64
24
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T17549 |
Biotin-EDA
|
Others; PROTAC Linker | Others; PROTAC |
Biotin-EDA 是一种属于 alkyl chain 类的 PROTAC linker,可用于 PROTAC 分子的合成。 | |||
T39373 |
PNU-EDA-Gly5
PNU-EDA-Gly5 |
||
PNU-EDA-Gly5 is a DNA topoisomerase I inhibitor-based oligo-glycine linker-payload used for the synthesis of antibody-drug conjugates (ADCs). It consists of the DNA topoisomerase I inhibitor PNU-159682 and the linker EDA-Gly5. | |||
T18247 | Mal-C2-Gly3-EDA | Others | Others |
Mal-C2-Gly3-EDA is a cleavable antibody-drug conjugate (ADC) linker equipped with a Maleimide moiety. It serves the purpose of facilitating the synthesis of ADCs. | |||
T18246 |
Mal-C2-Gly3-EDA-PNU-159682
|
Others | Others |
Mal-C2-Gly3-EDA-PNU-159682, a drug-linker conjugate for antibody-drug conjugates (ADC), combines the cleavable ADC linker Mal-C2-Gly3-EDA with the potent ADC cytotoxin PNU-159682. | |||
T75354 | RH-EDA | ||
RH-EDA 是一种基于罗丹明的开启式荧光探针,用于检测生命系统中的羟基自由基。 | |||
T74555 |
EDA-DA
|
||
EDA-DA 是一种 N 末端标记的二肽探针,可用于标记细菌的肽聚糖 (PG)。肽聚糖 (PG) 是绝大多数细菌细胞壁中的一种基本结构,对于分裂和维持细胞形状和静水压力至关重要。 | |||
T82842 |
BODIPY FL EDA free base
|
||
ODIPY FL EDA free base为绿色荧光胺类探针,能通过R-NH2与醛或酮反应形成可逆的席夫碱产物。使用如硼氢化钠或氰硼氢化钠等还原剂,ODIPY FL EDA free base可转化成稳定的胺衍生物,适用于检测修饰或未修饰脱氧核苷酸,以及评估DNA损伤和基因组DNA甲基化情况。 | |||
T3979 |
Emedastine
LY188695,依美斯汀,Emadine |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Emedastine (LY188695) 是一种可口服的,选择性和高亲和力的组胺 H1受体拮抗剂,Ki 值为 1.3 nM。它是苯并咪唑衍生物,可用于过敏性鼻炎、过敏性皮肤疾病和过敏性结膜炎的研究。 | |||
T36683 |
Vedaprofen
Quadrisol,PM 150,维达洛芬,CERM 10202 |
COX; Antibacterial; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Vedaprofen (PM 150) 抑制 COX-1 并通过抗炎活性减少前列腺素 H2 的合成。 Vedaprofen 是一种大肠杆菌滑动钳抑制剂,IC50 为 222 μM,Ki 为 131 μM。 | |||
T13110 |
Tedatioxetine hydrobromide
Lu AA 24530 hydrobromide |
Dopamine Receptor; 5-HT Receptor; Norepinephrine | GPCR/G Protein; Neuroscience |
Tedatioxetine hydrobromide (Lu AA 24530 hydrobromide) 是一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂 ,也是 5-HT2A、5-HT2C、5-HT3 和 α1A-肾上腺素能受体的拮抗剂,可用于治疗抑郁症和焦虑症。 | |||
T2410 |
Nedaplatin
奈达铂,NSC 375101D |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Nedaplatin (NSC-375101D) 是顺铂的衍生物,是肿瘤集落形成单位的 DNA 损伤剂,IC50为94 μM。 | |||
T22436 |
Takeda-6d
|
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Takeda-6d 是一种新型、有效的 DFG-out RAF/血管内皮生长因子受体 2 (VEGFR2) 抑制剂,IC50 分别为 7.0 nM 和 2.2 nM。 | |||
T24850 |
Takeda103A
CMPD103A,Takeda-103A,Takeda-103-A,CMPD-103A,Takeda 103 A |
GRK | GPCR/G Protein |
Takeda103A (CMPD103A) 是 GRK2抑制剂。G 蛋白偶联受体是许多生理过程的核心。Takeda103A 对研究心力衰竭具有潜在的研究价值。 | |||
T21023 |
Bedaquiline fumarate
TMC 207,R403323,TMC-207,TMC207,R-403323,贝达喹啉富马酸盐,R 403323 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bedaquiline fumarate (TMC207) 是二芳基喹啉抗生素,作用于 ATP 合成酶,常用于结核杆菌感染的研究。 | |||
T23445 |
Anxiolytic/nonsedative agent-1
