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Cat. No. | Product Name | Target | Signaling Pathways |
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T30098 |
Aplindore Fumarate
Aplindore,DAB-452 Fumarate,DAB-452 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Aplindore Fumarate (DAB-452)是一种小分子多巴胺 D2 受体部分激动剂,Aplindore Fumarate 对多巴胺D2 和D3 受体表现出高亲和力,对多巴胺D4、5-羟色胺(5-HT2)和α1-肾上腺素受体表现出低亲和力。Aplindore Fumarate 可用于研究帕金森和精神分裂症。 | |||
T25197 |
Bz-Dab(nbd)-awfpp-nle-NH2
Bz-Dab(nbd)-ala-trp-phe-pro-pro-nle-NH2 |
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Bz-Dab(nbd)-ala-trp-phe-pro-pro-nle-NH2 is a fluorescent NK2 antagonist. | |||
T21353 |
Fmoc-Dab(Boc)-OH
|
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Fmoc-Dab(Boc)-OH is a chemical intermediate used for chemical synthesis. | |||
TP2007 |
Lei-Dab7
Lei-Dab 7 |
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High affinity, selective KCa2.2 (SK2) channel blocker (Kd = 3.8 nM). Exhibits >200-fold selectivity for KCa2.2 over KCa2.1, KCa2.3, KCa3.1, IK, Kv and Kir2.1. Increases theta-burst responses and increases LTP in rat hippocampal slices in vitro. Convulsive | |||
T82620 |
DAB tetrahydrochloride dihydrate
3,3-Diaminobenzidine tetrahydrochloride dihydrate |
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3,3-Diaminobenzidine tetrahydrochloride dehydrate 作为染料,在组织化学(HC)及免疫组织化学(IHC)中应用广泛。该化合物主要用于过氧化物酶体染色和线粒体细胞色素c氧化酶活性的检测。 | |||
T23797 |
Bis(diazoacetyl)butane
1,4-Bis-diazoacetylbutane,Supermutagen,1,4-Bis(diazoacetyl)butane,DAB (mutagen) |
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Bis(diazoacetyl)butane is a mutagen and traditionally related to radio-mimetic chemical mutagens due to the similarity of appearance of mutagenic action of this mutagen and physical mutagens. It also has anti-tumor and carcinogenic activity. | |||
T81713 |
N-4′-(p-Trifluoromethylphenyl)butyl-DAB
|
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N-4′-(p-Trifluoromethylphenyl)butyl-DAB (compound 5g) 作为溶酶体酸 α-葡萄糖苷酶 (GAA) 的激动剂,在携带 M519V 突变的 Pompe 病患者成纤维细胞中,能剂量依赖性地提升细胞内 GAA 的活性。 | |||
T70071 |
SLM6031434 (free base)
|
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SLM6031434 (free base) is an inhibitor of sphingosine kinase type 2 (SphK2). It consists of pedant 1-guanidino-2-phenyloxadiazolylpyrrolidine group. | |||
T19270 |
DTPA-DAB2
|
Others | Others |
DAB2-DTPA is a conjugate of DTPA and two DABs used in the photooxidation experiment. | |||
T75946 |
Lei-Dab7 TFA
|
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Lei-Dab7 TFA, a selective and high-affinity blocker of the K Ca 2.2 (SK2) channel with a dissociation constant (K d) of 3.8 nM, demonstrates over 200-fold selectivity for K Ca 2.2 compared to K Ca 2.1, K Ca 2.3, K Ca 3.1, K v, and Kir2.1. Furthermore, Lei-Dab7 TFA enhances theta-burst responses and long-term potentiation (LTP) in rat hippocampal slices in vitro. | |||
T80137 |
