108
6
3
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6781 |
Benzenesulfonamide
Benzenesulphonamide,苯磺酰胺,Phenyl sulfonamide,Benzosulfonamide |
Carbonic Anhydrase | Metabolism |
Benzenesulfonamide (Benzosulfonamide) 是碳酸酐酶的抑制剂。 | |||
T14960 |
Chroman 1
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Chroman 1 是高效的的ROCK 选择性抑制剂,对 ROCK2 (IC50=1 pM) 的抑制作用强于 ROCK1 (IC50=52 pM) 。它对MRCK 也有抑制作用,IC50为 150 nM。 | |||
T0142 |
Brinzolamide
布林佐胺,AL-4862 |
Carbonic Anhydrase | Metabolism |
Brinzolamide (AL-4862) 是一种碳酸酐酶(carbonic anhydrase)II 抑制剂(IC50:3.19 nM)。 | |||
T6469 |
Dichlorphenamide
Diclofenamide,双氯非那胺,二氯苯二磺胺,Daranide,Antidrasi |
Carbonic Anhydrase | Metabolism |
Dichlorphenamide (Diclofenamide) 是一种碳酸酐酶抑制剂。 | |||
T0106 |
Methazolamide
L584601,醋甲唑胺,CL 8490 |
Carbonic Anhydrase | Metabolism |
Methazolamide (CL 8490) 是一种磺胺衍生物,用作碳酸酐酶 (carbonic anhydrase) 抑制剂,对人 carbonic anhydrase II 的 Ki=为 14 nM。它是降低眼压的药物,能够抑制由青光眼及其他眼病引起的眼压升高的作用。 | |||
T23782 |
Benzolamide
CL-11366,W 1803,CL 11366,CL11366,苯唑拉胺,W-1803 |
Carbonic Anhydrase | Metabolism |
Benzolamide (CL 11366) 是碳酸酐酶 (CA) 抑制剂,抑制hCA I(Ki:15 nM)、hCA II(Ki:9 nM)、EcoCAγ(Ki:94 nM)、VchCAγ(Ki:78 nM)、CAS3(Ki:54 nM)。它可用于研究青光眼和癫痫。 | |||
T20743 |
TG-46
TG46,TG 46 |
FLT; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
TG-46 (TG46) 对 JAK2, FLT3, RET, JAK3 具有抑制作用,可用于研究青光眼。 | |||
T0445 |
Promethazine
Proazamine,异丙嗪,Diphergan |
CaMK; Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Promethazine (Proazamine) 是抗青光眼前列腺素(PG)的类似物。 | |||
T68402 |
Falintolol
Falintololum |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Falintolol 是一种新型β-肾上腺素能拮抗剂,具有降压作用,可用于研究青光眼。 | |||
T6408 |
Betaxolol
Kerlone,SL 75212,Betoptic,倍他洛尔 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Betaxolol (Kerlone) 是 β1 肾上腺素受体阻断剂,可用于研究高血压和青光眼。 | |||
T19528 |
Propionylcarnitine
Propionyl carnitine |
Others | Others |
Propionylcarnitine (Propionyl carnitine) 是一种被广泛使用的膳食补充剂,有青光眼和难道破裂有关。 | |||
T8580 |
Bupranolol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bupranolol 是竞争性的、口服活性的、非选择性的β-adrenoceptor 拮抗剂,无固有的拟交感神经活性。 | |||
T32985 |
LX-7101 hydrochloride
LX7101 hydrochloride,LX 7101 hydrochloride |
ROCK; LIM Kinase; PKA | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells; Tyrosine Kinase/Adaptors |
LX-7101 hydrochloride是高效的 LIMK 和 ROCK2 抑制剂,具有降压活性,抑制 LIMK1/2, ROCK, PKA,可用于研究青光眼。 | |||
T7213 |
Demecarium bromide
地美溴铵,BC-48 |
AChE | Neuroscience |
Demecarium bromide (BC-48) 是一种有效的cholinesterase 抑制剂,Kiapp=0.15 μM,它可用研究于青光眼。 | |||
T19870 |
Aceclidine
3-Acetoxyquinuclidine,1-azabicyclo[2.2.2]octan-3-yl acetate,NSC657843,3-quinuclidinyl acetate,NSC-657843,Glaucostat,NSC 657843,Quinuclidin-3-yl acetate |
AChR | Neuroscience |
Aceclidine (1-azabicyclo[2.2.2]octan-3-yl acetate) 是M3 mAChR 的调节剂,可用于有关通过降低眼内压治疗青光眼的研究。 | |||
T31731 |
Evodenoson
