196
32
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5513 |
RO-3
|
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
RO3 是一种能透过大脑的P2X3和P2X2/3拮抗剂,口服有活性。它对人同型多聚体 P2X3和异型多聚体 P2X2/3受体的 pIC50分别为 5.9 和 7.0。 | |||
T26745 |
BAY 73-1449
BAY-73-1449,BAY73-1449 |
Others | Others |
BAY 73-1449 是前列环素受体选择性拮抗剂,在人 HEL 细胞和大鼠 DRG 的 cAMP 分析中具有很高的效价,IC50小于 0.1 nM。BAY 73-1449在降血压方面有研究的价值。 | |||
T1504 |
Silodosin
西洛多辛,KAD 3213,KMD 3213 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Silodosin (KAD 3213) 是有选择性的、强效的、口服活性的 α1A-adrenergic receptor 阻滞剂,是一种有效且耐受性良好的试剂,可用于研究 LUTS/BPH。它对 α1A-AR 表现出高度的亲和力,是 α1B-AR 和 α1D-AR 亲和力的 162 和 50 倍。 | |||
T6991 |
Nitroprusside disodium dihydrate
硝普钠二水合物,硝普钠,Sodium Nitroferricyanide(III) Dihydrate,Sodium Nitroprusside Dihydrate |
Guanylate cyclase; Autophagy | Autophagy; GPCR/G Protein |
Nitroprusside disodium dihydrate (Sodium Nitroprusside Dihydrate) 是一种血管扩张剂,通过在血液中自发释放 NO 发挥作用。它可在谷胱甘肽耗竭的成骨细胞中诱导自噬,用于急性高血压和心力衰竭的研究。 | |||
T0703 |
Flavoxate hydrochloride
Flavoxate HCl,盐酸黄酮哌酯,NSC-114649,DW61,Rec-7-0040 |
AChR | Neuroscience |
Flavoxate hydrochloride (DW61) 是一种毒蕈碱受体 AChR 拮抗剂, IC50为 12.2 μM。 | |||
T64006 |
Lipid-lowering agent-1
|
||
Lipid-lowering agent-1 是有效的降脂剂,能够明显抑制低密度脂蛋白胆固醇 (LDLC) 和促进高密度脂蛋白胆固醇 (HDLC) 产生的药理作用。Lipid-lowering agent-1 能够明显降低高脂饮食大鼠的脂肪。 | |||
T8529 |
WYC-210
|
Others | Others |
WYC-210 是一种视黄醇类化合物,是 Tazarotene 的衍生物,具有较低的抗癌活性。 | |||
T21478 |
Cromakalim
BRL-34915,BRL 34915,(±)-Cromakalim,BRL34915 |
||
Cromakalim, a potassium channel-opening vasodilator, acts on ATP-sensitive potassium channels and so causes membrane hyperpolarization, it can be used to treat hypertension as it will relax vascular smooth muscle to lower blood pressure. The active isomer | |||
T15102 |
Dexamethasone palmitate
地塞米松棕榈酸酯,DXP |
Glucocorticoid Receptor | Endocrinology/Hormones |
Dexamethasone palmitate (DXP) (DXP) 是 Dexamethasone 的前药。Dexamethasone 是糖皮质激素受体激动剂。与Dexamethasone 相比, DXP 对糖皮质激素受体的亲和力低 47 倍。DXP 显示出抗炎活性。 | |||
TP2104L |
UFP 803 acetate
|
Neurotensin Receptor | GPCR/G Protein |
UFP 803 acetate 是一种有效的 urotensin-II (UT) 受体配体。 UFP-803 显示较低残留激动剂的活性。 | |||
T22316 |
Doxazosin
UK 33274,多沙唑嗪 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Doxazosin (UK 33274) 是选择性的拮抗突触后的α1肾上腺素受体。 | |||
T19794 |
Temafloxacin
替马沙星,Omniflox |
Antibiotic | Microbiology/Virology |
Temafloxacin (Omniflox) 是一种喹诺酮类广谱抗菌剂,对革兰氏阳性菌、革兰氏阴性菌和厌氧菌均有效。 | |||
T20381 |
Cetyl glycol
NSC-71525,NSC 71525,1,2-十六烷二醇,NSC71525 |
Others | Others |
