Lipoxygenase
Lipoxygenase(脂氧合酶)
Lipoxygenases (LOXs) are dioxygenases that catalyze the formation of corresponding hydroperoxides from polyunsaturated fatty acids such as linoleic acid and arachidonic acid. Thre are six LOX isoforms have been found in the humans and mice. 5-Lipoxygenase (5-LOX) is a distinct isoform playing an important role in asthma and inflammation. 5-LOX causes the constriction of bronchioles in response to cysteinyl leukotrienes such as LTC4, thus leading to asthma. 5-LOX also induces neutrophilic inflammation by its recruitment in response to LTB4. 12-Lipoxygenase (12-LOX) is an isoform expressed in epithelial cells and myeloid cells including platelets. 12-LOX can be found in the epithelial cells of the skin. 12-LOX is a potential target for novel anti-platelet therapeutics.15-Lipoxygenase (15-LOX) is expressed in epithelial cells and leukocytes, has different substrate specificity in the humans and mice.15-LOX-1 is a target of nonsteroidal anti-inflammatory drug-induced apoptosis in colorectal cancer cells.
Lipoxygenase 相关产品(254)
- GC302774',5-DihydroxyflavoneCAS: 6665-67-4
4',5-Dihydroxyflavone inhibits soybean LOX-1 and yeast α-glucosidase.
- GC31947ICI 211965 (ZM-211965)CAS: 129424-08-4
ICI 211965 (ZM-211965) (ZM-211965) 是一种选择性和口服有效的 5-脂氧合酶 (5-LPO) 抑制剂。
- GC31978Lonapalene (RS4317)CAS: 91431-42-4纯度: >99.00%
Lonapalene (RS4317) (RS4317) 是一种局部有效的 5-脂氧合酶 (5-LO) 抑制剂。
- GC319975-Lipoxygenase-In-1CAS: 125235-15-6
5-Lipoxygenase-In-1是5-脂氧合酶抑制剂,来自专利EP331232A2,table4,化合物实例4.10。
- GC32038PGS-IN-1 (KME-4)CAS: 102271-49-8纯度: >99.50%
PGS-IN-1 (KME-4) 是一种有效的前列腺素合成酶 (PGS) 抑制剂,IC50 为 0.28 μM;也抑制 5-脂氧合酶,IC50 为 1.05 μM.
- GC36516LycopodineCAS: 466-61-5
Lycopodine,一种石松 (Lycopodium clavatumspores) 孢子重要的生物活性成分,通过调节难治性前列腺癌细胞中 5-脂氧合酶 (5-lipoxygenase),极化线粒体膜电位而不调节 p53 活性来诱导细胞凋亡。 Lycopodine 通过激活 caspase-3 诱导细胞凋亡来抑制 HeLa 细胞的增殖。
- GC36883PF-4191834CAS: 1029317-21-2纯度: >98.00%
PF-4191834 (PF-04191834) 是一种具有口服活性的,非铁螯合的,非氧化还原的 5-脂氧合酶 (5-LOX) 抑制剂(IC50=229 nM),PF-4191834 对 5-LOX 的选择性约是 12-LOX 和 15-LOX 的 300 倍,对环氧合酶没有活性,对炎症和疼痛有效。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC30277 | 4',5-Dihydroxyflavone | 6665-67-4 | - | |
4',5-Dihydroxyflavone inhibits soybean LOX-1 and yeast α-glucosidase. | ||||
| GC30610 | LY 178002 | 107889-32-7 | - | |
LY178002是一种有效的5-lipoxygenase,phospholipaseA2抑制剂,对5-lipoxygenase的IC50值为0.6μM,能够抑制人多形核白细胞产生LTB4,同时可相对较弱地抑制cyclooxygenase的活性。 | ||||
| GC31235 | Cirsiliol | 34334-69-5 | - | |
A flavonoid with diverse biological activities | ||||
