75
18
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T29909 |
ALS-I
ALS1,Acid-Liable Surfactant-1,ALS 1,ALS-1 |
||
ALS-1 is an acid-Liable surfactant. | |||
T14336 |
Allitinib
AST-1306,ALS 1306 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Allitinib (AST-1306) 是可口服的 EGFR 和 ErbB2不可逆抑制剂,IC50分别为 0.5 和 3 nM。它具有抗癌活性,抑制 ErbB4,IC50为 0.8 nM。 | |||
T14195 | ALS-8112 | Others | Others |
ALS-8112 is a inhibitor of respiratory syncytial virus (RSV) polymerase. The 5'-triphosphate form of ALS-8112 inhibits RSV polymerase (IC50: 0.02 μM). | |||
T26602 |
ALS-I-41
|
||
ALS-I-41 is a novel, potent and selective antagonist of oxytocin receptor. | |||
TQ0034 |
Lumicitabine
ALS-8176,ALS-008176 |
RSV | Microbiology/Virology |
Lumicitabine (ALS-008176) is an inhibitor of RSV polymerase. | |||
T29970 |
AMG-222
AMG 222,ALS-2-0426 free base,ALS-2-0426,ALS-20426 |
||
AMG-222 (ALS-2-0426, ALS-20426) is a DPP-4 inhibitor and may be used in the treatment of type 2 diabetes. | |||
T19859 |
Nicosulfuron
Milagro,Accent,Motivell,烟嘧磺隆 |
Others | Others |
Nicosulfuron (Milagro) 是一种磺酰脲类的选择性除草剂,常用作出苗后的除草剂,保护玉米作物免受杂草的侵害。它也能够降低乙酰乳酸合酶的活性。 | |||
T3198L |
PRE-084 hydrochloride
|
Sigma receptor | GPCR/G Protein |
PRE-084 hydrochloride 是 σ1 的选择性激动剂在sigma 受体检测中,IC50值为44 nM。 | |||
T39924 |
NF-κΒ activator 2
|
NF-κB | NF-κB |
NF-κΒ activator 2 是口服有效的 NF-ҡB 激活剂,EC50为 1.58 μM。它通过增加 NF-κB 的表达和激活来诱导 SOD2。它具有用于研究肌萎缩性侧索硬化症的价值。 | |||
T67848 |
Valsartan Methyl Ester
|
RAAS | Endocrinology/Hormones |
Valsartan Methyl Ester 是一种强效血管紧张素II 受体拮抗剂,IC50=0.06uM。 | |||
T0498 |
Salsalate
Disalicylic acid,Salicylsalicylic acid,Sasapyrine,NSC-49171,双水杨酸酯 |
Reactive Oxygen Species; COX | Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
Salsalate (Sasapyrine) 是一种有效的抗风湿药物,是一种非乙酰化水杨酸盐,可以绕过胃的吸收,也可以避免环氧合酶的抑制。它具有抗炎活性,降低血糖水平、胰岛素抵抗和细胞因子表达,可用于研究 2 型糖尿病。 | |||
TQ0277 |
Pralsetinib
普拉替尼,Blu667 |
c-RET | Apoptosis; Tyrosine Kinase/Adaptors |
Pralsetinib (Blu667) 是高效的、选择性的RET 抑制剂。它能够抑制 WT RET (IC50:0.4 nM),RET 突变体 V804L (IC50:0.3 nM),V804M (IC50:0.4 nM),M918T (IC50:0.4 nM) 和 CCDC6-RET (IC50:0.4 nM) 的融合。 | |||
T39350 |
Sebetralstat
KVD900 |
Others | Others |
Sebetralstat (KVD900) 是一种血浆激肽释放酶抑制剂,可用于代谢性疾病的研究。 | |||
T2318 |
Sacubitril/Valsartan
Sacubitril mixture with Valsartan,沙库必曲/缬沙坦,Valsartan,Sacubitril,LCZ696 |
Apoptosis; RAAS; Neprilysin | Apoptosis; Endocrinology/Hormones; Metabolism |
Sacubitril/Valsartan (LCZ696),以1:1摩尔比由Valsartan(一种ARB)和Sacubitril(AHU377)组成,为创新口服血管紧张素受体-脑啡肽酶(ARN)双重抑制剂,旨在治疗高血压与心力衰竭。其作用机制包括抑制炎症、氧化应激及细胞凋亡,有助于改善糖尿病心肌病。 | |||
T4615 |
Balsalazide sodium hydrate
巴柳氮钠水合物,Balsalazide disodium dihydrate,巴柳氮钠,Balsalazide disodium salt dihydrate,Balsalazide disodium |
STAT; Interleukin | Immunology/Inflammation; JAK/STAT signaling; Stem Cells |
Balsalazide sodium hydrate (Balsalazide disodium) 可通过调节IL-6/STAT3通路起抑癌作用,可用于治疗炎症性肠病。 | |||
T7426 |
ALSTERPAULLONE
|
Apoptosis; GSK-3; CDK | Apoptosis; Cell Cycle/Checkpoint; PI3K/Akt/mTOR signaling; Stem Cells |
Alsterpaullone 是高效的 CDK 抑制剂,是一种 ATP 竞争性的 GSK-3alpha/GSK-3beta 抑制剂,且作用的 IC50值都为 4 nM。它有用于神经退行性和增生性疾病的研究潜力,具有抗肿瘤活性,诱导白血病细胞凋亡。 | |||
