248
23
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14667 |
BLT-1
|
Others; HCV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
BLT-1 是一种氨基硫脲铜螯合剂,是一种选择性清除受体 B1 型 (SR-BI) 抑制剂,抑制高密度脂蛋白 (HDL) 和 SR-BI 介导的细胞之间的脂质转移。 | |||
T5326 |
Sugammadex sodium
Org25969,Sugammadex (sodium),舒更葡糖钠 |
Others | Others |
Sugammadex sodium (Org25969) 是合成的 γ 环糊精衍生物,是一种新型的神经肌肉阻断逆转剂。 | |||
T0370 |
Pheniramine maleate
Daneral,Inhiston,Trimetose,马来酸非尼拉敏 |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pheniramine maleate (Trimetose) 是一种具有抗组胺和血管扩张特性的烷基胺衍生物,可与组胺 H1 受体结合,从而抑制磷脂酶 A2 和内皮源性松弛因子一氧化氮的产生。 | |||
T6134 |
IEM 1754 2HBr
IEM 1754 dihydrobromide |
GluR | Neuroscience |
IEM 1754 2HBr (IEM 1754 dihydrobromide) 是一种选择性 AMPA/红藻氨酸受体阻滞剂,作用于 GluR1 和 GluR3,IC50 为 6 μM。 | |||
T11063 |
DMT1 blocker 1
|
Others | Others |
DMT1 blocker 1 是二价金属转运蛋白1 (DMT1) 的阻断剂,IC50 为 0.64 μM,可以阻断体内肠细胞的铁摄取。 | |||
T11064 |
DMT1 blocker 2
|
Others | Others |
DMT1 blocker 2 是一种二价金属转运蛋白 1 的直接抑制剂(IC50:0.83 μM)。它可以阻断体内肠细胞的铁摄取。 | |||
T26078 |
Rhodblock 6
Rhodblock6,Rhodblock-6 |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Rhodblock 6 是一种 Rho 激酶 (ROCK) 抑制剂,可抑制磷酸化 MRLC(肌球蛋白调节轻链)定位,通过特异性抑制 Rho 激酶的活性发挥作用。 | |||
T12504 |
(+)-KCC2 blocker 1
|
Potassium Channel | Membrane transporter/Ion channel |
(+)-KCC2 blocker 1 是 KCC2 的选择性阻断剂 (IC50 = 0.4 μM)。 | |||
T8741 |
MitoBloCK-10
3-fluoro-N'-[(E)-(5-nitrothiophen-2-yl)m |
Others | Others |
MitoBloCK-10 (3-fluoro-N'-[(E)-(5-nitrothiophen-2-yl)m) 是第一个能够减弱PAM 复合体活性的小分子调节剂,对 C 末端结构域的Tim44与前体和 Hsp70 结合具有抑制作用。 | |||
T8782 |
MitoBloCK-11 (MB-11)
|
Others | Others |
MitoBloCK-11 (MB-11) 是线粒体蛋白输入的小分子抑制剂,可能通过转运蛋白 Seo1 起作用,但不通过 Tom70 或 Tom20;抑制含有疏水片段的前体蛋白,以特定方式在缺乏尿嘧啶的培养基中促进生长,并影响斑马鱼的发育。 | |||
T10690 |
Cav 2.2 blocker 1
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Cav 2.2 blocker 1 是一种N 型钙离子通道 (Cav 2.2) 的阻断剂,IC50值为 1 nM,可用于治疗疼痛。 | |||
T60143 |
MitoBloCK-6
|
Apoptosis | Apoptosis |
MitoBloCK-6 是一种有效的Erv1/ALR 抑制剂,IC50分别为 900 nM 和 700 nM。MitoBloCK-6 还抑制Erv2,IC50值为1.4 μM。MitoBloCK-6 可通过释放细胞色素 c 诱导 hESCs 细胞凋亡。 | |||
T72170 |
NaV1.2/1.6 channel blocker-1
|
Sodium Channel | Membrane transporter/Ion channel |
NaV1.2/1.6 channel blocker-1 是一种有效的 NaV1.2/1.6 channel 阻滞剂,对 rNaV1.6 和 hNaV1.2 有抑制作用。NaV1.2/1.6 channel blocker-1 可用于研究全身性癫痫和运动障碍。 | |||
T12153 |
N-type calcium channel blocker-1
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
N-type calcium channel blocker-1 is an orally active analgesic agent,shows high affinity to functionally block N-type calcium channels. | |||
T26077 | Rhodblock 3 | ||
Rhodblock 3 is a potent small molecule Rho pathway inhibitor. | |||
T28132 |
NaV1.7 Blocker-801
|
||
NaV1.7 Blocker-801 is a potent NaV1.7 blocker. | |||
T69387 |
NMO-IgG blocker A-01
|
||