| GC31707 | Chebulagic acid | 23094-71-5 | >98.00% | |
A polyphenol with diverse biological activities | ||||
| GC31801 | Enazadrem | 107361-33-1 | - | |
Enazadrem是有效的5-脂氧合酶(5-lipoxygenase)抑制剂,具有抗炎功效。 | ||||
| GC31813 | RWJ 63556 | 190967-35-2 | - | |
RWJ63556是一种可口服的COX-2selective/5-lipoxygenase抑制剂,具有抗炎活性。 | ||||
| GC31835 | S-2474 | 158089-95-3 | - | |
S-2474是COX-2和5-lipoxygenase的抑制剂,在人完整的细胞中,对COX-2和COX-1的IC50值分别为11nM和27μM,为一种非甾体抗炎药。 | ||||
| GC31938 | A-69412 | 123606-23-5 | - | |
A-69412是一种特异性的、亲水性5-脂氧合酶(5-LO)的可逆抑制剂。 | ||||
| GC31940 | Docebenone (AA 861) | 80809-81-0 | >99.00% | |
A 5-LO inhibitor | ||||
| GC31947 | ICI 211965 (ZM-211965) | 129424-08-4 | - | |
ICI 211965 (ZM-211965) (ZM-211965) 是一种选择性和口服有效的 5-脂氧合酶 (5-LPO) 抑制剂。 | ||||
| GC31961 | CMI977 (LDP977) | 175212-04-1 | - | |
CMI977 (LDP977) 是一种有效的 5-脂氧合酶 (5-LO) 抑制剂。 | ||||
| GC31967 | COX/5-LO-IN-1 | 154355-75-6 | - | |
COX/5-LO-IN-1是cylooxygenase和5-lipoxygenase的抑制剂,用于炎症性和过敏性疾病的研究。 | ||||
| GC31978 | Lonapalene (RS4317) | 91431-42-4 | >99.00% | |
Lonapalene (RS4317) (RS4317) 是一种局部有效的 5-脂氧合酶 (5-LO) 抑制剂。 | ||||
| GC31997 | 5-Lipoxygenase-In-1 | 125235-15-6 | - | |
5-Lipoxygenase-In-1是5-脂氧合酶抑制剂,来自专利EP331232A2,table4,化合物实例4.10。 | ||||
| GC32002 | Bunaprolast (U66858) | 99107-52-5 | - | |
Bunaprolast (U66858) (U66858) 是人类全血中产生 LTB4 的有效抑制剂。 | ||||
| GC32035 | AZD 4407 (ZD 4407) | 166882-70-8 | - | |
AZD 4407 (ZD 4407) 是一种有效的 5-脂氧合酶抑制剂。 | ||||
| GC32038 | PGS-IN-1 (KME-4) | 102271-49-8 | >99.50% | |
PGS-IN-1 (KME-4) 是一种有效的前列腺素合成酶 (PGS) 抑制剂,IC50 为 0.28 μM;也抑制 5-脂氧合酶,IC50 为 1.05 μM. | ||||
| GC33905 | CMI-392 | 205654-37-1 | - | |
CMI-392是一种双重5-lipoxygenese抑制剂和血小板活化因子(PAF)受体拮抗剂,IC50值分别为100和10nM。 | ||||
| GC33907 | LP117 | 1056468-55-3 | - | |
LP117是一种新型且有效的5-脂氧合酶(5-LO)产品合成抑制剂,其IC50值为1.1μM。 | ||||
| GC35168 | 5-O-Demethylnobiletin | 2174-59-6 | >99.50% | |
A flavonoid with diverse biological activities | ||||
| GC35425 | Atreleuton | 154355-76-7 | - | |
A 5-LO inhibitor | ||||
| GC36516 | Lycopodine | 466-61-5 | - | |
Lycopodine,一种石松 (Lycopodium clavatumspores) 孢子重要的生物活性成分,通过调节难治性前列腺癌细胞中 5-脂氧合酶 (5-lipoxygenase),极化线粒体膜电位而不调节 p53 活性来诱导细胞凋亡。 Lycopodine 通过激活 caspase-3 诱导细胞凋亡来抑制 HeLa 细胞的增殖。 | ||||
| GC36628 | ML355 | 1532593-30-8 | >98.00% | |
A selective 12-LO inhibitor | ||||
| GC36883 | PF-4191834 | 1029317-21-2 | >98.00% | |
PF-4191834 (PF-04191834) 是一种具有口服活性的,非铁螯合的,非氧化还原的 5-脂氧合酶 (5-LOX) 抑制剂(IC50=229 nM),PF-4191834 对 5-LOX 的选择性约是 12-LOX 和 15-LOX 的 300 倍,对环氧合酶没有活性,对炎症和疼痛有效。 | ||||
