Other Apoptosis(其他细胞凋亡)
- Cat.No. 产品名称 Information
- GC25743 PIM447 (LGH447) PIM447 (LGH447) is a novel pan-PIM kinase inhibitor with Ki values of 6 pM, 18 pM, 9 pM for PIM1, PIM2, PIM3 respectively. It also inhibits GSK3β, PKN1, and PKCτ, but at a significantly lower potency with IC50 between 1 and 5 μM (>105-fold differential relative to the Ki on PIMs). PIM447 induces apoptosis.
- GC25691 OTS514 hydrochloride OTS514 is a highly potent TOPK(T-LAK cell-originated protein kinase) inhibitor with an IC50 value of 2.6 nM. OTS514 induces cell cycle arrest and apoptosis.
- GC25428 Foscenvivint (ICG-001) Foscenvivint (ICG-001) antagonizes Wnt/β-catenin/TCF-mediated transcription and specifically binds to CREB-binding protein (CBP) with IC50 of 3 μM, but is not the related transcriptional coactivator p300. ICG-001 induces apoptosis.
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GC19771
STM2457
N-[[6-[[(环己基甲基)氨基]甲基]咪唑并[1,2-A]吡啶-2-基]甲基]-4-氧代-4H-吡啶并[1,2-A]嘧啶-2-甲酰胺
An inhibitor of the METTL3/14 complex
- GC39620 AKOS-22 AKOS-22 是一种有效的线粒体蛋白电压依赖性阴离子通道 1 (VDAC1) 抑制剂 (Kd=15.4 μM)。AKOS-22 与 VDAC1 相互作用,抑制 VDAC1 齐聚和凋亡。AKOS-22 对线粒体功能的保护作用。
- GC50372 SK 216 Plasminogen activator inhibitor-1 (PAI-1) inhibitor
- GC50282 EC 19 Synthetic retinoid; induces differentiation of stem cells
- GC50223 MSC 2032964A Potent and selective ASK1 inhibitor; orally bioavailable
- GC50141 SMBA 1 High affinity and selective activator of Bax
- GC50118 S 07662 Constitutive androstane receptor (CAR) inverse agonist
- GC50112 NCL 00017509 A Nek2 inhibitor
- GC50063 rac-CCT 250863 rac-CCT 250863 (compound rac-21) 是一种选择性和可逆的 NEK 2 抑制剂,IC50 为 0.073 µM。 rac-CCT 250863 表现出良好的诱导细胞周期停滞的作用,并且还可以在细胞中进行抗增殖(Pomalidomide 敏感/抗性)。 rac-CCT 250863 与 Pomalidomide 结合时可诱导细胞凋亡。
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GC39182
Soyasaponin III
大豆皂苷 III
Soyasaponin III 是一类单链齐墩果烷三萜类化合物,是大豆 (Glycine max) 及其相关产品中发现的主要潜在生物活性皂苷之一。Soyasaponin III 可以诱导 Hep-G2 细胞凋亡。 - GC39175 SR-4835 SR-4835 is a highly selective dual inhibitor of CDK12 and CDK13 with IC50 of 99 nM and Kd of 98 nM for CDK12 and IC50 of 4.9 nM for CDK13. SR-4835 disables triple-negative breast cancer (TNBC) cells. SR-4835 promotes synergy with DNA-damaging chemotherapy and PARP inhibitors.
- GC39174 EC359 EC359 是一种有效的,选择性的,高亲和力的和口服的生物利用度白血病抑制因子受体 (LIFR) 抑制剂,其 Kd 值为 10.2 nM,可直接与 LIFR 相互作用以有效阻断 LIF/LIFR 相互作用。
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GC39169
CC-92480
CC-92480
A modulator of cereblon - GC39167 VBIT-4 VBIT-4 is a voltage-dependent anion channel (VDAC) oligomerization inhibitor that decreases mitochondrial DNA (mtDNA) release, type I interferon (IFN) signaling, neutrophil extracellular traps, and disease severity in a mouse model of systemic lupus erythematosus.
- GC39155 PI-273 PI-273, the first reversibly and specific phosphatidylinositol 4-kinase (PI4KIIα) inhibitor with an IC50 of 0.47 μM, can inhibit breast cancer cell proliferation, block the cell cycle and induce cell apoptosis.
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GC39152
9-ING-41
Elraglusib
A GSK3β inhibitor -
GC46027
IP7e
Isoxazolo-pyridinone 7e
An activator of Nurr1 signaling -
GC46008
(±)-Thalidomide-d4
沙利度胺 D4
An internal standard for the quantification of (±)-thalidomide - GC38864 TL02-59 TL02-59 is an orally active, selective Src-family kinase Fgr inhibitor with an IC50 of 0.03 nM.
- GC38863 TK216 TK216 is a potent inhibitor targeting E26 transformation specific (ETS) factors via blocking the protein-protein interaction with RNA helicases. TK216 exhibits antilymphoma activity.