NMO-IgG blocker A-01 is a idiotype-specific blocker of neuromyelitis opticaimmunoglobulin g (nmo-igg) binding to aquaporin-4 (aqp4) | |||
TP2195 |
Nitric Oxide Synthase (599-613) Blocking Peptide, Bovine Endothelial Cell
|
Others | Others |
Nitric Oxide Synthase (599-613) Blocking Peptide, Bovine Endothelial Cell (Ac-Pro-Tyr-Asn-Ser-Ser-Pro-Arg-Pro-Glu-Gln-His-Lys-Ser-Tyr-Lys-Cys) is a peptide that inhibits the function of NOSs as a result it blocks the production of NO. Because of the invol | |||
T80930 |
TRPV2-selective blocker 1
|
||
TRPV2-selective blocker 1 (compound IV2-1) 为选择性TRPV2通道阻断剂,具有6.3 μM IC50,不对TRPV1、TRPV3和TRPV4通道产生影响。该化合物能够抑制巨噬细胞中TRPV2介导的Ca2+流入,进而抑制其吞噬功能。 | |||
T39717 |
VGSC blocker-1
|
||
VGSC blocker-1 is a powerful small molecule that serves as a blocker for the neonatal isoform of the VGSC subtype known as Nav1.5 (nNav1.5). It effectively blocks INa peak currents by 34.9% at a concentration of 1 μM, and demonstrates a 0.3% inhibition of cell invasion at the same concentration in the MDA-MB-231 human breast cancer cell line, without compromising cell viability. | |||
T11927 |
M2 ion channel blocker
|
Others | Others |
M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel. | |||
T62586 |
Cav 2.2/3.2 blocker 1
|
||
Cav 2.2/3.2 blocker 1 (Compound 9e) 是一种神经钙离子通道 (neuronal calcium channel) 阻断剂,能够作用于 Cav2.2 (IC50: 1.22 μM) 和 Cav3.2 (IC50: 80 μM)。Cav 2.2/3.2 blocker 1 可以穿透中枢神经系统。 | |||
TP2485 |
difelikefalin acetate(1024828-77-0 Free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
difelikefalin acetate 是酮体和砌块。 | |||
T4542 |
Clonixin
Clonixic acid,氯尼辛 |
Others | Others |
Clonixin (Clonixic acid) 是一种非甾体抗炎药,具有口服活性。 | |||
T9160 |
4-Chloroquinolin-8-ol
|
Others | Others |
4-Chloroquinolin-8-ol 是一个组成部分。 | |||
T9537 |
N'-Nitro-D-arginine
N'-Nitro-D-arginine,H-D-Arg(NO2)-OH,(R)-2-Amino-5-(3-nitroguanidino)pentanoic acid,N'-硝基-D-精氨酸 |
Others | Others |
N'-Nitro-D-arginine (N'-Nitro-D-arginine) 是一种砌块。 | |||
T10101 |
Calcium channel-modulator-1
|
Others; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Others |
Calcium channel-modulator-1是钙离子通道调节剂(IC50:0.8 μM),具有阻塞主动脉收缩的专业化。 | |||
T50103 |
NFAT Inhibitor-2
|
Others | Others |
NFAT Inhibitor-2 是一种化学合成中的砌块。 | |||
T40020 |
Pomalidomide-C2-acid
|
Others | Others |
Pomalidomide-C2-acid 是 PROTAC 的组成部分。 | |||
T8361 |
Tetraethylammonium bromide
四乙基溴化铵,TEAB,TEA bromide |
Potassium Channel | Membrane transporter/Ion channel |
Tetraethylammonium bromide (TEA bromide) 可以选择性阻断钾通道。 | |||
T27400L |
Ganaplacide phosphate
Ganaplacide phosphate (1261113-96-5 Free base) |
Others | Others |
Ganaplacide phosphate 对疟原虫症状性无性血期感染具有多阶段抗疟活性,并且能够在动物模型中预防传播和阻断感染。 | |||
T34603 |
L-Selenocystine
L-Selenocystine,L-硒代胱胺基乙酸 |
Others | Others |