(d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin
d(CH2)5[Tyr(Me)2, Dab5]AVP |
Vasopressin Receptor | GPCR/G Protein |
(d(CH2)51,Tyr(Me)2,Dab5,Arg8)-Vasopressin (d(CH2)5[Tyr(Me)2, Dab5]AVP)作为针对加压素受体V1a的特异性拮抗剂,具有pA2值为6.71。 | |||
T80135 |
Tyr-(D-Dab4,Arg5,D-Trp8)-cyclo-Somatostatin-14 (4-11)
|
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Tyr-(D-Dab4,Arg5,D-Trp8)-cyclo-Somatostatin-14 (4-11),一种生长抑素激动剂,用于癌症研究。 | |||
T10952 |
Dabuzalgron
达布扎琼,Ro 115-1240 |
Apoptosis; Adrenergic Receptor | Apoptosis; GPCR/G Protein; Neuroscience |
Dabuzalgron (Ro 115-1240) 是一种口服活性选择性 α-1A 肾上腺素受体激动剂,用于治疗尿失禁。它通过维持线粒体功能来预防多柔比星引起的心脏毒性。 | |||
T5133 |
Dabigatran Etexilate Mesylate
甲磺酸达比加群酯,BIBR 1048MS,Dabigatran etexilate methanesulfonate |
Thrombin | Proteases/Proteasome |
Dabigatran Etexilate Mesylate (BIBR 1048MS) 是一种口服具有活性的 Dabigatran 前药,具有抗凝作用,能够预防心房颤动引起的静脉血栓栓塞和中风。 | |||
T6295 |
Dabigatran
BIBR 953,BIBR 953ZW,达比加群 |
Thrombin | Proteases/Proteasome |
Dabigatran (BIBR 953ZW) 是一种口服抗凝剂,是一种可逆的,竞争性的直接凝血酶 (thrombin) 抑制剂,Ki=4.5 nM。它也抑制凝血酶诱导的血小板聚集 (IC50=10 nM)。 | |||
T31175 |
Dabelotine
UNII-6RY56RB98P |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dabelotine (UNII-6RY56RB98P) 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T18962 |
Dabcyl acid, SE
Dabcyl, SE |
Others | Others |
Dabcyl acid, SE (Dabcyl, SE) 是Dabcyl acid (DABCYL)的氨基活性形式,普遍用于制备含有DABCYL 荧光探针。 | |||
T77795 |
L-DABA hydrobromide
L-2,4-Diaminobutyric acid hydrobromide |
Others; Endogenous Metabolite | Metabolism; Others |
L-DABA hydrobromide (L-2,4-Diaminobutyric acid hydrobromide) 是一种有效的 GABA 转氨酶抑制剂,具有抗肿瘤和抗惊厥活性,可用于研究神经系统疾病。 | |||
T8474 |
Dabrafenib Mesylate
达帕菲尼甲磺酸盐,甲磺酸达拉非尼,GSK 2118436B,GSK2118436 Mesylate |
Raf | MAPK |
Dabrafenib Mesylate (GSK2118436 Mesylate) 是一种ATP 竞争型Raf 抑制剂,抑制C-Raf 和B-RafV600E 的IC50分别为 5 和 0.6 nM。 | |||
T0389 |
Dabigatran etexilate
达比加群酯,BIBR 1048 |
Thrombin | Proteases/Proteasome |
Dabigatran etexilate (BIBR 1048) 是一种 Dabigatran 前药,具有口服活性。它具有抗凝作用,能够预防心房颤动引起的静脉血栓栓塞和中风。 | |||
T1903 |
Dabrafenib
GSK2118436A,GSK2118436,达拉非尼 |
Raf | MAPK |
Dabrafenib (GSK2118436A) 是一种 Raf 抑制剂,抑制 C-Raf 和 B-RafV600E (IC50=5/0.6 nM),具有 ATP 竞争性。Dabrafenib 具有抗肿瘤活性,可用于治疗 B-RafV600E 突变的黑色素瘤。 | |||
T32191 |
Irdabisant
CEP-26401,CEP 26401,CEP26401 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Irdabisant (CEP-26401) 是选择性、口服活性和血脑屏障渗透性的组胺 H3 受体 (histamine H3 receptor, H3R) 拮抗剂/逆激动剂。Irdabisant 显示人 H3R 和大鼠 H3R 的 Ki 分别为 2.0 nM 和 7.2 nM。Irdabisant 抑制 hERG 电流的活性相对较低 (IC50= 13.8 μM)。在大鼠社会认知模型中,Irdabisant 具有认知增强和唤醒作用。Irdabisant 可用于研究精神分裂症或认知障碍。 | |||
T10951 |
Dabigatran ethyl ester hydrochloride
N-[[2-[[[4-(氨基亚氨甲基)苯基]氨基]甲基]-1-甲基-1H-苯并咪唑-5-基]羰基]-N-(2-吡啶基)-BETA-丙氨酸乙酯盐酸盐 |
Others; Thrombin | Others; Proteases/Proteasome |
Dabigatran ethyl ester hydrochloride 是一种核糖基二氢烟酰胺脱氢酶抑制剂,IC50=0.8 μM,也是一种凝血酶的抑制剂。 | |||
T18964 |
Dabsyl chloride
磺酰氯,DABS-Cl |
Others | Others |
Dabsyl chloride (DABS-Cl) 是胺的衍生剂,能产生稳定的产品,可用于标记氨基酸。在 460 nm 的波长下使用分光光度法易于进行监测。 | |||
T5114 |
Pyridaben
