106
9
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T36220 |
2,3-dinor Thromboxane B1
2,3-dinor Thromboxane B1 |
||
Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2. In rats and rabbits, 2,3-dinor TXB1 has been identified as another urinary metabolite of TXB2. However in human urine, only trace amounts of 2,3-dinor TXB1 have been identified. In rats, 2,3-dinor TXB1 is excreted at a much higher rate than 2,3-dinor TXB2 (19.2 ± 4.9 ng/24 hr and 1.6 ± 0.3 ng/24 hr, respectively). Therefore, urinary 2,3-... | |||
T36208 |
15(R)-Pinane Thromboxane A2
15(R)-Pinane Thromboxane A2 |
||
15(R)-Pinane thromboxane A2 is the (R)-epimer of pinane thromboxane A2 . 15(R)-PTA2 does not inhibit collagen-induced platelet aggregation (IC50s = 120-130 μM). It does not affect gastric tone in isolated rat gastric fundus when used at concentrations of 0.5 or 1.5 μg/ml and is less effective than PTA2 at inhibiting prostaglandin-induced contraction of isolated rat stomach muscle. | |||
T41246 | Thromboxane B2 | ||
Thromboxane B2 是一种在过敏反应期间释放的前列腺素衍生物。Thromboxane B2 诱导动脉收缩和血小板聚集。 | |||
T36548 |
Carbocyclic Thromboxane A2
|
||
Carbocyclic Thromboxane A2 可用于生命科学领域的相关研究。其产品编号为 T36548,CAS号为 74034-56-3。 | |||
T34862 |
Thromboxane A2
Rabbit aorta contracting substance,TXA-2,TXA2,TXA 2 |
||
Thromboxane A2, as an unstable intermediate between the prostaglandin endoperoxides and thromboxane B2, is a potent inducer of platelet aggregation and causes vasoconstriction. | |||
T73855 |
Thromboxane B1
|
||
Thromboxane B1 (TXB1) 是TXB家族中的一员,属于类花生酸脂质家族。该家族因参与血栓形成而得名。 | |||
T12268 |
NTP42
|
Prostaglandin Receptor; PPAR | DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism |
NTP42 是血栓素 A2 (TXA2) 受体的拮抗剂,IC50为 3.278 nM,可用于肺动脉高压的相关研究。 | |||
T6236 |
Ozagrel
奥扎格雷,OKY-046,Domenan |
Thrombin; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Proteases/Proteasome |
Ozagrel (Domenan) 是血栓烷 A2(TXA2) 合酶抑制剂,可抑制哮喘。它也是一种抗血小板剂,可选择性抑制人血小板聚集,IC50为 53.12 μM。 | |||
T6625 |
Ozagrel hydrochloride
Ozagrel HCl,盐酸奥扎格雷,OKY-046 HCl |
Thrombin; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Proteases/Proteasome |
Ozagrel hydrochloride (OKY-046 HCl) 是一种选择性血栓素 A(2) 合成酶抑制剂,用于改善术后脑血管收缩和伴随的脑缺血。它是一种抗血小板剂,可选择性抑制人血小板聚集,IC50为 53.12 μM。 | |||
T11339 |
Furegrelate sodium
U-63557A |
PPAR | DNA Damage/DNA Repair; Metabolism |
Furegrelate sodium (U-63557A) 是口服有效的、血栓素合酶选择性抑制剂,抑制人血小板微粒体血栓素 A2 (TxA2) 合酶的 IC50为 15 nM。它正在开发作为抗血小板药物。 | |||
T17039 |
Terbogrel
BIBV 308SE |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Terbogrel 是一种可口服的 、具有选择性 thromboxane A2 受体拮抗剂(IC50 约为 10 nM),是一种 thromboxane A2 synthase 抑制剂(IC50 约为 10 nM)。Terbogrel 是一种抗血小板化合物,可抑制血小板聚集,是预防血栓的潜在化合物。 | |||
