547
20
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15374 |
Ipatasertib dihydrochloride
GDC-0068 dihydrochloride,RG-7440 dihydrochloride |
Akt; PKA | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Ipatasertib dihydrochloride (GDC-0068 dihydrochloride) 是ATP 竞争性的pan-Akt 选择性抑制剂,抑制Akt1,Akt2,Akt3,IC50分别为 5,18,8 nM。 | |||
T7821 |
DG172 dihydrochloride
DG172 (dihydrochloride),DG-172 dihydrochloride |
PPAR | DNA Damage/DNA Repair; Metabolism |
DG172 dihydrochloride (DG-172 dihydrochloride) 是一种 PPARβ/δ拮抗剂,IC50值为 27 nM。 | |||
T11345L |
Lerociclib dihydrochloride
G1T38 dihydrochloride |
CDK | Cell Cycle/Checkpoint |
Lerociclib dihydrochloride (G1T38 dihydrochloride) 是一种有效的选择性CDK4/CDK6抑制剂,抑制CDK6/CyclinD3和CDK4/CyclinD1,IC50值分别为 2 nM 和 1 nM。 | |||
T9012 |
Preq1-Dihydrochloride
pre-queuosine1 Dihydrochloride |
Others | Others |
Preq1-Dihydrochloride (pre-queuosine1 Dihydrochloride) 是 queuosine 途径的中间体,它以高亲和力结合 PreQ1 核糖开关的适体,从而减弱蛋白质表达。 | |||
T9172 |
Simufilam dihydrochloride
PTI-125 dihydrochloride |
Others | Others |
Simufilam dihydrochloride (PTI-125 dihydrochloride) 是口服具有活力的、毒性低的 filamin A 激活剂。它可优先结合改变的 FLNA,并恢复其天然构象,恢复受体和突触活性,并减少其与 a7nAChR/TLR4 的关联和下游病理作用。它可用于研究阿尔茨海默症。 | |||
T10358 |
Netarsudil Dihydrochloride
AR-13324 Dihydrochloride |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Netarsudil Dihydrochloride (AR-13324 Dihydrochloride) 是 Rho 相关蛋白激酶 (ROCK) 和去甲肾上腺素转运蛋白 (NET) 的抑制剂,可有效降低眼压 (IOP)。 | |||
T12374 |
PAβN dihydrochloride
MC-207,110 dihydrochloride,Phe-Arg-β-naphthylamide dihydrochloride |
Others; Antibacterial | Microbiology/Virology; Others |
PAβN dihydrochloride (MC-207,110 dihydrochloride) 是一种外排泵抑制剂。 | |||
T13675 |
Elacestrant dihydrochloride
RAD1901 dihydrochloride |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Elacestrant dihydrochloride (DA-DKRAD1901 dihydrochloride) 是一种具有口服活性的的选择性雌激素受体 (ER) 降解剂 (SERD),能够作用于 ERα (IC50:48 nM) 和 ERβ (IC50:870 nM)。 | |||
T22354 |
Levocetirizine Dihydrochloride
Xyzal Dihydrochloride,(-)-Cetirizine Dihydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Levocetirizine Dihydrochloride (Xyzal Dihydrochloride) is a third-generation peripheral H1-receptor antagonist. Acting as an antihistaminic agent, it specifically targets the histamine H1-receptor. Levocetirizine Dihydrochloride is the R-enantiomer of Cetirizine, which gives it a higher affinity for the H1-receptor than the S-enantiomer. Due to this enhanced affinity, Levocetirizine Dihydrochloride is effective in treating allergic rhinitis and chronic idiopathic urticaria. | |||
T4467 |
UAMC00039 dihydrochloride
UAMC 00039 dihydrochloride |
Proteasome | Proteases/Proteasome; Ubiquitination |
UAMC00039 dihydrochloride 是可逆、竞争性的 dipeptidyl peptidase II 高效抑制剂,IC50=为0.48 nM。 | |||