|
Calcium Channel; Parasite | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Pyridaben 是一种METI 杀螨剂,可抑制复合物 I 处的线粒体电子转运。它对多种螨虫具有活性,通过滤纸接触给药,在 25 mg/mL、100 mg/mL 和 200 mg/mL 的剂量下,分别诱导 100% 的C. malaccensis,D. farina 和T. putrescentia 死亡率。 | |||
T18963 |
Dabcyl acid
DABCYL,4-二甲胺偶氮苯-4’-羧酸,Para-methyl red |
Others | Others |
Dabcyl acid (DABCYL) 是一种最早的深色荧光猝灭剂。 | |||
T39287 |
Ledaborbactam
|
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Iedaborbactam, as a beta-lactamase inhibitor (WO2015191907, Example 62), can be used for the research of bacterial infections. | |||
T31174 |
DABA
diaminobenzoic acid |
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DABA (diaminobenzoic acid) can react with all aldehydes in the form of RCH(2)CHO, has the high serum stability of oligomers, and will develop new nanomaterials in biotechnology and biomedical applications. | |||
T76067 |
Dabcyl-KTSAVLQSGFRKME-Edans TFA
|
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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。 | |||
T10952L |
Dabuzalgron HCl
R1240,R-450,R450,RO-1151240,R-1240,RO1151240 |
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Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence. | |||
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。 | |||
T75369 |
DABCYL-Glu-Arg-Nle-Phe-Leu-Ser-Phe-Pro-EDANS
|
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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。 | |||
T31179 |
DABI
NSC-80087 |
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DABI 可用于生命科学领域的相关研究。其产品编号为 T31179,CAS号为 443-30-1。 | |||
T73161 |
HadAB-IN-1
|
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HadAB-IN-1 是一种有效的 HadAB 抑制剂。HadAB-IN-1 抑制 HadAB 酶复合物的活性,IC50值为 0.03 μM。HadAB-IN-1 还影响结核分枝杆菌(Mtb)中的分枝杆菌酸生物合成。HadAB-IN-1 可用于结核病(TB)的研究。 | |||
T82619 |
Dabsyl-Leu-Gly-Gly-Gly-Ala-Edans
|
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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。 | |||
T35615 |
Dabcyl-YVADAPV-EDANS
|
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Dabcyl YVADAPV EDANS 是一种荧光 IL-1β 转化酶 (interleukin-1β converting enzyme, ICE) 底物,可用于检测 ICE 样蛋白酶活性。Dabcyl YVADAPV EDANS 检测荧光的 λex=360 nm,λem=480 nm。 | |||
T31180 |
DABTH
|
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DABTH 可用于生命科学领域的相关研究。其产品编号为 T31180,CAS号为 72683-57-9。 | |||
T31177 |
Dabelotine, (S)-
UNII-494Y55877B |
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Dabelotine, (S)- 是 Dabelotine 的 S 型异构体。Dabelotine 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T61197 |
Irdabisant hydrochloride
|
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Irdabisant (CEP-26401) hydrochloride 是一种选择性、口服活性的组胺H3受体拮抗剂/逆激动剂,具备良好的血脑屏障渗透性。该化合物对大鼠和人类的H3受体具有高亲和力,其Ki值分别为7.2 nM和2.0 nM。此外,Irdabisant hydrochloride在抑制hERG电流方面表现出较低的活性,IC50为13.8 μM。在大鼠社会认知模型中,它展现了认知增强和唤醒的效果,可作为精神分裂症或认知障碍研究的潜在工具。 | |||
T31176 |
Dabelotine, (R)-
UNII-3NZJ1HNE7Y |