Cetyl glycol (NSC-71525) 有利于金属有机前体的分解、中间体 Co(2+)Fe(3+)-油酸配合物的形成以及纳米颗粒在较低温度下的成核。 Cetyl glycol 是一种可用于化妆品的还原剂。 | |||
T63166 |
LSN3318839
LSN-3318839,LSN 3318839 |
Glucagon Receptor | GPCR/G Protein |
LSN3318839 是一种有效且可口服的胰高血糖素样肽-1受体(GLP-1R)变构调节剂。LSN3318839可增强GLP-1R的G蛋白偶联信号传导,可用来降低血糖。 | |||
T15251 |
Etebenecid
乙磺舒,Urelim |
Others | Others |
Etebenecid (Urelim) 是促尿酸排泄药,能够抑制青霉素自肾小管分泌。 | |||
T6728 |
VUF 10166
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
VUF 10166 是一种新型的、有效的、竞争性的 5-HT3A 受体拮抗剂,Ki 为 0.04 nM,其对 5-HT3AB 受体的亲和力显着降低。 | |||
T6565 |
Levobetaxolol hydrochloride
Betaxon,左旋倍他洛尔,(S)-Betaxolol hydrochloride,AL-1577A,Levobetaxolol HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Levobetaxolol hydrochloride ((S)-Betaxolol hydrochloride) 是 β-肾上腺素能受体抑制剂 (β阻滞剂) 。它具有降低眼压的作用,可用于研究青光眼。 | |||
T1423 |
3-Methylsalicylic acid
Hydroxytoluic acid,3-甲基水杨酸,o-Cresotic acid,邻甲基水杨酸 |
COX | Immunology/Inflammation; Neuroscience |
3-Methylsalicylic acid (o-Cresotic acid) 是水杨酸衍生物,可作用于人血浆,激活纤维蛋白溶解系统,具有显著的纤溶活性。 | |||
T29037 |
UC-781
NSC 675186,UC781,UC 781 |
Antiviral; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
UC-781 (NSC-675186) 是一种高效且具有选择性的人类免疫缺陷病毒 HIV-1 非核苷类逆转录酶(NNRTI)I抑制剂 ,C50 值为 5 nM。UC-781 具有抗病毒活性和耐药性。UC-781状态稳定,较低的 PH 或不同温度对其影响较小。 | |||
T10000 |
(±)-Tazifylline
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
(±)-Tazifylline 是一种选择性的长效组胺 H1 受体拮抗剂。 Tazifylline 对 H2 受体、α- 和 β-肾上腺素能受体、5-羟色胺和毒蕈碱受体亚型的亲和力要低得多。 | |||
T14298 |
Rimiducid
|
Apoptosis; Others; Fatty Acid Synthase | Apoptosis; Metabolism; Others |
Rimiducid 是一种可渗透脂质的他克莫司类似物,是一种二聚剂,通过交联 FKBP 结构域起作用。它将 Caspase 9 自杀开关二聚化并迅速诱导细胞凋亡。 | |||
T3978 |
Linerixibat
GSK2330672,Iinerixibat |
HBV | Microbiology/Virology |
Linerixibat (GSK2330672) 是高效的、不可吸收的、具有口服活性的顶端钠依赖性胆汁酸转运蛋白 (ASBT) 抑制剂,对人ASBT 的IC50为 42 nM。它是一种降脂剂,具有用于 2 型糖尿病和原发性胆源性胆管炎的研究潜力。 | |||
T13140 |
Umbralisib R-enantiomer
TGR-1202 R-enantiomer,RP5264 R-enantiomer |
PI3K | PI3K/Akt/mTOR signaling |
Umbralisib R-enantiomer (RP5264 R-enantiomer) 是 PI3K 的δ型抑制剂,是 TGR-1202 活性较低的对映体。Umbralisib R-enantiomer 对δ型 pi3激酶的 IC50,至少比抑制剂对其他 PI3K 亚型(A, β和γ)的 IC50低20倍。 | |||
T40229 |
SR-0813
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
SR-0813 is a potent and selective inhibitor of the YEATS domain in ENL/AF9. It has an IC 50 of 25 nM and EC 50 of 205 nM for the ENL YEATS domain and an IC 50 of 311 nM and EC 50 of 76 nM (CETSA) for the AF9 YEATS domain. SR-0813 exhibits over 100-fold lower affinity (Kd =3.5 μM) for MAP3K19 compared to ENL YEATS (Kd =30 nM). It can be utilized in acute leukemia research. | |||
