140
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1092 |
Myelin Basic Protein (MBP) (68-82), guinea pig
MBP (68-82), guinea pig,豚鼠髓磷脂碱性蛋白片段68-82 |
Others | Others |
Myelin Basic Protein (MBP) (68-82), guinea pig 是一种髓鞘碱性蛋白 (MBP) 的片段。 | |||
TP2210 |
VIP(Guinea pig)
VIP (guinea pig) |
Others | Others |
Neuropeptide with many biological actions | |||
T80866 |
VIP(Guinea pig) TFA
Vasoactive Intestinal Peptide, guinea pig TFA |
||
VIP Guinea pig TFA,作为一种胃肠激素,兼具神经递质功能,能够刺激胚胎生长,起到营养和有丝分裂因子的作用。 | |||
T20570 |
Labetalol
Apo-Labetalol,Albetol,Trandate,Dilevalol,拉贝洛尔,Normodyne |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Labetalol (Apo-Labetalol) 是一种抗高血压药物,可用于心血管疾病的研究,如妊娠期高血压。它是一种口服具有活性的选择性 α1- 和非选择性 β-肾上腺素能受体 (adrenergic receptor) 竞争性拮抗剂。 | |||
T10537 |
BI-749327
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
BI-749327是高选择性、口服有效的TRPC6拮抗剂,对小鼠、人、豚鼠 TRPC6 作用的IC50值分别为 13 nM、19 nM 和 15 nM。BI-749327对小鼠 TRPC6 选择性比 TRPC3 高出 85 倍, 比TRPC7高出42 倍。 | |||
T16026 |
MCI826
|
P-gp; LTR | Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
MCI826 是一种具有有效性和选择性的 P-glycoprotein (P-gp)和肽白三烯 (p-LTs) 拮抗剂,在豚鼠晚期哮喘模型中显示出抗哮喘活性。 | |||
TP1819L |
Substance P 1-9 aceate
|
Neurotensin Receptor | GPCR/G Protein |
Substance P 1-9 aceate 是九肽,可减少豚鼠回肠和膀胱对 P 物质的失活。 | |||
T12267 |
NSP-805
|
PDE | Metabolism |
NSP-805 是一种强心剂,是一种选择性的 phosphodiesterase 3 抑制剂,具有舒张血管的作用。 | |||
T14941 |
CGP37157
7-Chloro-5-(2-chlorophenyl)-1,5-dihydro-4,1-benzothiazepine-2(3H)-one |
Na+/Ca2+ Exchanger | Membrane transporter/Ion channel |
CGP37157 (7-Chloro-5-(2-chlorophenyl)-1,5-dihydro-4,1-benzothiazepine-2(3H)-one) 是一种 Na+/Ca2+ 交换抑制剂,抑制 Na+ 诱导的豚鼠心脏线粒体中 Ca2+ 的释放,IC50 为 0.8 μM。 | |||
T26781 |
BF-1
BF1 |
||
BF-1 is a 5-Hydroxytryptamine receptor 2B antagonist. BF-1 was tested as potential migraine prophylactic drug by blocking BW723C86 (5-((thiophen-2-yl)methoxy)-α-methyltryptamine) or meta-chlorophenylpiperazine (mCPP) induced neurogenic dural plasma protei | |||
TP1572 |
GR-73632
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
GR-73632 强效和选择性速激肽 NK1 受体激动剂,可通过传递瘙痒信号的 NK1 受体直接作用于初级感觉神经元的外周末端。 | |||
T16564 |
PPADS tetrasodium
|
P2X Receptor; Na+/Ca2+ Exchanger | Membrane transporter/Ion channel; Neuroscience |
PPADS tetrasodiuma 是一种有效的 P2X 受体拮抗剂,也是是豚鼠气道平滑肌 Na/Ca²⁺ 交换逆模式的抑制剂,对谷氨酸/NMDA毒性有神经保护作用。PPADS tetrasodiuma 抑制 P2X1、P2X-2、P2X-3 和 P2X-5。 | |||
T27627 |
Iroxanadine
BRX005,BRX-235,BRX-005,BRX235,BRX 005,BRX 235 |
p38 MAPK | MAPK |
Iroxanadine (BRX-005) 是一种新型小分子MAPK p38 抑制剂,诱导p38 SAPK 的磷酸化,在用去氧肾上腺素预先收缩的豚鼠肺动脉制剂中诱导浓度依赖性松弛,可用于治疗动脉粥样硬化、糖尿病血管病,微血管心绞痛和外周动脉疾病等血管疾病。 | |||
T31195 |
Dalcotidine
KU 1257,KU-1257 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dalcotidine (KU 1257) 是一种新型组胺H2受体拮抗剂,具有组胺H9受体拮抗活性和抗分泌作用,与豚鼠大脑皮层结合的Ki 值为0.040 对分离性豚鼠右心房组胺诱导的正变时反应的拮抗作用的KB 值为0.041。Dalcotidine 提高了溃疡愈合的质量,可能有助于降低溃疡的复发率和复发率。 | |||
T3574 |
Sematilide hydrochloride
司美利特,CK-1752A,CK-1752,Sematilide HCl |