T17216 |
Valspodar
PSC 833 |
P-gp | Membrane transporter/Ion channel; Neuroscience |
Valspodar (PSC 833) 是一种特异性的 P-糖蛋白抑制剂和MDR调节剂,常被用作化学增敏剂,可用于研究晚期上皮卵巢癌。 | |||
T14358 |
Avoralstat
BCX4161 |
Others | Others |
Avoralstat (BCX4161) 是血浆激肽释放酶(PKK)抑制剂,具有口服活性,可用于遗传性血管性水肿的研究。 | |||
T6716 |
Valsartan
Diovan,缬沙坦,Tareg,CGP 48933 |
RAAS | Endocrinology/Hormones |
Valsartan (CGP 48933) 是一种血管紧张素 II 受体拮抗剂,有用于高血压和心力衰竭的研究潜力。 | |||
T13283 | Valsartan Ethyl Ester | Others | Others |
Valsartan Ethyl Ester is an impurity of Valsartan. Valsartan is an antagonist of the angiotensin II receptor and for the treatment of high blood pressure and heart failure. | |||
T4571 |
Balsalazide
巴柳氮,Balsalazido |
Lipoxygenase; STAT; Interleukin | Immunology/Inflammation; JAK/STAT signaling; Metabolism; Stem Cells |
Balsalazide (Balsalazido) 可通过调节IL-6/STAT3通路起抑癌作用,可用于治疗炎症性肠病。 | |||
T31379 |
deOxy-DALSiR
deOxy DALSiR |
||
deOxy-DALSiR is a selective and sensitive near-infrared fluorescent probe for visualization of endogenous nitric oxide in living cells and animals. | |||
T124585 |
rac Salsolinol, Hydrobromide
|
||
rac Salsolinol, Hydrobromide 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 T124585,CAS号为 59709-57-8。 | |||
T23417 |
Talsupram hydrochloride
|
Others | Others |
noradrenalin re-uptake inhibitor | |||
T123974 |
Salsoloside C
|
||
Salsoloside C 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 T123974,CAS号为 89827-13-4。 | |||
T81560 |
Palsucibep pegol
|
||
Palsucibep pegol为工程化人类lipocalin-2结合蛋白,与hepcidin发生结合。 | |||
T68890 |
Desvaleryl Valsartan
|
||
Desvaleryl valsartan is a potential impurity found in commercial preparations of the angiotensin II type 1 (AT1) receptor antagonist valsartan. It is a degradation product formed under acidic conditions. | |||
T35869 |
Berotralstat
|
||
Berotralstat (BCX7353) is a second-generation, synthetic, and orally active plasma kallikrein inhibitor with low toxicity. It is highly specific and effectively used in the research of hereditary angioedema (HAE) attacks. Berotralstat functions by inhibiting the enzymatic activity of plasma kallikrein, which is responsible for the release of bradykinin. This blocking mechanism targets the major biologic peptide involved in the promotion of swelling and pain associated with HAE attacks[1][2]. | |||
T29911L |
Alstonidine acetate
O-Acetylalstonidine |
||
Alstonidine acetate is a biochemical. | |||
T131406 |
Venalstonine
|
||
Venalstonine 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 T131406。 | |||
T76917 | Balstilimab | ||
Balstilimab (AGEN2034) 是一种针对PD-1的完全人单克隆IgG4抗体。 | |||
T78287 |
Alsevalimab
|
||
Alsevalimab为针对B7-H4的人源化单克隆抗体。 | |||
T13282 |
Valsartan-d9
CGP-48933 D9,缬沙坦 D9 |
Others | Others |
Valsartan D9 is a deuterium-labeled valsartan. Valsartan is an antagonist of the angiotensin II receptor and for the treatment of high blood pressure and heart failure. | |||
T131396 |
Carnegine (Pectenine, N-Methylsalsolidine)
|
||