T22029 | AL 34662 | 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
AL 34662 是一种具有选择性和高效性的 5-HT2A 受体激动剂,对大鼠和人 5-HT2 受体的IC50 分别为 0.77 nM 和 1.5 nM。AL 34662 还是一种亲和力较低的 α-1D 肾上腺素能激动剂,EC50 值为 0.4 μM。AL 34662 可用于降低眼压。 | |||
TQ0271 |
Falnidamol
BIBX 1382 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Falnidamol (BIBX 1382) 是一种具有口服活性的,选择性的 EGFR 酪氨酸激酶抑制剂,IC50 为3 nM。Falnidamol 对 ErbB2 (IC50=3.4 μM) 和其他一系列相关酪氨酸激酶 (IC50>10 μM) 的选择性 >1000倍。Falnidamol 是嘧啶-嘧啶化合物,具有抗癌活性。 | |||
T3625 |
Bempedoic acid
ETC1002,ESP-55016,ETC 1002,ETC-1002 |
ATP Citrate Lyase; AMPK | Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling |
Bempedoic acid (ETC1002) 是一种 ATP-柠檬酸裂解酶抑制剂,可激活AMPK。它是脂质和碳水化合物代谢的调节剂。 | |||
T11174 |
(R)-Elagolix
恶拉戈利,NBI-56418 |
GNRH Receptor | GPCR/G Protein |
(R)-Elagolix (NBI-56418) 是口服具有活性的、选择性高的非肽类促性腺激素释放激素受体短期有效拮抗剂 (KD = 54 pM)。 | |||
T2119 |
Venetoclax
GDC-0199,ABT 199,维奈妥拉,ABT-199,ABT199 |
BCL; Autophagy | Apoptosis; Autophagy |
Venetoclax (ABT-199) 是一种 Bcl-2 抑制剂 (Ki<0.01 nM),具有高效性、选择性和口服活性。Venetoclax 与 Bcl-xL 和 Bcl-W 的亲和力降低了 3 个数量级(Kis=48/245 nM)。Venetoclax 可以诱导自噬和凋亡。 | |||
T7218 |
Endomorphin 2
内吗啡肽 2 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Endomorphin 2 是一种高亲和力和选择性的 μ-阿片受体激动剂,对 kappa3 结合位点具有合理的亲和力 ,Ki 为 20 到 30 nM 之间。 | |||
T15300 |
Fluorofenidone
AKF-PD |
Others | Others |
Fluorofenidone (AKF-PD) 是 AMR69 的类似物,抗纤维化活性与 AMR69相同,但 Fluorofenidone 的毒性更低,半衰期长。它部分通过 PI3K/Akt 信号通路抑制 NADPH 氧化酶和细胞外基质 (ECM) 的沉积,能够减少肾间质纤维化的发生。 | |||
T0197 |
Terazosin hydrochloride
盐酸特拉唑嗪,Terazosin HCl,Terazosine,Blavin,Hytrin,Zayasel,Fosfomic |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Terazosin hydrochloride (Hytrin) 是一种竞争性和口服活性的 α1-肾上腺素受体拮抗剂,是一种喹唑啉衍生物。它通过舒张血管和打开膀胱来起作用。它可用于良性前列腺增生和高血压的研究。 | |||
T9417L |
gamma-preprotachykinin amide (72-92) acetate
gamma-preprotachykinin amide (72-92) acetate (114882-65-4 Free base) |
Others | Others |
gamma-preprotachykinin amide (72-92) acetate 是一种 21 个氨基酸的肽,属于速激肽 (TK) 家族,在其 C 末端序列中包括神经激肽 A (NKA)。它对中枢 NK-2 受体的亲和力高于 NKA;它对 NK-1 受体的亲和力较低,但是,它有效地刺激唾液分泌,这是由 NK-1 受体激活介导的。 | |||
T0006 |
Methylene Blue trihydrate
碱性亚甲蓝三水合物,Methylthionine chloride,Basic blue 9,亚甲蓝三水合物,Methylene Blue |
Guanylate cyclase; Microtubule Associated; NO Synthase; Parasite; Monoamine Oxidase | Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Methylene Blue trihydrate (Basic blue 9) 是鸟苷酸环化酶,单胺氧化酶 A 和 NO 合酶抑制剂。它是血管加压药,在医疗中通常用作染料。它具有抗伤害感受,抗疟疾,抗抑郁和抗焦虑作用,可用于高铁血红蛋白血症,神经退行性疾病和异环磷酰胺引起的脑病的研究。 | |||
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。 | |||
T0918 |
Trimebutine
