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Cat. No. | Product Name | Target | Signaling Pathways |
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T38128 |
Leukotriene D4
Leukotriene D4 MaxSpec® Standard,LTD4 |
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Leukotriene D4 (LTD4) is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A) produced by the metabolism of LTC4 by γ-glutamyl transpeptidase. It is the first cysteinyl-leukotriene metabolite of LTC4 . Like LTC4, LTD4-induced bronchoconstriction and enhanced vascular permeability contribute to the pathogenesis of asthma and acute hypersensitivity. LTD4 is equipotent to LTC4 in its biological activities, except that LTD4 is nearly 100-fold more effective in the contraction of... | |||
T37261 |
14,15-Leukotriene D4
14,15-Leukotriene D4 |
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14,15-Leukotriene D4 (14,15-LTD4) is a member of an alternate class of LTs synthesized by a pathway involving the dual actions of 15- and 12-lipoxygenases (15- and 12-LOs) on arachidonic acid via 15-HpETE and 14,15-LTA4 intermediates. 14,15-LTD4 is classified as an eoxin (EXD4), because it is formed mostly by eosinophils. However, mast cells and nasal polyps can synthesize 14,15-LTD4 as well. Little is known about the physiological actions of 14,15-LTD4. It has weak contractile activity on both ... | |||
T37493 |
11-trans Leukotriene D4
11-trans Leukotriene D4 |
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11-trans Leukotriene D4 (11-trans LTD4) is a C-11 double bond isomer of LTD4. LTD4 undergoes slow temperature-dependent isomerization to 11-trans LTD4 during storage. 11-trans LTD4 retains about 10-25 % of the potency for contraction of guinea pig ileum, trachea and parenchyma compared to LTD4. It exhibits an ED50 ranging between 12-60 nM for contraction of guinea pig trachea. | |||
T28529 |
RG 7152
RG7152,RG-7152 |
Leukotriene Receptor | GPCR/G Protein |
RG 7152 是白三烯 D4 拮抗剂,具有抗哮喘作用,可作用于研究哮喘。 | |||
T27979 |
Masilukast
ICI-D-3523,ZD-3523,ICI D-3523,MCC-847,SA-09012,D-3523 |
Leukotriene Receptor | GPCR/G Protein |
Masilukast(MCC-847) 是一种口服的白三烯D4 (LTD4) 受体拮抗剂,可用于研究与炎症相关的疾病。 | |||
T2583 |
Cilastatin
西司他丁,MK0791 |
Proteasome; Antibacterial; Antibiotic | Microbiology/Virology; Proteases/Proteasome; Ubiquitination |
Cilastatin (MK0791) 是一种可逆的竞争性的肾脏脱氢肽酶 I 抑制剂,IC50为 0.1 μM。它抑制细菌金属叶内酰胺酶CphA 的IC50为 178 μM,可用作抗菌辅助剂。 | |||
T23390 |
SR 2640 hydrochloride
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Leukotriene Receptor | GPCR/G Protein |
SR 2640 hydrochloride 是白三烯 D4 和 E4 的竞争性拮抗剂,可用于研究人类哮喘中的白三烯。 | |||
T6736 |
Zafirlukast
Vanticon,ICI 204219,Accolate,扎鲁司特 |
Leukotriene Receptor | GPCR/G Protein |
Zafirlukast (ICI 204219) 是一种可口服的白三烯 D4受体拮抗剂,具有平喘、抗炎和抗菌作用。 | |||
T1639 |
Amlexanox
氨来呫诺,CHX3673,Amoxanox,氨来诺,AA673 |
IL Receptor; FGFR; Others; IκB/IKK | Angiogenesis; Immunology/Inflammation; NF-κB; Others; Tyrosine Kinase/Adaptors |
Amlexanox (AA673) 是一种特异性的 IKKε和 TBK1抑制剂,其 IC50=1-2 μM。 | |||
T67959 |
Pirodomast
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Thrombin; Serine Protease | Proteases/Proteasome |
Pirodomast 是血栓素 A(TXA2)合成酶抑制剂。Pirodomast 能抑制白三烯(LT)D4、C4、E4 的形成和血栓素 B2(TXB2)的活性,但对组胺、甲氧胆碱、血清素、LTC4 或血小板活化因子诱导的豚鼠支气管痉挛的拮抗作用较弱或无效。Pirodomast 在体外对豚鼠气管只有微弱的松弛活性。Pirodomast 是一种潜在的抗过敏化合物,在体外可抑制胰蛋白酶的蛋白水解活性,在体内可阻止抗原诱发过敏绵羊的即时和晚期哮喘反应,抑制抗原诱导的过敏绵羊对组胺和卡巴胆碱的气道高反应性。 | |||
T27893 |
LY 203647
LY203647,LY-203647 |
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LY 203647 is a antagonist of leukotriene D4 and E4 receptor. | |||
T24304 |
L 648051
4-Apsob,L48051,L-648051 |
