201
56
3
1
17
Cat. No. | Product Name | ||
---|---|---|---|
L4710 | 非甾体类抗炎化合物库 | 530 compounds | |
530 种非甾体类的抗炎相关化合物,可用于高通量和高内涵筛选; | |||
L6710 | 中药抗炎分子库 | 1246 compounds | |
1246 种具有抗炎活性或靶向炎症相关靶点的中药单体集合,是药物开发、药理研究的有效工具; | |||
L4700 | 免疫/炎症分子化合物库 | 4720 compounds | |
4720 种具有抗炎症活性的化合物的特有集合,可用于高通量筛选和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2550 |
Tolmetin
Tolectin,托麦汀 |
COX | Immunology/Inflammation; Neuroscience |
Tolmetin (Tolectin) 是非甾体类抗炎药,是可口服的 COX 抑制剂,对人 COX-1 和 COX-2 的 IC50值分别为 0.35 和 0.82 µM。 | |||
T11399 |
Giredestrant
GDC-9545 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Giredestrant (GDC-9545) 是一种口服有效的、选择性的、非甾体的雌激素受体 (ER) 拮抗剂,具有抗肿瘤作用。它可以在 ER 配体结合域内与雌二醇 (Estradiol) 竞争结合并诱导构象变化。 | |||
T0380 |
Bicalutamide
比卡鲁胺,ICI-176334 |
Androgen Receptor; Autophagy | Autophagy; Endocrinology/Hormones |
Bicalutamide (ICI-176334) 是一种具有口服活性的非甾体雄激素受体拮抗剂,可研究前列腺癌。 | |||
T22371 |
Mivacurium dichloride
米库氯铵,Mivacurium chloride,二氯美维库铵 |
AChR | Neuroscience |
Mivacurium dichloride (Mivacurium chloride) 是苄基异喹啉衍生物,可与 nAChR 偶联,以减少或抑制乙酰胆碱对肌肉细胞末端盘的去极化作用。它也是非去极化短效的神经肌肉阻滞剂和骨骼肌松弛剂。 | |||
T6737 |
Zaltoprofen
CN100,扎托布洛芬,Soleton |
COX | Immunology/Inflammation; Neuroscience |
Zaltoprofen (Soleton) 是一种非甾体类抗炎剂,具有强大的抗炎作用和对炎性疼痛的止痛作用。它是可口服的COX-2抑制剂,对COX-1和COX-2的IC50值分别为 1.3 和 0.34 μM。 | |||
T26539 |
AC-262536
AC262536,4-(3-内型-羟基-8-氮杂双环[3.2.1]辛烷-8-基)萘-1-甲腈 |
Androgen Receptor | Endocrinology/Hormones |
AC-262536 是非甾体雄激素受体选择性调节剂,具有有益的合成代谢作用。它可以强效激动雄激素受体,亲和力为1-10 nM。 | |||
T0383 |
Fenspiride hydrochloride
Fenspiride HCl,Pneumorel,Fluiden,Decaspiride,盐酸芬司必利 |
Adrenergic Receptor; PDE; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Fenspiride hydrochloride (Decaspiride) 是一种口服活性的非甾体抗炎剂,是 H1-组胺受体的拮抗剂,可用于呼吸系统疾病的研究。 | |||
T4602 |
Hydrocortisone hemisuccinate
Hydrocortisone 21-he,氢化可的松琥珀酸酯,hydrocortisone 21-hemisuccinate*free acid,Hydrocortisone 21-hemisuccinate |
Glucocorticoid Receptor; Others; Interleukin | Endocrinology/Hormones; Immunology/Inflammation; Others |
Hydrocortisone hemisuccinate (hydrocortisone 21-hemisuccinate*free acid) 是糖皮质激素, 是口服有活性的甾体抗炎剂。它能够降低IL-6(IC50:6.7 μM)、IL-3(IC50:21.4 μM)的生物活性,可用于研究溃疡性结肠炎。 | |||
T61444 |
Nonsteroidal aromatase inhibitor 1
|
Others | Others |
Nonsteroidal aromatase inhibitor 1 (Compound 13h) effectively inhibits the enzyme CYP19A1 with an IC50 value of 0.09 nM. Due to its potent inhibitory activity, Nonsteroidal aromatase inhibitor 1 holds promise for research in the field of breast cancer [1]. | |||
T33414 |
MK 0434
MK-434,MK0434,MK-0434,MK 434,MK434 |
Reductase | Endocrinology/Hormones; Metabolism |
MK 0434 是一种具有口服活性的类固醇 5 α-还原酶抑制剂。 | |||
T26109 |
Robenacoxib
Onsior |
COX | Immunology/Inflammation; Neuroscience |
Robenacoxib (Onsior) 是一种对环氧化酶-2 有很强的选择性的非甾体化合物,具有抗炎活性。 | |||
T19679 |
Benoxaprofen
氧苯恶唑丙酸,NSC 299582,LY-90459,Benoxaphen. Compound 90459 |
COX | Immunology/Inflammation; Neuroscience |
Benoxaprofen (NSC-299582) 是长效的、强效的抗炎和解热化合物,在体外具有较弱的对环氧合酶的抑制作用,也可以抑制脂氧合酶,在一些炎症动物模型中抑制单核细胞迁移。 | |||
T6498 |
