93
27
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14007 |
PAF-AN-1
|
PAFR | GPCR/G Protein |
PAF-AN-1是一种新型有效的血小板激活因子受体 (PAF) 拮抗剂,参与研究过敏性死亡。 | |||
T21547 |
PAF (C16)
C16-PAF |
ERK; MEK; MAPK; Endogenous Metabolite | MAPK; Metabolism |
PAF (C16) 是有效的 MAPK 和 MEK/ERK 激活剂,可诱导血管通透性增加。PAF (C16) (PAF (C16)) 是血小板活化因子,是一种磷脂衍生介质,也是 PAF G 蛋白偶联受体 (PAFR) 的配体。PAF (C16) 在体外实验中显示出抗凋亡和抗炎活性,通过与其受体 (PAF-R) 相互作用以执行细胞信号传导来抑制 caspase 依赖性凋亡。 | |||
T36180 |
Azelaoyl PAF
|
||
Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPARγ. One of these substances was recently isolated and purified from oxLDL, and identified as azelaoyl PAF. Azelaoyl PAF is a potent PPARγ agonist which competes for the thiazolidinedione binding site. Azelaoyl PAF is more potent than 15-deoxy-δ12,14-prostaglandin J2, and equipotent with rosiglitazone as a ligand for this receptor. | |||
T36763 |
PAF C-18
|
||
PAF C-18 is a naturally occurring phospholipid produced upon stimulation through two distinct pathways known as the remodeling" and 'de novo' pathways. It is less potent than PAF C-16 in the induction of platelet aggregation | |||
T36764 |
PAF C-18:1
|
||
PAF C-18:1 is a naturally occurring phospholipid produced by cells upon stimulation and plays a role in the establishment and maintenance of the inflammatory response. It is less potent than PAF C-16 and PAF C-18 in the induction of neutrophil chemotaxis, but is equipotent to PAF C-16 and PAF C-18 in promoting eosinophil migration. PAF C-18:1 activates the PAF receptor and has been used in antibody binding experiments to determine the importance of an acyl linkage at the sn-2 position for recogn... | |||
T36205 |
Methylcarbamyl PAF C-16
|
||
Methylcarbamyl PAF C-16 is a stable analog of PAF C-16 with a half-life greater than 100 minutes in platelet poor plasma due to its resistance to degradation by PAF-AH. It is nearly equipotent with PAF C-16 in its ability to induce platelet aggregation both in isolated platelets and in platelet-rich plasma. In NRK-49 cells overexpressing the PAF receptor, both PAF C-16 and methylcarbamyl PAF C-16 cause the induction of c-myc and c-fos and the activation of mitogen-activated protein kinase. Methy... | |||
T37268 |
PAF C-16 Carboxylic Acid
|
||
PAF C-16 is a naturally occurring phospholipid produced upon stimulation through two distinct pathways known as the remodeling" and 'de novo' pathways. It is a potent mediator of neutrophil migration and the production of reactive oxygen species and IL-6. Pathological processes involving PAF include necrotizing enterocolitis | |||
T19104 |
2-Thio-PAF
|
Others | Others |
2-Thio-PAF is a synthetic analog of PAF used in a colorimetric assay for PAF acetylhydrolase. | |||
T29308 |
Lyso-PAF C-16
|
||
Lyso-PAF C-16 is a biologically inactive precursor of platelet activating factor. | |||
T6242 |
Rupatadine Fumarate
富马酸卢帕他定,Rinialer,Rupafin,Alergoliber |