DE 112,DE-112,ATL 313,DE112,ATL313,ATL-313 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Evodenoson (ATL313) 是一种有效的选择性腺苷 A2a 受体(A2aR)激动剂,可用于治疗眼部疾病、肿瘤和免疫系统疾病,可用于研究开角型青光眼和血液肿瘤。 | |||
T34914 |
Trabodenoson
INNO-8875,INO-8875,PJ875,PJ-875,INNO 8875,INNO8875,PJ 875 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Trabodenoson (INO-8875) 是一种具有选择性和有效性的的腺苷 A1 受体激动剂,是一种腺苷类似物,可用于研究原发性开角型青光眼。 | |||
T9847 |
TLC2976-0103
|
Others | Others |
ROCK1-IN-1 是一种ROCK1抑制剂,Ki 值为 540 nM。ROCK1-IN-1 可用于高血压、青光眼、勃起功能障碍的研究。 | |||
T16132 |
MRE3008F20
|
cAMP; Adenosine Receptor | GPCR/G Protein; Neuroscience |
MRE3008F20 是一种具有种属选择性和高效性的腺苷 A3 受体(AA3R)拮抗剂,抑制 Cl-IB-MECA 诱导的 cAMP 的产生,可用于研究青光眼和哮喘。 | |||
T20157 |
Brimonidine
AGN190342,溴莫尼定,Bromoxidine,AGN 190342,AGN-190342 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Brimonidine (Bromoxidine) 是一种完全的α2肾上腺素受体激动剂。 | |||
T6422 |
Brimonidine Tartrate
AGN190342 tartrate,304 tartrate,酒石酸溴莫尼定,AGN190342 (tartrate),UK 14304 (tartrate),UK14304 tartrate |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Brimonidine Tartrate (AGN190342 tartrate) 是一种 alpha2 Adrenergic Receptor (alpha2-AR) 受体激动剂。 | |||
T16389 |
Omidenepag
UR-7276 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Omidenepag (UR-7276) 是一种具有选择性和高效性的前列腺素 E2 受体 2 (EP2)激动剂,也是一种新型局部眼部降压药。Omidenepag可用于研究青光眼和高眼压症。 | |||
T0103 |
Dipivefrin hydrochloride
盐酸地匹福林,Dipivefrin HCL |
Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Dipivefrin hydrochloride (Dipivefrin HCl) 是抗青光眼前体药物,被角膜中的酯酶水解为其活性化合物肾上腺素。 | |||
T2538 |
Bimatoprost
AGN 192024,比马前列素 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Bimatoprost (AGN 192024) 是一种氯前列醇衍生的酰胺,用作治疗开角型青光眼和高眼压症的抗高血压药。 | |||
T3174 |
Taprenepag
CP-544326 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Taprenepag (CP-544326) 是一种有效的选择性前列腺素 E2 受体激动剂,EC50为 2.8 nM,可用于研究开角治疗高眼压和青光眼的试验。 | |||
T6565 |
Levobetaxolol hydrochloride
Betaxon,左旋倍他洛尔,(S)-Betaxolol hydrochloride,AL-1577A,Levobetaxolol HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Levobetaxolol hydrochloride ((S)-Betaxolol hydrochloride) 是 β-肾上腺素能受体抑制剂 (β阻滞剂) 。它具有降低眼压的作用,可用于研究青光眼。 | |||
T71138L |
Binospirone
MDL 73005EF |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Binospirone (MDL 73005EF) 是一种 5-HT1A 受体激动剂,具有抗焦虑活性,可用于研究青光眼和与神经功能障碍相关的运动障碍。 | |||
T5841 |
Travoprost
曲伏前列素,Flu-Ipr,Fluprostenol isopropyl ester,AL6221 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Travoprost (Fluprostenol isopropyl ester) 是一种异丙基酯前药,是一种高亲和力的,选择性的 FP 前列腺素全受体激动剂。它能够降低眼压,有潜力应用于青光眼和眼高压。 | |||
T60351 |
Acetazolamide sodium
OT-302 sodium |
Carbonic Anhydrase | Metabolism |
Acetazolamide sodium (OT-302 sodium) 是一种高效的碳酸酐酶 (CA)IX抑制剂,具有利尿、抗淋球菌和降压活性,可用于癫痫、青光眼、水肿和高原反应等适应症。 | |||
T21371 |
Apraclonidine hydrochloride
Iopidine,ALO 2145,Apraclonidina,P-aminoclonidine,4-Aminoclonidine,Apraclonidine HCl,Apraclonidinum |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Apraclonidine hydrochloride (ALO 2145) 是一种 α2-肾上腺素能激动剂和弱的 α-1 肾上腺素能受体激动剂。 Apaclonidine hydrochloride 可降低人眼的眼内压,可用于青光眼治疗的研究。 | |||
