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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8133 |
SulfadiMethoxine sodium
|
Anti-infection; Antibacterial; Antibiotic | Microbiology/Virology |
SulfadiMethoxine sodium 是一种磺胺类抗生素,可研究由多种感染引起的疾病。 | |||
T1078 |
Sulfadimethoxine
Sulphadimethoxine,磺胺二甲氧嗪 |
Antibacterial; Antibiotic | Microbiology/Virology |
Sulfadimethoxine (Sulphadimethoxine) 是一种磺胺类抗生素,用于多种感染引起的疾病的研究。 | |||
T7808 |
Alacepril
Cetapril,阿拉普利,DU-1219 |
RAAS | Endocrinology/Hormones |
Alacepril (DU-1219) 是一种具有口服活性血管紧张素转换酶 (ACE) 抑制剂,具有长效抗高血压作用。 | |||
T12732 |
Rezafungin
棘白菌素,SP-3025,CD101,Biafungin |
Others; Antifungal | Microbiology/Virology; Others |
Rezafungin (SP-3025) 是一种长效的广谱棘皮菌素,对念珠菌、曲霉和肺孢子菌具有强效抗真菌活性。 | |||
T5376 |
Aranidipine
阿雷地平,MPC1304 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Aranidipine (MPC1304) 是一种钙通道拮抗剂,具有强效和持久的抗高血压作用。 | |||
T22316 |
Doxazosin
UK 33274,多沙唑嗪 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Doxazosin (UK 33274) 是选择性的拮抗突触后的α1肾上腺素受体。 | |||
T1470L |
Fexofenadine hydrochloride
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Fexofenadine hydrochloride 是 terfenadine 的羧化代谢衍生物和长效选择性组胺 H1 受体拮抗剂,具有抗组胺活性。 | |||
T3407L |
Rapastinel acetate
Rapastinel acetate (117928-94-6 Free base) |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Rapastinel acetate 是 N-甲基-D-天冬氨酸 (NMDA) 受体的调节剂和甘氨酸位点的部分激动剂,具有长效抗抑郁作用。 | |||
T0231 |
Amlodipine Besylate
Amlodipine benzenesulfonate,苯磺酸氨氯地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Amlodipine Besylate (Amlodipine benzenesulfonate) 是可口服的二氢吡啶钙通道阻滞剂,有抗心绞痛作用。它通过阻断电压依赖性的 L 型钙通道,从而抑制钙离子内流,用于高血压和癌症的研究。 | |||
T27636 |
Ispronicline
AZD-3480,RJR-1734,AZD 3480,TC 1734,AZD3480,TC-01734,TC-1734-112 |
AChR | Neuroscience |
Ispronicline (TC-1734) 是一种具有口服活性、选择性和有效性的 α4β2 nAChR 部分激动剂,具有抗抑郁、神经保护和持久的认知作用。Ispronicline 对 α4β2 nAChR 具有很高的亲和力,Ki= 11 nM。 | |||
T8536 |
Filastatin
|
Antifungal | Microbiology/Virology |
Filastatin 是一种长效的白色念珠菌丝状体抑制剂,具有强大的抗真菌作用。它抑制真菌与聚苯乙烯和人类细胞的粘附,从酵母到菌丝的形态转变,抑制菌丝特异性 HWP1 启动子。 | |||
T6999 |
Teneligliptin hydrobromide
Teneligliptin hydrobromide anhydrous,MP-513 (hydrobromide) |
Others; Proteasome; DPP-4 | Others; Proteases/Proteasome; Ubiquitination |
Teneligliptin hydrobromide (MP-513(hydrobromide)) 是β2肾上腺素能受体 (β2AR) 阻滞剂,具有抗高血压、抗氧化、清除自由基的活性。 | |||
T2180 |
Hexythiazox
|
Parasite | Microbiology/Virology |
Hexythiazox 是一种螨类生长调节剂和噻唑烷类杀螨剂,对多种螨类具有长效杀虫作用,适用于植物从萌芽到结果的任何生长阶段。 | |||
T24932 |
Vatanidipine
AE-0047,AE 0047,AE0047 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Vatanidipine (AE0047) 是一种新型的双氢吡啶(DHP)型钙通道阻滞剂,具有缓慢起效的药理作用。在各种实验性高血压模型中观察到缓慢起效和持久的降压作用。 | |||
T15432 |
GSK256073
|
GPR; Others | Endocrinology/Hormones; GPCR/G Protein; Others |
GSK256073 是一种口服有活性的GPR109A 选择性激动剂,也是一种持久的人HCA2激动剂(pEC50:7.5) 。它能够减少脂降解,而显著改善葡萄糖稳态,对 2 型糖尿病和血脂异常具有潜在的研究价值。 | |||
T38192 |
Unifiram
|
Others | Others |
Unifiram 是一种认知增强剂。 Unifiram 诱导大鼠海马 CA1 区场兴奋性突触后电位 (fEPSP) 幅度的持久增加 (EC50= 27 nM) 并增加大鼠大脑皮层中乙酰胆碱 (ACh) 的释放。 | |||
T68129L1 |
Picumeterol FA
Picumeterol FA(130641-36-0 Free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
picumeterol FA 是一种有效的选择性β2肾上腺素能受体激动剂。在体外和体内试验中,picumeterol FA 可产生持久的气道平滑肌松弛作用。picumeterol FA 是一种纯 R 对映异构体,可用于改善哮喘患者的肺功能和降低气道高反应性。 | |||
T6707 |
Tiotropium Bromide hydrate