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GC38853
Tandutinib hydrochloride
MLN518 hydrochloride; CT53518 hydrochloride
An antagonist of PDGFRβ, FLT3, and c-Kit -
GC38848
Se-Methylselenocysteine
L-硒甲基硒代半胱氨酸,Methylselenocysteine; Se-Methylseleno-L-cysteine
A selenium-containing amino acid -
GC38817
Minerval
2-羟基乳清酸,2-Hydroxyoleic acid; 2-OHOA
A synthetic monounsaturated hydroxylated fatty acid
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GC38772
DIM-C-pPhOH
4(二(1H-吲哚-3-基)甲基)苯酚
A Nur77 antagonist -
GC45723
Macitentan-d4
马其顿D4,ACT-064992-d4
An internal standard for the quantification of macitentan - GC38710 TVB-3166 A FASN inhibitor
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GC38683
Benzyl isothiocyanate
苄基异硫氰酸酯
Benzyl isothiocyanate (BITC, Benzoylthiocarbimide, Isothiocyanic Acid Benzoyl Ester) is an isothiocyanate originally found in cruciferous vegetables that exhibits immunomodulatory, anti-parasitic, antibiotic, antioxidative, anti-atherosclerotic, anti-angiogenic, anti-metastatic, anticancer chemotherapeutic, and chemopreventive activities. -
GC38653
Selumetinib sulfate
司美替尼硫酸盐,AZD6244 sulfate; ARRY-142886 sulfate
Selumetinib (AZD6244) 是一种高效选择性的,非 ATP 竞争性的 MEK1/2 抑制剂, 抑制 MEK1 的 IC50 为 14 nM。Selumetinib (AZD6244) 抑制 MEK1/2 磷酸化水平。 -
GC38620
Dihydrorotenone
二氢鱼藤酮
Dihydrorotenone 是一种天然杀虫剂,是一种线粒体 (mitochondrial) 抑制剂。Dihydrorotenone 可能诱发帕金森综合症。Dihydrorotenone 通过触发内质网应激并激活 p38 信号通路来诱导人浆细胞凋亡 (apoptosis) -
GC38617
Dihydrokaempferol
香橙素
A flavone with diverse biological activities -
GC38609
Rotundic acid
铁冬青酸
Rotundic acid (Rutundic acid), a natural compound, exhibit cytotoxic activities toward human hepatocellular carcinoma (HepG2), malignant melanoma (A375), SCLC (NCI-H446), breast cancer (MCF-7), and colon cancer (HT-29) cell lines.RA induces cell cycle arrest, DNA damage, and apoptosis by modulating the AKT/mTOR and MAPK pathways. -
GC38606
Glaucocalyxin A
蓝萼甲素
Glaucocalyxin A is a biologically active ent-kauranoid diterpenoid isolated from Rabdosia japonica var. glaucocalyx with antitumor and anti-inflammatory activity. Glaucocalyxin A induces G2/M cell cycle arrest and apoptosis through the PI3K/Akt pathway in human bladder cancer cells. -
GC38592
PTC596
PTC596
A BMI1 inhibitor -
GC38566
Ilexsaponin A
毛冬青皂苷A
Ilexsaponin A 是从冬凌草的根中分离出的,通过抗凋亡途径减轻缺血再灌注引起的心肌损伤。Ilexsaponin A 可以减少心肌梗塞的大小,降低 LDH,AST 和 CK-MB 的血清水平,增加细胞活力并抑制缺氧/复氧心肌细胞的凋亡。 -
GC38564
Deoxypodophyllotoxin
脱氧鬼臼毒素
A flavolignan with diverse biological activities -
GC38545
Polygalacin D
远志皂苷D
Polygalacin D (PGD) 是从桔梗 Platycodon grandiflorum 中分离的具有抗癌和抗增殖特性的生物活性化合物。Polygalacin D 抑制 IAP 蛋白家族的表达,包括存活蛋白,cIAP-1 和 cIAP-2 蛋白,并通过抑制 GSK3β,Akt 的磷酸化和PI3K 的表达来阻断 PI3K/Akt 途径。Polygalacin D 通过 PI3K/Akt 途径诱导凋亡 (apoptosis)。 - GC38467 BTdCPU BTdCPU is a potent activator of heme regulated inhibitor kinase (HRI), one of eukaryotic translation initiation factor 2α kinases (eIF2α-kinases).
- GC38447 Eriosematin Eriosematin 是一种来自 Flemingia philippinensis 的根的化合物,具有抗增殖活性和诱导细胞凋亡的特性。
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GC38437
Fangchinoline
防己诺林碱
An alkaloid with diverse biological activities -
GC38425
Sophoridine
槐定碱
A quinolizidine alkaloid with diverse biological activities -
GC38419
Cyclovirobuxine D
黄杨碱
An alkaloid with diverse biological activities -
GC38408
Diosgenin glucoside
延龄草苷
A steroidal saponin with diverse biological activities - GC38406 MN58b MN58b 是一种选择性的 choline kinase α (CHKα) 抑制剂,可抑制磷酸胆碱的合成。MN58b 通过诱导凋亡来减少细胞生长,并具有抗肿瘤活性。
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GC38392
Euscaphic acid
野鸦椿酸
A triterpene with diverse biological activities -
GC38374
Uvarigrin
大花紫玉盘素
Uvarigrin 可从Uvaria calamistrata 根部分离得到,可诱导肿瘤多药耐药细胞凋亡和 Caspase-9 的激活。 -
GC38318
2-Methoxycinnamaldehyde
2'-甲氧基肉桂醛,o-Methoxycinnamaldehyde
2-methoxycinnamaldehyde (O-methoxycinnamaldehyde), found in ceylan cinnamon, is a flavouring ingredient. -
GC38237
Higenamine hydrochloride
盐酸去甲乌头碱,Norcoclaurine hydrochloride
Higenamine (Norcoclaurine, (+-)-Demethylcoclaurine), also known as Norcoclaurine HCl, is a non-selective β2 adrenoceptor agonist which is a chemical compound naturally occurring in a number of plants.