T76828 |
Sonepcizumab
LT 1009 |
LPL Receptor | GPCR/G Protein |
Sonepcizumab (LT 1009) 是一种完全人源化的抗 S1P 单克隆抗体。Sonepcizumab 具有抗癌活性,可用于研究转移性肾细胞癌 (mRCC) ,可预防青光眼滤过手术后的眼部瘢痕形成。 | |||
T15719 |
Latanoprostene bunod
LBN,NCX116 |
Others | Others |
Latanoprostene bunod (LBN) 是一氧化氮 (NO) 供体前列腺素 F2a 类似物,有用于开角型青光眼或高眼压 (OHT) 患者降低眼压 (IOP) 的局部眼科的研究潜力。 | |||
T77513 |
2-Chlorophenylboronic acid
|
FAAH | Metabolism; Neuroscience |
2-Chlorophenylboronic acid 是一种单卤代苯硼酸,是一种重要的医药中间体,在新药合成中应用广泛。2-Chlorophenylboronic acid 对脂肪酸酰胺酶有抑制作用,Ki 值为0.01-1 µM,可用于研究抑郁症、青光眼、神经性疼痛、焦虑、偏头痛、I 型糖尿病和胃炎等疾病。 | |||
T29708 |
Aganepag isopropyl
AGN-210961,AGN 210961,AGN210961 |
Others | Others |
Aganepag isopropyl can be used to treat Glaucoma. | |||
T32699 |
Levobunolol
Levobunololum,Liquifilm,AK-Beta,Betegan |
Others | Others |
Levobunolol is a nonselective beta-blocker. It is used topically to treat glaucoma. | |||
T0103L |
Dipivefrin
K 30081,K-30081,Dipivefrinum,Dipivefrina,K30081 |
Others | Others |
Dipivefrin is a prodrug of epinephrine, and is used to treat open-angle glaucoma. | |||
T28457 |
Proxodolol hydrochloride
|
Others | Others |
Proxodolol, a β-adrenergic receptor antagonist, is used potentially for the treatment of glaucoma, hypertension and angina. | |||
T71249 |
NCX-278
|
Others | Others |
NCX-278 is a ROCK inhibitor and NO-donating anti-glaucoma agent. | |||
T27518 |
GW-876167
PRX-00933,PNU-183933,GW876167,BVT933,BVT-933 |
Others | Others |
GW-876167, a 5-HT2C agonist, is used potentially for the treatment of obesity and glaucoma. | |||
T29811 |
AL-16049
AL 16049,AL16049 |
Others | Others |
AL-16049 is an FP-Class prostaglandin analog which may be useful in the treatment of glaucoma and ocular hypertension. | |||
T22743 |
Dorzolamide
|
Others | Others |
Dorzolamide is an anti-glaucoma agent and is a carbonic anhydrase inhibitor. | |||
T34644 |
Simenepag isopropyl
AGN210669,AGN-210669,AGN 210669 |
Others | Others |
Simenepag isopropyl can be used for the treatment of Glaucoma, Ocular Hypertension. | |||
T31600 |
Echothiophate Iodide
Phospholine iodide,Ecostigmini Sodidum,Iodide, Echothiophate,Echodide,Ecothiophate iodide |
Others | Others |
Echothiophate iodide is an effective long-acting cholinesterase inhibitor for the treatment of glaucoma. | |||
T71250 |
NCX-274
|
Others | Others |
NCX-274 is a ROCK inhibitor and NO-donating anti-glaucoma agent | |||
T31054 |
CP-432
CP432,CP734432,CP 734432,CP-734432 |
Others | Others |
CP-432 (CP-734432) is an EP4 prostaglandin agonist for the treatment of glaucoma and ocular hypertension. | |||
T20644 |
Unoprostone isopropyl
UF021,Rescula,UF-021,UF 021 |
Others | Others |
Unoprostone isopropyl, a prostanoid and synthetic docosanoid, is approved for the treatment of ocular hypertension and open-angle glaucoma. | |||
T19682 |
Levobetaxolol
(S)-(-)-Betaxolol,(S)-Betaxolol |
Others | Others |