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L 648051 is a leukotriene D4 receptor antagonist. | |||
T2583L |
Cilastatin sodium
Cilastatinum,Cilastatin Monosodium Salt ;Cilastatin Sodium,Cilastatin Monosodium Salt,MK 791,Cilastatine,Cilastatin,Cilastatin Sodium,MK 0791 |
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Cilastatin is a renal dehydropeptidase-I and leukotriene D4 dipeptidase inhibitor. | |||
T71411 |
U 19052
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U 19052 is a Leukotriene D4 antagonist. | |||
T68195 |
SC 39070
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SC 39070 is a leukotriene D4 antagonist. | |||
T35112 |
WAY 126299A
WAY126299A,WAY-126299A |
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Way 126299a is a dual-acting 5-lipoxygenase inhibitor and leukotriene D4 antagonist. | |||
T10873 |
CP-96486
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Others | Others |
CP-96486 is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor (PAF) receptor (Kis: 20 and 24 nM). | |||
T11764 |
KP496
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Others | Others |
KP496 is a selective, dual antagonist for Thromboxane A2 receptor and Leukotriene D4 receptor. | |||
T10057 |
LTD4 antagonist 1
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Others | Others |
LTD4 antagonist 1 is a potent and orally active antagonist of leukotriene D4 (LTD4; Ki: 0.57 nM). | |||
T71039 |
MDL-28753
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MDL-28753 is an antagonist of leukotriene D4 and antagonist of leukotrine C4. | |||
T10872 |
CP-96021 hydrochloride
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Others | Others |
CP-96021 hydrochloride is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor receptor (Kis: 34 nM and 37 nM). | |||
T10054 | CI-949 | Others | Others |
CI-949 is an allergic mediator release inhibitor, which inhibits leukotriene C4/D4 (LTC4/LTD4), histamine, and thromboxane B2 (TXB2) release (IC50s: 0.5 μM, 11.4 μM and 0.1 μM). | |||
T12771 |
RS-601
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Leukotriene Receptor; Thrombin | GPCR/G Protein; Proteases/Proteasome |
RS-601 是一种有效的 leukotriene D4/thromboxane A2 双重抑制剂,对抗原诱导的气道高反应性 (AHR)有抑制作用且在豚鼠哮喘模型中显示出平喘作用。 | |||
T19674 |
Verlukast
MK 0679,MK-679,L 668,019,MK 679,L 668019,L-668,019 |
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Verlukast is an (R)-enantiomer of MK-571 and a potent and selective LTD4 receptor antagonist. Verlukast showed [3H]leukotriene D4 binding in guinea-pig (IC50 = 3.1 +/- 0.5 nM) and human (IC50 = 8.0 +/- 3.0 nM) lung homogenates and dimethyl sulfoxide diffe | |||
TMIH-0609 |
Zafirlukast-d7
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Zafirlukast-d7 是 Zafirlukast 的氘代化合物。Zafirlukast 的 CAS 号为 107753-78-6。Zafirlukast 是一种可口服的白三烯 D4受体拮抗剂,具有平喘、抗炎和抗菌作用。 | |||
T36618 |
Rupatadine
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Rupatadine (UR-12592) is a potent dual PAF/H1 antagonist with Ki of 0.55/0.1 uM(rabbit platelet membranes/guinea pig cerebellum membranes).IC50 value:Target: PAF/H1 antagonistin vitro: Rupatadine competitively inhibited histamine-induced guinea pig ileum contraction (pA2 = 9.29 +/- 0.06) without affecting contraction induced by ACh, serotonin or leukotriene D4 (LTD4). It also competitively inhibited PAF-induced platelet aggregation in washed rabbit platelets (WRP) (pA2 = 6.68 +/- 0.08) and in hu... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN5180 |
Triptinin B
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Others | Others |
Triptinin A and triptinin B are leukotriene D4 antagonist constituents. |