PAFR; Autophagy; Histamine Receptor | Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Rupatadine Fumarate (Rinialer) 是一种可口服的长效PAF/H1受体的双抑制剂,Ki 值分别为 0.55 μM 和 0.1 μM。它可研究过敏性鼻炎和荨麻疹。 | |||
T80312 |
PAF26
|
||
PAF26为针对植物病原真菌Penicillium digitatum、Penicillium italicum及Botrytis cinerea具有活性的抗菌肽。 | |||
T15338 |
Foropafant
SR27417,福罗帕泛 |
Others; Platelet aggregation | Others |
Foropafant (SR27417) 是一种高效和特异性的血小板活化因子 (PAF) 受体拮抗剂 (Ki: 57 pM)。 Foropafant 有效抑制 PAF 诱导的兔和人血小板聚集。 | |||
T28607 |
Rocepafant
LAU 8080,LAU8080,BN 50730,LAU-8080,BN50730,BN-50730 |
Platelet aggregation | Others |
Rocepafant (LAU8080) 是一种血小板活化因子(PAF)拮抗剂,可减轻新生大鼠缺氧缺血性脑损伤。Rocepafant 抑制肿瘤坏死因子-Afa 介导的小鼠 L929 肿瘤细胞的细胞毒性。 | |||
T17178 |
Tulopafant
RP 59227 |
PAFR | GPCR/G Protein |
Tulopafant(RP 59227) 是一种有效的血小板活化因子 (PAF) 拮抗剂,可增加毛细血管通畅性并延长异体心脏移植的生存期。 | |||
T68124 |
Pafenolol
|
Adrenergic Receptor; P-gp | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Pafenolol 是一种 P-糖蛋白调节剂,Ki 值为5.5 µM。Pafenolol 是一种可口服的且具有选择性的β肾上腺素受体拮抗剂。 | |||
T0866 |
Propafenone
Rythmol,普罗帕酮,Propafenonum |
Potassium Channel; MRP; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel |
Propafenone (Propafenonum) 是钠通道阻滞剂,它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ,具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡,从而抑制食管癌增殖。 | |||
T1280 |
Nepafenac
AL 6515,AHR 9434,奈帕芬胺 |
COX | Immunology/Inflammation; Neuroscience |
Nepafenac (AHR 9434) 是一种非甾体抗炎药,可抑制COX-2,是Amfenac 的原药。 | |||
T9445 |
Vepafestinib
|
c-RET | Apoptosis; Tyrosine Kinase/Adaptors |
Vepafestinib 是 RET 的抑制剂,具有潜在的抗癌活性。 | |||
T6955 |
Propafenone hydrochloride
Propafenone HCl,Arythmol,SA-79 (hydrochloride),Rytmonorm,盐酸普罗帕酮,Rythmol |
Sodium Channel | Membrane transporter/Ion channel |
Propafenone hydrochloride (Arythmol8) 具有抗心律不齐的功效,可用于心房和心室性心律不齐。 | |||
T14300 |
Apafant
WEB 2086,阿帕泛 |
Others | Others |
Apafant is a potent antagonist of platelet-activating factor (PAF), inhibits PAF binding to human PAF receptors(Ki : 9.9 nM). | |||
T33466 | Modipafant | ||
Modipaafant is a potent dihydropyridine PAF (platelet activating factor) antagonist. | |||
T28081 |
(Rac)-Modipafant
UK-74505,Modipafant racemate,UK74505,UK 74505 |
||
Modipafant racemate is a potent and specific oral platelet activating factor (PAF) receptor antagonist. | |||
T27821 |
Lexipafant
ISV-611,GR-167089,DO-6,BB-882,DO6,BB882 |
||
Lexipafant is a platelet-activating factor (PAF) receptor antagonist. | |||
T27638 |
Israpafant
Y-24180,Y 24180,Y24180 |
||
Israpafant is a selective antagonist for the platelet-activating factor receptor ( IC50 = 0.84nM). Israpafant inhibits PAF-induced human platelet aggregation. Israpafant inhibits the activation of eosinophil cells and consequently delays the development o | |||
T26775 |
Bepafant
WEB-2170,WEB2170,STY 2108,STY-2108,WEB 2170 |
||
Bepafant is a platelet activating factor (PAF) antagonist. Bepafant may produce significant anti-inflammatory effects. Bepafant triggered apoptosis in NB4, KG1, and NB4-MR4 cells where PTEN was expressed, but not in THP1 and U937 cells where PTEN was abse | |||
