63
16
2
17
4
Cat. No. | Product Name | ||
---|---|---|---|
L7700 | 神经再生化合物库 | 524 compounds | |
524 种神经再生相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L5100 | 含氟化合物库 | 574 compounds | |
574 个含氟化合物的独特集合,可用于高通量筛选和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8580 |
Bupranolol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bupranolol 是竞争性的、口服活性的、非选择性的β-adrenoceptor 拮抗剂,无固有的拟交感神经活性。 | |||
T1944 |
LDN-214117
|
ALK; TGF-beta/Smad | Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors |
LDN214117 是一种高效的 ALK2 选择性抑制剂(IC50:22nM),也是一种 BMP6 抑制剂(IC50:100nM),对ALK5抑制力弱100倍。 | |||
T24381 |
L-822179
L822179,L 822,179,L 822179,L822,179,L-822,179 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
L-822179 (α5IA) 是 GABAA 受体 Α5 亚型的选择性反向激动剂,在 A5 亚型中具有比其他药物更高的内在活性。 | |||
T10631L |
Bucindolol Formate
Bucindolol Formate (71119-11-4 Free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bucindolol Formate 是一种具有内源性拟交感活性的β1 肾上腺素能受体 (β1-adrenergic receptor) 阻滞剂。Bucindolol 可用于心力衰竭疾病研究。 | |||
T38563 |
Raptinal
|
Caspase | Apoptosis; Proteases/Proteasome |
Raptinal 直接激活 caspase-3 并在多种细胞系中启动内在的 caspase 依赖性细胞凋亡途径。 | |||
T22128 |
OU749
|
Transferase | Metabolism |
OU749 是一种 γ-谷氨酰转移酶 (GGT) 抑制剂,固有 Ki 值为 17.6 μM。 | |||
T0342 |
Carvedilol phosphate hemihydrate
Carvedilol phosphate,BM 14190 (phosphate hemihydrate),卡维地洛磷酸盐 |
VEGFR; Others; Potassium Channel; LDL; Integrin; Gap Junction Protein; NADPH; Adrenergic Receptor; Autophagy | Angiogenesis; Autophagy; Cytoskeletal Signaling; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience; Others; Tyrosine Kinase/Adaptors |
Carvedilol phosphate hemihydrate (BM 14190 phosphate hemihydrate) 是一种外消旋混合物,是一种非选择性β/α-1受体阻断剂,具有抗高血压活性且缺乏内在拟交感神经活性。 | |||
T28124 |
N106
N-106,N 106 |
E1/E2/E3 Enzyme | Ubiquitination |
N106 是 SUMO 激活酶 E1 连接酶的激活剂,并触发 SERCA2a 的内在 sumoylation。 N106 可用于有关心力衰竭的研究。 | |||
T6191 |
Tasisulam
LY573636,他司磺胺 |
Apoptosis; Caspase | Apoptosis; Proteases/Proteasome |
Tasisulam (LY573636) 是一种小分子抗肿瘤药物,通过内在途径诱导细胞凋亡,导致细胞色素 c 释放和 caspase 依赖性细胞死亡。它抑制有丝分裂进程并诱导血管正常化。 | |||
T67917 |
ML353
VU0478006 |
Potassium Channel | Membrane transporter/Ion channel |
ML353 (VU0478006)是 TREK-1和 TREK-2的选择性激活剂,是 mGlu5 沉默变构调节剂 (SAM) 的选择性配体(Ki =18.2 nM)。 ML353 有作为解决 SAM 体内固有活性或药物阻断的潜力。 | |||
T9014 |
SKI-178
|
Apoptosis; S1P Receptor | Apoptosis; GPCR/G Protein |
SKI-178 是一种鞘氨醇激酶-1(SphK1)和 SphK2抑制剂,以 CDK1 依赖性方式诱导人急性髓性白血病细胞凋亡。 | |||
T1282 |
Carteolol hydrochloride
Arteoptic,Abbott-43326,OPC-1085 hydrochloride,盐酸卡替洛尔,Carteolol HCl,Mikelan |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Carteolol hydrochloride (Abbott-43326) 是一种非选择性的β肾上腺素受体阻断剂。 | |||
T1012 |
Acebutolol hydrochloride
盐酸醋丁洛尔,Acebutolol HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Acebutolol hydrochloride (Acebutolol HCl) 是一种 β-肾上腺素受体拮抗剂,用于研究高血压、心绞痛和心律失常。 | |||
T9836 |
(E)-SI-2
|
Others | Others |
(E)-SI-2 是类固醇受体 coactivator-3(SRC-3 或 AIB1)的有效小分子抑制剂,可选择性抑制 SRC-3 的内在转录活性,也抑制 SRC-1 和 SRC-2。它选择性地降低 SRC-3 的细胞蛋白水平,但不降低 CARM-1 的细胞蛋白水平,阻断 MDA-MB-468 细胞生长,IC50 值为 3.4 nM,但不影响正常细胞。 | |||
T26762 |
Befunolol HCl
BFE60,Bentox,Befunolol hydrochloride,BFE-60,BFE 60 |
Others | Others |
Befunolol is a beta blocker with intrinsic sympathomimetic activity and also acts as a β adrenoreceptor partial agonist. | |||
T8456 |
GALNON
|
Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
Galnon 是一种甘丙肽受体激动剂,可改善内在的皮质骨组织特性。 | |||
T5450 |
DL-071-IT
Afurolol Hydrochloride,DL 071 IT |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
DL-071-IT (Afurolol Hydrochloride) 是一种有效的非选择性β-肾上腺素受体拮抗剂。 DL-071-IT 表现出内在的拟交感神经活性和弱的膜稳定活性。 | |||
