148
9
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22746 |
Tesmilifene fumarate
DPPE fumarate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Tesmilifene fumarate (DPPE fumarate) 是一种 H1C 受体拮抗剂,可增强化疗的细胞毒性且保护正常细胞。 | |||
T35346 |
Tiamulin fumarate
Thiamutilin fumarate |
Antibacterial | Microbiology/Virology |
Tiamulin fumarate (Thiamutilin fumarate)是一种半合成的二萜类抗生素,具有抗菌活性,抑制蛋白质合成,可用于研究气囊炎。 | |||
T13241 |
UB 165 fumarate
UB-165 fumarate,UB165 fumarate |
AChR | Neuroscience |
UB 165 fumarate 是 nAChR 的激动剂,α4β2 亚型的部分激动剂,是 α3β2 亚型的全激动剂,其在大鼠脑中测得的结合到 [3H]-nicotine 的 Ki 值为 0.27 nM,可用于研究神经系统疾病。 | |||
T39214L |
LXE408 fumarate
LXE408 fumarate (1799330-15-6 Free base) |
Proteasome | Proteases/Proteasome; Ubiquitination |
LXE408 fumarate 是一种口服有效的,非竞争性的,动素体选择性蛋白酶体 (proteasome) 抑制剂。LXE408 fumarate 抑制 L. donovani 蛋白酶体 (IC50=0.04 μM) 和 L. donovani (EC50=0.04 μM)。LXE408 fumarate 具有较弱的透过血脑屏障能力。LXE408 fumarate 具有用于内脏利什曼病 (VL) 研究的潜力。 | |||
T0147 |
Clemastine fumarate
HS-592 (fumarate),富马酸氯马斯汀,Meclastine fumarate,Meclastine (fumarate) |
Autophagy; Histamine Receptor | Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Clemastine fumarate (Meclastine (fumarate)) 是一种合成乙醇胺,具有抗胆碱能、镇静和组胺 H1 拮抗作用。 | |||
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。 | |||
T0001 |
Iron(II) fumarate
Ferrous fumarate,Iron Fumarate,富马酸铁 (II),富马酸亚铁 |
Others | Others |
Iron(II) fumarate (Ferrous fumarate) 是一种口服活性膳食补充剂,是一种富马酸的铁 (II) 盐,可用于研究缺铁性贫血。 | |||
T41249 |
Tenofovir alafenamide fumarate
GS-7340 fumarate |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Tenofovir alafenamide fumarate (GS-7340 fumarate) 是一种可口服的 Tenofovir 前体化合物。Tenofovir alafenamide fumarate 具有抗 HIV 活性,可用于预防 HIV 感染。 | |||
T13385 |
Zamifenacin fumarate
扎非那星富马酸盐,UK-76654 fumarate |
AChR | Neuroscience |
Zamifenacin fumarate (UK-76654 fumarate) 是肠道选择性毒蕈碱M3受体的有效拮抗剂, 可显著降低肠易激综合症的结肠蠕动。 | |||
T6541 |
Ibutilide Fumarate
Corvert Fumarate,U70226E,富马酸伊布利特 |
Calcium Channel; Sodium Channel | Membrane transporter/Ion channel; Metabolism |
Ibutilide Fumarate (U70226E) 是一种 III 类抗心律失常药物,可作用于急性心梗阻塞。 | |||
T0994 |
Ketotifen fumarate
HC 20511 fumarate,富马酸酮替芬 |
PDE; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Ketotifen fumarate (HC 20511 fumarate) 是组胺 H1 受体和炎症介质释放的环七噻吩阻滞剂。 | |||
T28453L |
Propiram fumarate HCl
Propiram fumarate HCl(15686-91-6 Free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Propiram fumarate HCl是一种可口服的Opioid receptors激动剂,具有镇痛活性,可用于研究肌肉骨骼疼痛。 | |||
T37807 |
JTV 519 fumarate
|
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Ryanodine receptor (RyR) inhibitor; stabilizes RyR2 in a closed conformation. Exhibits antiarrhythmic and cardioprotective properties in vivo. Hunt et al (2007) K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 association. Biochem.J. 404 431 PMID:17313373 |Chen et al (2008) Effect of K201, a novel antiarrhythmic drug on calcium handling and arrhythmogenic activity of pulmonary vein cardiomyocytes. Br.J.Pharmacol. 153 915 PMID:17994112 |... | |||