T12548 |
Propafenone D7 hydrochloride
盐酸普罗帕酮 D7,SA-79 (D7 hydrochloride) |
Others | Others |
Propafenone D7 hydrochloride is the deuterium labeled Propafenone, and is a classic anti-arrhythmic medication. | |||
T16874 |
Setipafant
BN-50727,司替帕泛,LAU-0901 |
Others | Others |
Setipafant is an antagonist of the platelet-activating factor. | |||
T39103 |
Pafolacianine
OTL 38 |
||
Pafolacianine (OTL 38) is a near-infrared dye-based fluorescent marker utilized for identifying ovarian cancer lesions during surgeries. | |||
T81111 |
SPPHPSPAFSPAFDNLYYWDQ TFA
|
||
SPPHPSPAFSPAFDNLYYWDQ TFA,一种II类大鼠HER2/neu多表位肽,应用于II类HER2-DC1疫苗的研究。 | |||
T81112 |
SPPHPSPAFSPAFDNLYYWDQ
|
||
SPPHPSPAFSPAFDNLYYWDQ 为多表位 II 类大鼠HER2/neu 肽,适用于 HER2-DC1 II 类疫苗研究。 | |||
T81270 |
Ripafollitropin alfa (bovine)
|
||
Ripafollitropin alfa (bovine)为一种结合了重组促卵泡激素(FSH)与绒毛膜促性腺激素(HCG)的融合蛋白。 | |||
T19153 |
5-Hydroxy Propafenone D5 Hydrochloride
GPV-129 D5 Hydrochloride |
Others | Others |
5-Hydroxy Propafenone D5 HCl is the deuterium labeled 5-Hydroxy Propafenone. | |||
T70999 |
Aspafilioside B
|
||
Aspafilioside B is a steroidal saponin extracted from Asparagus filicinus that inhibits the growth and proliferation of HCC cell lines. | |||
T12811 |
(S)-Propafenone
(S)-SA-79 |
Others | Others |
(S)-Propafenone ((S)-SA-79) is the S-enantiomer of Propafenone. It possesses beta-blocking properties and exhibits class 1 antiarrhythmic activity reliant on sodium channel blockade. | |||
T31996 |
Grepafloxacin Hydrochloride
DSSTox_CID_26692,OPC-17116,DSSTox_RID_81826,DSSTox_GSID_46692 |
||
Grepafloxacin Hydrochloride is an antimicrobial agent, oral broad-spectrum fluoroquinolone. It is used to treat bacterial infections. | |||
T23951 |
Dacopafant
UNII-H1T03Z1G60 |
||
Dacopafant is an antagonist of platlet activationg factor receptor. | |||
T24587 |
Pafuramidine maleate
DB-289,DB289,DB 289 |
||
Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis. | |||
T20840 |
Apaflurane
FM200,FM-200,FM 200 |
||
Apaflurane is a chemical fire extinguishing agent. | |||
T12208 |
Nepafenac-d5
奈帕芬胺 D5,AHR-9434 D5,AL-6515 D5 |
Others | Others |
Nepafenac D5 is the deuterium labeled Nepafenac, which is a selective inhibitor of COX-2 . | |||
T16428 |
Pafuramidine
DB289 |
Others | Others |
Pafuramidine is an orally bioavailable prodrug of furamidine. It has activity against Pneumocystis pneumonia (IC50 value: 4.5 nM) | |||
T38586 |
Grepafloxacin
dl-Grepafloxacin,OPC-17116 |
||
Grepafloxacin (OPC-17116) is a fluoroquinolone antibiotic that is administered orally. It possesses strong efficacy against community-acquired respiratory pathogens, notably Streptococcus pneumonia. Grepafloxacin exhibits excellent tissue penetration and demonstrates a promising pharmacodynamic profile. | |||
T25461 |
Grepafloxacin, (S)-