Fenoprofen calcium hydrate
Feprona dihydrate,Fenoprofen calcium salt dihydrate,Progesic dihydrate,非诺洛芬钙二水合物 |
Apoptosis; Others; COX | Apoptosis; Immunology/Inflammation; Neuroscience; Others |
Fenoprofen calcium hydrate (Progesic dihydrate) 是一非甾体类抗炎症化合物。 | |||
T30161 |
EN3356
AS N001,ASN-001 |
P450 | Metabolism |
EN3356 是一种可口服且具有选择性的类固醇 17-α- 羟化酶/C17,20 裂解酶(CYP17A1 或 CYP17)抑制剂,是一种非甾体类裂解酶选择性化合物,具有潜在的抗雄激素和抗肿瘤活性。 | |||
T25985 |
Prifelone
R-830,R830,S-16820,S 16820,R 830 |
Others | Others |
Prifelone (R 830) 是一种非甾体抗炎化合物,具有抗氧化活性。 | |||
T0321 |
Indoprofen
吲哚洛芬,(±)-Indoprofe,茚酮苯丙酸 |
COX | Immunology/Inflammation; Neuroscience |
Indoprofen ((±)-Indoprofe) 是非甾体类抗炎药, 可用于研究脊髓性肌萎缩。 | |||
T30150 |
AS-601811
AS601811,AS 601811,UNII-LIV8A6AE5F |
Androgen Receptor | Endocrinology/Hormones |
AS-601811 是类固醇 5α还原酶抑制剂和雄激素受体调节剂,可用于研究脱发和痤疮。 | |||
T21740 |
RD162
|
Androgen Receptor | Endocrinology/Hormones |
RD162 是一种与雄激素受体 (AR) 特异性结合的非甾体抗雄激素 (NSAA)。 | |||
T6540 |
Ibuprofen Lysine
布洛芬赖氨酸盐,Neoprofen |
COX | Immunology/Inflammation; Neuroscience |
Ibuprofen Lysine (Neoprofen) 是一种非甾体抗炎药。 | |||
T14546 |
Bermoprofen
AD-1590,AJ-1590 |
Others | Others |
Bermoprofen (AD-1590) 是一种口服活性非甾体抗炎化合物, 具有抗炎镇痛活性,可用于研究胃溃疡。 | |||
T7839 |
Lasofoxifene Tartrate
CP-336156,酒石酸拉索昔芬 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Lasofoxifene Tartrate (CP-336156) 是一种非甾体类的雌激素受体选择性调节剂 (SERM)。 | |||
T22307 |
Diclofenac Epolamine
diclofenac hydroxyethylpyrrolidine,DHEP,2-((2,6-二氯苯基)氨基)苯乙酸 1-吡咯烷乙醇盐,DIEP |
Others | Others |
Diclofenac Epolamine (DHEP) 是一种非甾体抗炎药 (NSAID),具有镇痛和解热作用。 | |||
T11340 |
Furprofen
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Furprofen 是一种非甾体类抗炎剂,抑制前列腺 (PGE) 合成,可用于研究类风湿关节炎和骨关节炎。 | |||
T0184 |
Fenoprofen calcium dihydrate
|
COX | Immunology/Inflammation; Neuroscience |
Fenoprofen calcium dihydrate 是一种丙酸衍生物,用作非甾体抗炎剂。 | |||
T27209 |
Droxicam
Droxicamum,屈昔康 |
Others | Others |
Droxicam (Droxicamum) 是一种非甾体抗炎化合物,可用于缓解肌肉骨骼疾病的炎症和疼痛的研究。 | |||
T27635 |
Isoxepac
伊索克酸,Olopatadine USP Related Compound C |
Others | Others |
Isoxepac (Olopatadine USP Related Compound C) 是非甾体抗炎剂,显示出抗炎、镇痛和解热活性,已在多种动物模型中进行了相关研究。 | |||
T19694 |
Hydronidone
F351,F-351,F 351 |
Others | Others |
Hydronidone (F-351) 是一种 pyridine 衍生物。Hydronidone 对肝纤维化具有潜在的治疗作用。 | |||
T1720 |
Amfenac Sodium Hydrate
一水氨芬酸钠,Amfenac Sodium Monohydrate,氨芬酸钠水合物 |
COX | Immunology/Inflammation; Neuroscience |
Amfenac Sodium Hydrate 是一种含有乙酸部分的非甾体镇痛抗炎药,是 COX-2抑制剂。 | |||
T15246 |
Esaxerenone
艾沙利酮,XL-550,CS-3150 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Esaxerenone (XL-550) 是高效的、选择性的非类固醇盐皮质激素受体拮抗剂。 | |||
T14666 |
BL-1249
|
Potassium Channel | Membrane transporter/Ion channel |
BL-1249 是一种具有选择性和有效性的非甾体钾通道激活剂,具有抗炎活性,可激活 K2P2.1 (TREK-1) 和 K2P10.1 (TREK-2)。 | |||
T7313 |
Enclomiphene citrate
恩氯米芬柠檬酸盐,Enclomifene citrate,(E)-Clomiphene citrate,trans-Clomiphene citrate |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Enclomiphene citrate (trans-Clomiphene citrate) 是口服具有活力的 oestrogen receptor 拮抗剂,具有抗雌激素活性。 | |||