T75688 |
1-Stearoyl-2-arachidonoyl-sn-glycero-3-phosphoinositol
|
Others | Others |
1-Stearoyl-2-arachidonoyl-sn-glycero-3-phosphoinositol 是一种内源性代谢物,是细胞膜成分。 | |||
T40658 |
[D-Asn5]-Oxytocin
[D-Asn5]-Oxytocin |
||
[D-Asn5]-Oxytocin exhibits minimal specific oxytocic and vasodepressor effects. Comparative cumulative dose-response investigations reveal that [D-Asn5]-Oxytocin demonstrates a similar intrinsic activity to oxytocin in terms of oxytocic activity. | |||
T40596 |
Tasisulam sodium
LY 573636 sodium,Tasisulam sodium |
Others | Others |
Tasisulam is an anti-cancer compound that induces apoptosis through the intrinsic pathway, leading to the release of cytochrome c and caspase-dependent cell death. Additionally, tasisulam inhibits mitotic progression and triggers vascular normalization. | |||
T79921 |
Moloney murine leukemia virus RT
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Moloney murine leukemia virus RT为源自Moloney小鼠白血病病毒的逆转录酶,作为复制聚合酶在逆转录病毒生命周期中扮演关键角色。 | |||
T36928 |
ICI 215,001 hydrochloride
|
Others | Others |
ICI 215,001 hydrochloride 在其内在激动剂活性较低的情况下可充当 β1 和 β2 肾上腺素受体的拮抗剂。 | |||
T1244 |
Celiprolol hydrochloride
Selecor,Selectrol,盐酸塞利洛尔 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Celiprolol hydrochloride (Selectrol) 是一种选择性肾上腺素受体调节剂,是一种选择性的和具有口服活性的β1肾上腺素受体拮抗剂,具有部分β2激动剂活性,具有降压和抗心绞痛的作用。 | |||
T0143 |
Bisoprolol hemifumarate
富马酸比索洛尔,(±)-Bisoprolol hemifumarate,Bisoprolol fumarate,Bisoprolol hemifumarate salt,EMD33512,(±)-Bisoprolol (hemifumarate) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bisoprolol hemifumarate 是一种 β1 肾上腺素受体阻断剂。 | |||
T35947 |
17(S)-HDHA
|
Others | Others |
17(S)-HDHA is a primary mono-oxygenation product of docosahexaenoic acid in human whole blood, human leukocytes, and mouse brain. 17(S)-HDHA serves as a precursor to 17(S)-resolvins and has intrinsic biological activity, such as the inhibition of TNF-α-induced interleukin-1β expression in human glioma cells and inhibition of TNF-α-induced leukocyte trafficking to the mouse air pouch. | |||
T62814 |
Antitumor agent-77
|
Others | Others |
Antitumor agent-77 对癌细胞的生长和迁移具有抑制作用,具有抗癌作用。Antitumor agent-77 能够抑制 GPx-4 和提高 COX2 引发铁下垂。Antitumor agent-77 可以激活肿瘤细胞固有凋亡通路 (Bax-Bcl-2-caspase-3),阻碍肿瘤细胞上皮间质转化 (EMT) 过程。 | |||
T73778 |
cis-5-Tetradecenoic acid
|
Others | Others |
cis-5-Tetradecenoic acid,一种存在于血液中的内源性代谢物,主要用于研究长链3羟酰基CoA脱氢酶缺乏症。 | |||
T60553 |
Tetrahydrouridine dihydrate
|
Others | Others |
Tetrahydrouridine dihydrate (THU dihydrate) 是有效的胞苷脱氨酶抑制剂。Tetrahydrouridine dihydrate 比内在胞苷更有效地竞争性阻断酶的活性位点。 | |||
TP2126 |
R 892
|
||
Potent and selective bradykinin B1 receptor antagonist (ID50 values are 2.8 and > 600 nM at B1 and B2 receptors respectively). Exhibits no intrinsic agonist activity and is resistant to aminopeptidase and kininase II (ACE) cleavage. Displays hypertensive | |||
T76214 |
5′-Nucleotidase
|
Others | Others |
5′-Nucleotidase (CD73) 是一种作为胞外酶存在的内在膜糖蛋白。5′-Nucleotidase 催化 5-核苷酸水解成相应的核苷。 | |||
T68869 |
TP-110
|
Others | Others |
TP-110 is a new proteasome inhibitor, which shows potent growth inhibition in various tumor cell lines. Treatment with TP-110 for 24 h in vitro induced apoptosis in multiple myeloma cell line RPMI8226. TP-110 reduced the intrinsic inhibitor of apoptosis proteins (IAPs), cIAP-1 and XIAP, that suppress executioner caspases. | |||
T38099 |
APF
|
||