T2409L |
Tenofovir Disoproxil Fumarate
GS-1278 Disoproxil Fumarate,Tenofovir DF,富马酸替诺福韦酯 |
HBV; HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Tenofovir Disoproxil Fumarate (GS-1278 Disoproxil Fumarate) 是一种核苷酸逆转录酶抑制剂,有潜力研究艾滋病和慢性乙型肝炎。 | |||
T13324 |
VUF11207 fumarate
|
CXCR; Arrestin | Autophagy; GPCR/G Protein; Immunology/Inflammation |
VUF11207 fumarate 是一种 CXCR7激动剂和高效CXCR7配体,pKi 为 8.1。它可诱导CXCR7的β-arrestin2募集和随后的内在化,pEC50分别为 8.8 和 7.9。 | |||
T17038 |
Tepilamide fumarate
XP-23829 |
Others | Others |
Tepilamide fumarate (XP-23829) 是一种口服具有活性的延胡索酸酯,可用于研究中度到重度慢性斑块银屑病。 | |||
T11071 |
Dofequidar fumarate
MS-209 |
P-gp | Membrane transporter/Ion channel; Neuroscience |
Dofequidar fumarate (MS-209) 是口服活性的喹啉化合物,通过抑制 ABCB1/P-gp 和 ABCC1/MDR 相关蛋白 1 来克服 MDR。 | |||
T1771 |
Ro 48-8071 fumarate
|
Others | Others |
Ro 48-8071 fumarate 是一种氧化鲨烯环化酶抑制剂(IC50:6.5 nM)。 | |||
T22810 |
GR 89696 fumarate
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
GR 89696 fumarate 是一种高效选择性的κ2 opioid receptor 受体激动剂(IC50 = 0.04 nM),具有预防瘙痒、体内抗伤害和神经保护作用。 | |||
T28258 |
Org-13011 fumarate
Org13011,Org 13011 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Org-13011 fumarate1 是 5-HT1A 受体的激动剂,可用于研究神经系统疾病。 | |||
T2404 |
Vonoprazan fumarate
富马酸沃诺拉赞,TAK-438 |
ATPase | Membrane transporter/Ion channel |
Vonoprazan fumarate (TAK-438) 是一种新型 P-CAB(钾竞争性酸阻滞剂),可可逆地抑制 H+/K+、ATP 酶。 | |||
T4271 |
Diroximel fumarate
Diroximel Fumarete |
Others | Others |
Diroximel fumarate (Diroximel Fumarete) 是一种控释制剂,是口服具有活力的富马酸单乙酯的前体药物。它被认为与其活性代谢物富马酸二甲酯的活性等效。它具有良好的安全性和有效性,具有研究多发性硬化的潜力。 | |||
T27753 |
KT-362 fumarate
KT 362,KT362,KT-362 |
Potassium Channel; Calcium Channel; Sodium Channel | Membrane transporter/Ion channel; Metabolism |
KT-362 fumarate 是一种新型化合物,可作为钙通道、钾通道和钠通道的拮抗剂.KT-362 fumarate 通过影响心房肌肉细胞内钙动员导致血管舒张。KT-362 fumarate 对兔子的股动脉和基底动脉条有放松作用。 | |||
T11337 |
Fumarate hydratase-IN-1
|
Others | Others |
Fumarate hydratase-IN-1 has antiproliferative activity against several cancer cell lines with a mean IC50 of 2.2 μM. Fumarate hydratase-IN-1 is a cell-permeable fumarate hydratase inhibitor. | |||
T6242 |
Rupatadine Fumarate
富马酸卢帕他定,Rinialer,Rupafin,Alergoliber |
PAFR; Autophagy; Histamine Receptor | Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Rupatadine Fumarate (Rinialer) 是一种可口服的长效PAF/H1受体的双抑制剂,Ki 值分别为 0.55 μM 和 0.1 μM。它可研究过敏性鼻炎和荨麻疹。 | |||
T21254 |
Vonoprazan Fumarate
TAK-438,TAK 438,Vonoprazan Fumurate,TAK438,富马酸沃诺拉赞 |
Proton pump | Membrane transporter/Ion channel |
Vonoprazan Fumarate (TAK438) 是质子泵的有效抑制剂,是口服有效的高效钾竞争性酸阻断剂,具有抗分泌活性。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50为 19 nM。它被开发用于研究酸相关疾病,如消化性溃疡和胃食管反流病。 | |||
T1475 |
Fesoterodine fumarate
Toviaz,SPM 907,富马酸非索罗定 |
AChR | Neuroscience |