T7389 |
G15
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
G15 是一种高亲和力的、选择性的 G 蛋白偶联雌激素受体(GPER/GPR30)拮抗剂(Ki:20 nM)。 | |||
T7293 |
EC330
|
Others | Others |
EC330 是一种白血病抑制因子抑制剂。 | |||
T0448 |
(S)-(+)-Ibuprofen
左旋布洛芬,Dexibuprofen,(S)-Ibuprofen,(S)-(+)-布洛芬 |
BCL; Thrombin; Cysteine Protease; COX; PPAR | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience; Proteases/Proteasome |
(S)-(+)-Ibuprofen (Dexibuprofen) 是 Ibuprofen 的 S(+)-对映异构体,能够有效的抑制COX-1(IC50:2.1 μM)和COX-2(IC50:1.6 μM),。它具有抗癌、退热、止痛,抗炎的效果。 | |||
T27798 |
Lapisteride
CS891B,CS-891,CS-891B,CS891 |
Others | Others |
Lapisteride (CS-891) 一种类固醇5α-还原酶抑制剂,可用于治疗良性前列腺增生(BPH)和雄激素性脱发,可有效预防或治疗AGA 。 | |||
T1258 |
Nabumetone
BRL14777,萘丁美酮 |
COX; Glutathione Peroxidase | Immunology/Inflammation; Metabolism; Neuroscience |
Nabumetone (BRL14777) 是一种非甾体抗炎药,是选择性COX-2抑制剂,其活性代谢物 6MNA 可抑制环加氧酶 I 和 II。 | |||
T0285 |
Isoxicam
伊索昔康,Isoxicamum,Isoxicamo,Maxicam |
COX | Immunology/Inflammation; Neuroscience |
Isoxicam (Isoxicamum) 是可口服的非甾体抗炎剂,可通过抑制环氧合酶 1 和 2 来阻断前列腺素的合成,可用于关节炎的研究。 | |||
T17217 |
Vamorolone
地塞米松EP杂质E,VBP15 |
Glucocorticoid Receptor; NF-κB | Endocrinology/Hormones; NF-κB |
Vamorolone (VBP15) 是一种首创的,具有口服活性的解离性类固醇 (dissociative steroidal) 抗炎药和膜稳定剂。它抑制 (NF-κB) 抑制作用,并降低了激素的影响。它改善肌营养不良,无副作用。 | |||
T0637 |
2-Acetyl-6-methoxynaphthalene
|
Others | Others |
2-Acetyl-6-methoxynaphthalene 是naphthalene tome 和naproxen 的关键中间体,用于合成非甾体抗炎镇痛药。 | |||
T1421 |
Aceclofenac
醋氯芬酸,Preservex,Airtal |
COX | Immunology/Inflammation; Neuroscience |
Aceclofenac (Preservex) 是一种可口服的非甾体抗炎药,可用于缓解疼痛、骨关节炎、强直性脊柱炎、类风湿性关节炎的研究。 | |||
T4561 |
Tiaprofenic acid
Tiaprofensaeure,噻洛芬酸,Acido tiaprofenico,Surgam |
Others; COX | Immunology/Inflammation; Neuroscience; Others |
Tiaprofenic acid (Acido tiaprofenico) 是可口服的非甾体抗炎药,通过抑制环氧化酶抑制前列腺素合成,可用于风湿性疾病的研究。 | |||
T0319 |
Suxibuzone
琥布宗,Calibene,Suxibuzonum,Suxibuzona |
COX | Immunology/Inflammation; Neuroscience |
Suxibuzone (Suxibuzona) 是非甾体类抗炎药 Phenylbutazone 的前药,可用于关节和肌肉疼痛研究。 | |||
T4542 |
Clonixin
Clonixic acid,氯尼辛 |
Others | Others |
Clonixin (Clonixic acid) 是一种非甾体抗炎药,具有口服活性。 | |||
T19967 |
Fendosal
芬度柳,HP 129,P 71-0129,P71-0129,P-71-0129,HP129,HP-129 |
Immunology/Inflammation related | Immunology/Inflammation |
Fendosal (HP-129) 是一种非甾体抗炎药。在预防性和治疗性辅助诱导的慢性炎症多关节炎模型中,它的活性是阿司匹林的 6.9 至 9.5 倍。 | |||
T12361 |
Parcetasal
MR-897 |
Others | Others |
Parcetasal (MR-897) 是一种非甾类体抗炎剂,在缓解疼痛方面具有研究价值。 | |||
T5843 |
Tarenflurbil
MPC7869,(R)-Flurbiprofen,R-flurbiprofen,氟比洛芬,R-氟比洛芬 |
Retinoid Receptor; Autophagy | Autophagy; Metabolism |
Tarenflurbil ((R)-Flurbiprofen) 是 Flurbiprofen 的 R 型对映体,可抑制 [3H]9-cis-RA 结合到 RXRαLBD,IC50为 75 μM。它可研究阿尔兹海默症。 | |||
T26926 |
Butibufen
FF 105,FF-106,FF 106,FF106 |
Lipoxygenase | Metabolism |
Butibufen (FF-106) 是一种具有口服活性的非甾体抗炎化合物,是潜在的环氧合酶抑制剂,具有止痛和解热活性,抑制尿素合成。Butibufen 可用于研究风湿性疾病。 | |||
T27254 |
Eltenac
B78820,B 78820,B-78820,BY-820,BY820,BY 820 |
COX | Immunology/Inflammation; Neuroscience |
Eltenac (B78820) 是一种非甾体抗炎剂,是 COX 抑制剂,具有镇痛活性。Eltenac 抑制 COX-1 和 COX-2 ,可用于研究急性呼吸窘迫综合征(ARDS)。 | |||