Potassium Channel | Membrane transporter/Ion channel |
Sematilide hydrochloride (CK-1752) 是一种选择性的 IKr 通道阻滞剂。Sematilide 以浓度依赖性抑制延迟整流钾通道 (K+current),IC50为 25 μM。Sematilide 是一种 III 类抗心律不齐剂。 | |||
T0173 |
Nylidrin hydrochloride
Buphenine HCl,布芬宁盐酸盐 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Nylidrin hydrochloride (Buphenine HCl) 是被动致敏大鼠腹腔肥大细胞中IgE 介导的组胺释放抑制剂,具有抗过敏的功效。它也是被动致敏的豚鼠肺切片中 IgG1 介导的组胺释放抑制剂。 | |||
T23265 |
RS 67333 hydrochloride
RS 67333 (hydrochloride),RS 67333 HCl,盐酸RS67333 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
RS 67333 hydrochloride (RO5203648) 是一种有效的、选择性的5-HT4 受体 (5-HT4R) 部分激动剂,在豚鼠纹状体中的 pKi 为 8.7。RS 67333 hydrochloride 对其他几种受体的亲和力较低,包括 5-HT1A、5-HT1D、5-HT2A、5-HT2C、多巴胺 D1、D2 和毒蕈碱 M1-M3 受体。RS 67333 hydrochloride 具有神经保护作用,可用于阿尔茨海默病研究。 | |||
T39039 |
FSCPX
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
FSCPX是一种针对A1 腺苷受体(A1AR)的强效、选择性不可逆拮抗剂,显示出低纳摩尔级的结合效能。此外,FSCPX能有效降低豚鼠心房中的间质腺苷水平,进而改变核苷转运抑制剂NBTI的效果。 | |||
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。 | |||
T68138 |
Saterinone
|
Adrenergic Receptor; PDE | GPCR/G Protein; Metabolism; Neuroscience |
Saterinone 是一种强效且具有选择性的磷酸二酯酶III 抑制剂,是血管α - 1-肾上腺素受体的有效拮抗剂。Saterinone 具有血管舒张作用,可用于慢性心力衰竭的急性治疗。Saterinone 对豚鼠右心室匀浆中粗cAMP 磷酸二酯酶(PDE)活性具有抑制作用,ic50值为2.3 × 10(-5) mol/l。 | |||
T6707 |
Tiotropium Bromide hydrate
BA-679 BR hydrate,BA 679BR,噻托溴铵一水合物 |
AChR | Neuroscience |
Tiotropium Bromide hydrate (BA-679 BR hydrate) 是长效的毒蕈碱受体拮抗剂,可用于治疗慢性阻塞性气道疾病 (COPD)。 | |||
T67956L |
Litoxetine HCl
litoxetine HCL(86811-09-8 Free base) |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Litoxetine HCl 是一种选择性5-羟色胺(5-HT)再摄取抑制剂(SSRI)和混合5-羟色胺拮抗剂,可用于治疗尿失禁。Litoxetine HCl 在没有抗毒蕈碱特性的浓度下(10 nM-1 microM)引起大鼠离体食道肌肉粘膜的浓度依赖性松弛,使卡巴胆碱张力降低达37%,更高浓度的Litoxetine HCl(3微摩-300微摩)与明显的松弛有关,直至取消卡巴胆碱张力。以前在离体豚鼠肠道中证明的利托西汀的抗心律失常活性,在浓度大于1 microM 时在大鼠离体食道肌肉粘膜中发挥了作用。 Litoxetine HCl 的5-HT 释放作用可以解释利托西汀对未处理的大鼠组织中的5-HT 诱导的松弛的效力,这种效力被pCPA 处理所逆转。 | |||
T14326 |
AS-35
|
Others | Others |
AS-35 is an orally effective, potent and selective antagonist of leukotrienes, antagonizes LTC4-, LTD4 and LTE4-induced contractions of the ileum. With IC50 values of 8 nM, 4 nM and 3 nM, respectively. It has antiallergic activities. | |||
T15487 |
HMR 1556
|
Others | Others |
HMR 1556 is a chromanol derivative and is an IKs blocker (IC50s of 10.5 nM and 34 nM in canine and guinea pig left ventricular myocytes, respectively). | |||
T10360 |
AR-A 2
AR-A 000002 |
Others | Others |
AR-A 2 is a selective 5-HT1B receptor antagonist, with a high affinity to guinea pig cortex 5HT1B/1D and recombinant guinea pig 5-HT1B receptors (Ki: 0.24 and 0.47 nM) and with 10-fold lower affinity to guinea pig 5-HT1D receptor (Ki: 5 nM). | |||
T27364 |
FR 75513
FR-75513,FR75513 |
||
FR 75513 inhibits the contraction of guinea pig detrusor muscle . | |||
T13163 |
Tiotidine
ICI 125211 |
Others | Others |