曲美布汀,Mebutin |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Trimebutine (Mebutin) 是阿片受体激动剂,有抗毒蕈碱活性。它是解痉剂,可调节肠道和结肠运动,并通过抗毒蕈碱和弱μ-阿片受体激动剂作用缓解腹痛。 | |||
T0267 |
Zonisamide
AD 810,唑尼沙胺,CI 912 |
Calcium Channel; Sodium Channel; Carbonic Anhydrase | Membrane transporter/Ion channel; Metabolism |
Zonisamide (AD 810) 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂,对人类线粒体同工酶 hCA II 和 hCA V 作用的 Ki 值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性,在癫痫、癫痫发作和帕金森病的研究中具有价值。 | |||
T27437 |
GS-462808
GS462808,GS 462808 |
||
GS-462808 is a late sodium current inhibitor of the cardiac Nav1.5 channel. GS-462808 had lower brain penetration and serendipitously lower activity at the brain isoforms. | |||
T32691 | Levamlodipine hydrochloride | ||
Levamlodipine hydrochloride is a medication used to lower blood pressure and prevent chest pain. | |||
T32692 |
Levamlodipine hydrobromide
Levamlodipine HBr |
||
Levamlodipine hydrobromide is a medication used to lower blood pressure and prevent chest pain. | |||
T29999 | Amlodipine camsylate | ||
Amlodipine camsylate is a medication used to lower blood pressure and prevent chest pain. | |||
T29997 |
Amlodipine adipate
CJ11828,CJ 11828,CJ-11828 |
||
Amlodipine adipate is a medication used to lower blood pressure and prevent chest pain. | |||
T0231L3 |
Amlodipine besylate monohydrate
|
||
Amlodipine besylate monohydrate is a medication used to lower blood pressure and prevent chest pain. | |||
T11018 |
DHMEQ racemate
rel-DHMEQ |
NF-κB | NF-κB |
DHMEQ racemate is an NF-κB inhibitor. The activity of DHMEQ racemate is lower than (-)-DHMEQ. | |||
T32504 |
L-732531
L732531,L 732531 |
||
L-732531 is a tacrolimus-related immunosuppressant with lower toxicity. | |||
T8663L |
Nifenalol
|
||
Nifenalol is an adrenergic beta-blocker with good antiarrhythmic properties. It tends to lower blood pressure and provide protection against angina. | |||
T30001 |
Amlodipine besylate, (R)-
|
||
Amlodipine besylate, (R)- is a medication used to lower blood pressure and prevent chest pain. | |||
T27418 |
Glybuzole
Desaglybuzole,Sulfamidothiodiazol,Gludiase,Glybuzolum |
||
Glybuzole is a sulfonamide derivative, it is able to lower blood glucose levels by increasing the release of insulin from pancreatic beta cells. | |||
T30000 |
Amlodipine hydrobromide
Amlodipine HBr |
||
Amlodipine hydrobromide is a salt of Amlodipine --- a medication used to lower blood pressure and prevent chest pain. | |||
T13442 | (R)-BAY1238097 | Others | Others |