L-Grepafloxacin |
||
Grepafloxacin, (S)- is an oral broad-spectrum fluoroquinolone antibacterial used for the treatment of bacterial infections. | |||
T77039 | Ipafricept | ||
Ipafricept (OMP-54F28; FZD8-Fc) 是一类重组融合蛋白,由人卷曲 8 受体胞外部分融合到结合Wnt 配体的人IgG1Fc 片段组成。Ipafricept 具有实体瘤抑制活性,耐受性良好。 | |||
T24586 |
PAFAH1b2
PAFAH-1-b-2,3-IN-P11,3INP11,3 IN P11,PAFAH 1 b 2 |
||
PAFAH1b2 is a selective platelet-activating factor acetylhydrolases 1b2 and 1b3 inhibitor that acts by impairing cancer cell survival. | |||
T68101 |
minopafant
|
||
minopafant 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T68101,CAS号为 790174-16-2。 | |||
T19686 |
SCH-37370
乙酰地氯雷他定 |
Platelet aggregation | Others |
SCH-37370 是一种有效且具有口服活性的血小板活化因子和组胺双重拮抗剂。 Sch 37370 阻断 [3H]pyrilamine 与大鼠脑膜中组胺-H1 受体的结合。 Sch 37370 选择性地抑制 PAF 诱导的人血小板聚集(IC50:0.6 mM),并且还与 PAF 竞争与人肺膜制剂中特定位点的结合(IC50:1.2 mM)。 | |||
T27159 |
DF-1111301
DF1111301,DF 1111301 |
Platelet aggregation; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience; Others |
DF-1111301 是一种具有抗组胺 H1和抗PAF活性的新型抗过敏化合物。 | |||
T27102 |
CV-6209
|
||
CV-6209 is a potent antagonist of the platelet-activating factor (PAF) receptor. | |||
T4511 |
ST271
ST 271 |
Phospholipase; Tyrosine Kinases | Metabolism; Tyrosine Kinase/Adaptors |
ST271 是蛋白质酪氨酸激酶 (PTK) 抑制剂,抑制 fMet-Leu-Phe 和 PAF 引起的 phospholipase D 活化的IC50值分别为 6.7 和 9 μM。 | |||
T10844 | CMI-392 | Others | Others |
CMI-392 is a dual 5-lipoxygenase inhibitor and platelet-activating factor (PAF) receptor antagonist (IC50s: 100 and 10 nM). |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN4222 |
Homoeriodictyol 7-O-β-D-glucoside
高圣草素-7-O-Β-D-葡萄糖苷,Homoeriodictyol 7-O-glucoside |
Others; Platelet aggregation | Others |
Homoeriodictyol 7-O-β-D-glucoside (Homoeriodictyol 7-O-glucoside) 是 Viscum coloratum(Kom.)Nakai 的天然产物。Homoeriodictyol 7-O-β-D-glucoside 是血小板活化因子 (PAF) 的拮抗剂。 | |||
T30170 |
Aspafilioside A
|
||
Aspafilioside A is a steroidal saponin isolated from the root of Asparagus filicinus. | |||
TN1170 |
1-Cinnamoylpyrrolidine
|
Platelet aggregation | Others |
1-Cinnamoylpyrrolidine 是从 Piper caninum 制备的天然产物,可作为一种 DNA 链断裂剂,在Cu2+ 存在下诱导质粒 pBR322 DNA 超螺旋的松弛。1-Cinnamoylpyrrolidine 对 PAF 诱导的血小板聚集有抑制作用,IC50 值为 37.3 μM。 | |||
TN2322 |
Yangambin
|
Calcium Channel; PAFR | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
Yangambin 是从诸如番荔枝科植物中分离出来的呋喃木脂素,是选择性PAF 受体拮抗剂,通过调控Ca2+通道抑制 Ca2+流入,导致 [Ca2+]i 在血管平滑肌细胞和随后的外周血管舒张中减少,具有降压作用。 | |||
T2749 |
Ginkgolide A
银杏内酯A,BN-52020 |
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Ginkgolide A (BN-52020) 是从银杏叶提取出来的一种天然产物,是 GABA 拮抗剂,有用于多种炎症和免疫疾病的研究潜力。 | |||
T7030 |
anemarsaponin B
知母皂苷B,知母皂苷 B |
p38 MAPK; NF-κB; MEK; COX; NO Synthase | Immunology/Inflammation; MAPK; Neuroscience; NF-κB |
Anemarsaponin B 是一种甾体皂苷,可降低iNOS 和COX-2的蛋白和 mRNA 水平,减少促炎细胞因子的表达和产生。它通过阻断 IκBα 的磷酸化来抑制NF-κB 的 p65 亚基的核转位,还抑制 MAP 激酶激酶 3/6 (MKK3/6) 和混合谱系激酶 3 的磷酸化。 | |||
TN3161 |
6-Deoxyjacareubin
|