T1582 |
Naproxen
萘普生,(S)-Naproxen |
COX; Autophagy | Autophagy; Immunology/Inflammation; Neuroscience |
Naproxen ((S)-Naproxen) 是COX-1和COX-2的抑制剂,在细胞试验中IC50值分别为8.72 和5.15 μM。它是丙酸衍生物和非甾体抗炎药,具有抗炎、解热和镇痛活性。 | |||
T0463 |
Loxoprofen
Loxoprofene,洛索洛芬,Loxoprofeno,Koloxo |
COX | Immunology/Inflammation; Neuroscience |
Loxoprofen (Koloxo) 是一种非甾体类抗炎药,具有解热作用,可用于缓解疼痛的研究。它是非选择性COX 抑制剂,对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3901 |
Solasonine
|
Others | Others |
Solasonine 是一种甾体糖苷生物碱,从龙葵中分离获得,对人胃癌细胞有细胞毒性。 | |||
T4035 |
Khasianine
|
Others | Others |
Khasianine 是一种从茄属植物Solanum Nigrum L 中提取的甾体糖生物碱,具有抗肿瘤作用。 | |||
T3S1251 |
Neoruscogenin
|
ROR | Metabolism |
Neoruscogenin 是甾体 sapogenin 家族的成员,是一种可生物利用且具有高亲和力的核受体RORα (NR1F1)激动剂。 | |||
T3S0509 |
Gaultherin
|
COX | Immunology/Inflammation; Neuroscience |
Gaultherin 是一种分离自 Gaultheria yunnanensis 中的天然水杨酸酯衍生物。它是一种非甾体类抗炎药,具有止痛和抗炎作用,与 Aspirin 相比没有胃溃疡作用。 | |||
T3S1265 |
Liriopesides B
山麦冬皂苷B,Nolinospiroside F |
Others | Others |
Liriopesides B (Nolinospiroside F) 是一种甾体皂苷,分离自 Ophiopogon japonicas 中,具有抗氧化和抗衰老活性。 | |||
T7024 |
Qingyangshengenin
青阳参甙元,Qingyangshengenin A,Cynanchagenin |
Others | Others |
Qingyangshengenin (Cynanchagenin) 是一种孕烷糖苷,是一种分离自Cychuchumot ophyllum(Asclepiadaceae) 的根中的 C21 类固醇糖苷配基。它具有抗癌作用。 | |||
T0301 |
Ethisterone
炔孕酮,17α-Ethynyltestosterone,Pregneninolone |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Ethisterone (17α-Ethynyltestosterone) 是一种口服活性类固醇避孕药,是一种合成类固醇雌激素。据报道,它具有雄激素活性,用于妇科疾病的研究。 | |||
T4036 |
Solasodine
Solancarpidine,Purapuridine,澳洲茄铵,Solasodin |
Apoptosis; Others; E1/E2/E3 Enzyme; Antifungal | Apoptosis; Microbiology/Virology; Others; Ubiquitination |
Solasodine (Purapuridine) 是存在于茄科植物中的一种类固醇生物碱。它具有神经保护、降压、抗真菌、抗癌、抗动脉粥样硬化、抗雄激素和抗炎活性。 | |||
T2S0250 |
Pseudoprotogracillin
伪原纤细薯蓣皂苷 |
Others | Others |
Pseudoprotogracillin 是一种从薯蓣科中提取的甾体皂苷类天然产物。 | |||
T10233 |
Acetylarenobufagin
|
HIF | Angiogenesis; Chromatin/Epigenetic |
Acetylarenobufagin 是一种类固醇缺氧诱导因子-1 (HIF-I) 调节剂。 | |||
T8094 |
16-Dehydroprogesterone
16-Dehydroprogesterone,16-去氢黄体酮 |
Endogenous Metabolite | Metabolism |
16-Dehydroprogesterone 是甾体孕激素。 | |||
T2S2295 |
Timosaponin A1
知母皂苷A1 |
Others | Others |
Timosaponin A1 是一种黄酮类甾体皂苷,分离自知母中。 | |||
TN2329 |
Zingiberen newsaponin
Zingiberensis saponin I,盾叶新苷 |
PARP; PAFR; Caspase | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Proteases/Proteasome |
Zingiberen newsaponin 是分离自盾叶薯 (Dioscorea zingiberensis) 中。 它能够诱导血小板聚集。 | |||
T2S1749 |
Protogracillin
原纤细薯蓣皂甙 |
Others | Others |
Protogracillin 是一种甾体皂苷,分离自Dioscorea zingiberensisWright (DZW) 中。从 DZW 根状茎中获得的甾体皂苷具有抗血栓作用,同时由降低心血管疾病风险的潜力。 | |||
T2962 |
5α-Cholestan-3β-ol
Dihydrocholesterol,Zymostanol,5α-Cholestanol,5alpha-Cholestanol,NSC 18188,Beta-Cholestanol,二氢胆甾醇 |
Others; Endogenous Metabolite | Metabolism; Others |
Dihydrocholesterol 是衍生化的类固醇化合物的一种,抑制胆固醇吸收。 | |||
TN6712 |
yibeissine
|
Others | Others |
Yibeissine 是一种甾体生物碱,分离自贝母球茎中。 | |||
T2825 |
Cyclopamine