T11727 |
JPH203 dihydrochloride
KYT-0353 dihydrochloride |
Others | Others |
JPH203 dihydrochloride (KYT-0353 dihydrochloride) 是一种酪氨酸类似物,可作为 L 型氨基酸转运蛋白 1 (LAT1) 的选择性抑制剂,用于癌症研究。 | |||
T12241 |
Norbinaltorphimine dihydrochloride
nor-BNI dihydrochloride,Nor-BNI dihydrochloride,nor-Binaltorphimine dihydrochloride,Nor-Binaltorphimine dihydrochloride |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Norbinaltorphimine dihydrochloride是一种具有选择性和有效性的κ阿片受体 (κ opioid receptor) 拮抗剂,可在小鼠中诱导瘙痒相关反应。 | |||
T4676 |
Sardomozide dihydrochloride
CGP 48664 dihydrochloride,Sardomozide dihydrochloride |
Others | Others |
Sardomozide dihydrochloride (CGP 48664 dihydrochloride) 是 S-腺苷甲硫氨酸脱羧酶 (SAMDC) 的抑制剂 (IC50 = 5 nM)。 | |||
T21648 |
CP-31398 dihydrochloride
CP 31398 dihydrochloride |
p53 | Apoptosis |
CP-31398 dihydrochloride 是一种 p53 稳定剂,可稳定 p53 的活性构象并促进具有突变型或野生型 p53 的癌细胞系中的 p53 活性。 | |||
T10459 |
Banoxantrone dihydrochloride
AQ4N dihydrochloride,AZD1689 2HCl |
NOS | Immunology/Inflammation |
Banoxantrone dihydrochloride (AQ4N dihydrochloride) 是一种新型缺氧细胞毒素,通过 iNOS 依赖机制选择性地杀死缺氧细胞。 | |||
T3597 |
Cutamesine dihydrochloride
AGY94806 dihydrochloride,库他美新二盐酸盐,SA4503 (dihydrochloride),SA4503 dihydrochloride |
Sigma receptor | GPCR/G Protein |
Cutamesine dihydrochloride (SA4503 dihydrochloride) 是一种选择性 σ1 受体激动剂,IC50值为 17.4 nM。 | |||
T6720 |
Vatalanib dihydrochloride
CGP-797870 dihydrochloride,ZK-222584 dihydrochloride,Vatalanib 2HCl,PTK787 dihydrochloride,Vatalanib (PTK787) 2HCl,CGP-79787 dihydrochloride,瓦他拉尼 |
Apoptosis; VEGFR; PDGFR | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Vatalanib dihydrochloride (PTK787 dihydrochloride) 是一种VEGFR2/KDR 的抑制剂,其IC50值为37nM。 | |||
T5135 |
Flupentixol dihydrochloride
盐酸氟哌噻吨,Fupentixol Dihydrochloride,Flupenthixol dihydrochloride,(E/Z)-Flupentixol Dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Flupentixol dihydrochloride 是噻克西酮类试剂,能够用于研究精神分裂症以及抗焦虑和抑郁障碍。 | |||
T26240 |
Surfen dihydrochloride
Aminokinuride dihydrochloride,Aminoquinuride dihydrochloride,NSC-12155,Aminokinuride 2HCl,Aminoquinuride 2HCl |
FGFR; Antiviral; Antibiotic | Angiogenesis; Immunology/Inflammation; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Surfen dihydrochloride (Aminoquinuride dihydrochloride) 是一种有效的硫酸肝素小分子拮抗剂,具有抗菌和抗病毒活性,抑制炭疽致死因子、凝血因子 X 和致死因子。Surfen dihydrochloride 可抑制普通肝素和低分子量肝素的抗凝活性,抑制肝素的硫酸化和肝素裂解酶的降解。Surfen dihydrochloridn 抑制阻断硫酸乙酰肝素介导的 FGF2 结合和信号转导。Surfen 抑制 SEVI 和精液介导的 HIV 1 型感染增强。 | |||
T4327 |
Prexasertib dihydrochloride
LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368 |
Apoptosis; Chk; S6 Kinase | Apoptosis; Cell Cycle/Checkpoint; MAPK; PI3K/Akt/mTOR signaling |
Prexasertib dihydrochloride (LY2606368) 是一种选择性的,ATP 竞争性的细胞周期检测点激酶 1 抑制剂,Ki 为 0.9 nM,IC50为 <1 nM。它抑制 CHK2(IC50=8 nM) 和 RSK1 (IC50=9 nM)。它引起双链 DNA 断裂和复制突变,导致细胞凋亡,有抗肿瘤活性。 | |||