T25741 |
Linotroban
HN 11500,CL-871502 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Linotroban(CL-871502) 是一种有效的选择性血栓素(TXA2)受体拮抗剂,具有抗血栓活性。 | |||
T67958 |
Pirmagrel
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
pirmagrel 是一种强效的血栓素合酶抑制剂。 | |||
T15049 |
Daltroban
BM-13505,SKF 96148 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Daltroban (SKF 96148) (BM-13505) 是选择性和特异性的血栓素 A2 (TXA2) 受体拮抗剂。Daltroban 可以增加血管平滑肌细胞内钙。Daltroban 显示对再灌注损伤的保护作用。 | |||
T5505 |
Terutroban
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Terutroban 是有效的血栓素-前列腺素受体拮抗剂。 | |||
T7968 |
Dazoxiben
UK-37248,达唑氧苯 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Dazoxiben (UK-37248) 是口服具有活性的血栓烷合酶抑制剂。 | |||
T31213 |
Dazmegrel
UK-38,485,UK 38485,UK 38,485,UK38,485,UK-38485 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Dazmegrel (UK 38,485) 是一种强效特异性血栓素 A2(TXA2)合成酶抑制剂,可用于预防正常妊娠中全血小板聚集增加。 | |||
T24542 |
NP-313
NP 313,NSC 4264,NSC-4264,NSC4264 |
||
NP-313 (NSC-4264) 是一种有效的抗血栓剂,对血栓素 A 2 合成和选择性抑制由 SOCC 介导的 Ca 2+ 内流有抑制作用,可以抑制血小板的聚集和活化。 | |||
T11339L |
Furegrelate
|
PPAR | DNA Damage/DNA Repair; Metabolism |
FUREGRELATE 是一种血栓素 A2 (TxA2) 合酶抑制剂,可减缓新生仔猪肺动脉高压的发展。 | |||
T15577 |
Indobufen
Ibustrin,吲哚布芬 |
COX | Immunology/Inflammation; Neuroscience |
Indobufen (Ibustrin) 是一种血小板聚集抑制剂,是下调单核细胞中的组织因子,可逆抑制血小板环氧合酶 (Cox) 的活性和血栓素 A2 (TxA2) 的合成。 | |||
T27630 |
Isbogrel
CV4151,CV-4151,CV 4151 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Isbogrel (CV4151)是一种小分子血栓素A2合成酶(TXA2 synthase)抑制剂,可用来研究心律失常、短暂性脑缺血发作和血栓形成。 | |||
T68022L |
Sulotroban potassium
BM 13177 potassium,Sulotroban potassium(72131-33-0 Free base) |
PPAR | DNA Damage/DNA Repair; Metabolism |
Sulotroban potassium 是一种小分子血栓素A2受体(TXA2R)拮抗剂,可用于研究心肌梗塞和血栓形成。 | |||
T0839 |
Ketoprofen
酮基布洛芬,RP-19583,酮洛芬 |
Apoptosis; COX; MRP | Apoptosis; Immunology/Inflammation; Neuroscience |
Ketoprofen (RP-19583) 是一种非甾体抗炎剂,能够有效地抑制COX 的活性,在人血单核细胞中,对 COX-1 和 COX-2 的IC50值分别为 2 nM 和 26 nM。 | |||
T11825 |
LCB-2853
|
PPAR | DNA Damage/DNA Repair; Metabolism |
LCB-2853 是一种有效的血栓素 A2/前列腺素 H2 (TXA2/PGH2) 受体拮抗剂,具有抗血小板聚集、抗血管痉挛和抗血栓作用。 | |||
T0212 |
Seratrodast
塞曲司特,AA 2414,ABT-001 |
COX; Prostaglandin Receptor; PPAR | DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Seratrodast (ABT-001) 是一种血栓素 A2 受体 (TP) 拮抗剂,用于治疗哮喘。 | |||
T2396 |
Ramatroban
BAY u3405,雷马曲班 |
GPR; Prostaglandin Receptor; PPAR | DNA Damage/DNA Repair; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism |
Ramatroban (BAY u3405) 是一种血栓素 A(2) (TxA(2)) 拮抗剂,IC50为 14 nM。它还通过抑制PGD2结合从而拮抗CRTH2,IC50为113 nM。它用于治疗过敏性鼻炎,可用于治疗哮喘的研究。 | |||
TQ0145 |