Carnegine (Pectenine, N-Methylsalsolidine) 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 T131396。 | |||
T35725 |
4-hydroxy Valsartan
|
||
4-hydroxy Valsartan is a major metabolite of the angiotensin II type 1 (AT1) receptor antagonist valsartan . It reduces platelet aggregation induced by epinephrine and collagen but not ADP in human whole blood. | |||
T68555 |
Alsterpaullone, 2-Cyanoethyl
|
||
Alsterpaullone, 2-Cyanoethyl is a selective dual inhibitor of Cdk1/cyclin B and GSK-3β. | |||
T68829 | (+/-)-Salsolinol Hydrochloride | ||
(+/-)-Salsolinol hydrochloride is a full Gi protein agonist of the μ-opioid receptor (μOR). | |||
T29910 |
Alseroxylon
Egalin |
||
Alseroxylon can be used to treat hypertension. | |||
T76297 |
Alsactide
|
||
Alsactide,一种ACTH激动剂七肽类似物,主要应用于中枢神经系统的研究。 | |||
TQ0277L |
Pralsetinib HCl (2097132-94-8 free base)
Pralsetinib HCl,Pralsetinib hydrochloride,BLU-667,BLU667,BLU 667 |
||
Pralsetinib is a selective and next-generation RET inhibitor (IC50: 0.3-0.4 nM for WT RET, RET mutants V804L, V804M, M918T, and CCDC6-RET fusion). BLU-667 is an effective and selective inhibitor of RET mutations, fusions, and predicted resistant mutants. | |||
T13071 |
Talsaclidine
|
Others | Others |
Talsaclidine is an agonist of muscarinic with preferential neuron-stimulating properties. Talsaclidine is a full agonist at the M1 subtype, and as a partial agonist at the M2 and M3 subtypes. | |||
T29911 |
Alstonidine
|
||
Alstonidine is a biochemical. | |||
T70161 |
Berotralstat HCl
|
||
Berotralstat HCl is a novel selective inhibitor of plasma kallikrein, blocking the enzymatic activity of plasma kallikrein in releasing bradykinin, the major biologic peptide that promotes swelling and pain associated with attacks of HAE. | |||
T131573 |
Isosalsolidine
|
||
Isosalsolidine 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 T131573。 | |||
T29912 |
Alstonidine acetate trihydrate
Alstonidine acetyl deriv trihydrate |
||
Alstonidine acetate trihydrate is a biochemical. | |||
T20564 |
Valsartan benzyl ester
Valsartan impurity B,Valsartan related compound C |
||
Valsartan benzyl ester is a intermediate of Valsartan. | |||
T63507 |
Feniralstat
|
||
Feniralstat 是吡唑衍生物,是一种激肽释放酶 (kallikrein) 的有效抑制剂,能够抑制人血浆激肽释放酶 (pKal) (IC50: 6.7 nM)。Feniralstat 不抑制人 KLK1、人 FXIa 和人因子 Xlla (IC50均 >40 μM)。 | |||
T10823 |
trans-Pralsetinib
cis-Pralsetinib,cis-BLU-667 |
c-RET | Apoptosis; Tyrosine Kinase/Adaptors |
trans-Pralsetinib (trans-BLU-667) is an inhibitor of rearranged during transfection (RET). | |||
T60507 |
Utreloxastat
|
||
Utreloxastat 是一种用于 α-突触核蛋白病、tau 蛋白病、渐冻症、创伤性脑损伤和缺血再灌注相关损伤等疾病研究的化合物。 | |||
T15562 |
Imazamox
CL29926,甲氧咪草烟,(±)-Imazamox |
Others | Others |
Imazamox ((±)-Imazamox) 是一种具有高选择性、高活性、安全性、广谱活性的全身性除草剂,能够抑制植物中乙酰乳酸合酶(ALS) 的产生,进而抑制植物生长并最终导致植物死亡。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2830 |
Betulinic acid
白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid |
Apoptosis; Mitophagy; NF-κB; HIV Protease; Topoisomerase; Endogenous Metabolite; Aminopeptidase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Betulinic acid (ALS-357) 是从白桦树皮中分离出来的一种五环三萜类天然产物,是真核细胞拓扑异构酶 I 的抑制剂,IC50值为 5 μM,具有抗逆转录病毒、抗疟疾、抗癌和抗炎特性。 | |||