环巴胺,11-Deoxojervine |
Hedgehog/Smoothened; Endogenous Metabolite; Smo | GPCR/G Protein; Metabolism; Stem Cells |
Cyclopamine (11-Deoxojervine) 是Hedgehog 通路的拮抗剂,细胞实验中IC50=46 nM。它还是选择性Smo 抑制剂。 | |||
T2321 |
Protodioscin
Furostanol I,原薯蓣皂苷 |
Androgen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Protodioscin (Furostanol I) 是一种山药根茎中的主要甾体皂苷,具有抗高血脂、抗癌活性。 | |||
TN2282 |
trans-Stilbene
反式-1,2二苯乙烯,1,2-Diphenylethylene (trans),(E)-Stilbene |
Others | Others |
trans-Stilbene (1,2-Diphenylethylene (trans)) 可用于制备荧光增白剂、染料激光器、非甾体合成雌激素。 | |||
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。 | |||
T3150 |
Caudatin
告达亭苷元,告达庭 |
Apoptosis; Others | Apoptosis; Others |
Caudatin 是白首乌中的一种甾体类天然产物,具有抗肿瘤和抗血管生成作用。它是一种 C-21 甾体糖苷,可使细胞周期停滞,诱导细胞凋亡。 | |||
T5751 |
Tigogenin
|
Others | Others |
Tigogenin 是甾体皂甙元,普遍用于甾体类药物的合成。它能够阻碍小鼠骨髓基质细胞脂肪细胞分化,促使成骨细胞的分化。 | |||
T16338 |
Norgestimate metabolite Norelgestromin
17-Deacetyl norgestimate,17-Deacylnorgestimate,甲基孕酮 |
Drug Metabolite | Metabolism |
Norgestimate metabolite Norelgestromin (17-Deacylnorgestimate) 是norgestimate 的一种活性代谢物。它是用于避孕贴片的甾体孕激素,与雌激素乙炔雌二醇结合使用。 | |||
TN1383 |
Timosaponin B III
Anemarsaponin BIII,知母皂苷B3,知母皂苷BIII |
Others; Platelet aggregation | Others |
Timosaponin B III (Anemarsaponin BIII) 是一种具有生物活性的甾体皂苷,从知母中分离出来。Timosaponin B III 具有抗炎、抗血小板聚集和抗抑郁作用。 | |||
T1048 |
Estradiol
雌二醇,E2,17β-Estradiol,17β-Oestradiol,β-Estradiol |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Estradiol (E2) 是一种天然的类固醇性激素,对于女性生育能力和第二性征的维持至关重要。Estradiol 通过雌激素受体 β (ERβ) 上调 IL-6 表达。 | |||
T2733 |
Sarsasapogenin
Parigenin,知母皂苷元,Sarsagenin |
Apoptosis; NF-κB; Endogenous Metabolite | Apoptosis; Metabolism; NF-κB |
Sarsasapogenin (Parigenin) 是一种甾体皂苷元,从中草药知母中分离到,具有抗糖尿病、抗氧化、抗癌、抗炎等作用。 | |||
T4034 |
Solamargine
Solamargin,δ-Solanigrine,澳洲茄边碱 |
Apoptosis; p38 MAPK; P-gp; STAT | Apoptosis; JAK/STAT signaling; MAPK; Membrane transporter/Ion channel; Neuroscience; Stem Cells |
Solamargine (δ-Solanigrine) 是一种来源于茄属植物的类固醇 Solasodine 的衍生物,诱导非选择性细胞毒性和 P-gp 抑制作用。它通过下调 MMP-2 和 MMP-9 的表达和活性来显著抑制 HepG2 细胞的迁移和侵袭,在多种癌症中均表现出抗癌活性。 | |||
TMS1461 |
Qingyangshengenin B
青阳参甙元B,青阳参苷元B,Otophylloside B |
Beta Amyloid | Neuroscience |
Qingyangshengenin B (Otophylloside B) 是一种分离自 Qingyangshen 的 C-21 甾体苷。它能够在 mRNA 水平上抑制 Aβ 的表达来减少 Aβ 的沉积,对 Aβ 的毒性有保护作用。它具有抗癫痫作用。 | |||
T4000 |
(±)-Equol
Equol,(±)-雌马酚,(R,S)-Equol |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Drug Metabolite | Endocrinology/Hormones; Metabolism |
(±)-Equol ((R,S)-Equol) 是 equol 的外消旋体。它对 ERα 和 ERβ 的 EC50s of 分别为 200 和 74 nM。Equol 是大豆异黄酮黄豆苷和大豆黄素的代谢产物。 | |||
T6491 |
(-)-(S)-Equol
(−)-Equol,Equol,4',7-Dihydroxyisoflavan,4',7-Isoflavandiol,雌马酚 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
(-)-(S)-Equol (4',7-Dihydroxyisoflavan) 是雌激素受体β的高亲和力配体。 | |||
T34584 |
Scillaren A
Transvaalin,Scillaglykosid A |
Others | Others |
Scillaren A is a a crystalline steroidal glycoside from Scilla maritima. | |||
T33926 |
Penupogenin
|
||
Penupogenin is a steroidal aglycone isolated from the roots of Cynanchum auriculatum. | |||
