找到约 36 条 “CaLL” 相关结果 （用时 0.088 秒）
| 目录号 | 产品名称 | 中文名称 | 靶点 |
|---|---|---|---|
| M45241 | Ecallantide | 艾卡拉肽 | Others |
| Ecallantide是一种有效的，选择性的重组血浆激肽释放酶抑制剂，能抑制缓激肽的产生。 | |||
| M17356 | Callosin | Callosin | Phenols |
| Callosin | |||
| M17662 | 3-Oxo-24,25,26,27- tetranortirucall-7-en-23,21-olide | 3-Oxo-24,25,26,27- tetranortirucall-7-en-23,21-olide | Triterpenoids |
| 3-Oxo-24,25,26,27- tetranortirucall-7-en-23,21-olide | |||
| M17676 | 3-Oxotirucalla-7,24-dien-21-oic acid | 3-Oxotirucalla-7,24-dien-21-oic acid | Triterpenoids |
| 3-Oxotirucalla-7,24-dien-21-oic acid | |||
| M17678 | 24,25-Epoxytirucall-7-en-3,23-dione | 24,25-Epoxytirucall-7-en-3,23-dione | Triterpenoids |
| 24,25-Epoxytirucall-7-en-3,23-dione | |||
| M17735 | Triptocallic acid A | Triptocallic acid A | Triterpenoids |
| Triptocallic acid A | |||
| M17990 | 3alpha-Hydroxytirucalla-7,24-dien-21-oic acid | 3alpha-Hydroxytirucalla-7,24-dien-21-oic acid | Others |
| 3α-Hydroxytirucalla-7,24-dien-21-oic acid 是一种三萜化合物，可从 Protium hebetatum Daly 的油树脂中分离得到。 | |||
| M39869 | 3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone | 3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone | Others |
| 3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone 是从大叶蝉的茎皮中分离出的一种细胞毒性的 tirucallane C26 三萜类化合物。 | |||
| M44559 | Caffeoylcalleryanin | 咖啡酰基鹿梨苷 | Others |
| 咖啡酰基鹿梨苷 | |||
| M44572 | Calleryanin | 鹿梨苷 | Others |
| 鹿梨苷 | |||
| M44611 | Protocatechuoylcalleryanin-3-O-beta-glucopyranoside | 原儿茶酰鹿梨苷-3-O-beta-葡萄糖苷 | Others |
| 原儿茶酰鹿梨苷-3-O-beta-葡萄糖苷 | |||
| M53550 | CaLL | CaLL | Antibiotic |
| CaLL 是一种抗菌肽。 | |||
M55374
|
Recombinant Human Neprilysin (HEK293, N-8His) | 重组人Neprilysin 蛋白 (HEK293, N-8His) | Cytokines and Growth Factors |
| MME; Atriopeptidase; CALLA; Enkephalinase; SFE; CD10 | |||
| Neprilysin/CD10 (MME; NEP) is a zinc metallopeptidase expressed at the cell surface of a variety of cells. Neprilysin/CD10 (MME) has been shown to be involved in the degradation of enkephalins in the mammalian brain and the inactivation of circulating atrial natriuretic peptide. | |||
| M2538 | Colistin methanesulfonate sodium salt | Colistin methanesulfonate sodium salt | Antibiotic |
| Colistimethate Sodium | |||
| Colistin methanesulfonate sodium salt is the inactive prodrug of colistin, has been given intrathecally and intraventricularly in Acinetobacter baumanii and Pseudomonas aeruginosa meningitis/ventriculitis. | |||
| M2939
|
Physostigmine Salicylate | 水杨酸毒扁豆碱 | AChR/AChE |
| Eserine Salicylate | |||
| Physostigmine is a parasympathomimetic alkaloid, specifically, a reversible cholinesterase inhibitor. | |||
| M40957
|
Recombinant Human IL-22 Protein (HEK293) | 重组人IL-22蛋白 (HEK293) | Cytokines and Growth Factors |
| Interleukin-22 | |||
| Interleukin-22(IL-22) belongs to a group of cytokines called the IL-10 family or IL-10 superfamily. IL-22 is produced by activated DC and T cells and initiates innate immune responses against bacterial pathogens in epithelial cells such as those in the lung and gut. | |||
| M7328 | SR 33805 oxalate | SR 33805 oxalate | Others |
| SR 33805 oxalate is a ca 2+ channel blocker; binds allosterically to distinct site on L-type channels. | |||
| M7368 | TC-E 5008 | TC-E 5008 | Others |
| TC-E 5008 is a selective mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor; phenotypically lethal. | |||
| M7731 | CHIC-35 | CHIC-35 | Others |
| CHIC-35 is cell-permeable, metabolically stable, and very potent inhibitor of SIRT1; IC50 of S-isomer is 60 nM; IC50 of mixed isomers is 124 nM. | |||