TCS 1205 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Anxiolytic/nonsedative agent-1 (TCS 1205) 是一种有效的选择性 GABAA 激动剂。Anxiolytic/nonsedative agent-1 对牛脑膜中的 BzR 显示出明显的亲和力,对 α1β2γ2、α2β2γ2、α5β3γ2 的 Kis 分别为 14、121、239 nM。Anxiolytic/nonsedative agent-1 在体外表现出 α2 选择性功效,在体内表现出抗焦虑选择性作用。 | |||
TD0082 |
EDANS sodium
EDANS sodium salt,EDANS sodium salt [5-((2-Aminoethyl)amino)naphthalene-1-sulfonic acid, sodium salt],5-(2-氨乙基氨)-1-萘磺酸钠盐,5-(2-Aminoethylamino)-1-naphthalenesulfonic acid sodium salt,N-(Aminoethyl)-5-naphthylamine-1-sulfonic Acid Sodium Salt |
Others | Others |
EDANS sodium (5-(2-Aminoethylamino)-1-naphthalenesulfonic acid sodium salt) 是开发基于 FRET 的核酸探针的供体,该探针广泛用于实时 PCR 测定。 | |||
T1777 |
Nintedanib
BIBF 1120,Intedanib,尼达尼布 |
VEGFR; FGFR; FLT; PDGFR; Src | Angiogenesis; Tyrosine Kinase/Adaptors |
Nintedanib (Intedanib) 是一种三重血管激酶抑制剂,抑制 VEGFR1、VEGFR2、VEGFR3 (IC50=34/13/13 nM),FGFR1、FGFR2、FGFR3 (IC50=69/37/108 nM),PDGFRα、PDGFRβ (IC50=59/65 nM)。Nintedanib 具有抗肿瘤活性,通过抑制血管生成来抑制肿瘤生长。 | |||
T34795 |
Tedatioxetine
Lu AA 24530,Lu AA-24530,Lu AA24530 |
||
Tedatioxetine (Lu AA24530) 是一种血清素-去甲肾上腺素-多巴胺再摄取抑制剂(SNDRI),具有抗抑郁作用。Tedatioxetine 可作为 CYP2D6 底物。 | |||
T1970 |
Gedatolisib
PF-05212384,PKI-587 |
PI3K; mTOR | PI3K/Akt/mTOR signaling |
Gedatolisib (PF-05212384) 是一种高效的双重 PI3Kα (IC50:0.4 nM),PI3Kγ (IC50:5.4 nM) 和 mTOR (IC50:1.6 nM)抑制剂。它在 mTOR 复合物mTORC1和mTORC2中同样有效。 | |||
T38514 |
PMEDAP
|
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
PMEDAP 是有效的人类免疫缺陷病毒 (HIV) 复制抑制剂。它具有抗小鼠巨细胞病毒活性。它有效抑制莫罗尼鼠肉瘤病毒诱导的肿瘤形成和相关死亡率。 | |||
T1073 |
Dronedarone hydrochloride
Dronedarone HCl,SR33589,决奈达隆盐酸盐,盐酸决奈达隆 |
Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Dronedarone hydrochloride (SR33589) 是一种胺碘酮类似物,可抑制 Na+,K+andCa2+的电流,有可能治疗心房颤动。 | |||
T26972 |
Cedazuridine
西达尿苷,(4R)-2'-Deoxy-2',2'-difluoro-3,4,5,6-tetrahydrouridine |
DNA Methyltransferase | Chromatin/Epigenetic |
Cedazuridine ((4R)-2'-Deoxy-2',2'-difluoro-3,4,5,6-tetrahydrouridine) 是一种口服的胞苷脱氨酶抑制剂,具有抗肿瘤特性。 | |||
TD0081 |
EDANS
EDANS acid [5-((2-Aminoethyl)amino)naphthalene-1-sulfonic acid],EDANS酸,1,5-EDANS,EDANS acid [5-((2-Aminoethyl)amino)napht |
Others | Others |
EDANS (EDANS acid [5-((2-Aminoethyl)amino)naphthalene-1-sulfonic acid]) 是新型的淬灭荧光底物 (fluorogenic substrate),可利用共振能量转移,分析逆转录病毒蛋白酶。 | |||
T15198 |
Edasalonexent
CAT-1004 |
NF-κB | NF-κB |
Edasalonexent is an orally bioavailable inhibitor of NF-κB. | |||
T2585 |
Bedaquiline
R207910,TMC207,贝达喹啉 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bedaquiline (R207910) 是一种二芳基喹啉药物,能同时靶向 c-亚基和 ε-亚基,抑制结核分枝杆菌 (Mtb) F1FO-ATP 合酶。它具有解偶联活性和有用于耐多药结核病的潜力。 | |||
T5001 |
Nintedanib esylate
Intedanib,乙磺酸尼达尼布,BIBF 1120 (esylate),尼达尼布乙磺酸盐,Nintedanib Ethanesulfonate Salt,BIBF 1120 |
VEGFR; FGFR; PDGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Nintedanib esylate (BIBF 1120 esylate) 是一种有效的三重血管激酶抑制剂,能够抑制 VEGFR1 (IC50:34 nM)、VEGFR2 (IC50:13 nM)、VEGFR3 (IC50:13 nM),FGFR1 (IC50:69 nM)、FGFR2 (IC50:37 nM)、FGFR3 (IC50:108 nM),PDGFRα (IC50:59 nM)、PDGFRβ (IC50:65 nM)。 | |||