BA-679 BR hydrate,BA 679BR,噻托溴铵一水合物 |
AChR | Neuroscience |
Tiotropium Bromide hydrate (BA-679 BR hydrate) 是长效的毒蕈碱受体拮抗剂,可用于治疗慢性阻塞性气道疾病 (COPD)。 | |||
T22659 |
Chlorisondamine diiodide
|
Others | Others |
long lasting nicotinic antagonist | |||
T28914 |
Tak 187
Tak-187,Tak187 |
Others | Others |
Tak 187 is a long-lasting inhibitor of ergosterol biosynthesis. | |||
T71189 |
RX 809055AX
|
Others | Others |
RX 809055AX is a long lasting opioid antagonist at mu and delta receptors. | |||
T23965 |
DAT 582
DAT582,DAT-582 |
Others | Others |
DAT 582 is a novel serotonin3 receptor antagonist. It is also an effective and long-lasting antiemetic agent | |||
T11755 |
KF 13218
|
Histone Demethylase | Chromatin/Epigenetic |
KF 13218 is a selective, potent and long lasting thromboxane B2 (TXB2) synthase inhibitor with an IC50 value of 5.3±1.3 nM. | |||
T26305 |
U 67827E
N-Ac-Asp-tyr(So3H)-nle-gly-trp-nle-asp-phe-NH2,U-67827E,U67827E |
Others | Others |
U 67827E is a long-lasting cholecystokinin agonist. It acts by decreases food intake. | |||
T29182 |
YM-358 potassium hydrate
YM-358,YM358,YM 358 |
Others | Others |
YM-358 potassium hydrate is an orally active and long-lasting antagonist of angiotensin type 1 receptor. | |||
T70749 |
TY 11223
|
Others | Others |
TY 11223 is a chemically stable homoisocarbacyclin analog. It has showed potent and long-lasting activities in inhibiting platelet aggregation and a good selectivity in biological activities. | |||
T71229 |
NA 0346
|
Others | Others |
NA 0346 is a derivative of SF 2370 that shows long lasting antihypertensive action as well as potent protein kinases inhibitory activity. | |||
T68066 |
Eptastigmine
|
Others | Others |
Eptastigmine,一种有效且持久的胆碱酯酶抑制剂,用于治疗与年龄相关的记忆缺陷。 | |||
T25669 |
Lercanidipine, (S)-
(S)-Lercanidipine,(+)-Lercanidipine |
Others | Others |
Lercanidipine, (S)-是 Lercanidipine 的异构体,一种降压化合物。Lercanidipine 是二氢吡啶类的钙通道阻滞剂,具有持久的降压作用和肾脏保护作用。 | |||
T70294 |
KAA-276 free base
|
Others | Others |
KAA-276 free base is a novel potent and long-lasting histamine HI-receptor antagonist with less-topical irritation, and can be topically administered by inhalation for the treatment of bronchial asthma. | |||
T69475 |
Dinalbuphine sebacate
|
Others | Others |
Dinalbuphine sebacate is a long-lasting prodrug of nalbuphine, acting as a moderate-efficacy partial agonist or antagonist of the μ-opioid receptor and as a high-efficacy partial agonist of the κ-opioid receptor. | |||
T12732L |
Rezafungin acetate
Biafungin acetate,SP-3025 acetate,CD101 acetate |
Others | Others |
Rezafungin acetate is an advanced echinocandin compound that exhibits broad-spectrum antifungal activity against Candida spp, Aspergillus spp, and Pneumocystis spp. This long-lasting next-generation medication showcases potent efficacy in combating fungal infections. | |||
TP1202 |
Calcitonin Gene Related Peptide (CGRP) II, rat
CGRP II, rat |
||
Calcitonin Gene Related Peptide II is a potent, long-lasting vasodilator; activation of CGRP receptors on pancreatic β-cells increases plasma levels of pancreatic enzymes. | |||
T70293 |
KAA-276 HCl
|
Others | Others |
KAA-276 HCl is the salt form of KAA-276 free base, a novel potent and long-lasting histamine HI-receptor antagonist with less-topical irritation, and can be topically administered by inhalation for the treatment of bronchial asthma. | |||