| M7987
|
N-Oleoylglycine | N-Oleoylglycine | Metabolite/Endogenous Metabolite |
| Enzymatically produced in mammals. | |||
| M8143 | Razoxane | 丙亚胺；抗癌散 | Others |
| Razoxane is clinically active against angiogenesis and metastasis. | |||
| M8313
|
CZC-25146 hydrochloride | CZC-25146 hydrochloride | LRRK2 |
| CZC-25146 is a potent selective and metabolically stable inhibitor of leucine-rich repeat kinase-2 (LRRK2) also known as dardarin or PARK8, a kinase with mutations linked to Parkinson’s disease. | |||
| M8320 | CUR61414 | CUR61414 | Others |
| CUR61414 specifically binds to, and antagonizes the activity of smoothened (Smo) in the hedgehog signaling pathway. | |||
| M8378 | DCAP | DCAP | Others |
| DCAP is a potent broad-spectrum antibiotic that specifically targets the membranes of both Gram-positive and Gram-negative bacteria. | |||
| M8610 | UPCDC30245 | UPCDC30245 | Others |
| UPCDC30245 is an allosteric inhibitor of AAA ATPase p97, also called valosine containing protein (VCP). | |||
| M8644 | Beraprost sodium | 贝前列素钠 | Others |
| Beraprost sodium is a chemically stable analog of prostacyclin PGI2. | |||
| M9472
|
Hydroxyhexamide | Hydroxyhexamide | Metabolite/Endogenous Metabolite |
| (±)-Hydroxyhexamid | |||
| Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents. | |||
| M15001 | Noreugenin | Noreugenin | Others |
| Noreugenin，是一种色酮，源于 Hymenocallis littoralis Salisb (石蒜科)。 | |||
| M17955 | (13alpha,14beta,17alpha,20S)-5alpha-Lanosta-8,24-Dien-3beta-Ol | 表大戟二烯醇 | Others |
| Tirucallol 是一种从 Euphorbia lacteal 乳胶中分离得到的四环三萜。 | |||
| M18025 | Quercetin 3-O-rutinoside-7-O-glucoside | 槲皮素3-O-芸香苷-7-O-葡萄糖苷 | Others |
| Quercetin 3-O-rutinoside-7-O-glucoside (化合物 8) 是一种抗氧化剂，存在于 Hemerocallis fulva 中。 | |||
| M19873
|
Sulfacetamide | Sulfacetamide | Antibiotic |
| Sulfacetamide Sodium is an anti-infective agent that is used topically to treat skin infections and orally for urinary tract infections. | |||
| M20408 | 2-Methoxy-1,4-naphthoquinone | 2-Methoxy-1,4-naphthoquinone | PKC |
| 2-Methoxy-1,4-naphthoquinone, isolated from the leaves of Impatiens glandulifera, specifically suppressed the expression of PKC βI, δ, and ζ in a concentration-dependent manner in Raji cells. | |||
| M20409 | Levamlodipine | Levamlodipine | Calcium Channel |
| S-amlodipine | |||
| Levamlodipine is a pharmacologically active enantiomer of amlodipine which belongs to the dihydropyridine group of calcium channel blocker. It acts on the L-type of calcium channels and its treatment results in vasodilation and a fall in blood pressure. | |||
| M20431 | Menadiol Diacetate | Menadiol Diacetate | Vitamin |
| Vitamin K4, Acetomenaphthone, Kapilin | |||
| Menadiol Diacetate (Vitamin K4) is a synthetic hydrophilic menadione compound, which is clinically used as hemostasis medicine. It induces caspase-3-related apoptosis pathway via mitochondrial dysfunction and DNA fragmentation. | |||
| M20464
|
Atrazine | Atrazine | Others |
| Chromozin, Oleogesaprim, Aktikon, Gesaprim | |||
| Atrazine is a selective triazine herbicide. Atrazine is also a potent endocrine disruptor that is active at low, ecologically relevant concentrations. | |||
| M20518 | Orphenadrine Hydrochloride | Orphenadrine Hydrochloride | Others |
| A muscarinic receptor antagonist, specifically an H1 histamine receptor antagonist. This compound is a muscle relaxant. Orphenadrine has also been reported to inhibit the noradrenergic transporter and to block the NMDA receptor ion channel. | |||