L-Selenocystine (L-Selenocystine) 可用作生物活性硒醇化合物的组成部分。 | |||
T64341 |
H-β-Ala-AMC TFA
|
Others | Others |
H-β-Ala-AMC TFA 是氨基肽酶的底物之一。 | |||
T67830 |
p38α inhibitor 3
|
p38 MAPK | MAPK |
p38α inhibitor 3是一种丝裂原活化蛋白激酶P38α的抑制剂,可以有效阻断成肌细胞分化。 | |||
T22305 |
Dexrazoxane
右雷佐生,ICRF-187 |
Others | Others |
Dexrazoxane (ICRF-187) 是一种心脏保护剂。 | |||
T3543 |
NS-638
NS 638 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
NS-638 是一种 Ca2+ 通道阻滞剂,可阻断 K+ 刺激的细胞内 Ca2+ 升高,IC50值为3.4 μM。 | |||
T67910 |
2,4,5-Trichlorobenzenesulfonyl chloride
|
Others | Others |
2,4,5-Trichlorobenzenesulfonyl chloride (TCBSC) 是合成各种有机化合物(如胺、醇和羧酸)的通用构件。 | |||
T7470 |
6-Chloropurine
6-氯嘌呤,6-Chloro-9H-purine |
Others | Others |
6-Chloropurine (6-Chloro-9H-purine) 是一种制备9-烷基嘌呤和6-巯基嘌呤的中间体,是化学合成的砌块,具有抗肿瘤作用。 | |||
T50099 |
HIF-2α-IN-4
|
Others; HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism; Others |
HIF-2a translation inhibitor 是一种有效的HIF-2α翻译抑制剂,IC50=5 μM,能够抑制组成型和缺氧诱导的 HIF-2α 蛋白表达。其中 HIF-2α-IN-4 将 5'UTR 铁响应元件与氧传感联系起来。 | |||
T5828 |
MS21570
5-(苄基硫代)-N-甲基-1,3,4-噻二唑-2-胺 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
MS21570 作为 GPR171 拮抗剂基于其阻断能力,IC50 为 220 nM,可减少小鼠的焦虑样行为和恐惧条件反射。 | |||
T22353 |
Lanthanum(III) chloride heptahydrate
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lanthanum(III) chloride heptahydrate 是一种无机化合物,用于生化研究,阻断二价阳离子通道,尤其是钙通道的活性。 | |||
TNU0864 |
HUP30
|
Potassium Channel; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
HUP30是一种强效的血管舒张剂。HUP30可以刺激可溶性鸟苷酸环化酶,激活 K+离子通道,阻断细胞外 Ca2+的内流。 | |||
T50051 |
1,3-diethyl 2-(3-methoxyphenyl)propanedioate
|
Others | Others |
1,3-diethyl 2-(3-methoxyphenyl)propanedioate 是一种用作分子结构单元的化合物,可用于多种化合物的合成。 | |||
T9082 |
1,3-Benzoxazole-6-carboxylic acid
|
Others | Others |
1,3-Benzoxazole-6-carboxylic acid 被用作药物合成中的催化剂,以及其他化合物合成中的构建块。 | |||
T6762 |
AS1842856
|
Autophagy; FOXO1 | Apoptosis; Autophagy |
AS1842856 是一种特异性的Foxo1抑制剂,IC50为 30 nM。它抑制自噬,直接与 FoxO1 结合而降低 FoxO1 的活性。 | |||
T4985 |
Neticonazole Hydrochloride
|
Antifungal | Microbiology/Virology |
Neticonazole hydrochloride 是一种咪唑衍生物,具有抗感染和抗癌作用。它也是一种长效抗真菌剂。 | |||
T7329 |
C-178
|
STING | Immunology/Inflammation |
C-178 是 STING 选择性共价抑制剂,与 Cys91 结合抑制小鼠中由不同的激活剂引起的 STING 反应。 | |||
T25212 |
CCCI-01
CCCI 01,CCCI01,Centrosome Clustering Chemical Inhibitor-01 |
Apoptosis | Apoptosis |
CCCI-01(Centrosome Clustering Chemical Inhibitor-01) 是一种中心体簇抑制剂。 CCCI-01 具有抗癌活性,可诱导细胞凋亡,可用于阻断中心体聚类的非交叉耐药抗癌化合物的研究。 | |||
T4207 |
(S,R,S)-AHPC hydrochloride
VHL Ligand 1 hydrochloride,ULM-1,Protein degrader 1 hydrochloride |
Others; Ligand for E3 Ligase | Others; PROTAC |
(S,R,S)-AHPC hydrochloride (Protein degrader 1 hydrochloride) 是基于 VH032 的 VHL 配体,可用于募集 von Hippel-Lindau (VHL) 蛋白。它能够利用 linker 与靶蛋白配体连接,得到 PROTAC 分子。 | |||
T6074 |
KPT276
KPT-276,KPT 276 |