APF is an aromatic amino-fluorescein derivative and fluorescent probe for highly reactive radicals. It has low intrinsic fluorescence, however, upon oxidation by hydroxyl radical, hypochlorite ion, and certain peroxidase intermediates, it is converted to the highly fluorescent molecule fluorescein, facilitating the detection of highly reactive biological radicals. APF is not oxidized by nitric oxide (NO), hydrogen peroxide (H2O2), or other oxidants. Fluorescein displays excitation/emission maxim... | |||
T36042 |
17(R)-HDHA
|
Others | Others |
Resolvins are a group of polyhydroxylated metabolites of docosahexaenoic acid (DHA) found in the inflammatory exudates of aspirin-treated experimental animals. 17(R)-HDHA is the primary oxygenation product of DHA when exposed to aspirin-inhibited cyclooxygenase-2. 17(R)-HDHA serves as a precursor to resolvins and has intrinsic biological activity, such as the inhibition of TNFα-induced IL-1β expression in human glioma cells. | |||
T60756 |
NLRP3 antagonist 1
|
Others | Others |
NLRP3 antagonist 1 具有癌症疾病的研究潜力,是NLRP3的有效拮抗剂。NLRP3 参与机体对应激损伤和病原体感染的内在免疫,主要表达在巨噬细胞和中性粒细胞。 | |||
T60990 |
U92016A hydrochloride
|
Others | Others |
U92016A hydrochloride 是口服有效的5-HT1A 受体激动剂,代谢稳定。U92016A hydrochloride 表现出极高的内在活性,能够以高亲和力结合中国仓鼠卵巢细胞中表达的人 5-HT1A 受体,Ki 值为0.2 nM。 | |||
T85194 |
N-Deacetylcolchicine
NSC 201400 |
Others | Others |
Trimethylcolchicinic acid methyl ether (HAN 76504), an antimitotic agent, blocks microtubule assembly by attaching to tubulin and inhibiting its polymerization. It enhances tubulin's intrinsic GTPase activity, induces apoptosis across various normal and tumor cell lines, and activates the JNK/SAPK pathway. Currently unnamed, it is referred to by a provisional code name in line with MedKoo Chemical Nomenclature (https://www.medkoo.com/page/naming) for ease of communication. | |||
T62850 |
IRAK4-IN-13
|
Others | Others |
IRAK4-IN-13 (compound 21) 是一种选择性的、有效的 IRAK4 抑制剂 (IC50: 0.6 nM)。IRAK4-IN-13 具有高代谢清除率,人肝微粒体 (HLM) 固有清除率为 96 μL/min/mg。 | |||
T84919 |
M4K2163 dihydrochloride
|
Others | Others |
M4K2163二盐酸盐是一种高效、选择性的ALK2抑制剂,具有血脑屏障(BBB)渗透能力,IC50为19 nM。该化合物主要用于弥漫性内源性脑桥胶质瘤(DIPG)的研究。 | |||
T71033 |
ZD7114 free base
|
Others | Others |
ZD7114, also known as ICI-D7114, is a selective adrenoceptor agonist of brown fat and thermogenesis. ICI D7114 stimulates thermogenesis at doses that have little effect on beta 1 or beta 2 adrenoceptors. Treatment with ICI D7114 activates BAT and thermogenesis even in species and situations where the intrinsic capacity is low. ICI D7114 has beneficial effects in animal models of obesity and disturbed glucose and lipid homeostasis. | |||
T63262 |
IRAK4-IN-15
|
Others | Others |
IRAK4-IN-15 是选择性的、有效的 IRAK4 抑制剂 (IC50: 0.002 μM),具有良好的人类 PK 预测且具有低内在清除率。IRAK4-IN-15 与 Acalabrutinib 联用对 MyD88/CD79 双突变体 ABC-DLBCL 的表现出强大的协同体外活性。 | |||
T84648 |
2-Linoleoyl Glycerol
2-LG |
Others | Others |
2-Arachidonoyl glycerol (2-AG), a natural endocannabinoid ligand for the CB1 receptor, was isolated from porcine brain and characterized. Its congener, 2-linoleoyl glycerol (2-LG), which has a linoleoyl group instead of an arachidonoyl group, also exists alongside 2-AG in vivo. While 2-LG exhibits low intrinsic activity, it enhances the activity of 2-AG and other endocannabinoids through an "entourage" effect, attributed to the inhibition of breakdown and reuptake pathways that typically decreas... | |||
T71284 |
Glimepiride urethane
|
Others | Others |