Fesoterodine fumarate (Toviaz) 是可口服的,非亚型选择性的竞争性毒蕈碱受体拮抗剂,用于膀胱过度活动症,对 M1、M2、M3、M4 和 M5 受体的pKi 值分别为 8.0、7.7、7.4、7.3 和 7.5。 | |||
T6505 |
Formoterol fumarate
Formoterol Hemifumarate,NSC 299587,Eformoterol Hemifumarate,CGP 25827A,Eformoterol,福美特罗富马酸盐,YM 08316 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Formoterol fumarate (Eformoterol Hemifumarate) 是一种长效的 β2-肾上腺素受体激动剂。 | |||
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。 | |||
T72526 |
Aliskiren fumarate
CGP 60536 fumarate,SPP 100 fumarate,CGP 60536 fumarate ; CGP60536B fumarate ; SPP 100 fumarate,CGP60536B fumarate |
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Aliskiren fumarate是一种口服有效、选择性的肾素(renin)抑制剂,IC50值为1.5 nM。适用于高血压、心血管疾病和癌症恶病质的研究。 | |||
T40358 |
Ensitrelvir fumarate
S-217622 fumarate |
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Ensitrelvir (S-217622) fumarate is a novel orally active inhibitor, targeting the SARS-CoV-2 3CL protease (IC50 = 13 nM). It demonstrates non-covalent and non-peptidic characteristics. This compound represents a pioneering advancement in the development of effective antiviral agents against the SARS-CoV-2 virus. | |||
T37622 |
F13714 fumarate
F13714 fumarate |
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F13714 fumarate, a selective biased agonist of the 5-HT1A receptor, exhibits antidepressant-like effects upon single administration in the mouse model of chronic mild stress[1]. | |||
T10772L |
Cevipabulin fumarate
TTI-237 fumarate |
Others | Others |
Cevipabulin (TTI-237) fumarate is a microtubule-active antitumor compound and inhibits the binding of [3H] vinblastine to tubulin (IC50: 18-40 nM in the human tumor cell line). | |||
T27047 |
Clovoxamine fumarate
DU23811 fumarate,DU 23811 fumarate,DU-23811 fumarate |
5-HT Receptor; Serotonin Transporter; Norepinephrine | GPCR/G Protein; Neuroscience |
Clovoxamine fumarate (DU 23811 fumarate) 是一种 5-羟色胺再摄取、血清素和去甲肾上腺素抑制剂,具有抗抑郁和抗惊厥活性。 | |||
T11045 |
Dimethyl fumarate-d6
Dimethyl fumarate D6,DMF D6 |
Others | Others |
Dimethyl fumarate D6 is a deuterium labeled Dimethyl fumarate. can induces upregulation of antioxidant gene expression. | |||
T10319L |
Anamorelin Fumarate
ONO-7643 Fumarate,RC1291 Fumarate,富马酸阿拉莫林 |
Others | Others |
Anamorelin Fumarate is a novel ghrelin receptor agonist (EC50: 0.74 nM in the FLIPR assay). | |||
T6364L |
Desfesoterodine fumarate
PNU-200577 fumarate,UNII-607O3D83YQ |
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Desfesoterodine fumarate is a bio-active chemical. Detailed information has not been published. | |||
T12618 |
Quetiapine-d4 fumarate
Quetiapine D4 fumarate,富马酸奎硫平 D4 |
Others | Others |
Quetiapine D4 fumarate is the deuterium labeled Quetiapine fumarate. Quetiapine fumarate is a agonist of 5-HT receptors and a antagonist of dopamine receptor,with antidepressant and anxiolytic. | |||
T19435 |
Monomethyl fumarate-d3