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Dabelotine, (R)- 是 Dabelotine 的 R 型异构体。Dabelotine 是一种肾上腺素能受体激动剂,可用于研究痴呆症。 | |||
T39288 |
Ledaborbactam etzadroxil
VNRX-7145 |
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Ledaborbactam etzadroxil (VNRX-7145) is an orally active inhibitor of Ambler class A, C, and D β-lactamase enzymes. | |||
TMIH-0174 |
Dabigatran-d3
|
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Dabigatran-d3 是 Dabigatran 的氘代化合物。 | |||
T10950 |
Dabigatran D4 hydrochloride
BIBR-953 D4 hydrochloride |
Others | Others |
Dabigatran D4 hydrochloride is deuterium-labeled dabigatran, which is a reversible and selective direct thrombin inhibitor (DTI) with a Ki value of 4.5 nM. | |||
T31178 |
Dabequin
dabechin,G 800 |
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Dabequin is a derivative of aminoquinoline. It is said to have pharmacological activity against Plasmodium fukiparum. | |||
T83873 |
Dabigatran Acyl-β-D-Glucuronide TFA
Dabigatran β-1-O-Acyl Glucuronide |
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Dabigatran acyl-β-D-glucuronide是凝血酶抑制剂dabigatran的一种活性代谢产物,主要通过UDP-葡萄糖醛酸转移酶(UGT)的UGT2B15亚型形成。在人体去除血小板的贫血浆中,Dabigatran acyl-β-D-glucuronide (0.46 µM) 能增加活化部分凝血活酶时间(aPTT)。 | |||
T80128 |
RE(EDANS)EVNLDAEFK(DABCYL)R
|
Beta-Secretase | Neuroscience |
RE(EDANS)EVNLDAEFK(DABCYL)R为具有EDANS和DABCYL双标记的肽,作为BACE1的荧光底物(Em=360nm,Ex=528nM)。该化合物主要用于评估BACE1酶活性,其活性水平正相关于荧光产生的强度。 | |||
T15046 |
Dabigatran ethyl ester
Dabigatran (ethyl ester),Dabigatran ethyl ester |
Thrombin | Proteases/Proteasome |
Dabigatran ethyl ester (Dabigatran (ethyl ester)) 是新型的口服抗凝化合物和凝血酶抑制剂。 | |||
T35939 |
Dabigatran Acyl-β-D-Glucuronide
|
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Dabigatran acyl-β-D-glucuronide is a major active metabolite of the thrombin inhibitor dabigatran . The prodrug of dabigatran, dabigatran etexilate , is hydrolyzed by plasma esterases to form dabigatran, which is metabolized primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT2B15 to form dabigatran acyl-β-D-glucuronide. Dabigatran acyl-β-D-glucuronide increases activated partial thromboplastin time (aPTT) in isolated human platelet-poor plasma equipotently to dabigatran. | |||
TMIH-0173 |
Dabigatran-d4 HCl
|
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Dabigatran-d4 HCl 是 Dabigatran HCl 的氘代化合物。Dabigatran HCl 的 CAS 号为 211914-51-1。Dabigatran 是一种口服抗凝剂,是一种可逆的,竞争性的直接凝血酶 (thrombin) 抑制剂,Ki=4.5 nM。它也抑制凝血酶诱导的血小板聚集 (IC50=10 nM)。 | |||
T73697 |
Denileukin diftitox
|
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Denileukin diftitox (DAB 389IL-2) 是一种融合蛋白毒素,将白喉毒素 (DT) 与白细胞介素 2 (IL-2) 结合,专门针对表达高亲和力IL-2受体 (IL-2R)、CD25 的细胞。它通过与IL-2R阳性细胞结合并利用白喉毒素片段的内化作用来抑制蛋白质合成,从而达到耗尽目标细胞的效果。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T7595 |
L-DABA
L-2,4-Diaminobutyric acid,L-2,4-二氨基丁酸氢溴酸盐,L-DAB HBR |
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
L-DABA (L-2,4-Diaminobutyric acid) 是GABA 转氨酶的弱抑制剂,IC50值大于500 μM,具有抗肿瘤活性。 |