Glimepiride urethane is a third generation sulfonylurea compound, which increases the release of insulin from pancreatic beta cells. In addition, glimepiride increases the activity of intracellular insulin receptors. Glimepiride increases osteoblast proliferation and differentiation, which is thought to be related to its ability to activate the PI3K and Akt pathway. Furthermore, Glimepiride enhances intrinsic peroxisome proliferator-activated receptor γ activity. Glimepiride also increases prote... | |||
T80963 |
TPEQM-DMA
|
||
TPEQM-DMA为近红外二区光敏剂,能在癌性线粒体中积累,抑制癌细胞生长。其显著I型光疗效果,有助于克服光动力疗法(PDT)治疗低氧肿瘤的限制。 | |||
T28449 |
Pradefovir
ICN-2001-3,MB-6866,帕拉德福韦,ICN-20013,MB-06866,Remofovir |
HBV | Microbiology/Virology |
Pradefovir (Remofovir) 是一种逆转录酶抑制剂,可能用于治疗慢性 HBV 感染。它也是阿德福韦的肝脏靶向前药。代谢激活后,它在人肝微粒体中转化为 PMEA(9-(2-膦酰基甲氧基乙基)腺嘌呤),Km 为 60 microM,最大代谢速率为 228 pmol/min/mg 蛋白质,以及内在的清除率约为 359 ml/min。 | |||
T84457 |
DC4 Crosslinker
|
Others | Others |
DC4 crosslinker, an 18Å mass spectrometry-cleavable crosslinking reagent, features two intrinsic positive charges facilitating the fragmentation of cross-linked peptides into their constituent peptides through collision-induced dissociation or in-source decay. Initial fragmentation leads to cleavage adjacent to the positive charges, enabling the identification of cross-linked peptides as pairs of ions with precise mass separation. Furthermore, the resultant intact peptide fragments can undergo f... | |||
T84891 |
TM5441 sodium
|
Others | Others |
TM5441是一种口服生物可利用的PAI-1(纤溶酶原激活物抑制剂-1)抑制剂,其对多种癌症细胞系的IC50值介于13.9到51.1μM之间,能诱导人类癌症细胞的内在凋亡(apoptosis)。此外,TM5441还可减轻Nω-硝基-1-精氨酸甲酯引发的心脏高血压和血管老化。 | |||
T70352 |
PH11
|
Others | Others |
PH11 is a novel Focal Adhesion Kinase (FAK) inhibitor. PH11 restores TRAIL apoptotic pathway in PANC-1 cells through down-regulation of c-FLIP via inhibition of FAK and the phosphatidylinositol-3 kinase (PI3K)/AKT pathways. Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) emerges as one of the most-promising experimental cancer therapeutic drugs and is currently being tested in clinical trials. However, both intrinsic and acquired resistance of human cancer cells to TRAIL... | |||
T70506 |
Bupranolol HCl
|
Others | Others |
Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity. Its potency is similar to propranolol. Bupranolol is quickly and completely absorbed from the gut. Over 90% undergo first-pass metabolism. Bupranolol has a plasma half life of about two to four hours, with levels never reaching 1 µg/l in therapeutic doses. The main metabolite is carboxybupranolol, 4-chloro-3-[3-(1,1-dimethylethylamino)-2-hydroxy-propyloxy]be... | |||
T78877 |
MTX-241F
|
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
MTX-241F是一种选择性小分子抑制剂,针对EGFR和PI3激酶家族。其具备穿透血脑屏障的能力,能够持续控制肿瘤生长。在来源于患者的DIPG神经球中,MTX-241F展示了与放射疗法协同增效的特性,适用于研究弥漫性内源性桥脑胶质瘤(DIPG)。 | |||
T84653 |
17-phenyl trinor Prostaglandin F2α diethyl amide
Bimatoprost diethyl amide |
Others | Others |
17-Phenyl trinor Prostaglandin F2αdiethyl amide (17-phenyl trinor PGF2αdiethyl amide) is a Prostaglandin F2α(PGF2α) analog characterized by the substitution of the C-1 carboxyl group with an N-diethyl amide. Prostaglandin (PG) esters and N-ethyl amides have demonstrated ocular hypotensive properties, with N-ethyl amides introduced as alternative options for PG hypotensive prodrugs. Studies indicate that both bovine and human corneal tissues can convert N-ethyl amides of various PGs into their fr... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1019 |
Beta-mangostin
β-Mangostin,beta-倒捻子素 |
Apoptosis; Antibacterial; Parasite | Apoptosis; Microbiology/Virology |
Beta-mangostin (β-Mangostin) 是存在 Cratoxylum arborescens 中的一种氧杂蒽酮类天然产物,有抗癌和抗菌活性,对结核分枝杆菌的 MIC 值为 6.25 μg/mL。它在体外有抗疟活性,对恶性疟原虫的 IC50值为 3.00 μg/mL。 | |||