(R)-(+)-Bay-K-8644
(R)-(+)-Bay K 8644 |
Calcium Channel; PPAR | DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
(R)-(+)-Bay-K-8644 是一种 Ca2+ 通道激动剂,是二氢吡啶激动剂,抑制 Ba2+电流 (IBa),诱导猫的中枢性呼吸抑制,通过竞争性拮抗血栓素 A2-前列腺素 H2 受体抑制血小板活化。 | |||
T1002 |
Etodolac
Ultradol,AY-24236,依托度酸,Etodolic acid,Lodine |
Retinoid Receptor; COX | Immunology/Inflammation; Metabolism; Neuroscience |
Etodolac (AY-24236) 是一种吡喃羧酸和非甾体抗炎药,具有解热和镇痛活性,对 COX 的 IC50为53.5 nM。 | |||
T68086 |
Imitrodast
|
Thrombin | Proteases/Proteasome |
Imitrodast是一种小分子血栓素A2合成酶(TXA2 synthase)抑制剂,可用于治疗免疫系统疾病、呼吸系统疾病和心血管疾病,可用于研究动脉血栓形成、哮喘和冠状血管痉挛。 | |||
T68130 |
Pobilukast
SKF 104353 Z2,SKF 104353 |
Leukotriene Receptor | GPCR/G Protein |
Pobilukast (SKF 104353) 是一种选择性半胱氨酰白三烯受体拮抗剂,可阻断磷脂酰肌醇代谢和白三烯D诱导的血栓素合成,可用于研究过度心肌再灌注损伤 (MI/R) 大鼠限制心肌损伤。 | |||
T67959 |
Pirodomast
|
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。 | |||
T34986 |
UK 14819
UK-14819,UK14819 |
||
UK 14819 is a selective thromboxane inhibitor. | |||
T70936 |
CGS 22652
|
||
CGS 22652 has thromboxane receptor antagonism combined with thromboxane synthase inhibition. | |||
T24298 |
L 641953
L-641953,L641953 |
||
L 641953 is an antagonist of the thromboxane receptor. | |||
T22896 |
L-655,240
|
Others | Others |
L-655,240 is a thromboxane A2/prostaglandin endoperoxide receptor antagonist. | |||
T68199 | Nafagrel | ||
Nafagrel is a thromboxane A2 synthetase inhibitor. | |||
T68754 |
N.0096
|
||
N.0096 is a thromboxane synthesis inhibitor. | |||
T71027 | KDI-792 hydrochloride | ||
KDI-792 hydrochloride is a thromboxane dual blocker. | |||
T70541 | IS-145 | ||
IS-145 is a thromboxane A2 receptor antagonist. | |||
T71511 |
ICI-185282
|
||
ICI-185282 is a potent thromboxane receptor antagonist. | |||
T23670 |
AH 22921
AH22921,AH-22921 |
||
AH 22921 is an antagonist of thromboxane A2. | |||
T68287 |
Indobufen sodium
|
||
Indobufen sodium is a Thromboxane A2 antagonist and Cyclooxygenase inhibitor. | |||
T15252 |
Etersalate
Etherylate,Eterylate |
Others | Others |
Etersalate inhibits platelet function. It also reduces thromboxane A2 (TXA2) levels. | |||
T25710 |
LG 82-4-01
LG-82-4-01,L82401,Lg-82401,LG82-4-01 |
||
LG 82-4-01 is an inhibitor of thromboxane (TX) synthetase. | |||
T70871 | Mipitroban | ||
Mipitroban is a thromboxane A2/prostaglandin H2 antagonist. | |||
T70966 |
GR-36246
|
||
GR-36246 is a Thromboxane A2-receptor blocker. | |||
T28176 |
Nizofenone
Y9179,Y-9179,Ekonal,Y 9179 |
||
Nizofenone, a thromboxane A2 (TXA2) biosynthesis inhibitor, is used as a neuroprotective drug and used to treat stroke. | |||
T70561 | FCE-24265 | ||
FCE-24265 is a calcium & thromboxane A2 synthase inhibitor. | |||