Tiotidine is a selective histamine H2-receptor antagonist (pA2=7.3-7.8 for guinea-pig right atrium). | |||
T23918 |
Cularine
|
||
Cularine is an isoquinoline alkaloid from the Fumariaceae family. It displays non-specific antispasmodic activity on guinea-pig and human airways. | |||
T4250 |
Bilastine
比拉斯汀,Bilaxten |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Bilastine (Bilaxten) 是新型抗组胺药,对H1组胺受体具有高度选择性,起效快,作用时间长的特性,可用于变应性鼻结膜炎和荨麻疹。 | |||
T25010 |
AK-2-38
AK -2-38,AK2-38 |
||
AK-2-38 is a nifedipine analogue with potent smooth muscle calcium antagonist action and partial agonist effects on isolated guinea pig left atrium. | |||
T12756 |
ROS 234 dioxalate
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
ROS 234 dioxalate is a potent antagonist of H3(pKB of 9.46 for Guinea-pig ileum H3-receptor) | |||
T37493 |
11-trans Leukotriene D4
11-trans Leukotriene D4 |
||
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. | |||
T19674 |
Verlukast
MK 0679,MK-679,L 668,019,MK 679,L 668019,L-668,019 |
||
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 | |||
T15101 |
Devazepide
L-364,718,地伐西匹,MK-329 |
Others | Others |
Devazepide is a competitive and orally active nonpeptide antagonist of cholecystokinin (CCK) receptor (IC50s: 81 pM, 45 pM, and 245 nM for rat pancreatic, bovine gallbladder and guinea pig brain CCK receptors, respectively). | |||
T33449 |
ML 1035
ML103,ML-1035 |
||
ML 1035 is a benzamide that elicits contractions from guinea-pig non-stimulated ileum. | |||
T12771 |
RS-601
|
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。 | |||
T26757 |
BDF 9148
BDF-9148,BDF9148 |
||
BDF 9148, a Na(+)-channel modulator, increases the contractile force of guinea-pig atria and papillary muscles. | |||
T24145 |
Hns 32
Hns32,Hns-32 |
||
Hns 32 possesses antiarrhythmic properties in dog and guinea pig hearts. It also has vasodilator action. | |||
T27435 |
GS 283
GS283,GS-283 |
||
GS 283 is a Ca(2+) antagonist. GS 283 is also a weak histamine and muscarinic receptor blocker in rat and guinea pig tracheal smooth muscles. | |||
T68904 | GW-833972A free base | ||
GW833972 is a CB2 Agonist. GW 833972A inhibited capsaicin-induced depolarization of the human and guinea-pig and prostaglandin E(2) (PGE(2)) and hypertonic saline-induced depolarization of the guinea-pig isolated vagus nerve in vitro. GW 833972A also inhibited citric acid-induced cough but not plasma extravasation in the guinea-pig and this effect was blocked by a CB(2) receptor antagonist. | |||
TP2119 |
Sarafotoxin S6a
|
||
Endothelin receptor agonist (EC50 values are 7.5 and > 150 nM for contraction of pig coronary artery and guinea pig aorta respectively). Nociceptive in vivo. | |||
T29034 |
U75302
U 75302,U-75302 |
||
U75302 is an antagonist of thymosin beta-4 (TB4) receptor with a Ki value of 159 nM on guinea pig lung membranes. | |||
T13065 |
TAK-024
|
Others | Others |