T0407 |
Edaravone
依达拉奉右莰醇,依达拉奉,MCI-186 |
Apoptosis; MMP; Free radical scavengers | Apoptosis; oxidation-reduction; Proteases/Proteasome |
Edaravone (MCI-186) 是一种新型自由基清除剂,能够抑制大鼠与 MMP-9有关的脑出血。 | |||
T76067 |
Dabcyl-KTSAVLQSGFRKME-Edans TFA
|
||
Dabcyl-KTSAVLQSGFRKME-Edans TFA 是一种用于测量蛋白酶酶促活性的荧光肽,具有研究2019-nCoV (COVID-19) 感染潜力的特性。该化合物作为底物,用于相关蛋白酶活性的测定。 | |||
T76369 |
CEDAEVFKDSMVPGEK
|
||
CEDAEVFKDSMVPGEK 为大鼠辣椒素受体亚型 1 (VR1) 的多肽序列片段,适用于探测 VR1 的存在、分布及分子形态。 | |||
T26818 |
Binedaline
binodaline. Ixprim,SCHA 1059,SCHA1059,Sgd-Sch-1059,SCHA-1059 |
||
Binedaline is a selective norepinephrine reuptake inhibitor with Ki value of 25 nM. | |||
T20673 |
Clofedanol
NSC113595,NSC 113595,NSC-113595 |
||
Clofedanol, also known as chlophedianol or antitussin, is used in the treatment of pediatric pertussis. | |||
T39287 |
Ledaborbactam
|
||
Iedaborbactam, as a beta-lactamase inhibitor (WO2015191907, Example 62), can be used for the research of bacterial infections. | |||
T131569 |
Allosedamine
|
||
Allosedamine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T131569。 | |||
T31092 |
Credazine
BRN 0880257,NIA 20439,SW-670,H-722,Kusakira |
||
Credazine is a bio-active chemical. Detailed information has not been published. | |||
T17027 |
Tedalinab
GRC-10693 |
Cannabinoid Receptor | GPCR/G Protein |
Tedalinab is an effective and selective cannabinoid receptor 2 agonist. Tedalinab has the potential for neuropathic pain and osteoarthritis treatment. Tedalinab has >4700-fold functional selectivity for CB2 over CB1. | |||
T60708 | Cedazuridine hydrochloride | ||
Cedazuridine (E7727) (Compound 7a) hydrochloride 是一种可用于研究癌症的,口服有效的胞苷脱氨酶 (CDA) 抑制剂 (IC 50 = 0.4 μM)。 | |||
T77082 | Melredableukin alfa | ||
Melredableukin alfa (RO-7049665)是一种由人IgG1-κ通过多肽连接子与人突变白细胞介素2(IL2 mutin)融合形成的融合蛋白。它适用于乙型肝炎和溃疡性结肠炎的研究。 | |||
T76239 | Efrilacedase alfa | ||
Efrilacedase alfa 是一种活性化合物。Efrilacedase alfa 可用于各种生化研究。 | |||
T82619 |
Dabsyl-Leu-Gly-Gly-Gly-Ala-Edans
|
||
Dabsyl-Leu-Gly-Gly-Gly-Ala-Edans为标记有Dabsyl荧光基团的肽类化合物。该化合物用于鉴定铜绿假单胞菌LasA蛋白酶的肽酶活性,并呈现酶特异性,适用于相关生物医学研究。 | |||
T75369 |
DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS
|
||
DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS 为一种用于人类疟原虫天冬氨酰蛋白酶的荧光底物,属于荧光染料类。储存条件:需避光。 | |||
T26549 |
Acedapsone
Atilon,BA 2650,Rodilon,Camilan,Acetamin |
||
Acedapsone has antimalarial and antimicrobial action, but is mainly used as a depot leprostatic agent. | |||
T21388 |
Emedastine Difumarate
Rapimine,DSSTox_CID_26911,AL-3432A,富马酸依美斯汀,KB-2413,Emedastine fumarate,KB 2413 |
||
Emedastine Difumarate is a selective histamine H1 receptor antagonist with anti-allergic activity, prescribed for allergic conjunctivitis. Upon ocular administration, emedastine causes a dose-dependent inhibition of histamine-stimulated vascular permeabil | |||
T39288 |
Ledaborbactam etzadroxil
VNRX-7145 |
