124
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0432 |
Diclofenac diethylamine
|
Apoptosis; COX | Apoptosis; Immunology/Inflammation; Neuroscience |
Diclofenac diethylamine 是非选择性抗炎剂,通过活化 caspase 级联反应来诱导神经干细胞凋亡。它是一种COX 抑制剂,在 CHO 细胞中,对人COX-1和COX-2的IC50值分别为 4 和 1.3 nM。它对绵羊COX-1和COX-2的IC50值分别为 5.1 μM 和0.84 μM。 | |||
T2667 |
PIK-75
|
Apoptosis; DNA-PK; PI3K | Apoptosis; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
PIK75 是一种可逆的DNA-PK 和p110α-选择性的抑制剂,抑制 DNA-PK、p110α 和 p110γ,IC50分别为 2、5.8 和 76 nM。它诱导凋亡,抑制 p110α 效果比抑制 p110β 高 200 多倍,p110β的IC50为 1.3 μM。 | |||
T1555 |
Diclofenac sodium
GP 45840,双氯芬酸钠 |
Apoptosis; COX | Apoptosis; Immunology/Inflammation; Neuroscience |
Diclofenac sodium (GP 45840) 是一种非选择性抗炎剂,是 COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的 IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的 IC50值分别为 5.1 μM,0.84 μM。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。 | |||
T0196 |
Diclofenac
双氯芬酸,奥尔芬,Diclofenacum,Voltaren |
Apoptosis; COX | Apoptosis; Immunology/Inflammation; Neuroscience |
Diclofenac (Diclofenacum) 是一种具有抗炎活性的非甾体苯乙酸衍生物,是 COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的 IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的 IC50值分别为 5.1 μM,0.84 μM。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。 | |||
T6470 |
Diclofenac Potassium
双氯芬酸钾,CGP-45840B,Cataflam,Voltfast |
Apoptosis; Others; COX | Apoptosis; Immunology/Inflammation; Neuroscience; Others |
Diclofenac Potassium (CGP-45840B) 是一种非甾体抗炎药,用于减轻炎症并在某些情况下作为镇痛剂减轻疼痛。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。它是一种COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的IC50值分别为 5.1 μM 和0.84 μM。 | |||
T1566 |
Aripiprazole
阿立哌唑,OPC-14597 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Aripiprazole (OPC-14597) 是血清素受体 5-HT1A 和多巴胺 D2 受体的部分激动剂,还用作突触后拮抗剂和血清素受体 5-HT2A 的拮抗剂。 | |||
T23386 |
SR 142948
|
Neurotensin Receptor | GPCR/G Protein |
SR 142948 是一种神经降压素 (NT) 受体拮抗剂。 | |||
T2287 |
PIK-75 hydrochloride
PIK-75 HCl,2-甲基-5-硝基苯磺酸 [(6-溴咪唑并[1,2-a]吡啶-3-基)亚甲基]甲基肼盐酸盐,PIK-75 |
Apoptosis; DNA-PK; PI3K | Apoptosis; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
PIK-75 hydrochloride (PIK-75 HCl) 是一种可逆的 DNA-PK 和 p110α-选择性抑制剂,抑制 DNA-PK,p110α和 p110γ,可诱导凋亡。 | |||
TQ0227 |
Etrasimod
APD334 |
S1P Receptor; LPL Receptor | GPCR/G Protein |
Etrasimod (APD334) 是一种特异性和口服的S1P1受体拮抗剂,在CHO 细胞中的IC50值为1.88 nM。 | |||
T4626L |
TC-O 9311
TCO-9311,TC-O9311,TCO 9311,TC-O 9311,TCO9311,TC-O-9311 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
TC-O 9311 (TCO-9311) 是一种孤儿 G 蛋白偶联受体 139 激动剂,EC50值为 39 nM。 | |||
T8449 |
TC-I2000
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