Monomethyl fumarate D3 |
Others | Others |
Monomethyl fumarate D3 is a deuterium labeled Monomethyl fumarate. | |||
T69434 | Methapyrilene fumarate | ||
Methapyrilene fumarate is a histamine H1 antagonist with sedative action used as a hypnotic and in allergies. It is a hepatocarcinogen in sufficiently high doses, inducing mutations through an indirect genotoxic mechanism; e.g., via an oxidative mechanism or interaction with chromosomal proteins. | |||
T28759 |
Sesamodil
Sesamodil fumarate,SD-3211,SD 3211,SD3211,DS-4823 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Sesamodil(SD 3211) 是一种新型钙拮抗剂,可用于研究高血压。 | |||
T36639 | Donecopride (fumarate hydrate) | ||
Donecopride is a partial agonist of the serotonin (5-HT) receptor subtype 5-HT4E(Ki= 8.5 nM) and an inhibitor of acetylcholinesterase (AChE; IC50= 16 nM).1It is selective for AChE over butyrylcholinesterase (BChE; IC50= 3,530 nM) but does bind to 5-HT2Band sigma-2 (σ2) receptors (Ki= 1.6 nM for both) in a panel of 42 neurotransmitter receptors and transporters. Donecopride induces release of soluble amyloid precursor protein-α (sAPP-α) in COS-7 cells transiently expressing 5-HT4with an EC50value... | |||
T9450 |
NS3861 fumarate
|
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NS3861 fumarate 是烟碱型乙酰胆碱受体 (nAChRs) 的激动剂。NS3861 fumarate 是α3β4 nAChR 的部分激动剂。与α3β4、α3β2、α4β4、α4β2 的结合Ki 值分别为 0.62、25、7.8、55 nM。 | |||
T68397 | Xamoterol fumarate | ||
Xamoterol fumarate is a selective beta-1-adrenergic partial agonist. Because it is a partial agonist, it acts as an agonist when sympathetic activity is low and as an antagonist when sympathetic activity is high. It reduces myocardial ischemia and improves ventricular function in patients with mild to moderate heart failure. In patients with severe heart failure it has been shown to produce benefits in systolic and diastolic function. | |||
T68960 |
F-15599 Fumarate
|
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F-15599 Fumarate is a highly selective post-synaptic 5-HT(1A) receptor agonist: in-vivo profile in behavioural models of antidepressant and serotonergic activity. | |||
T69576 |
J-104129 fumarate
|
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J-104129 fumarate is a potent M3 muscarinic receptor antagonist. | |||
T69306 | Lubabegron fumarate | ||
Lubabegron, also known as LY591281; LY488756 fumarate, is a veterinary drug used to reduce ammonia emissions from animals and their waste. Ammonia emissions are a concern in agricultural production because of detrimental effects on the environment, human health, and animal health. Lubabegron was approved by the U.S. Food and Drug Administration in 2018 for use in feedlot cattle. Lubabegron is a beta-adrenergic receptor agonist that has the effect of increasing the breakdown of fats and increasin... | |||
T36721 |
Dehydro Amlodipine (fumarate)
|