T41006 |
TFAX 488,TFP
|
||
TFAX 488,TFP is a green fluorescent dye that demonstrates pH-insensitivity across an extensive range (pH 4-10). It provides highly intense and long-lasting conjugates with proteins or antibodies, such as goat anti-mouse IgG and streptavidin. | |||
T63434 |
Abiraterone decanoate
|
Others | Others |
Abiraterone decanoate 是 Abiraterone 的前药,能够利用肌肉内 (IM) 递送提供 Abiraterone 的受控释放和长效 CYP17 抑制。 | |||
T61300 |
RBP4 inhibitor 1
|
Others | Others |
RBP4 inhibitor 1 (compound 43b) is an orally active and potent inhibitor of retinol-binding protein 4 (RBP4), exhibiting IC50 values of 28 nM and 110 nM for human and mouse RBP4, respectively. It effectively reduces blood RBP4 levels in mice, providing a long-lasting effect [1]. | |||
TP1885 |
[(pF)Phe4]Nociceptin(1-13)NH2
|
||
Highly potent and selective nociceptin/orphanin FQ receptor (OP4) agonist peptide (pKi = 10.68; pEC50 = 9.80). Displays > 8000-fold selectivity over δ, κ, and μ opioid receptors and has relatively long lasting pronociceptive, hypotensive, negative inotrop | |||
T25819 |
ML350
SR-2311,SR 2311,SR2311,ML-350,ML 350 |
Others | Others |
ML350 (CYM-50202) is a KOR (IC50: 12.6 nM) antagonist with good and moderate selectivity against the DOR and MOR. CYM-50202 displayed high solubility and excellent CNS penetration. CYM-50202 did not display long-lasting pharmacodynamic effects observed wi | |||
T37748 |
Ivermectin B1b
|
Others | Others |
Ivermectin B1b is the minor component . It produces antiparasitic activity by binding to glutamate-gated chloride channels expressed on nematode neurons and pharyngeal muscle cells, inducing irreversible channel opening and very long-lasting hyperpolarization/depolarization of the neuron/muscle cell, thereby blocking further function. | |||
T26452 |
A 80b
A80b,A-80b |
Others | Others |
A-80b is a synthesized pyridazino[4,5-b]indole derivate with potent and long-lasting antihypertensive activity. The decrease in diastolic pressure was greater than the decrease in systolic pressure and cardiac frequency was not modified significantly. A-8 | |||
T61654 |
PI3Kα-IN-9
|
Others | Others |
PI3Kα-IN-9 (compound 27) is a highly specific, orally active, and long-lasting inhibitor of PI3Kα, demonstrating potent inhibitory effects with IC50 values of 4.4, 128, 146, and 153 nM against PI3Kα, PI3Kγ, PI3Kδ, and PI3Kβ, respectively. Additionally, PI3Kα-IN-9 exhibits antiproliferative properties and effectively induces apoptosis. Given its characteristics, PI3Kα-IN-9 holds great potential for cancer research [1]. | |||
TP2012 |
JMV 449
|
||
Potent, metabolically stable neurotensin receptor agonist peptide (IC50 = 0.15 nM for inhibition of [125I]-NT binding to neonatal mouse brain; EC50 = 1.9 nM for contraction of guinea pig ileum). Produces long-lasting hypothermic, neuroprotective and analg | |||
T41250 |
Teneligliptin hydrobromide hydrate
|
Others | Others |
Teneligliptin hydrobromide hydrate 是一种有效的 DPP-4抑制剂,可在体外竞争性抑制人血浆、大鼠血浆和重组人 DPP-4 ,IC50值约为 1 nM。 | |||
T75919 |
PL-017 TFA
|
||
PL-017 TFA 是高效、选择性的 μ 阿片受体(μopioid receptor)激动剂,具有 5.5 nM 对125I-FK 33,824 与 μ 位点结合的 IC50 值。该化合物在大鼠中展现出持久且可逆的缓解疼痛效果。 | |||
T27799 |