T2S2321 |
Pennogenin
|
Others | Others |
Pennogenin steroidal saponins could be utilized to develop anticancer medicines. | |||
T32610 |
Laxogenin
6-Oxotigogenin |
||
Laxogenin is a new steroidal sapogenin extracted from Smilax sieboldi Miq. | |||
T13757 |
Lirioprolioside B
|
Others | Others |
Lirioprolioside B is a steroidal glycoside isolated from the underground organs of Liriope spicata var. prolifera. | |||
T40890 |
Proprotogracillin
|
Others | Others |
Proprotogracillin is a steroidal glycoside isolated from the bulbs of lilium speciosum. | |||
T30170 |
Aspafilioside A
|
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Aspafilioside A is a steroidal saponin isolated from the root of Asparagus filicinus. | |||
T13577 |
β-Zearalenol
|
Others | Others |
β-Zearalenol, a non-steroidal estrogenic mycotoxin synthesized by Fusarium species, potentially influences transcription and affects gene expression on the translational level. | |||
T39854 |
Cycloposine
|
Others | Others |
Cycloposine, a steroidal alkaloid present in the roots and rhizomes of Veratrum californicum, is known to possess teratogenic properties. | |||
T13641 |
Dehydrotomatine
|
Others | Others |
Dehydrolycopene is a major steroidal sugar alkaloid (SGAs), which is mainly found in mature green fruits, leaves and flowers of tomatoes. Dehydrotomato is targeted at bacteria, fungi, insects and animals. | |||
T82544 |
Disporoside C
|
||
Disporoside C, 分子式为C41H66O12, 是一种甾体皂苷,可从植物Disporopsis pernyi中提取。 | |||
T10913 |
Cyclobuxine D
|
Others | Others |
Cyclobuxine D is a steroidal alkaloid extracted from Buxus microphylla. Cyclostatin D has obvious bradycardia effect on rat heart, and inhibits acetylcholine and Ba ++ induced longitudinal muscle contraction isolated from rabbit jejunum. | |||
T40193 |
Ebeiedinone
|
Others | Others |
Ebeiedinone, a steroidal alkaloid derived from Fritillaria species, effectively inhibits the activity of human whole blood cholinesterase (ChE) at a concentration of 0.1 mM, resulting in a significant inhibitory effect of 69.0%. | |||
T81545 |
Parisyunnanoside H
|
||
Parisyunnanoside H,一种甾体皂苷,可从Paris polyphylla Smith var. yunnanensis分离提取。 | |||
T13805 |
Ophiopogonin C
Ophiopogonin C,麦冬胶原蛋白 C |
Others | Others |
Ophiopogonin C is a natural product isolated from the tubers of Ophiopogon japonicus, is a rare naturally occurring C29 steroidal glycoside. | |||
T81093 |
Sterebin F
|
||
Sterebin F, 一种甾类化合物,来源于Stevia rebaudiana叶的分离提取,表现出降血糖的活性。 | |||
T83259 |
6β-Hydroxystigmasta-4,22-dien-3-one
|
||
6β-Hydroxystigmasta-4,22-dien-3-one为一类固醇化合物,可从Hedychium coronarium中提取。 | |||
T81097 |
Stauntoside M
|
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Stauntoside M是一种从Cynanchum stauntonii的根中分离得到的类固醇糖苷。 | |||
T82480 |
Elephanoside D
|
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Elephanoside D(化合物8)是从丝兰(Yucca elephantipes Regel)茎部分离出的一种甾体皂苷。 | |||
T82549 |
Diosgenin-3-O-rhamnosyl(1→2)[glucosyl(1→6)]glucoside