Levobetaxolol, also known as AL-1577A and Betaxon, is a cardioselective β-adrenergic receptor inhibitor. It has been demonstrated to reduce intraocular pressure in patients affected by ocular hypertension and primary open-angle glaucoma. | |||
T27739 |
KR-31378
MSH1001,DNB 001,DNB-001,DNB001,MSH-1001,KR31378 |
Others | Others |
KR-31378, a K(ATP) channel activator, is used potentially for the treatment of ocular hypertension and glaucoma. | |||
T68756 |
Naboctate
|
Others | Others |
Naboctate is a synthetic cannabinoid receptor agonist. It has antiemetic, sedative, anxiolytic and anti-glaucoma properties. | |||
T71120 |
AR-13503
|
Others | Others |
AR-13503, is an metabolite of Netarsudil (AR-11324), is a Rho-associated protein kinase inhibitor. Netarsudil is potential useful for treating glaucoma and/or reducing intraocular pressure. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1540 |
Cyanidin-3,5-O-diglucoside chloride
|
Others | Others |
Cyanidin-3,5-O-diglucoside chloride 具有抗氧化活性。 Cyanidin-3,5-O-diglucoside 抑制高压诱导的 GLAST 降低,可用于青光眼研究。 Cyanidin-3,5-O-diglucoside chloride 在 >40°C 的温度下很容易通过水解和/或氢化降解。 | |||
T1287 |
Synephrine
辛弗林,Oxedrine |
Endogenous Metabolite; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Synephrine (Oxedrine) 是来自 Citrus aurantium 的α-adrenergic 和β-adrenergic 激动剂,是一种生物碱。它也是一种拟交感神经化合物,能够用于减肥。 | |||
T1231 |
Pilocarpine nitrate
匹鲁卡品硝酸盐,Pilagan,硝酸毛果芸香碱,Pilofrin |
AChR | Neuroscience |
Pilocarpine nitrate (Pilagan) 是 M3 型毒蕈碱乙酰胆碱受体激动剂,可用于治疗青光眼。 | |||
TN1465 |
Cannabigerol
|
NOS; 5-HT Receptor; ROS | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cannabigerol 是一种植物大麻素,是一种高亲和力 α2-肾上腺素能受体激动剂、中度亲和力 5-HT1A 受体拮抗剂和低亲和力 CB1/CB2受体拮抗剂。它可降低眼压,有潜力治疗青光眼。 | |||
T39168 |
Epsilon-(gamma-glutamyl)-lysine
Epsilon-(gamma-glutamyl)-lysine,γ-Glu-ε-Lys,H-Glu(H-Lys-OH)-OH |
Others | Others |
Epsilon-(gamma-glutamyl)-lysine is an N(6)-acyl-L-lysine derivative that forms bonds between extracellular matrix (ECM) components with the assistance of the enzyme tissue transglutaminase (tTg). These bonds are implicated in the pathogenesis of certain diseases like non-diabetic kidney and glaucoma filtration. | |||
T20636 |
Latrunculin B
LAT-B,LATB,NSC 339663,NSC339663,NSC-339663,LAT B,INS115644 |
Antifungal | Microbiology/Virology |
Latrunculin B 是一种 来自红海海绵的生物碱,是一种肌动蛋白聚合 (actin polymerization) 抑制剂,具有抗真菌和抗原生动物活性。Latrunculin B 调节肺静脉电生理特征并减轻牵张性心律失常的发生,可用于研究青少年青光眼。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02248 |
Myocilin Protein, Human, Recombinant (His)
myocilin, trabecular meshwork inducible glucocorticoid respo... |
Human | HEK293 Cells |
Myocilin, also known as Trabecular meshwork-induced glucocorticoid response protein, MYOC, and GLC1A, is a protein that contains one olfactomedin-like domain. Myocilin / MYOC may participate in the obstruction of fluid outflow in the trabecular meshwork. Myocilin / MYOC is expressed in large amounts in various types of muscle, ciliary body, papillary sphincter, skeletal muscle, heart, and other tissues. Myocilin / MYOC is expressed predominantly in the retina. In normal eyes, it is found in the ... | |||