T22288 |
(1E)-CFI-400437 dihydrochloride
CFI-400437 dihydrochloride |
PLK | Cell Cycle/Checkpoint |
(1E)-CFI-400437 dihydrochloride (CFI-400437 dihydrochloride) 是一种选择性和有效的 polo 样激酶 4 (PLK4) 抑制剂,IC50为 0.6 nM。它还抑制 Aurora A、 Aurora B、 KDR 和 FLT-3,IC50分别为 0.37、0.21、0.48 和 0.18 μM,具有抗增殖活性。 | |||
T11500L |
GSK3368715 dihydrochloride
EPZ019997 dihydrochloride,GSK3368715 2HCl,EPZ019997 2HCl |
Histone Methyltransferase | Chromatin/Epigenetic |
GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) 是一种具有口服活性和高效性的 I 型蛋白精氨酸甲基转移酶 (PRMTs) 抑制剂 ,具有抗癌和抗肿瘤活性,抑制PRMT1,PRMT3,PRMT4,PRMT6,PRMT8的活性,可用于研究晚期实体肿瘤。 | |||
T7153 |
Vanoxerine dihydrochloride
GBR-12909 dihydrochloride,伐诺司林二盐酸盐,I893 dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Vanoxerine dihydrochloride (GBR-12909 dihydrochloride) 是一种竞争性的、有效的、选择性的多巴胺再摄取抑制剂,能够与多巴胺转运体 (DAT) 上的靶点结合。 | |||
T11227L |
Eravacycline dihydrochloride
TP-434-046,TP-434 dihydrochloride |
Antibacterial | Microbiology/Virology |
Eravacycline dihydrochloride (TP-434-046) 是一种有效的广谱抗菌剂,可对抗六种大肠杆菌(MIC:0.125-0.25 mg/L)。 | |||
T2501 |
Canertinib dihydrochloride
CI-1033 dihydrochloride,PD-183805 dihydrochloride,Canertinib,卡奈替尼二盐酸盐 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Canertinib dihydrochloride (PD-183805 dihydrochloride) 是一种可口服的喹唑啉盐酸盐,具有潜在的抗肿瘤和放射增敏活性,抑制细胞 EGFR 和 ErbB2自身磷酸化的 IC50值分别为 7.4 和 9 nM。 | |||
T19069 |
TMB dihydrochloride
3,3',5,5'-四甲基联苯胺盐酸盐,BM blue dihydrochloride,Sure Blue TMB dihydrochloride,3,3',5,5'-Tetramethylbenzidine dihydrochloride |
Others | Others |
TMB dihydrochloride (Sure Blue TMB dihydrochloride) 是一种免疫组化和 ELISA 的显色底物。 | |||
T11011 |
Dexpramipexole dihydrochloride
普拉克索杂质D,KNS-760704 dihydrochloride,R-(+)-Pramipexole dihydrochloride,右旋普拉克索二盐酸盐,(R)-Pramipexole dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Dexpramipexole dihydrochloride (KNS-760704 dihydrochloride) 是一种神经保护剂,是一种弱的非麦角类多巴胺受体激动剂。 | |||
T60248 |
4-Aminobenzamidine dihydrochloride
p-Aminobenzamidine dihydrochloride |
Serine Protease | Proteases/Proteasome |
4-Aminobenzamidine dihydrochloride (p-Aminobenzamidine dihydrochloride) 是一种强胰蛋白酶 (trypsin)抑制剂,也是一种相对较弱的尿激酶型纤溶酶原激活剂 (uPA) 抑制剂 (Ki=82 μM)。4-Aminobenzamidine 可抑制 SCID 小鼠体内前列腺肿瘤的生长。 | |||
T2663 |
GTS-21 dihydrochloride
GTS 21 dihydrochloride,DMXB-A,DMBX-anabaseine |
5-HT Receptor; AChR | GPCR/G Protein; Neuroscience |
GTS-21 dihydrochloride (DMBX-anabaseine) 是一种选择性 α7 烟碱乙酰胆碱受体激动剂,具有抗炎和增强认知的活性。它也是一种拮抗剂,对人α4β2的 Ki 为20 nM,对5-HT3A 受体的 IC50为3.1 μM。 | |||
T7505 |
Azimilide Dihydrochloride
NE-10064 Dihydrochloride,盐酸阿齐利特 |
Potassium Channel | Membrane transporter/Ion channel |
Azimilide Dihydrochloride (NE-10064 Dihydrochloride) 是 I(Ks) 和 I(Kr) 抑制剂,具有抗心律失常活性。 | |||