Antioxidant; PAFR; Platelet aggregation; Antifection | GPCR/G Protein; Microbiology/Virology; Others; oxidation-reduction |
6-Deoxyjacareubin 具有有效的抗氧化和抗真菌活性。 6-Deoxyjacareubin 抑制血小板活化因子 (PAF) 受体,IC50 为 29.0 microM,可用于天然 PAF 受体拮抗剂的研究。 | |||
TN4795 |
Piperenone
|
PAFR | GPCR/G Protein |
Piperenone is an insect antifeeding substance. It has anti-platelet-activating factor(PAF) activities, is a PAF-acether antagonist. | |||
TN3520 | Bisdethiobis(methylthio)gliotoxin | PAFR | GPCR/G Protein |
Bisdethiobis(methylthio)gliotoxin is a platelet activating factor (PAF) antagonist. | |||
TN2763 |
2-Hydroxy-3-methoxybenzoic acid glucose ester
|
PAFR | GPCR/G Protein |
2-Hydroxy-3-methoxybenzoic acid glucose ester shows a potent antagonistic activity against platelet activating factor (PAF), it can prevent the mice from the PAF-induced death at a dose of 300 micrograms/mouse. | |||
TN4181 |
Hancinone C
|
PAFR | GPCR/G Protein |
Hancinone C shows inhibitory activity against the platelet aggregation caused by PAF. | |||
TN5045 | Spiradine F | PAFR | GPCR/G Protein |
Spiradine F can significantly inhibit platelet-activating factor(PAF)-induced platelet aggregation in a concentration-dependent manner. | |||
TN4821 |
Pregomisin
|
PAFR | GPCR/G Protein |
Pregomisin shows platelet-activating factor (PAF) antagonistic activity and the IC 50 value is 4.8x10(-5) M. | |||
TN4794 |
Pinusolidic acid
|
PAFR | GPCR/G Protein |
Pinusolidic acid shows a potent inhibitory effect on platelet activating factor (PAF) binding to rabbit platelets (IC50 = 2.3 x 10(-5) M, 7.48 +/- 2.11 micrograms/ml). | |||
T68233 |
Kadsurenone
|
||
Kadsurenone is a platelet-activating factor receptor antagonist from Chinese herbal plant, haifenteng. It is a useful and promising treatment strategy for breast cancer bone metastases by blocking the PAF/PTAFR signaling pathway. | |||
TN6056 |
Zanthobungeanine
8-Methoxy-N-methylflindersine |
||
Zanthobungeanine has anti-inflammatory activity, it shows moderate NO production inhibitory activity with an IC50 value of 37.26 mg /L.It shows obviously inhibitoryactivity to platelet aggregation caused by platelet-activating factor (PAF). Zanthobungeani | |||
T83460 |
11-O-β-D-glucopyranosyl thamnosmonin
|
||
11-O-β-D-glucopyranosyl thamnosmonin是一种香豆素苷,能够从Angelica apaensis根部提取。该化合物对PAF、AA和ADP诱发的兔血小板聚集表现出轻度的抑制效果。 | |||
TN1815 | Kadsulignan L | HBV; PAFR | GPCR/G Protein; Microbiology/Virology |
Kadsulignan L shows in vitro antiviral effects on hepatitis B virus. It also shows moderate platelet-activating factor (PAF) antagonistic activities with the IC50 value of 2.6 x 10(-5) M. | |||
T79948 |
Kadsurenin B
|
||
Kadsurenin B为PAF(platelet-activating factor)拮抗剂,展现出神经保护作用。该化合物在药理学领域显示出广泛的研究潜力,包括抗菌、抗炎、神经保护、抗氧化、抗血小板聚集、细胞毒性和抗寄生虫等效能。 | |||
T13716 | (+)-Guaiacin | Others | Others |