TMPY-03501 |
Optineurin Protein, Human, Recombinant (His & GST)
optineurin,HIP7,ALS12,HYPL,TFIIIA-INTP,FIP2,NRP,GLC1E |
Human | Baculovirus Insect Cells |
OPTN (Optineurin) is a Protein Coding gene. The Optineurin gene encodes the coiled-coil containing protein optineurin. Optineurin is a multifunctional adaptor protein intimately involved in various vesicular trafficking pathways. Through interactions with an array of proteins, such as myosin VI, huntingtin, Rab8, and Tank-binding kinase 1, as well as via its oligomerization, optineurin can act as an adaptor, scaffold, or signal regulator to coordinate many cellular processes associated with the ... | |||
TMPJ-00680 |
ANGPTL7 Protein, Human, Recombinant (His)
CDT6,Cornea-derived transcript 6 protein,Angiopoietin-like p... |
Human | HEK293 Cells |
Angiopoietin-like 7 (ANGPTL7) is a secreted glycoprotein that is structurally related to the angiopoietins. Members of this protein family contain an N-terminal coiled coil domain and a C-terminal fibrinogen-like domain. ANGPTL7 shares 89% aa sequence identity with mouse and rat ANGPTL7. It is secreted as a 45-50kDa monomer that forms disulfide-linked homotrimers and tetramers via the coiled coil domain. ANGPTL7 is expressed in the corneal stroma, trabecular meshwork, and sclera and is elevated ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10544 |
Bimatoprost D5
AGN 192024 D5 |
Others | Others |
Bimatoprost (AGN 192024) D5 is a deuterium-labeled Bimatoprost. Bimatoprost is a topical hypotensive agent frequently used for treating glaucoma and ocular hypertension. | |||
T70186 |
Methazolamide-d6
|
||
Methazolamide-d6 is intended for use as an internal standard for the quantification of methazolamide by GC- or LC-MS. Methazolamide is a carbonic anhydrase inhibitor. It reduces intraocular pressure and cerebrospinal fluid flow in a rat model of glaucoma. Methazolamide reduces electroshock-induced seizures in rats with an ED50 value of 19.2 mg/kg. It also inhibits production of reactive oxygen species (ROS) in a primary cortical neuron (PCN) cellular model of subarachnoid hemorrhage (SAH) and re... | |||
T36059 |
Dichlorphenamide-13C6
Dichlorphenamide-13C6 |
||
Dichlorphenamide-13C6is intended for use as an internal standard for the quantification of dichlorphenamide by GC- or LC-MS. Dichlorphenamide is a sulfonamide and an orally bioavailable carbonic anhydrase (CA) inhibitor (Kis = 1.20, 38, 50, and 50 nM for the human CA isoforms CAI, CAII, CAIX, and CAXII, respectively).1It lowers intraocular pressure in rabbits when 50 μl of a 10% solution is applied topically to the eye.2Dichlorphenamide rescues the potassium deficiency and prevents insulin-induc... |