CRM1 | Membrane transporter/Ion channel |
KPT276 (KPT 276) 是一种口服生物可利用的核输出选择性抑制剂(SINE),不可逆地与 CRM1 结合并阻断 CRM1 的功能。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5275 |
2,5-Furandicarboxylic acid
Dehydromucic Acid,2,5-Dicarboxyfuran,2,5-呋喃二甲酸 |
Others; Endogenous Metabolite | Metabolism; Others |
2,5-Furandicarboxylic acid (Dehydromucic Acid) 是重要的能够再生生物技术基础,能够在人类尿液中检测到,在聚酯生产中能够作为对苯二甲酸的环保替代品。 | |||
T3006 |
Cinnamylideneacetic acid
Beta-Styrylacrylic acid,5-苯基戊烷-2,4-双酸,5-Phenyl-2,4-pentadienoic acid,5-Phenylpenta-2,4-dienoic acid |
Others; Antibacterial | Microbiology/Virology; Others |
Cinnamylideneacetic acid (Beta-Styrylacrylic acid) 用作合成结构单元、抗疟疾剂。 | |||
T4896 |
D-Lyxose
来苏糖,D-(-)-Lyxose |
Others; Endogenous Metabolite | Metabolism; Others |
D-Lyxose (D-(-)-Lyxose) 是内源性代谢产物的一种。 | |||
T8084 |
Dimethyl 4-hydroxyisophthalate
二甲基 4-羟基异邻苯二甲酸酯,Dimetghyl 4-Hydroxyisophthalate |
Others | Others |
Dimethyl 4-hydroxyisophthalate (Dimetghyl 4-Hydroxyisophthalate) 是水杨酸甲酯类似物。 | |||
T19382 |
Isoguanine
2-羟基-6-氨基嘌呤,异鸟嘌呤 |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Isoguanine 是一种嘌呤碱基,是鸟嘌呤的异构体,可作为有机合成的砌块。 | |||
T2A2476 |
L-Hydroxyproline
羟脯氨酸,trans-4-Hydroxy-L-proline,L-Hydroxyprolin,Trans-4-Hydroxyproline |
Endogenous Metabolite | Metabolism |
L-Hydroxyproline (L-Hydroxyprolin) 是羟脯氨酸的异构体之一,是药物生产中有用的手性结构单元。 | |||
T5650 |
2,2':5',2''-Terthiophene
alpha-三联噻吩,α-Terthienyl,Trithiophene |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
2,2':5',2''-Terthiophene (Trithiophene) 是杂环噻吩的低聚物,可用作有机合成的砌块 。 | |||
T4842 |
1H-pyrazole
1,2-Diazole,Pyrazole,吡唑 |
Others; Endogenous Metabolite | Metabolism; Others |
1H-pyrazole (1,2-Diazole) 是内源性代谢产物的一种。 | |||
TN1828 |
Kahweol
|
Apoptosis; NF-κB; AMPK | Apoptosis; Chromatin/Epigenetic; NF-κB; PI3K/Akt/mTOR signaling |
Kahweol 是小果咖啡的成分之一,可诱导细胞凋亡,具有抗炎、抗血管生成和抗癌活性。它通过激酶的活化抑制的脂肪生成和增加葡萄糖摄取。 | |||
TMO2713 |
4(3H)-Quinazolinone
Quinazolin-4-ol,4-Hydroxyquinazoline,4-羟基喹唑啉,4-Quinazolinol,4-Quinazolone,4-Quinazolinone |
Antibacterial; Platelet aggregation | Microbiology/Virology; Others |
4(3H)-Quinazolinone (4-Hydroxyquinazoline) 是化学合成中的砌块,是一种生物活性氮杂环化合物。它具有多种生物学特性,如抗菌,抗真菌,抗惊厥,抗炎,抗 HIV,抗癌和缓解疼痛活性。 | |||
T3S1729 |
Dihydrolycorine
|
Others | Others |
Dihydrolycorine 是分离自Lycoris radiate 草药中,是一种真核细胞中蛋白质合成的抑制剂。 | |||
Fr16741 |
Oxindole
2-吲哚酮,板蓝根,Indolin-2-one |
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Oxindole (Indolin-2-one) 是一种芳族杂环砌块,其衍生物是激酶抑制剂研究中的主要成分。 | |||
TN1275 |
p-Hydroxyphenethyl anisate
4-Hydroxyphenethylanisate |
Others | Others |
p-Hydroxyphenethyl anisate (4-Hydroxyphenethylanisate) 是一种来自 Notopterygium forbe-siiBoiss 的天然产品,是一种新型聚合物缓释材料,与 AAPBA 嵌段共聚后, 制备的纳米颗粒具有良好的 Ph 敏感性、葡萄糖敏感性、胰岛素负载速率和稳定性。 | |||
T2732 |
(-)-Epicatechin gallate