T3916 |
Ginsenoside F2
人参皂苷F2 |
Apoptosis; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Metabolism |
Ginsenoside F2 是 Ginsenoside Rb1 的代谢物,通过激活内在的凋亡途径和线粒体功能障碍来诱导乳腺的凋亡,对乳腺癌干细胞具有抗增殖活性。 | |||
TN1248 |
3-Epioleanolic acid
|
AChR | Neuroscience |
3-Epioleanolic acid 是一种分离自马鞭草的有效成分,具有抗炎作用。 | |||
TN2097 |
Pomolic acid
坡模酸 |
Apoptosis; Caspase; HIV Protease; AMPK | Apoptosis; Chromatin/Epigenetic; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Pomolic acid 是从野鸦椿中分离出来的一种五环三萜烯。它抑制肿瘤细胞的生长,诱导细胞凋亡,有用于前列腺癌的潜力。 | |||
T3386 |
Kaempferitrin
Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷 |
cell cycle arrest; Glucokinase; IGF-1R | Cell Cycle/Checkpoint; Metabolism; Tyrosine Kinase/Adaptors |
Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物,具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用,可激活胰岛素信号传导。 | |||
T4746 |
Purine
7H-Imidazo(4,5-d)pyrimidine,嘌呤 |
Others; Endogenous Metabolite | Metabolism; Others |
Purine (7H-Imidazo(4,5-d)pyrimidine) 是内源性代谢产物的一种。 | |||
T7032 |
Eupatorin
|
Others; P450 | Metabolism; Others |
Eupatorin 是天然存在的黄酮,可捕获 G2-M 细胞周期,激活多个 caspase、细胞色素 C 的释放、多聚 (ADP-核糖) 聚合酶的裂解,促使凋亡细胞死亡。 | |||
T1040 |
Vitamin B12
Cyanocobalamin,Cobalamin,维生素B12 |
Endogenous Metabolite | Metabolism |
Vitamin B12 (Cobalamin) 是一种维生素,在维持血流形成和脑、神经系统正常功能等方面发挥关键作用。 | |||
T28122 |
Myrtenal
NSC-54384,NSC 54384,NSC54384,Benihinal |
||
Myrtenal is a natural monoterpene. It is found to attenuate diethylnitrosamine-induced hepatocellular carcinoma in rats by stabilizing intrinsic antioxidants and modulating apoptotic and anti-apoptotic cascades. Myrtenal also inhibits acetylcholinesterase | |||
TN6059 |
Demethoxyfumitremorgin C
|
||
Demethoxyfumitremorgin C and tryprostatin B are fungal inhibitors of mammalian cell cycle progression at the G(2)/M transition. Demethoxyfumitremorgin C inhibits the proliferation of PC3 human prostate cancer cells via the intrinsic (mitochondrial) and ex | |||
T78466 |
Erythronic acid potassium
|
Endogenous Metabolite | Metabolism |
Erythronic acid potassium为糖类内源性代谢物,关键作用于高尿酸血症发病及改善过程,并与转醛缩酶缺乏症相关的线粒体功能障碍有关,常用于代谢性疾病研究。 | |||
T13797 |
Nivalenol
|
Caspase | Apoptosis; Proteases/Proteasome |
Nivalenol 是一种由禾谷镰刀菌产生的真菌代谢物。 Nivalenol 通过 caspase 和内在凋亡途径诱导细胞死亡,从而影响免疫系统并引起呕吐、生长迟缓和生殖障碍。 | |||
T78471 |
α,α-Trehalose 6-phosphate potassium
Tre6P potassium |
Endogenous Metabolite | Metabolism |
α,α-Trehalose 6-phosphate (Tre6P) potassium 是一种α,α′-trehalose的6-磷酸衍生物及内源代谢物。在Tre6P磷酸酶 (T6PP) 的催化下,α,α-Trehalose 6-phosphate可被高效转化为α,α′-trehalose。 | |||
T73717 |
cGAMP diammonium
|
Others | Others |
cGAMP (Cyclic GMP-AMPP) diammonium 是一种内源性第二信使,通过触发干扰素的产生来响应胞浆 DNA。它通过激活干扰素基因刺激因子(STING),启动信号级联,进而导致I型干扰素及其他免疫介质的生成。 | |||
TN4877 | Quercetin 3,4'-dimethyl ether | ERK; BCL; MAPK; Caspase; JNK | Apoptosis; MAPK; Proteases/Proteasome |
Quercetin 3,4'-dimethyl ether shows anti-lipid peroxidation activity (IC 50 values of 0.3 uM), it also shows anti-inflammatory activity. Quercetin 3,4'-dimethyl ether could be useful in the development of novel anticancer agents, it has high cytotoxic aga | |||
T73403 |
Aviculin
|
Others | Others |
Aviculin 是一种木聚糖苷,是一种有效的抗癌剂 (anticanceragent)。Aviculin 可降低 MCF-7 细胞代谢活性到 50% 以下,IC50为 75.47 μM。Aviculin 通过内在凋亡途径诱导乳腺癌细胞凋亡 (apoptosis)。Aviculin 增加了 caspase-9、caspase-7和 PARP 的表达。Aviculin 使 Bax/Bcl-2 的比值升高。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-03221 |
Intrinsic Factor Protein, Human, Recombinant (His)
IF,IFMH,gastric intrinsic factor (vitamin B synthes... |
Human | HEK293 Cells |