T22911 |
β-N-methylamino-L-alanine hydrochloride
L-BMAA hydrochloride |
Others | Others |
β-N-methylamino-L-alanine hydrochloride (L-BMAA hydrochloride) 是由蓝细菌产生的一种神经毒素,既有导致肌萎缩性侧索硬化症 (ALS) 以及其他可能的神经退行性疾病可能性。 | |||
TN2267 |
Tetrahydroalstonine
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Tetrahydroalstonine 是从 Rhazya stricta 的果实中提取出来的吲哚类生物碱,是一种具有选择性的 α2-肾上腺素受体拮抗剂。Tetrahydroalstonine 在Rauwolfia tetraphylla 中表现出抗精神病活性。 | |||
TN2112 |
Przewalskinic acid A
|
Others | Others |
Przewalskinic acid A is a rare, water-soluble, and highly biologically active ingredient found, thus far, only in the Salvia przewalskii Maxim herb. | |||
T23305 | Salsolinol-1-carboxylic acid | Others | Others |
amino acid that occurs naturally in the CNS | |||
TN6032 | Alstoyunine E | ||
Alstoyunine E shows selective inhibition of Cox-2 (>75%). | |||
TN5204 |
Uralsaponin C
|
Others | Others |
Uralsaponin C shows the cytotoxic activity against the human cancer cell lines MGC-803, SW620, and SMMC-7721 with IC50 > 100 μmol/L. | |||
TN4835 |
Przewalskin
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Przewalskin A and Przewalskin B showed modest anti-HIV-1 activity with EC50 = 41 and 30 microg/mL, respectively. | |||
TN5931 |
Alstonic acid B
|
||
Alstonic acid B是一种天然产物,属于夹竹桃科鸡骨常山属,其产品编号为 TN5931,CAS号为 1159579-45-9。Alstonic acid B可用作对照参考。 | |||
TN3398 | Alstolenine | Others | Others |
Alstolenine是一种天然产物,属于夹竹桃科鸡骨常山属,其产品编号为 TN3398,CAS号为 85769-33-1。Alstolenine可用作对照参考。 | |||
T8429 |
Salsolidine hydrochloride
6,7-DIMETHOXY-1-METHYL-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE, 99 |
||
TN5251 |
Walsuralactam A
|
Others | Others |
Walsuralactam A in the formula I, which is used as an active ingredient, and is used for treating and preventing the tumour. | |||
TN5937 |
Walsuronoid B
|
||
Walsuronoid B shows weak antimalarial activity. | |||
TN5205 | Uralsaponin D | Others | Others |
Uralsaponin D displayed the inhibition on the growth of cancer cells with IC50 at 18.3-41.6 μmol/L, it could significantly increase the cytotoxic activity after hydrolysis. | |||
T40576 |
(S)-Salsolidine
|
||
(S)-Salsolidine, a chemical compound, functions as a weak inhibitor of monoamine oxidase (MAO), exhibiting an inhibition constant (K i ) of 63 μM. R enantiomer demonstrating a greater efficacy than (S)-Salsolidine, boasting a K i value of 26 μM compared to the S form. | |||
TN3399 |
Alstonic acid A
|
Others | Others |
Alstonic acid A是一种天然产物,属于夹竹桃科鸡骨常山属,其产品编号为 TN3399,CAS号为 1159579-44-8。Alstonic acid A可用作对照参考。 | |||
T75527 | Chrexanthomycin C | ||
Chrexanthomycin C 是一种具有显著生物活性的海洋天然产物,具有口服活性。Chrexanthomycin C 对 DNA (G4C2)4 G4 具有结合亲和力,Kd 值为 2.8 mM。Chrexanthomycin C 可用于肌萎缩侧索硬化症 (ALS) 等神经退行性疾病的研究。 | |||
T82822 | Brassicanate A sulfoxide | ||
Brassicanate A sulfoxide 表现出除草效果,它能抑制植物中必需氨基酸的生物合成路径。该化合物通过结合并抑制多种酶的活性来发挥其作用,包括二羟酸脱水酶 (DHAD)、羟甲基丙酮酸双加氧酶 (HPPD)、乙酰乳酸合酶 (ALS)、PYL家族蛋白及转运抑制剂响应 1 (TIR1)。Brassicanate A sulfoxide 可以从甘蓝 (Brassica oleracea) 中提取获得。 |