T5495 |
Decloxizine dihydrochloride
盐酸去氯羟嗪,UCB 1402 dihydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Decloxizine dihydrochloride (UCB 1402 dihydrochloride) 是组胺 1 受体拮抗剂。 | |||
T35528L |
TD52 dihydrochloride
TD52 dihydrochloride(1798328-24-1 Free base),TD52 2HCl |
Others | Others |
TD52 dihydrochloride (TD52 2HCl), a derivative of Erlotinib, is a potent and orally active inhibitor of protein phosphatase 2A (CIP2A). It exhibits strong anti-cancer properties by regulating the CIP2A/PP2A/p-Akt signaling pathway, resulting in the induction of apoptosis in triple-negative breast cancer (TNBC) cells. Mechanistically, TD52 dihydrochloride disrupts the binding of Elk1 to the CIP2A promoter, effectively reducing CIP2A levels. Notably, TD52 dihydrochloride demonstrates powerful anti... | |||
T6562 |
Latrepirdine dihydrochloride
Dimebolin dihydrochloride,Latrepirdine,Latrepirdine 2HCl,Dimebolin |
Beta Amyloid; 5-HT Receptor; Adrenergic Receptor; GluR; Autophagy; Histamine Receptor | Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Latrepirdine dihydrochloride (Dimebolin dihydrochloride) 是一种具有口服活性和神经活性的多种药物靶点的拮抗剂,可刺激淀粉样前体蛋白分解代谢和 β-淀粉样蛋白分泌。 | |||
T35328 |
H-1152 dihydrochloride
H-1152 2HCl,H-1152 dihydrochloride |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
H-1152 dihydrochloride (H-1152 2HCl) 是 Rho 相关蛋白激酶 (ROCK) 的特异性抑制剂,IC50 为 12 nM,Ki 为 1.6 nM。 H-1152 dihydrochloride 抑制 PKA、PKC、PKG、Aurora A 和 CaMKII,IC50 值分别为 3.03 μM、5.68 μM、0.360 μM、0.745 μM 和 0.180 μM。 | |||
T38034 |
MAO-IN-M30 dihydrochloride
M 30 dihydrochloride |
Monoamine Oxidase | Neuroscience |
MAO-IN-M30 dihydrochloride (M 30 dihydrochloride) 是一种口服活性,可通过血脑屏障的,脑选择性不可逆 MAO-A (IC50=37 nM) 和 MAO-B (IC50=57 nM) 抑制剂。MAO-IN-M30 dihydrochloride 是有效的铁螯合剂、自由基清除剂。MAO-IN-M30 dihydrochloride 对 Dexamethasone 诱导的脑细胞凋亡具有神经保护作用。MAO-IN-M30 dihydrochloride 在 MPTP 和 lactacystin 帕金森病模型中也显示出神经恢复活性。 | |||
T4167 |
Raf inhibitor 1 dihydrochloride
B-Raf inhibitor 1 dihydrochloride |
Raf | MAPK |
Raf inhibitor 1 dihydrochloride (B-Raf inhibitor 1 dihydrochloride) 是 Raf 激酶抑制剂,对 B-RafWT、B-RafV600E 和 C-Raf 的Ki 分别为 1、1 和 0.3 nM。 | |||
T25268L |
Coblopasvir dihydrochloride
Coblopasvir dihydrochloride(1312608-46-0 Free base) |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Coblopasvir dihydrochloride 是一种泛基因型非结构蛋白 5A(NS5A)抑制剂。本品可用于慢性丙型肝炎病毒感染的研究。 | |||
T1786 |
Daclatasvir dihydrochloride
BMS-790052 dihydrochloride,盐酸达拉他韦 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Daclatasvir dihydrochloride (BMS-790052 dihydrochloride) 是有机阴离子转运多肽 1B(OATP1B) 和 OATP1B3抑制剂,IC50分别为 1.5 µM 和 3.27 µM。它也具有口服活性的 HCV NS5A 蛋白抑制剂,多种 HCV 复制子基因型的 EC50范围为 9-146 pM。 | |||
T23132 |
Pentamidine dihydrochloride
喷他脒二盐酸盐,MP-601205 dihydrochloride |