TAK-024 is an inhibitor of platelet(IC50s of 31, 79 and 51 nM in human, monkey and guinea pig, respectively). | |||
T68495 |
Ganciclovir triphosphate
|
||
Ganciclovir triphosphate is a synthetic analog of 2'-deoxy-guanosine which is used to treat or prevent cytomegalovirus (CMV) infections. It inhibits the replication of human CMV with an IC50 value of 0.01 μM and is effective against strains of CMV from human, monkey, mouse, and guinea pig. | |||
TP1988 |
[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2
|
||
Potent agonist of the nociceptin (ORL1) receptor, demonstrated both in vitro and in vivo. Selective, competitive antagonism at the nociceptin receptor has also been reported (pA2 = 7.02 and 6.75 in the guinea pig ileum and mouse vas deferens respectively) | |||
T67885 |
Camlipixant
BLU-5937 |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
Camlipixant (BLU-5937) 是一种具有口服活性的嘌呤P2X3受体拮抗剂,具有有效性、选择性和竞争性。Camlipixant 对 hP2X3 同型三聚体的 IC50 为 25 nM。Camlipixant 可用于治疗呼吸系统疾病和免疫系统疾病,研究难治性慢性咳嗽和特应性皮炎。Camlipixant 具有较强的止咳效果。 | |||
T22946 |
LY255283
LY 255283 |
Leukotriene Receptor | GPCR/G Protein |
LY255283 是白三烯 B4 (LTB4) 受体的特异性拮抗剂,抑制人外周血多形核白细胞和由钙离子载体 A23187 激活的单核细胞中 LTB(4) 的产生。 | |||
T8437 |
3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox
|
Others | Others |
3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox 拮抗 2-methyl-5-HT 诱导的豚鼠回肠收缩。 | |||
T37652 |
5(S),6(R)-DiHETE
|
||
5(S),6(R)-DiHETE is a dihydroxy polyunsaturated fatty acid and a nonenzymatic hydrolysis product of leukotriene A4 (LTA4). Mouse liver cytosolic epoxide hydrolase catalyzes the conversion of LTA4 to 5(S),6(R)-DiHETE. It is a weak LTD4 receptor agonist in guinea pig lung membranes. It induces guinea pig ileum contraction with an ED50 value of 1.3 μM. | |||
T37189 |
BTCP maleate
|
||
BTCP 与豚鼠脑膜一起预孵育可增加 [3H]TCP 从 PCP 位点的解离速率。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1266 |
3-O-Methylquercetin
|
IL Receptor; cAMP; PDE | GPCR/G Protein; Immunology/Inflammation; Metabolism |
3-O-Methylquercetin 是分离自植物Rhamnus nakaharai 的天然产物,可抑制总 cAMP 和cGMP-phosphodiesterase (PDE)。它对PDE1、PDE5、PDE 和PDE4的IC50分别是31.9 μM、86.9 μM、18.6 μM 和1.6 μM。 | |||
T6S2025 |
8-O-Acetylharpagide
8-O-乙酰哈巴苷,8-Acetylharpagide,3-Acetylharpagide,Acetylharpagide,8-O-Acetylharpagide |
Antibacterial | Microbiology/Virology |
8-O-Acetylharpagide 是从 Ajuga reptans 中分离得到的一种环烯醚萜,有抗肿瘤、抗病毒、抗菌和抗炎作用。它对豚鼠的离体平滑肌有生物活性。 | |||
T4S1422 |
Praeruptorin E
白花前胡素 E,白花前胡素E |
Others; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Others |
Praeruptorin E 是白花前胡中的一种主要成分,是钙拮抗剂,pD2′值为 5.2。 | |||
PDK0014 |
3-Methylxanthine
|
Endogenous Metabolite | Metabolism |
3-Methylxanthine 是一种黄嘌呤衍生物和环磷酸鸟苷(GMP)抑制剂,在豚鼠分离的气管肌肉中测得其IC50值为 920 μM。 | |||
T6S0033 |
Crotonoside
巴豆苷;异鸟苷,巴豆苷,Isoguanosine,2-HYDROXYADENOSINE |
Others; FLT; HDAC | Angiogenesis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Others; Tyrosine Kinase/Adaptors |