Gastric intrinsic factor, also known as GIF, belongs to the of the cobalamin transport protein family. It is a glycoprotein produced by the parietal cells of the stomach. Gastric intrinsic factor plays a key role in the absorption of vitamin B12 on in the small intestine. Vitamin B12 bounds to haptocorrin after entry into the stomach. The resulting complex enters the duodenum, where pancreatic enzymes digest haptocorrin. In the less acidic environment of the small intestine, B12 can then bind to... | |||
TMPH-00580 |
Aquaporin Z Protein, E. coli, Recombinant (His)
Water channel AqpZ,bniP,Aquaporin Z,Bacterial nodulin-like <... |
E. coli | E. coli |
Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity. Aquaporin Z Protein, E. coli, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 27.7 kDa and the accession number is P60844. | |||
TMPY-05510 |
BDNF Protein, Mouse, Recombinant (His)
brain-derived neurotrophic factor |
Mouse | HEK293 Cells |
BDNF is a member of thenerve growth factorfamily. It is highly expressed in hippocampus, amygdala, cerebral cortex and cerebellum. It also can be detected in heart, lung, skeletal muscle, testis, prostate and placenta. BDNF is induced by cortical neurons, and is necessary for survival of striatal neurons in the brain. During development, BDNF promotes the survival and differentiation of selected neuronal populations of the peripheral and central nervous systems. It participates in axonal growth,... | |||
TMPY-01101 |
Coagulation factor X/F10 Protein, Human, Recombinant (His)
FXA,FX,coagulation factor X,coagulation factor 10 |
Human | Baculovirus Insect Cells |
Coagulation factor X, also known as FX, F10, Eponym Stuart-Prower factor, and thrombokinase, is an enzyme of the coagulation cascade. It is one of the vitamin K-dependent serine proteases, and plays a crucial role in the coagulation cascade and blood clotting, as the first enzyme in the common pathway of thrombus formation. Factor X deficiency is one of the rarest of the inherited coagulation disorders. FX deficiency among the most severe of the rare coagulation defects, typically including hema... | |||
TMPH-03057 |
Chorismate synthase Protein, Neurospora crassa, Recombinant (His)
B7F21.10,NCU05420,aro-2,5-enolpyruvylshikimate-3-phosphate p... |
Neurospora crassa | E. coli |
Bifunctional enzyme that possesses chorismate synthase and intrinsic flavin reductase activity, it uses NADPH to reduce FMN. | |||
TMPH-03381 |
Synaptoporin/SYNPR Protein, Rat, Recombinant (His)
Synaptoporin,Synpr |
Rat | E. coli |
Intrinsic membrane protein of small synaptic vesicles. Probable vesicular channel protein. Synaptoporin/SYNPR Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 35.2 kDa and the accession number is P22831. | |||
TMPH-01898 |
PARL Protein, Human, Recombinant (Myc)
Mitochondrial intramembrane cleaving protease PARL,Presenili... |
Human | E. coli |
Required for the control of apoptosis during postnatal growth. Essential for proteolytic processing of an antiapoptotic form of OPA1 which prevents the release of mitochondrial cytochrome c in response to intrinsic apoptotic signals. Required for the maturation of PINK1 into its 52kDa mature form after its cleavage by mitochondrial-processing peptidase (MPP). Promotes changes in mitochondria morphology regulated by phosphorylation of P-beta domain. PARL Protein, Human, Recombinant (Myc) is expre... | |||
TMPK-00188 |
JAM-A Protein, Mouse, Recombinant (His)
F11R,JCAM1,PAM-1,PAM-1KAT,JAM-1,JAM,JCAM,JAM-A,KAT,F11 recep... |
Mouse | HEK293 Cells |