Phosphatase; Antibacterial; Antibiotic; Parasite; Antifungal | Metabolism; Microbiology/Virology |
Pentamidine dihydrochloride (MP-601205 dihydrochloride) 是一种抗微生物剂,会干扰 DNA 的生物合成。它是选择性蛋白酪氨酸磷酸酶和再生肝磷酸酶抑制剂。它可用于冈比亚锥虫病,抗锑利什曼病和卡氏肺孢子虫肺炎的研究,有抗肿瘤活性,抗菌活性。 | |||
T6146 |
Dorsomorphin dihydrochloride
BML-275 2HCl,Compound C dihydrochloride,6-[4-[2-(1-哌啶基)乙氧基]苯基]-3-(4-吡啶基)吡唑并[1,5-A]嘧啶,Dorsomorphin (Compound C) 2HCl,Compound C 2HCl,BML-275 dihydrochloride |
AMPK; Autophagy; TGF-beta/Smad | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling; Stem Cells |
Dorsomorphin dihydrochloride (BML-275 2HCl) 是一种选择性和 ATP 竞争性的AMPK 抑制剂,Ki 为 109 nM。它诱导自噬,通过靶向抑制 I 型受体ALK2,ALK3和ALK6来抑制 BMP 途径。 | |||
T7309 |
TAS-103 dihydrochloride
6-[[2-(二甲基氨基)乙基]氨基]-3-羟基-7H-茚并[2,1-C]喹啉-7-酮二盐酸盐,TAS-103 (dihydrochloride),BMS-247615 dihydrochloride |
Topoisomerase | DNA Damage/DNA Repair |
TAS-103 dihydrochloride (BMS-247615 dihydrochloride) 是可用于癌症研究的一种 DNA 拓扑异构酶 I/II 双重抑制剂。 | |||
T16524 |
Philanthotoxin 74 dihydrochloride
PhTx-74 HCl,PhTx 74 dihydrochloride |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Philanthotoxin 74 dihydrochloride 是一种 AMPAR 拮抗剂,对 GluR3 和 GluR1 的 IC50 分别为 263 和 296 nM。 | |||
T12383 |
PD 168568 dihydrochloride
PD 168568 (dihydrochloride),二盐酸PD168568 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
PD 168568 dihydrochloride (PD 168568 (dihydrochloride)) 是一种口服有效的,选择性的 D4 受体拮抗剂,其 Ki 值为 8.8 nM。 | |||
T14490 |
Talipexole dihydrochloride
Domnin,盐酸他利克索,B-HT 920 dihydrochloride |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Talipexole dihydrochloride (Domnin) 是一种多巴胺 D2 受体激动剂、α2-肾上腺素受体激动剂和 5-HT3 受体拮抗剂,有抗帕金森病活性。 | |||
T2105 |
Veliparib dihydrochloride
维利帕尼二盐酸盐,ABT-888 dihydrochloride |
PARP; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Veliparib dihydrochloride (ABT-888 dihydrochloride) 是一种PARP1和PARP2抑制剂,Ki 分别为5.2 nM 和2.9 nM。 | |||
T3213 |
Hematoporphyrin dihydrochloride
血卟啉二盐酸盐,Hematoporphyrin IX dihydrochloride |
Apoptosis; Others; Endogenous Metabolite | Apoptosis; Metabolism; Others |
Hematoporphyrin dihydrochloride (Hematoporphyrin IX dihydrochloride) 是一种光敏剂,是血红素结合蛋白亲和色谱底物。它暴露在红光下时,可诱导 U87 胶质瘤细胞凋亡,并降低体内肿瘤的生长。 | |||
T61156 |
L-Lysyl-L-lysine dihydrochloride
Lysyllysine dihydrochloride |
Others | Others |
L-Lysyl-L-lysine dihydrochloride (Lysyllysine dihydrochloride) 是一种酶可裂解的接头。L-Lysyl-L-lysine dihydrochloride 可用作递送多种生物活性肽的简单接头。 | |||
T1791L |
Ceritinib dihydrochloride
LDK378 dihydrochloride,双盐酸盐色瑞替尼 |
IGF-1R; ALK | Angiogenesis; Tyrosine Kinase/Adaptors |
Ceritinib dihydrochloride (LDK378 dihydrochloride) 是一种选择性的、口服具有活性的、ATP 竞争性的ALK 酪氨酸激酶抑制剂 (IC50:200 pM)。它还抑制IGF-1R (IC50:8 nM),InsR (IC50:7 nM) 和 STK22D (IC50:23 nM)。它显示出良好的抗肿瘤作用。 | |||
T40711 |
H-D-Phe-Pip-Arg-pNA dihydrochloride