表儿茶素没食子酸酯,(−)-Epicatechin 3-gallate,Epicatechin gallate,(-)-Epicatechin 3-gallate,(-)-Epicatechin 3-O-gallate,ECG |
Virus Protease; COX; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
(-)-Epicatechin gallate ((-)-Epicatechin 3-O-gallate) 抑制环加氧酶-1 的IC50值为 7.5 μM。 | |||
T6S1699 |
Shogaol
[6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol |
Lipoxygenase; Autophagy | Autophagy; Metabolism |
6-Shogaol (6-Shogaol) 是从生姜中分离的一种天然产物,具有抗癌、抗炎和抗氧化的多种生物活性。 | |||
T5S1632 |
Barlerin
8-O-乙酰山栀苷甲酯,8-O-Acetylshanzhiside methyl ester,ND01 |
VEGFR; TNF; NF-κB; Akt; Caspase | Angiogenesis; Apoptosis; Cytoskeletal Signaling; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Tyrosine Kinase/Adaptors |
Barlerin (8-O-Acetylshanzhiside methyl ester) 是一种环孢菌素葡萄糖苷,从中国西藏民间药用植物中分离得到,能够抑制NF-κB 活性。 | |||
T12373 |
Paxilline
|
Others | Others |
Paxilline is an indole alkaloid mycotoxin from Penicillium paxilli, acts as a potent BK channels inhibitor by an almost exclusively closed-channel block mechanism. Paxilline possesses significant anticonvulsant activity. | |||
T78503 |
Tropone
|
||
Tropone作为分子构建块,在化学合成中具有重要应用。 | |||
T5614 |
3-Oxopentanedioic acid
1,3-丙酮二羧酸,1,3-Acetonedicarboxylic acid,3-Oxoglutaric acid |
Endogenous Metabolite | Metabolism |
3-Oxopentanedioic acid (1,3-Acetonedicarboxylic acid) 是二羧酸,能够用作有机化学合成的中间体。 | |||
T8267 |
Aspartic acid calcium
天冬氨酸钙,Calcium L-aspartate,Aspartic acid (calcium) |
Others | Others |
Aspartic acid calcium (Calcium L-aspartate) 是一种钙和 L-Aspartic acid (L-天冬氨酸) 连接的螯合物。其中L-Aspartic acid 是一种氨基酸,是体内蛋白质的结构单元。 | |||
T6981 |
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid
1-甲基-6-氧代-1,6-二氢吡啶-3-羧酸,Nudifloric Acid |
Others | Others |
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (Nudifloric Acid) 是来源于冬虫夏草,能够靶向阻断 AP-1 介导的荧光素酶活性,具有抗炎活性。其中冬虫夏草具有抗氧化,抗癌,抗炎,抗糖尿病,抗肥胖,抗血管生成和抗伤害感受活动。 | |||
TN4635 | Neoechinulin A | NADPH-oxidase; Beta Amyloid; ASK; IκB/IKK; p38 MAPK; TNF; NOS; NF-κB; COX; Prostaglandin Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; NF-κB |
Neoechinulin A has anti-inflammatory effect against LPS-stimulated RAW264.7 macrophages through inhibition of the NF-κB and p38 MAPK pathways, it may block the phosphorylation of mitogen-activated protein kinase (MAPK) molecule p38, apoptosis signal-regu | |||
TN2775 |
2-Methoxystypandrone
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MMP; BCL; IκB/IKK; GSK-3; TNF; NOS; NF-κB; Wnt/beta-catenin; COX; JAK; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
2-Methoxystypandrone displays an immunomodulatory effect in a cellular model, it blocks inflammatory responses by impairing NF-κB signaling to limit the inflammation and oxidative stress for preservation of BBB integrity. 2-Methoxystypandrone concomitant |