TC-I2000 是一款 TRPM8 通道阻断器。在表达 rTRPM8 的 CHO 细胞中抑制 icilin 诱导的 TRPM8 通道激活,IC50 为 53 nM。 | |||
T6329 |
3-Aminobenzamide
3-AB,INO1001,INO-1001,3-ABA,PARP-IN-1,INO 1001 |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
3-Aminobenzamide (PARP-IN-1) 是一种有效的 PARP 抑制剂,在 CHO 细胞中,对 PARP 的 IC50值约为 50 nM。它是再灌注过程中氧化剂诱导的肌细胞功能障碍的介质。 | |||
T9650 |
AZ12672857
|
Src; Ephrin Receptor | Angiogenesis; Tyrosine Kinase/Adaptors |
AZ12672857 是一种 EphB4 抑制剂,IC50 为 1.3 nM。 AZ12672857 抑制 Src 转染 3T3 细胞的细胞增殖,IC50 为 2 nM,抑制转染 CHO-K1 细胞中 EphB4 的自磷酸化,IC50 为 9 nM。 | |||
TP1199L |
Urotensin I acetate (83930-33-0 Free base)
|
CRFR | GPCR/G Protein |
Urotensin I acetate 是一种 CRF 样神经肽,可作为 CRF 受体激动剂,对 CHO 细胞中的人 CRF1、人 CRF2 和大鼠 CRF2α 受体的 pEC50 分别为 11.46、9.36 和 9.85,对 CHO 细胞的 Kis 分别为 0.4、1.8 和 5.7 nM hCRF1、rCRF2α 和 mCRF2β 受体分别为。 | |||
T12670 |
(Rac)-MGV354
MGV354,外消旋MGV354 |
Others | Others |
(Rac)-MGV354 (MGV354) 是 MGV354 的外消旋体,MGV354 是可溶性鸟苷酸环化酶活化剂,在 GTM-3E 和 CHO 细胞中 EC50分别为 5 nM 和小于 0.5 nM。 | |||
T12930 |
SKF89976A hydrochloride
d,l-SKF89976A hydrochloride |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
SKF89976A hydrochloride (d,l-SKF89976A hydrochloride) 是GABA 转运蛋白GAT-1的选择性抑制剂,抑制 CHO 细胞中的 GAT-1,GAT-2 和 GAT-3,IC50分别为 0.28 μM,137.34 μM 和 202.8 μM。 | |||
T14944 |
CGS 15943
|
PI3K; Adenosine Receptor | GPCR/G Protein; Neuroscience; PI3K/Akt/mTOR signaling |
CGS 15943 是一种可口服的非黄嘌呤腺苷受体拮抗剂。在转染的 CHO 细胞中,其对人 A1、A2A、A2B 和 A3 腺苷受体的 Ki 分别为 3.5、4.2、16 和 50 nM。 | |||
T22126 |
Org 25543 hydrochloride
|
GlyT | Neuroscience |
Org 25543 hydrochloride 是一种有效的选择性甘氨酸转运蛋白 2 型 (GlyT2) 抑制剂(hGlyT2 的 IC50 = 16 nM)。在 CHO 细胞的甘氨酸摄取测定中,对 GlyT1 或 56 种其他常见生物靶标 (≥ 100 μM) 没有显示活性。 | |||
T4317 |
PF 429242
|
NPC1L1; Lipid | Membrane transporter/Ion channel; Metabolism |
PF 429242 是甾醇调节元件结合蛋白 (SREBP) 位点 1 蛋白酶的竞争性抑制剂 (IC50 = 0.175 μM)。它对位点 1 蛋白酶对一组丝氨酸蛋白酶具有选择性。 PF-429242 抑制 CHO 细胞中胆固醇的合成速率 (IC50 = 0.53 μM)。 | |||
T30249 |
AZD 7009
AZD-7009,AZD7009 |
Sodium Channel | Membrane transporter/Ion channel |
AZD 7009是一种新型抗心律失常化合物,对CHO K1细胞中 hNav1.5的钠电流具有抑制作用,IC50为11 uM。AZD 7009 对离体兔心房和心室肌细胞的晚期钠电流具有抑制作用,对e -4031诱导的动作电位持续时间延长具有抑制作用,促使浦肯野纤维的早期后去极化(EADs)。 | |||
TP1940L1 |
Ac-RYYRIK-NH2 acetate
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Ac-RYYRIK-NH2 acetate 是 nociceptin/orphanin FQ(noc/OFQ) 受体的激动剂,影响自发运动活动。 它是转染在 CHO 细胞中的 ORL1 的部分激动剂,可拮抗大鼠脑膜和切片中 noc/OFQ 对 [35S]-GTPgammaS 与 G 蛋白结合的刺激。 | |||
T22986 |
MK 1903
|
GPR | Endocrinology/Hormones; GPCR/G Protein |
MK 1903 是一种有效的、具有选择性的羟基羧酸受体2 (HCA2) 的完全激动剂。HCA2也叫做G 蛋白偶联受体109A(GPR109A) 。MK 1903在使用表达人受体(ECso-12.9 nM)的 CHO 细胞进行的均匀时间分辨荧光(htf)测定中,它减少了福斯克林诱导的 cAMP 的产生。 | |||
TP2106L |
Urantide acetate(669089-53-6 free base)