S-2238 dihydrochloride,H-D-Phe-Pip-Arg-pNA dihydrochloride |
Others | Others |
H-D-Phe-Pip-Arg-pNA dihydrochloride (S-2238 dihydrochloride), a chromogenic substrate, mimics the N-terminal fragment of the A alpha chain of fibrinogen, the native substrate of thrombin. Specifically designed for thrombin detection, H-D-Phe-Pip-Arg-pNA dihydrochloride is employed for the quantification of antithrombin-heparin cofactor (AT-III). The AT-III assay utilizing this substrate is characterized by its sensitivity, accuracy, and ease of implementation. | |||
T1856 |
TPT-260 Dihydrochloride
TPT-260,TPT 260,NSC55712,TPT260,TPU-260 Dihydrochloride |
Others | Others |
TPT-260 Dihydrochloride (NSC55712) 是一种噻吩硫脲衍生物。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2920 |
Berbamine dihydrochloride
Berbamine,盐酸小檗胺,dihydrochloride |
Apoptosis; NF-κB; Bcr-Abl; Autophagy | Angiogenesis; Apoptosis; Autophagy; Cytoskeletal Signaling; NF-κB; Tyrosine Kinase/Adaptors |
Berbamine dihydrochloride (Berbamine) 是源自小檗植物的天然产物,是一种NF-κB 抑制剂,具有显著的抗骨髓瘤疗效。 | |||
TN1012L |
Febrifugine dihydrochloride
ISF-2123,Propyldazine hydrochloride,Atensil,(+)-Febrifugine dihydrochloride,常山乙素二盐酸盐,Pildralazine dihydrochloride |
Parasite | Microbiology/Virology |
Febrifugine dihydrochloride (Propyldazine hydrochloride) 是存在于常山的根和叶中的一种喹唑啉酮类生物碱,具有治疗疟疾、癌症、纤维化和炎症性疾病的活性。 | |||
T4754 |
Pyridoxylamine dihydrochloride
盐酸吡多胺,Pyridorin,Pyridoxamine dihydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Pyridoxylamine dihydrochloride (Pyridorin) 是一种糖基化终产物和脂质化终产物抑制剂,能够防止糖尿病引起的视网膜血管病变。 | |||
T0810 |
Ethambutol dihydrochloride
Ethambutol 2HCl,盐酸乙胺丁醇,Emb dihydrochloride,CL40881 |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Ethambutol dihydrochloride (CL40881) 能抗分枝杆菌,可抑制阿拉伯糖基转移酶活性来阻止细胞壁形成。 | |||
T7117 |
Sapropterin dihydrochloride
Sapropterin Hydrochloride,6R-Tetrahydro-L-biopterin dihydrochloride,(6R)-5,6,7,8-四氢生物蝶呤 二盐酸盐,6R-BH4 dihydrochloride,盐酸沙丙蝶呤 |
Hydroxylase | Metabolism |
Sapropterin dihydrochloride (6R-BH4 dihydrochloride) 是一种合成的 BH4 形式,已经被批准用于 BH4 反应的 PKU 研究。 | |||
T4895 |
Pentane-1,5-diamine dihydrochloride
5-diamine dihydrochloride,Cadaverine dihydrochloride,1,5-戊二胺盐酸盐,Pentane-1 |
Endogenous Metabolite | Metabolism |
Pentane-1,5-diamine dihydrochloride (Cadaverine dihydrochloride) 是内源性代谢产物的一种。 | |||
T2219 |
Puromycin dihydrochloride
CL13900 dihydrochloride,Puromycin 2HCl,嘌呤霉素二盐酸盐水合物,嘌呤霉素二盐酸盐 |
ribosome; DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Puromycin dihydrochloride (CL13900 dihydrochloride) 属于肉桂酰胺腺苷抗生素,是一种蛋白质合成的抑制剂。Puromycin dihydrochloride 通过与 RNA 结合来抑制蛋白质合成,具有抗肿瘤和抗锥虫活性。 | |||
T8790 |
1-Methylhistamine dihydrochloride
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Endogenous Metabolite | Metabolism |