||
Ledaborbactam etzadroxil (VNRX-7145) is an orally active inhibitor of Ambler class A, C, and D β-lactamase enzymes. | |||
T68661 |
Edatrexate
CGP 30694 |
||
Edatrexate (CGP 30694),即 10-乙基-10-去甲氨基蝶呤,是甲氨蝶呤Methotrexate 的类似物,对耐 MTX 肿瘤具有抗肿瘤活性。Edatrexate 是一种抗叶酸抗代谢物,可用于研究非小细胞肺癌,乳腺癌,非霍奇金淋巴瘤和头颈部癌症的研究。 | |||
T27239 |
Edaglitazone
Edaglitazone sodium,BM-13.1258,RO-2052349-602,依格列宗,R-483,RO-2052349-000 |
||
Edaglitazone is a PPARγ agonist. Edarglitazone restores acute inflammatory responses to cerebral hypoxia-ischemia in the diabetic ob/ob mouse. | |||
T69788 |
Daledalin
|
||
Daledalin is an antidepressant which was synthesized and trialed for depression in the early 1970s, but was never marketed. It is a selective norepinephrine reuptake inhibitor, with no significant effects on the reuptake of serotonin and dopamine, and no antihistamine or anticholinergic properties. | |||
T68229 |
Nintedanib esylate hemihydrate
|
||
Nintedanib esylate hemihydrate is a potent inhibitor of multiple receptor tyrosine kinases (RTKs) and non-receptor tyrosine kinases (nRTKs). | |||
T19273 |
Debutyldronedarone D7
SR-35021 D7 |
Others | Others |
Debutyldronedarone D7 is deuterium-labeled Debutyldronedarone, which is the main circulating active metabolite of dronedarone in the body. | |||
T29102 | Vedaclidine tartrate | ||
Vedaclidine tartrate is a muscarinic analgesic. | |||
T35712 |
Debutyldronedarone hydrochloride
SR35021 hydrochloride |
||
N-Desbutyl dronedarone is an active metabolite of the antiarrhythmic agent dronedarone .1,2,3It is formed from dronedarone by cytochrome P450s (CYPs) and monoamine oxidase (MAO) in human hepatocyte preparations.4N-Desbutyl dronedarone inhibits the binding of 3,3’,5-triiodo-L-thyronine to the thyroid hormone receptors TRα1and TRβ1(IC50s = 59 and 280 μM for the chicken and human receptors, respectively).1It inhibits CYP2J2-mediated formation of 14,15-EET from arachidonic acid and soluble epoxide h... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3862 |
Irigenin
|
NF-κB; Integrin | Cytoskeletal Signaling; NF-κB |
Irigenin 可通过特异性和选择性地阻断 Extra Domain A 域的 C-C 环上α9β1和α4β1整合素结合位点,介导其抗转移作用。可通过增强胃癌细胞中促凋亡分子的表达来敏化 TRAIL 诱导的凋亡,具有抗癌作用。 | |||
T3S0081 |
Oxypeucedanin
(+-)-Oxypeucedanin,氧化前胡素,Oxypeucadanin |
Potassium Channel | Membrane transporter/Ion channel |
Oxypeucedanin ((+-)-Oxypeucedanin) 是呋喃香豆素衍生物,分离自Angelica dahurica。它是选择性开放通道阻滞剂,可抑制hKv1.5通道电流,IC50值为 76 nM。它延长心脏动作电位持续时间,是潜在的抗心律失常试剂。它通过抑制癌细胞迁移来诱导细胞凋亡。 | |||
T7056 |
Dronedarone
决奈达隆,SR 33589 |
P450; Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; AChR; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Dronedarone (SR 33589) 是一种胺碘酮类似物,对治疗心房颤动可能有效。它是CYP3A4的底物和中度抑制剂。它是多种离子电流的有效阻滞剂,通过非竞争性结合到肾上腺素能受体显示出抗肾上腺素能的效果。 | |||
T6S0078 |
Oxypeucedanin hydrate
Prangolarin Hydrate,水合氧化前胡素 |
Antioxidant | oxidation-reduction |