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Dehydro amlodipine is a potential impurity found in commercial preparations of amlodipine. It is a degradation product formed during storage or when amlodipine is subjected to oxidative or acidic conditions or undergoes photo or electrochemical degradation. | |||
T71087 | Onvansertib fumarate | ||
Onvansertib fumarate is a A polo-like kinase 1 inhibitor, an antineoplastic | |||
T69808 | ABT-925 fumarate | ||
ABT-925, also known as A-37203, BSF-201640; DAT-201; Lu-201640; and A-437203, is a selective dopamine D3 receptor (DRD3) antagonist with an approximately 100-fold higher in vitro affinity for dopamine D₃ versus D₂ receptors. ABT-925 was tested in schizophrenia. ABT-925 is a selective dopamine D₃ receptor antagonist with an approximately 100-fold higher in vitro affinity for dopamine D₃ versus D₂ receptors. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2769 |
3-Aminopropionitrile fumarate (2:1)
Di-β-aminopropionitrile fumarate,3-Aminopropionitrile fumarate,3-氨基丙腈,β-Aminopropionitrile fumarate,3-Aminopropionitrile fumarate 2:1,Beta-Aminopropionitrile fumarate,β-Ammoniumpropionitrile hemifumarate |
Others | Others |
3-Aminopropionitrile fumarate (2:1) (β-Aminopropionitrile fumarate) 是一种能抑制胶原蛋白(collagen)交联的山黧豆素。 | |||
T40712 |
Diethyl fumarate
|
Others | Others |
Diethyl fumarate 是农药马拉硫磷的分解产物。 Diethyl fumarate 会在皮肤上引起非免疫性接触性荨麻疹。 | |||
T12095 |
Monomethyl fumarate
|
GPR; Drug Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism |
Monomethyl fumarate 是 Dimethyl fumarate 的活性代谢产物。Monomethyl fumarate 是一种 GPR109A 激动剂。Monomethyl fumarate 是一种 GPR109A 激动剂具有用于多种神经保护途径和其他视网膜疾病模型的潜力。 | |||
T0492 |
Dimethyl fumarate
富马酸二甲酯,DMF |
Reactive Oxygen Species; HIV Protease; Nrf2; Endogenous Metabolite; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Dimethyl fumarate (DMF) 是具有口服活性且可透过血脑屏障的Nrf2激活剂,可诱导抗氧化剂基因表达上调。它是一种富马酸盐衍生物,可作抗炎和免疫调节剂,可研究多发性硬化症。 | |||
TN6813 | Monoethyl fumarate | ||
Monoethyl fumaric acid is a natural product. | |||
T3763 |
Fumaric acid
Lichenic acid,Fumarate,2-Butenedioic acid,Trans-Butenedioic acid,反丁烯二酸,Donitic acid,Allomaleic acid,富马酸 |
Endogenous Metabolite | Metabolism |
Fumaric acid (2-Butenedioic acid) 与烟酸酶缺乏症相关,是癌症相关的内源性代谢物。 | |||
T20880 |
Mesaconic acid
中康酸,Methylfumaric acid,Mesaconate,Kyselina mesakonova |
Others | Others |
Mesaconic acid (Methylfumaric acid) 被用作阻燃剂,因为最近的研究表明这种酸是富马酸盐还原的竞争性抑制剂。 | |||
T4838 |
(S)-Malic acid
L-(-)-Malic acid,(S)-(-)-HYDROXYSUCCINIC ACID,(S)-2-Hydroxysuccinic acid,L-苹果酸 |
Others; Endogenous Metabolite | Metabolism; Others |
(S)-Malic acid ((S)-2-Hydroxysuccinic acid) 是天然存在的二羧酸,是水果酸甜味的来源,常用作食品添加剂。 | |||
T81570 |
Paecilaminol
FKI-0550 |
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Paecilaminol (FKI-0550) 为一种高效的 NADH 富马酸还原酶 (NADH-fumarate reductase) 抑制剂,其对蛔虫 (Ascaris suum) NADH 富马酸还原酶展现了 5.1 μM 的 IC50 值。 |