1-Methylhistamine dihydrochloride 是组胺代谢物。 | |||
T4333 |
Quinine dihydrochloride
盐酸奎宁,Quinine bimuriate |
Others | Others |
Quinine dihydrochloride (Quinine bimuriate) 是Cinchona(Rubiaceae) 各种物种的主要生物碱。它也是一种抗疟药和肌肉松弛剂(骨骼)。 | |||
T4940 |
3-Methylhistamine dihydrochloride
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Others; Endogenous Metabolite | Metabolism; Others |
3-Methylhistamine dihydrochloride 是一种组胺的降解产物,与免疫反应有关,并在接种过疫苗的小鼠中表现出上调作用。 | |||
T4899 |
L-Histidinol dihydrochloride
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Endogenous Metabolite | Metabolism |
L-Histidinol dihydrochloride 是内源性代谢产物的一种。 | |||
T19466 |
N8-Acetylspermidine dihydrochloride
N8-乙酰基亚精胺二盐酸盐 |
Endogenous Metabolite | Metabolism |
N8-Acetylspermidine dihydrochloride 是一种多胺物质。 | |||
T6534 |
Histamine dihydrochloride
组胺二盐酸盐,peremin,Ceplene,Histamine 2HCl |
Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Histamine dihydrochloride (Ceplene) 是 Histamine 的二盐酸形式。Histamine 是一种有机氮化合物,是一种强效的胃分泌兴奋剂,支气管平滑肌收缩剂,血管舒张剂,也是一种中枢作用的神经递质。 | |||
T0788 |
Spectinomycin dihydrochloride
淋必治,Spectinomycin 2HCl,盐酸奇霉素,Actinospectacin |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Spectinomycin dihydrochloride (Actinospectacin) 是一种能与细菌核糖体的30S 亚基结合,干扰蛋白质合成的抗生素。 | |||
T19394 |
L-hydroxylysine dihydrochloride
(2S,5R)-5-Hydroxylysine dihydrochloride |
Others | Others |
L-hydroxylysine dihydrochloride , is formed by posttranslational hydroxylation of some lysine residues. It is an amino acid, is exclusive to collagen protein. | |||
TQ0109 |
Cephaeline dihydrochloride
(-)-Cephaeline dihydrochloride,盐酸吐根酚碱,NSC 32944 |
P450 | Metabolism |
(-)-Cephaeline (dihydrochloride) is an enantiomer of Cephaeline. Cephaeline is a selective CYP2D6 inhibitor (IC50: 121 μM). | |||
T38541 | Chitobiose dihydrochloride | ||
Chitobiose dihydrochloride is a chitosan oligosaccharide consisting of β-1,4-linked glucosamine units. | |||
T22213 | 1,4-Diaminobutane Dihydrochloride | Others | Others |
1,4-Diaminobutane dihydrochloride, an endogenous metabolite, acts as an indicator of pollution-induced stress in higher plants: barley and rape stressed with Cr(III) or Cr(VI). In addition, 1,4-Diaminobutane dihydrochloride is an important source of GABA. | |||
T60789 |
L-Cystine dihydrochloride
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L-Cystine dihydrochloride 是合成谷胱甘肽 (GSH) 的含硫前体。L-Cystine dihydrochloride 的稳态对谷胱甘肽的功能很重要。L-Cystine dihydrochloride 可用作细胞培养组分。 | |||
TN7229 |
Baihuaqianhuoside
Praeroside |
Others | Others |
Baihuaqianhuoside (Praeroside) 是一种香豆素苷。Baihuaqianhuoside 可以从西番莲和 Hindenia solanacea 的根部分离出来,是首次从 P. japonicum 身上分离出来的。Baihuaqianhuoside 在体外具有抗炎活性,可以用于炎症的研究。Baihuaqianhuoside 对1,1-二苯基-2-丙烯酰肼自由基的清除作用,以及对2,2'-偶氮双(2-脒基丙烷)二盐酸盐诱导的脂质体氧化的抑制作用。 |