|
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Diosgenin-3-O-rhamnosyl(1→2)[glucosyl(1→6)]glucoside (compound 9) 为甾体皂甙类化合物,源自Paris polyphylla var. yunnanensis,具有特定的结构特征。 | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01640 |
MRGPRX2 Protein, Human, Recombinant (His)
Mas-related G-protein coupled receptor member X2,MRGPRX2 |
Human | E. coli |
Mast cell-specific receptor for basic secretagogues, i.e. cationic amphiphilic drugs, as well as endo- or exogenous peptides, consisting of a basic head group and a hydrophobic core. Recognizes and binds small molecules containing a cyclized tetrahydroisoquinoline (THIQ), such as non-steroidal neuromuscular blocking drugs (NMBDs), including tubocurarine and atracurium. In response to these compounds, mediates pseudo-allergic reactions characterized by histamine release, inflammation and airway c... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12336 |
Oxaprozin D4
Wy-21743 D4 |
Others | Others |
Oxaprozin D4 is the deuterium labeled Oxaprozin, is a non-steroidal anti-inflammatory drug (NSAID). | |||
T11998 |
Meloxicam-d3
Meloxicam D4 |
Others | Others |
Meloxicam D4 is deuterium labeled Meloxicam. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity,(Target:COX-1; IC50: 36.6 μM ;(Target:COX-2; IC50: 0.49 μM). | |||
T11754 |
Ketorolac-d5
Ketorolac D5 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Ketorolac D5, a deuterium-labeled version of Ketorolac, is a non-steroidal anti-inflammatory agent that functions as a nonselective COX inhibitor. It exhibits IC50 values of 20 nM for COX-1 and 120 nM for COX-2. | |||
T27210 |
DRX-065
DRX 065,DRX065,deuterated R-enantiomer of pioglitazone |
||
DRX-065 is a stabilized and deuterated R-enantiomer of pioglitazone. DRX-065 has pharmacological properties desirable for the treatment of NASH (mitochondrial function modulation, non-steroidal anti-inflammatory effects, and glucose lowering effects) with | |||
T11246 |
Etoricoxib-d4
MK-0663 D4,依托考昔 D4,L-791456 D4,Etoricoxib D4 |
Others | Others |
Etoricoxib D4 is a non steroidal anti-inflammatory agent, acting as a selective and orally active COX-2 inhibitor, with IC50s of 1.1 μM and 116 μM for COX-2 and COX-1 in human whole blood.Etoricoxib D4 is a deuterium labeled Etoricoxib. | |||
TMIH-0472 |
Rac Loxoprofen sodium-d3
|
||
Rac Loxoprofen sodium-d3 是 Rac Loxoprofen sodium 的氘代化合物。Rac Loxoprofen sodium 的 CAS 号为 68767-14-6。Loxoprofen 是一种非甾体类抗炎药,具有解热作用,可用于缓解疼痛的研究。它是非选择性COX抑制剂,对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。 | |||
TMIH-0325 |
MefenaMic Acid-d4
|
||
MefenaMic Acid-d4 是 MefenaMic Acid 的氘代化合物。MefenaMic Acid 的 CAS 号为 61-68-7。Mefenamic acid 是一种非甾体抗炎剂,可竞争性抑制hCOX-1和hCOX-2,IC50值分别为 40 nM 和 3 μM。 | |||
TMIJ-0211 |
Loxoprofen-d4
|
||
Loxoprofen-d4 是 Loxoprofen 的氘代化合物。Loxoprofen 的 CAS 号为 68767-14-6。Loxoprofen 是一种非甾体类抗炎药,具有解热作用,可用于缓解疼痛的研究。它是非选择性COX抑制剂,对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。 | |||
TMIH-0290 |
Ketorolac-d5-P1
|
||