junctional adhesion molecule A (JAM-A), a cell adhesion molecule, is highly elevated in human GBM cancer stem cells and predicts poor patient prognosis. While JAM-A is also highly expressed in other cells in the tumor microenvironment, specifically microglia and macrophages,JAM-A functions to suppress pathogenic microglial activation in the female tumor microenvironment, highlighting an emerging role for sex differences in the GBM microenvironment and suggesting that sex differences extend beyon... | |||
TMPY-03051 |
B3GNT2 Protein, Human, Recombinant (hFc)
B3GNT-2,B3GNT,UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosamin... |
Human | HEK293 Cells |
B3GNT2 belongs to the beta-1,3-N-acetylglucosaminyltransferase family. It is a type II transmembrane protein that prefers the substrate of lacto-N-neotetraose. Alternative splicing produced 2 isoforms of the human protein. B3GNT2 catalyzes the initiation and elongation of poly-N- acetyllactosamine chains. Enzymatic activities of some glycosyltransferases are markedly increased via complex formation with other transferases or cofactor proteins. B3GNT2 and beta3Gn-T8 can form a heterodimer in vitr... | |||
TMPJ-01071 |
Apolipoprotein H/APOH Protein, Mouse, Recombinant (His)
Beta-2-glycoprotein 1,Apoh,β-2-glycoprotein 1 |
Mouse | HEK293 Cells |
Apolipoprotein H (APOH), also known as Beta-2-glycoprotein 1, is a glycoprotein synthesized by liver cells and it is present in the blood associated with plasma lipoproteins. Its carbohydrate content is approximately 19% of the molecular weight and it is present in the blood associated with plasma lipoproteins. Mature mouse ApoH shares 76% and 42% aa sequence identity with human and rat ApoH, respectively. The activity of APOH appears to involve the binding of agglutenating, inhibits agglutinati... | |||
TMPJ-00715 |
FGF-19 Protein, Human, Recombinant (His)
FGF-19,Fibroblast growth factor 19,FGF19 |
Human | E. coli |
Fibroblast growth factor 19 (FGF19) is a secreted protein which belongs to the FGFs family. FGF19 is expressed in fetal brain, cartilage, retina, and adult gall bladder. FGFs modulate cellular activity via at least 5 distinct subfamilies of high-affinity FGF receptors (FGFRs): FGFR-1, -2, -3, and -4, all with intrinsic tyrosine kinase activity. FGFRs can be important for regulation of glucose and lipid homeostasis. FGF19 has important roles as a hormone produced in the ileum in response to bile ... | |||
TMPJ-00301 |
Coagulation Factor X Protein, Human, Recombinant (hFc)
Stuart-Prower factor,Stuart factor,Coagulation factor X |
Human | HEK293 Cells |
F10, also known as Coagulation factor X, belongs to the peptidase S1 family that is synthesized as a 488 amino acid (aa) with a signal peptide and a pro region (residues 1‑40). Both the intrinsic and extrinsic pathways activate Factor X to Xa, which consists of light (residues 41‑179) and heavy (residues 235‑488) chains linked by a disulfide bond. Coagulation factor X is initially synthesized in the liver. The two chains are formed from a single-chain precursor by the excision of two Arg residue... | |||
TMPJ-00192 |
CD32B Protein, Human, Recombinant (His)
FCG2,IgG Fc Receptor II-b,CDw32,Low Affinity Immunoglobulin ... |
Human | HEK293 Cells |
FcγRIIB is a low affinity receptor that recognizes the Fc portion of IgG. The human CD32 group consists of FcγRIIA, FcγRIIB, and FcγRIIC proteins that share 94-99% sequence identity in their extracellular domains but differ substantially in their transmembrane and cytoplasmic domains. FcγRII protein is expressed on cells of both myeloid and lymphoid lineages as well as on cells of non-hematopoietic origin. FcγRIIB has an intrinsic cytoplasmic immunoreceptor tyrosine-based inhibitory motif (ITIM)... | |||