|
Neurotensin Receptor | GPCR/G Protein |
Urantide acetate(669089-53-6 free base) 是一种选择性和竞争性的 urotensin-II (UT) 受体拮抗剂 (pKB = 8.3)。体外阻断 hU-II 诱导的胸主动脉收缩。对去甲肾上腺素或内皮素 1 诱导的收缩或乙酰胆碱诱导的松弛没有影响。在钙动员测定(在表达 hUT 受体的 CHO 细胞中)中表现为部分激动剂。 | |||
T27117 |
DA-6886
DA6886,DA 6886 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
DA-6886 是一种 5-羟色胺受体 4(5-HT4)激动剂。DA-6886 以 5-HT4 受体拮抗剂敏感的方式诱导大鼠食道制剂松弛。在表达 hERG 通道的 CHO 细胞中对 DA-6886 进行的评估显示,它抑制 hERG 通道电流的 pIC50 值为 4.3,表明该化合物对 5-HT4 受体的选择性比 hERG 通道高 1000 倍。 | |||
T38240 |
2,6-Dichlorodiphenylamine
|
Antibacterial | Microbiology/Virology |
2,6-Dichlorodiphenylamine 是双氯芬酸钠的一种结构类似物,显示出抗白色念珠菌活性。2,6-Dichlorodiphenylamine 是非选择性抗炎剂,为COX 的抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的IC50分别为 4 和 1.3 nM。 | |||
T3483 |
FTIDC
|
GluR | Neuroscience |
FTIDC 是非竞争性和选择性的口服变构代谢型谷氨酸受体 1 拮抗剂,对人 mGluR1a 的IC50为 5.8 nM。 | |||
T76341L |
[DPro10] Dynorphin A (1-11)acetate,porcine
[DPro10] Dynorphin A (1-11)acetate,porcine(94596-26-6 Free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
[DPro10] Dynorphin A (1-11)acetate,porcine 是一种高效的 κ-阿片受体激动剂,其 Ki 值为 0.13 nM。[DPro10] Dynorphin A (1-11), porcine 是一种 N-烷基化衍生物,具有镇痛活性。 | |||
T36008 |
Nebentan potassium
|
||
Nebentan potassium (YM598) is a potent, selective and orally active non-peptide endothelin ETA receptor antagonist through the modification of Bosentan . Nebentan potassium inhibits [125I] endothelin-1 binding to cloned human endothelin ETA and ETB receptor, with Ki of 0.697 nM and 569 nM, respectively[1]. YM598 can ameliorate the progression of cor pulmonale and myocardial infarction in vivo[2]. Nebentan potassium inhibits the specific binding of [125I] endothelin-1 to endothelin ETA and ETB re... | |||
T7549 |
Talnetant
SB 223412 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Talnetant (SB 223412) 是一种选择性、竞争性、脑渗透性 NK3 受体拮抗剂,Ki 为1.4 nM。它比对hNK-2受体的抑制性高100倍,具有调节中脑边缘和中脑皮质多巴胺能神经传递的能力。 | |||
T14202 | AM-4668 | GPR | Endocrinology/Hormones; GPCR/G Protein |
AM-4668 is a type 2 diabetes GPR40 agonist. For GPR40, in A9 cells (GPR40 IP3 assay) and CHO cells (GPR40 aequorin assay), the EC50s are 3.6 nM and 36 nM, respectively. | |||
T11655 |
Indomethacin-D4
Indometacin-D4,吲哚美辛-D4 |
CDK | Cell Cycle/Checkpoint |
Indomethacin-D4 is a deuterium labeled Indomethacin. Indomethacin is a potent and nonselective inhibitor of COX1 and COX2, with IC50s of 18 nM and 26 nM for human COX-1 and COX-2, respectively, in CHO cells. | |||
T41069 |
CHO-C-PEG2-C-CHO
CHO-C-PEG2-C-CHO |
||
CHO-C-PEG2-C-CHO is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T29233 |
Z-LLNle-CHO
|
||