Oxypeucedanin hydrate (Prangolarin Hydrate) 是一种分离自D. anethifolia 中的天然香豆素化合物,存在于几种植物中,具有抗感染和抗真菌活性。 | |||
T5808 |
(-)-Oxypeucedanin hydrate
水合氧化前胡素,OXYPEUCEDANIN HYDRATE |
Others | Others |
(-)-Oxypeucedanin hydrate 是一种呋喃香豆素衍生物,分离自Ducrosia anethifolia 中。 | |||
T13816 |
(+)-Peusedanol
(+)-白花前胡醇,白花前胡醇 |
Others | Others |
(+)-Peusedanol 是一种香豆素,从滨海前胡中分离出来。 | |||
T5763 |
Sedanolide
|
Others; Autophagy | Autophagy; Others |
Sedanolide 是从伞形科的种子油中分离出的一种天然苯酞,具有抗炎和抗氧化活性。 | |||
TN4758 | Peucedanol 3'-O-glucoside | Others | Others |
Peucedanol 3'-O-glucoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4758,CAS号为 65891-61-4。 | |||
T75620 | (+)-Oxypeucedanin methanolate | ||
(+)-Oxypeucedanin methanolate (compound 9) 是一种天然产物,可抑制前列腺素 E2 的产生。 | |||
TN5212 |
Uvedalin
|
Others | Others |
Uvedalin shows cytotoxicity against HeLa, HL-60, and Murine B16-F10 melanoma cell lines. | |||
TN3645 |
Chlorouvedalin
|
Others | Others |
Chlorouvedalin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3645,CAS号为 24694-80-2。 | |||
TC0029 |
Peucedanin
|
||
Peucedanin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TC0029,CAS号为 133-26-6。 | |||
TN4755 |
Peucedanocoumarin I
|
Others | Others |
Peucedanocoumarin I是一种天然产物,属于伞形科前胡属,其产品编号为 TN4755,CAS号为 130464-55-0。Peucedanocoumarin I可用作对照参考。 | |||
TMA2563 | Pedalitin | Tyrosinase | Proteases/Proteasome |
Pedalitin is a mixed-type inhibitor of tyrosinase. In the assay of α-glucosidase inhibition, rosmarinic acid is a competitive inhibitor, whereas both methyl rosmarinate and Pedalitin are mixed-type inhibitors. | |||
TN4757 | Peucedanocoumarin III | Others | Others |
Peucedanocoumarin Ⅲ can induce rice resistance to blast disease. | |||
T41136 | Azedarachol | ||
Azedarachol possesses antifeedant activity. | |||
TN6851 | Iso-oxypeucedanin | ||
Iso-oxypeucedanin is a natural product. | |||
TN4756 |
Peucedanocoumarin II
|
Others | Others |
Peucedanocoumarin II shows only partial relaxation. | |||
TN4759 |
Peucedanol 7-O-glucoside
|
Others | Others |
Peucedanol 7-O-glucoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4759,CAS号为 65853-04-5。 | |||
T81532 |
Pedaliin 6''-acetate
|
||
Pedaliin 6''-acetate (compound 10) 为甘青青兰中分离得到的天然产物,具有抗氧化活性,并能对抗DOX诱导的H9c2心肌细胞毒性,表现出细胞保护效应,其EC50为19.1 μM。 | |||
T81505 | Peucedanoside A | ||
Peucedanoside A,一种从Peucedanum praeretorum Dunn根部分离得到的苷类化合物。 | |||
TN6027 |
Pedatisectine F
2-Methyl-6-(1,2,3,4-tetrahydroxybutyl)pyrazine |
||
Pedatisectine F是一种天然产物,属于天南星科半夏属,其产品编号为 TN6027,CAS号为 206757-32-6。Pedatisectine F可用作对照参考。 | |||
TN5546 |
Pedaliin
Pedalin,Pedalitin 6-O-glucoside,Glucosyl-6-pedalitin |
Antioxidant | oxidation-reduction |
Pedaliin 是从芝麻 (Sesamum indicum L)和藏药Dracocephalum tanguticum Maxim 地上部分提取的一种黄酮类化合物。Pedaliin 在体外显示出抗氧化和抗结肠癌作用,可用于研究心脑血管疾病。 | |||
T83521 |
(S)-7-O-Methylpeucedanol 3′-O-β-D-glucopyranoside
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(S)-7-O-Methylpeucedanol 3'-O-β-D-glucopyranoside 为一种香豆素糖苷[sup][1]。 |