TMPY-02106 |
GAP43 Protein, Human, Recombinant (His)
B-50,PP46,growth associated protein 43 |
Human | HEK293 Cells |
Neuromodulin, also known as Axonal membrane protein GAP-43, Growth-associated protein 43, Neural phosphoprotein B-5, pp46 and GAP43, is a cell membrane protein which belongs to theneuromodulin family. Neuromodulin / GAP43 contains oneIQ domain. Neuromodulin / GAP43 is associated with nerve growth. It is a major component of the motile "growth cones" that form the tips of elongating axons. Neuromodulin / GAP43 is involved in neurite outgrowth, a crucial process for the differentiation of n... | |||
TMPY-01632 |
Serpin B4 Protein, Mouse, Recombinant (His)
Serpinb4,1110001H02Rik,1110013A16Rik,Serpinb3c,Scca2,serine ... |
Mouse | Baculovirus Insect Cells |
Serpins are the largest and most diverse family of serine protease inhibitors which are involved in a number of fundamental biological processes such as blood coagulation, complement activation, fibrinolysis, angiogenesis, inflammation and tumor suppression and are expressed in a cell-specific manner. Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. The acronym serpin was originally coined because many serpins inhi... | |||
TMPY-02220 |
HRAS Protein, Human, Recombinant (His)
HAMSV,Harvey rat sarcoma viral oncogene homolog,C-H-RAS,C-HA... |
Human | Baculovirus Insect Cells |
HRas, also known as HRAS, belongs to the small GTPase superfamily, Ras family, and is widely expressed. It functions in signal transduction pathways. HRas can bind GTP and GDP, and they have intrinsic GTPase activity. It undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Defects in HRAS are the cause of faciocutaneoskeletal syndrome (FCSS). FCSS is a rare condition characterized by prenatally increase... | |||
TMPH-01239 |
XPC Protein, Human, Recombinant (His)
Xeroderma pigmentosum group C-complementing protein,p125,XPC... |
Human | E. coli |
Involved in global genome nucleotide excision repair (GG-NER) by acting as damage sensing and DNA-binding factor component of the XPC complex. Has only a low DNA repair activity by itself which is stimulated by RAD23B and RAD23A. Has a preference to bind DNA containing a short single-stranded segment but not to damaged oligonucleotides. This feature is proposed to be related to a dynamic sensor XPC can rapidly screen duplex DNA for non-hydrogen-bonded bases by forming a transient nucleoprotein i... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMID-0236 |
Bisoprolol-d7 hemifumarate
|
||
Bisoprolol-d7 hemifumarate 是 Bisoprolol hemifumarate 的氘代化合物。Bisoprolol hemifumarate 的 CAS 号为 104344-23-2。Bisoprolol hemifumarate 是一种 β1 肾上腺素受体阻断剂。 | |||
TMIJ-0175 |
Bisoprolol-d5 Hemifumarate
|
||
Bisoprolol-d5 Hemifumarate 是 Bisoprolol Hemifumarate 的氘代化合物。Bisoprolol Hemifumarate 的 CAS 号为 104344-23-2。Bisoprolol hemifumarate 是一种 β1 肾上腺素受体阻断剂。 | |||
TMID-0245 |
Pindolol-d7
|
||
Pindolol-d7 是 Pindolol 的氘代化合物。Pindolol 的 CAS 号为 13523-86-9。Pindolol 是一种非选择性β-阻断剂,局部的β-肾上腺素能受体激动剂活性,也作为5-HT1A受体部分拮抗剂,Ki为33nM。它是非心脏选择性的,具有内在的拟交感神经作用。 | |||
TMIJ-0426 |
Celiprolol-d9 Hydrochloride
|
||
Celiprolol-d9 Hydrochloride 是 Celiprolol Hydrochloride 的氘代化合物。Celiprolol Hydrochloride 的 CAS 号为 57470-78-7。Celiprolol hydrochloride 是一种选择性肾上腺素受体调节剂,是一种选择性的和具有口服活性的β1肾上腺素受体拮抗剂,具有部分β2激动剂活性,具有降压和抗心绞痛的作用。 |