Ketorolac-d5-P1 是 Ketorolac 的氘代化合物。Ketorolac 的 CAS 号为 74103-06-3。Ketorolac 是非甾体抗炎剂,是非选择性的COX抑制剂,对 COX-1 和 COX-2 的IC50值分别为 20 和 120 nM。 | |||
TMIH-0291 |
Ketorolac-d5-P2
|
||
Ketorolac-d5-P2 是 Ketorolac 的氘代化合物。Ketorolac 的 CAS 号为 74103-06-3。Ketorolac 是非甾体抗炎剂,是非选择性的COX抑制剂,对 COX-1 和 COX-2 的IC50值分别为 20 和 120 nM。 | |||
TMID-0276 |
MAA-d3
|
||
MAA-d3 是 MAA 的氘代化合物。MAA 的 CAS 号为 519-98-2。4-Methylamino antipyrine 是 Metamizole 的活性代谢产物,可用于疼痛和发烧的研究。Metamizole 是吡唑啉酮类非甾体抗炎药,可抑制COX。 | |||
TMIJ-0135 |
Abiraterone-d4
|
||
Abiraterone-d4 是 Abiraterone 的氘代化合物。Abiraterone 的 CAS 号为 154229-19-3。Abiraterone 是不可逆的CYP17A1抑制剂,具有抗雄激素作用,抑制细胞色素 p450 酶 CYP17 的 17α-羟化酶 (IC50:2.5 nM) 和 17,20-裂合酶 (IC50:15 nM) 活性。 | |||
T71288 |
Phenylbutazone-d9
|
||
Phenylbutazone-d9 is intended for use as an internal standard for the quantification of phenylbutazone by GC- or LC-MS. Phenylbutazone is a non-steroidal anti-inflammatory drug and an inhibitor of the peroxidase activity of COX (IC50 = ~100 µM in the presence of hydrogen peroxide). It also inhibits prostaglandin I synthase (IC50 = ~25 µM in the presence of hydrogen peroxide). Phenylbutazone (2 mg/kg) reduces increases in type II collagen levels in the inflamed joints of an equine model of LPS-in... | |||
TMIJ-0207 |
(S)-Ketoprofen-d3
|
||
(S)-Ketoprofen-d3 是 (S)-Ketoprofen 的氘代化合物。(S)-Ketoprofen 的 CAS 号为 22161-81-5。S-(+)-Ketoprofen 抑制COX-1和COX-2的IC50值分别为 1.9 和 27 nM。 | |||
T71212 |
Lornoxicam-d4
|
||
Lornoxicam-d4 is intended for use as an internal standard for the quantification of lornoxicam by GC- or LC-MS. Lornoxicam is a COX inhibitor and non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory and analgesic properties. It inhibits production of thromboxane B2 from arachidonic acid in HEL human erythroleukemic cells, which endogenously express COX-1, as well as inhibits LPS-induced formation of prostaglandin F1α from arachidonic acid in Mono-Mac-6 cells, which endogenously e... | |||
T71303 |
Flufenamic Acid-d4
|
||
Flufenamic acid-d4 is intended for use as an internal standard for the quantification of flufenamic acid by GC- or LC-MS. Flufenamic acid is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor (IC50s = 3 and 9.3 µM for human COX-1 and COX-2, respectively). Flufenamic acid inhibits TNF-α-induced increases in COX-2 levels and NF-κB activation in HT-29 colon cancer cells in a concentration-dependent manner. It inhibits calcium influx induced by fMLP or A23187 in human polymorphonuclear... | |||
T71141 |
Fenspiride-d5
|
||
Fenspiride-d5 is intended for use as an internal standard for the quantification of fenspiride by GC- or LC-MS. Fenspiride is an antagonist of histamine H1 receptors and a non-steroidal anti-inflammatory drug (NSAID). It inhibits histamine-induced contraction of isolated guinea pig trachea but not histamine-induced inotropy of isolated guinea pig heart. It also inhibits phosphodiesterase 4 (PDE4), PDE5, and PDE3 (IC50s = 69, ~158, and 363 µM, respectively, in isolated human bronchi derived from ... |