Z-LLNle-CHO is a cell permeable inhibitor of gamma-secretase. Z-LLNle-CHO induces apoptosis of human glioblastoma tumor-initiating cells by proteasome inhibition and mitotic arrest response. | |||
T16134 |
MRS-1191
|
Others | Others |
MRS-1191 is an effective and selective A3 adenosine receptor antagonist (KB: 92 nM, a Ki: 31.4 nM for human A3 receptor and an IC50: 120 nM for CHO cells). | |||
T7499 |
TAK-779
Takeda 779 |
HIV Protease; CXCR; CCR | Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
TAK-779 (Takeda 779) 是一种非肽类CCR5和CXCR3 拮抗剂,对CCR5的Ki 值为 1.1 nM,并选择性抑制R5 HIV-1。 | |||
T80624 |
Ac-VAD-CHO
Ac-Val-Ala-Asp-CHO |
Caspase | Apoptosis; Proteases/Proteasome |
Ac-VAD-CHO (Ac-Val-Ala-Asp-CHO)是一款caspase抑制剂,能够阻止缺氧细胞内MMP的降解以及细胞色素c的释出。 | |||
T36118 |
3-hydroxy Darifenacin
|
||
3-hydroxy Darifenacin is a metabolite of darifenacin . It is an antagonist of M1-5 muscarinic receptors (Kis = 17.78, 79.43, 2.24, 36.31, and 6.17 nM, respectively, in CHO cells). | |||
T37112 |
YNT-185 dihydrochloride
|
||
Potent and selective orexin OX2 receptor agonist (EC50 = 28 nM at human OX2 expressed in CHO cells). Displays approximately 100-fold selectivity for OX2 over OX1 (EC50 = 2.75 μM at human OX1 expressed in CHO cells). Depolarizes OX2-expressing histaminergic neurons in mouse brain slices. Increases wake time in wild type mice. Suppresses cataplexy-like symptoms in OX knockout mice. Nagahara et al (2015) Design and synthesis of non-peptide, selective orexin receptor 2 agonists. J.Med.Chem. 58 7931 ... | |||
T80596 |
Coprelotamab
GB-221 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Coprelotamab (GB-221) 为针对EGFR2的IgG-κ类单克隆抗体。该化合物通常在CHO DG44 (中国仓鼠卵巢) 细胞中表达。 | |||
T80602 |
Dovanvetmab
ZTS-00521505 |
||
Dovanvetmab (ZTS-00521505),一种IgG1-κ型抗体,专一性靶向Felcat IL31,由CHO(Chinese Hamster Ovary)细胞主要表达。 | |||
T78083 |
CB-25
|
Cannabinoid Receptor | GPCR/G Protein |
CB-25是一种CB1大麻素受体的部分激动剂配体。它能增强Forskolin诱导的癌细胞中cAMP的形成,但在Forskolin诱导的hCB1-CHO细胞中则不显示增强作用。 | |||
T80608 |
Ebronucimab
AK102 |
||
Ebronucimab (AK102)为一种针对PCSK9的IgG1-λ2单克隆抗体,其主要源自经过工程化改造的CHO DG44细胞系。 | |||
T36651 |
Anti-MERS-2E6 mAb
Anti-MERS-2E6 mAb |
||
Anti-MERS-2E6 mAb (MERS-2E6), a human IgG1 neutralizing antibody, is expressed in CHO cells. It effectively competes with the virus Spike protein for binding to the CD26 receptor, consequently inhibiting viral invasion into host cells. | |||
T41144 |
CYM5442 hydrochloride
CYM 5442 hydrochloride |
||
CYM 5442 hydrochloride is a potent and selective S1P1agonistin vitro(EC50 = 1.35 nM). Activates S1P1-mediated p42/p44 MAPK phosphorylation in CHO-K1 cells transfected with S1P1. Induces acute lymphopenia in mice. Brain penetrant. | |||