Crotonoside (Isoguanosine) 是从中草药巴豆中分离出来的一种天然产物。 它抑制 FLT3 和 HDAC3/6,有治疗急性髓性白血病 (AML)的研究潜力。 | |||
T3S2259 |
Methyl eugenol
4-allylveratrole,eugenyl methyl ether,O-methyleugenol,Eugenol Methyl ether,丁香酚甲醚,丁子香酚甲醚 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Methyl eugenol (4-allylveratrole) 是一种苯丙类化合物,存在于植物叶子、果实、根茎中,当植物相应的部位因食草动物进食而受损时,就会释放。它可用于消灭雄性东方果蝇。 | |||
TN4486 |
Magnolianin
|
Others | Others |
Magnolianin can inhibit strongly (IC50 = 0.45 uM) 5-HETE formation by die cytosol of guinea pig polymorphonuclear leukocytes. | |||
TN4540 | Methyl demethoxycarbonylchanofruticosinate | Others | Others |
Methyl demethoxycarbonylchanofruticosinate exhibits significant antitussive activity in a citric acid induced guinea pig cough model. | |||
TMA0955 |
Thunberginol C
|
Antifection | Microbiology/Virology |
Thunberginol C exhibits antimicrobial activity against oral bacteria. It shows antiallergic activity in the in vitro bioassay using the Schults-Dale reaction in sensitized guinea pig bronchial muscle. | |||
TN4713 |
Onitisin
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Onitisin, onitinoside and onitin can inhibit the contraction of isolated guinea-pig ileum. | |||
TN4345 |
Jacobine
|
Others | Others |
Jacobine induces significant dose-dependent DNA-DNA interstrand cross-linking over the entire range of doses. It was catalyzed by guinea pig hepatic glutathione-S-transferase enzymes in in vitro experiments. | |||
TN4812 |
Pluviatolide
|
AChR | Neuroscience |
(-)-Pluviatolide can inhibit electrically-induced and acetylcholine-induced contraction in the isolated guinea-pig ileum. | |||
TN2517 |
1,7-Dihydroxy-2,3-dimethoxyxanthone
|
Others | Others |
1,7-Dihydroxy-2,3-dimethoxyxanthone may have medicinal use in the management of inflammation, asthma and allergy, it antagonises in a non competitive but, reversible manner the contractions induced by chemical inflammatory mediators in the guinea pig trac | |||
TN4303 |
Isokaempferide
|
ATPase; Potassium Channel; Calcium Channel; TNF; Prostaglandin Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Isokaempferide shows hepatoprotective, antiproliferative, and anti-inflammatory effects, the anti-inflammatory effects can be explained, at least in part, by reducing neutrophil degranulation, myeloperoxidase activity, mediators as well as TNF-alpha secretion. Isokaempferide is used as a bronchodilator, can induce relaxation of guinea-pig isolated trachea. | |||
TN6952 |
Hexadecane
n-Hexadecane |
||
Hexadecane (n-Hexadecane) 可作为真菌的碳源,与厌氧生物生物降解有关。Hexadecane 在豚鼠皮肤实验中抑制皮肤过度角质化。 | |||
T4S0083 |
Protostemonine
|
Others | Others |
Protostemonine 是一种主要从 Stemona sesslifolia 根中分离得到的生物碱,对哮喘及革兰氏阴性菌所致急性肺损伤有抗炎作用。 | |||
T20712 |
Conessine
Conessinum,Wrightine,地麻素,Roquessine,Neriine,Konessin |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Conessine (Conessinum) 是一种具有抗疟活性的甾体生物碱,是高效选择性H3 受体拮抗剂,对于人、狗、豚鼠和大鼠 H3受体的Ki 分别为 5.4、6.0、5.7 和 25 nM。 |