(+)-Guaiacin is a compound isolated from the bark of Machilus wangchiana Chun. It shows potent in vitro activities against the release of β-glucuronidase in rat polymorphonuclear leukocytes (PMNs) induced by platelet-activating factor (PAF). | |||
TN5414 |
Wallichinine
|
||
Wallichinine shows inhibitory activity on platelet aggregation caused by platelet activating factor (PAF). Wallichinine with ABCB1 presents valuable clues for the development of novel MDR reversal reagents from natural products, wallichinine can significa | |||
TN3723 | Cryptomeridiol | PAFR; Antifection | GPCR/G Protein; Microbiology/Virology |
Cryptomeridiol is a potential skin-whitening agent, exhibits melanogenesis inhibitory activity on α-MSH-stimulated B16 melanoma cells. Cryptomeridiol has low activity against A. niger, T. mentagrophytes, and C. albicans. (-)-Cryptomeridiol also exhibits a significant and concentration-dependent inhibitory effect on PAF receptor binding, with inhibitory concentration (IC)(50) values of 17.5 uM. | |||
TN4088 |
Futoenone
|
PAFR | GPCR/G Protein |
Futoenone and a series of its derivatives have shown inhibitory activities against matrix metalloproteinases, the molecular modelings of these compounds indicate the preferred binding of the P2' site of the enzymes. Neolignan derivative compounds of the 2,4-diaryl-1,3-dithiolane and futoenone variety exhibit both platelet activating factor receptor(PAF)and 5-lipoxygenase antagonist activity. | |||
T38015 |
Herquline A
|
||
Herquline A is an alkaloid fungal metabolite originally isolated from P. herquei. It inhibits cell death induced by influenza A strain A/PR/8/34 in MDCK cells with an IC50 value of 10 μg/ml and inhibits viral replication in a plaque assay in a concentration-dependent manner. Herquline A also inhibits platelet aggregation induced by ADP and platelet-activating factor (PAF) in vitro (IC50s = 180 and 240 μM, respectively). | |||
TL0014 | Pinusolide | ERK; p38 MAPK; Calcium Channel; Lipoxygenase; PAFR; Caspase; JNK; AMPK | Apoptosis; Chromatin/Epigenetic; GPCR/G Protein; MAPK; Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Pinusolide is a platelet activating factor ( PAF) antagonist, it may prove of therapeutic value in the treatment of hypotension, it has antileukemic potential, and could be used to treat neurodegenerative diseases. Pinusolide attenuates blockade of insulin signaling by enhancing IRS-1 tyrosine phosphorylation by the activating the AMPK pathway, indicates the targeting of AMPK represents a new therapeutic strategy for hyperglycemia-induced insulin resistance and type 2 diabetes. | |||
TN4664 |
Norarmepavine
|
Others | Others |
N-norarmepavine shows significant cytotoxic activities against HL-60 carcinoma cell line with inhibitory ratios of 51.43% at concentration of 1 x 10(-5) M. Norarmepavine shows inhibition against Trypanosoma cruzi. D-(+)- N-norarmepavine exhibits significa | |||
T38330 |
Collinin
|
||
Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a... |