethanolamide, 19,20-EDP-EA, 19,20-EDP epoxide
An ω-3 endocannabinoid epoxide and CB receptor agonist - GC41653 (±)16(17)-DiHDPA An epoxygenase metabolite of DHA
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GC41648
(±)13(14)-DiHDPA
13(14)-DiHDPA, 13(14)-DiHDoPE, 13,14-DiHDPE
A metabolite of DHA -
GC41625
Oroxylin A
千层纸素A; Baicalein 6-methyl ether; 6-Methoxybaicalein
A flavonoid with diverse biological activities -
GC41212
(±)10(11)-EpDPA
(±)10,11-EDP, (±)10,11-EpDPE, (±)10,11-epoxy DPA, (±)10,11-epoxy Docosapentaenoic Acid
A DHA epoxygenase metabolite -
GC41203
(±)7(8)-EpDPA
(±)7,8-EDP, (±)7,8-EpDPE, (±)7,8-epoxy DPA, (±)7,8-epoxy Docosapentaenoic Acid
A DHA epoxygenase metabolite -
GC41191
(±)13(14)-EpDPA
13,14-EpDPE
A DHA epoxygenase metabolite - GC40963 Spirolaxine A phthalide antibacterial agent
- GC40865 LYG-202 A synthetic flavonoid with anticancer and anti-angiogenic activities
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GC40466
(±)11(12)-EET
11,12-EET
A racemic version of a CYP450 metabolite of arachidonic acid - GC34709 PF-06250112 PF-06250112是一种有效的、高度选择性、口服有效的BTK抑制剂,IC50值为0.5nM,对BMX非受体酪氨酸激酶和TEC同样有抑制作用,IC50值分别为0.9nM和1.2nM。
- GC34595 GN44028 GN44028 是一种有效且具有口服活性的缺氧诱导因子 (HIF)-1α 抑制剂,IC50 为 14 nM。 GN44028 抑制缺氧诱导的 HIF-1α 转录活性,而不抑制 HIF-1α mRNA 表达、HIF-1α 蛋白积累或 HIF-1α/HIF-1β 异二聚化。 GN44028可用于癌症研究。
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GC40213
Regorafenib-13C-d3
瑞戈非尼-13C-D3,BAY 73-4506-13C,d3
An internal standard for the quantification of regorafenib -
GC40085
Pazopanib-d6
培唑帕尼-d6,GW786034-d6
An internal standard for the quantification of pazopanib -
GC34402
RGD Trifluoroacetate
(S)-2-(2-((S)-2-氨基-5-胍基戊酰胺基)乙酰氨基)琥珀酸三氟乙酸盐
RGDTrifluoroacetate是一种三肽,能够有效的引起细胞黏着,定位某种特定细胞系并产生特定的细胞反应;RGDTrifluoroacetate能够与integrins结合。 -
GC34301
ILK-IN-2
OSU-T315 analog
An ILK inhibitor - GC34265 GRGDSP TFA GRGDSP(TFA)是一种整联蛋白(integrin)抑制剂。
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GC34211
Vedolizumab
维多珠单抗; Anti-Human lymphocyte α4β7 integrin, Humanized Antibody
Vedolizumab (anti-α4β7-integrin) is a humanized IgG1 monoclonal antibody that targets the α4β7 integrin for the treatment of ulcerative colitis and Crohn's disease.