LAS191859
LAS-191859,LAS 191859 |
Others | Others |
LAS191859 is a CRTH2/DP2 antagonist with IC50 values of 7.6, 9.58, 14 and 15.5nM for recombinant guinea pig, human, rat and mouse CRTH2/DP2 receptors, respectively. LAS191859 has a residence time half-life of 21h at CRTh2 that translates into a long-lasti | |||
T62985 |
Cofrogliptin
|
Others | Others |
Cofrogliptin (HSK7653) (compound 2) 是一种四氢吡喃衍生物,是一种口服具有活力的 DPP-4 抑制剂,具有长效降糖作用。Cofrogliptin (compound 2) 具有潜力进行 2 型糖尿病 (T2DM) 的研究。 | |||
T27595 |
Imarikiren HCl
TAK-272 hydrochloride,TAK-272 HCl. Imarikiren HCl |,TAK272,TAK 272,TAK-272 |
Others | Others |
Imarikiren is a potent, selective and orally active direct renin inhibitor. TAK-272 shows potent inhibitory activity against human renin (IC50 = 2.1 nM) in hPRA assay and excellent selectivity against other aspartic proteases, such as cathepsin D (IC50 > | |||
T75868 |
JMV 449 acetate
|
Others | Others |
JMV 449 acetate 是一种有效的神经降压素受体 (neurotensin receptor) 激动剂。JMV 449 acetate 显示抑制125I-neurotensin 与新生小鼠脑结合的 IC50为 0.15 nM,对收缩豚鼠回肠的 EC50为 1.9 nM。JMV 449 acetate 对小鼠具有高效、持久的降温和缓解疼痛作用。 | |||
T68129 |
Picumeterol
GR 114297A |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Picumeterol(GR 114297A) 是一种有效的选择性β2肾上腺素能受体激动剂。在体外和体内试验中,Picumeterol 可产生持久的气道平滑肌松弛作用。Picumeterol 是一种纯 R 对映异构体,可用于改善哮喘患者的肺功能和降低气道高反应性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T68746 |
Chaetochromin
|
Others | Others |
Chaetochromin also known as 4548-G05 and NSC 345647, is an orally active, small-molecule, selective agonist of the insulin receptor. It has potent and long-lasting antidiabetic activity in vivo in mice. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00780 |
CACNA1C Protein, Guinea Pig, Recombinant (His)
CACNA1C,CACNL1A1,CACH2,CACN2,Voltage-dependent L-type calciu... |
Guinea pig | E. coli |
Pore-forming, alpha-1C subunit of the voltage-gated calcium channel that gives rise to L-type calcium currents. Mediates influx of calcium ions into the cytoplasm, and thereby triggers calcium release from the sarcoplasm. Plays an important role in excitation-contraction coupling in the heart. Required for normal heart development and normal regulation of heart rhythm. Required for normal contraction of smooth muscle cells in blood vessels and in the intestine. Essential for normal blood pressur... | |||
TMPH-02264 |
RANKL/TNFSF11/CD254 Protein, Human, Recombinant (His)
Tumor necrosis factor ligand superfamily member 11,Osteoprot... |
Human | HEK293 Cells |
Cytokine that binds to TNFRSF11B/OPG and to TNFRSF11A/RANK. Osteoclast differentiation and activation factor. Augments the ability of dendritic cells to stimulate naive T-cell proliferation. May be an important regulator of interactions between T-cells and dendritic cells and may play a role in the regulation of the T-cell-dependent immune response. May also play an important role in enhanced bone-resorption in humoral hypercalcemia of malignancy. Induces osteoclastogenesis by activating multipl... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13121 |
Teneligliptin D8
MP-513 D8 |
Others | Others |
Teneligliptin D8 a deuterium labeled Teneligliptin (MP-513). Teneligliptin is a potent, orally available, competitive, and long-lasting inhibitor of DPP-4. |