T36652 |
Anti-MERS-3A1 mAb
Anti-MERS-3A1 mAb |
||
Anti-MERS-3A1 mAb (MERS-3A1) is a high-affinity human monoclonal IgG1 antibody derived from CHO cells. It effectively inhibits the interaction between the MERS-CoV spike protein and the DPP4 receptor[1]. | |||
T82511 |
Ebdarokimab
|
||
Ebdarokimab (AK101),一种人源化IgG1-κ抗体,其表达系统主要选用CHO(中国仓鼠卵巢)细胞。 | |||
T27779 |
L-759,656
L 759,656,L759,656 |
||
L-759,656 is highly selective CB2 receptor agonist (CB1 Ki = 4888 nM, CB2 Ki = 11.8 nM). L-759,656 potently inhibits forskolin-stimulated cAMP production in CHO cells (EC50 = 3.1 nM). | |||
T36656 | Anti-Spike-RBD Single Domain mAb | ||
The Anti-Spike-RBD Single Domain mAb is a monoclonal antibody derived from CHO cells in Alpaca. It is composed of VHH-huFc and exhibits a strong affinity for the SARS-CoV-2 RBD. [1] | |||
T64298 | Turoctocog alfa | ||
Turoctocog alfa 是一种来源于中国仓鼠卵巢 (CHO) 细胞的重组凝血因子 VIII (FVIII)。Turoctocog alfa 能够用于研究 A 型血友病。 | |||
T82696 |
Cofetuzumab
PF-06523435,hu24 |
||
Cofetuzumab (PF-06523435)为针对PTK7的人源化IgG1-κ亚型单克隆抗体,常在CHO(中国仓鼠卵巢)细胞表达体系中生产。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5081 |
Adenine monohydrochloride hemihydrate
腺嘌呤盐酸盐,Adenine hydrochloride hydrate,6-Aminopurine hydrochloride hydrate |
Endogenous Metabolite; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Adenine monohydrochloride hemihydrate 是内源性代谢产物的一种。 | |||
T5214 |
Cholesteryl linoleate
CE(18:2(9Z,12Z)),Cholesterol Linoleate,Linoleic Acid cholesteryl ester,胆甾烯基亚油酸酯 |
Others; Endogenous Metabolite | Metabolism; Others |
Cholesteryl linoleate (Linoleic Acid cholesteryl ester) 是低密度脂蛋白和动脉粥样硬化病变中主要的胆固醇酯。它存在于 LDL 中的胆固醇酯,利用 LDL 受体相关蛋白转移到表达 15-脂氧合酶的巨噬细胞和 CHO 细胞的质膜,被氧化形成胆固醇亚油酸氢过氧化物。 | |||
TN1929 |
Methyl sinapate
芥子酸甲酯 |
Others | Others |
Methyl sinapate can increase the frequency of cells with chromosome aberrations in the CHO K-1 cells treated with MMC, 4NQO or UV. | |||
T19122 | 3-Methylvaleric Acid | Others; Endogenous Metabolite | Metabolism; Others |
3-Methylvaleric Acid 是一种食用级香料,存在于烟草中。3-Methylvaleric Acid 可增强 CHO-K1细胞和HEK293细胞中的细胞内cAMP 积累和CRE-荧光素酶活性。 | |||
T38262 |
Sphingosine (d14:1)
|
||
Sphingosine (d14:1) is a bioactive sphingolipid that has been found in B. mori (silkworm), P. clarkii (crayfish), and A. aurita (jellyfish) extracts. It increases the germination rate of N. rileyi, an entomopathogenic fungus, with an EC50 value of 10.2 nM. Sphingosine (d14:1) inhibits protein kinase C (PKC) in vitro (IC50 = 7.3 mol%) as well as superoxide generation induced by phorbol 12-myristate 13-acetate in neutrophils and reduces growth of CHO cells (IC50s = 19 and 8 μM, respectively). |