T70737 | HN 11500 | ||
HN 11500 is an antithrombotic agent and thromboxane A2 receptor antagonist. | |||
T71568 |
Wy 27569
|
||
Wy 27569 is is a combined calcium channel blocker and thromboxane synthetase inhibitor. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2964 |
2,3,5,4'-Tetrahydroxystilbene 2-O-β-D-glucoside
芪多酚,2,3,4',5-Tetrahydroxystilbene 2-O-D-glucoside,2,3,5,4'-Tetrahydroxystilbene-2-O-b-D-glucopyranoside,Astragalus polyphenols |
Others | Others |
2,3,5,4'-Tetrahydroxystilbene 2-O-β-D-glucoside (Astragalus polyphenols) 是分离自蓼属植物物种的根中,对5-HETE、HHT、thromboxane B2的形成具有抑制作用。 | |||
TN1957 |
Mulberrofuran Q
MulberrofuranQ |
||
Mulberrofuran Q是一种有活性的化合物,可抑制12-羟基-5,8,10-十七碳三烯酸(HHT)和血栓烷B2(环加氧酶产物)的形成 ,可保护神经细胞免受缺氧-缺糖(OGD)诱导的氧化应激的影响。 | |||
T7053 |
p-Hydroxycinnamic acid
p-Coumaric acid,p-Cumaric acid,p-Hydroxy-cinnamic acid,对羟基肉桂酸,NSC 59260 |
Thrombin; Endogenous Metabolite; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Proteases/Proteasome |
p-Hydroxycinnamic acid (NSC-59260) 是常见的食用酚,可抑制血小板活性,对血栓素 B2 和前列腺素 E2 的 IC50值分别为 371 和 126 μM。 | |||
T4740 |
Elaidic acid
反油酸,trans-Oleic Acid |
Endogenous Metabolite | Metabolism |
Elaidic acid (trans-Oleic Acid) 是在氢化植物油中发现的主要反式脂肪,能够被用作药物溶剂。在与花生四烯酸孵育的人类血小板中,反油酸抑制 HHT 和 HETE 的形成,同时诱导前列腺素和血栓素的合成。 | |||
T36831 |
9-Oxononanoic Acid
9-ONA |
Phospholipase; CPT | Metabolism |
9-Oxononanoic Acid是一种氧化脂肪酸,由亚油酸自氧化形成,它能提高磷脂酶 A2(PLA2)的活性,并增加离体人体血浆中血栓素 B2 的生成。9-Oxononanoic Acid 能减少肝脏新脂肪酸的合成,并提高大鼠肝脏肉碱棕榈酰转移酶(β-氧化的标志物)的活性。 | |||
TN5939 |
Glutinone
赤杨酮,5-Glutinen-3-one |
||
Glutinone (IC50=24 microM) shows a significant effect on thromboxane B2 (TXB2)-release induced by calcium ionophore in human platelets. | |||
TN2040 |
Panaxynol
|
BCL; Caspase; HIF | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Proteases/Proteasome |
Panaxynol is the most potent antiplatelet agent in ginseng and its mechanism of action is chiefly due to the inhibition of thromboxane formation. | |||
TMA1944 |
Protopine hydrochloride
|
EGFR; cAMP | Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Protopine has antiplatelet effects,which is due to inhibition on thromboxane formation and phosphoinositides breakdown and then lead to the decrease of intracellular calcium concentration.Protopine seems to inhibit the heterotypic cell adhesion between MD | |||
TN4586 |
Mulberrofuran A
|
COX | Immunology/Inflammation; Neuroscience |
Mulberrofuran A can inhibit the formations of 12-hydroxy-, 8, 10-heptadecatrienoic acid (HHT) and thromboxane B2, but it can increase the formation of 12-hydroxy-5, 8, 10, 14-eicosatetraenoic acid (12-HETE). |