(R)-BAY1238097 is the R-isomer with lower activity of BAY1238097. BAY1238097 is a selective BET inhibitor. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19056 |
Safflower yellow
Saffron powder,Carthamas yellow,红花黄 |
Others | Others |
Safflower yellow (Saffron powder) 是提取自植物红花的花中,可用于研究心脑血管疾病。 | |||
T6263 |
Safflower-yellow
|
Others | Others |
Safflower-yellow 是从植物红花(Carthamus tinctorius)的花中提取的,作为中药已广泛用于治疗心脑血管疾病。 | |||
T1134 |
Clofoctol
叔辛酚氯,氯福克酚 |
Antibacterial; Antibiotic | Microbiology/Virology |
Clofoctol 是一种抗生素,,可研究革兰氏阳性菌感染。它仅对革兰氏阳性菌起作用, 可渗透入人类肺组织。 | |||
T6000 |
Delta-Tocopherol
(+)-DELTA-生育酚,D-DELTA-TOCOPHEROL |
Endogenous Metabolite | Metabolism |
Delta-Tocopherol 是维生素 E 的异构体,具有抗氧化活性。 | |||
T5735 |
Methyl deacetylasperulosidate
Deacetyl asperulosidic acid methyl ester,6α-Hydroxygeniposide,去乙酰车叶草苷酸甲酯 |
Others | Others |
Methyl deacetylasperulosidate (6α-Hydroxygeniposide) 是环烯醚萜类化合物,能够降低正常小鼠的血糖水平,对小鼠具有通便作用。 | |||
T0254 |
Probucol
DH-581,普罗布考 |
Virus Protease; ABC; Lipid | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Probucol (DH-581) 是一种抗高脂血症药物,可通过增加 LDL 分解代谢率来降低血液中的胆固醇水平。 | |||
T21383 |
D-Thyroxine
Dethyrona,Detyroxin,Dextroid,Dextrothyroxine;Biotirmone,Dextroxin,Biotirmone,Debetrol,Dextrothyroxine |
Others | Others |
D-Thyroxine (Dextroxin) 是一种甲状腺激素,对 TSH 的分泌具有抑制作用,可用于研究高胆固醇血症。 | |||
TN2230 |
Soyasaponin Ba
大豆皂苷 BA,大豆皂苷Ba |
Others | Others |
Soyasaponin Ba 是一种大豆皂苷,分离自菜豆类,可用作醛糖还原酶抑制剂。 | |||
TN1622 |
Ermanin
堪非醇3,4'-二-O-甲醚 |
NOS; Influenza Virus; COX; HIV Protease; Antibacterial; Antibiotic | Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Ermanin 是一种从 Tanacetum microphyllum 中分离出来的类黄酮。Ermanin抑制血小板聚集,具有抗结核和抗病毒/细菌特性。Ermanin 可抑制 iNOS 和 COX-2 的表达,从而具有抗炎活性。Ermanin 可能具有抗 HIV-1 活性。Ermanin 在较低浓度下可有效地抑制 Dione juno 幼虫。 | |||
T5S1982 |
Periplocin
Periplocoside,杠柳毒苷 |
Apoptosis; Others | Apoptosis; Others |
Periplocin (Periplocoside) 是从黑龙骨中分离出的一种强心类固醇。它可促进肿瘤细胞凋亡并抑制肿瘤生长。它通过激活 Na/K-ATPase 介导的 Src/ERK 和 PI3K/Akt 途径,具有促进伤口愈合的潜力。 | |||
T2698 |
Asperosaponin VI
Akebia saponin D,Asperosaponin Ⅵ,川续断皂苷 VI |
Apoptosis; Others; Caspase | Apoptosis; Others; Proteases/Proteasome |
Asperosaponin VI (Akebia saponin D) 是一种来自续断壁的皂苷组分。它通过增加 Bcl-2/Bax 比值,降低活性 caspase-3 表达,以及增强 p-Akt 和 p-CREB,从而抑制缺氧诱导的心肌细胞凋亡。它通过 BMP-2/p38 和 ERK1/2 信号途径诱导成骨细胞分化。 | |||
T41095 |
(E)-3-(4-Methoxyphenyl)acrylic acid
(E)-3-(4-甲氧基苯基)丙烯酸 |
Glucosidase | Metabolism |
(E)-3-(4-Methoxyphenyl)acrylic acid 是从 Etlingera pavieana (Pierre ex Gagnep.) R. M. Sm. 的根茎中分离出来的一种小分子化合物。它是一种新型 α-葡萄糖苷酶抑制剂。(E)-3-(4-甲氧基苯基)丙烯酸具有保肝活性、抗失水活性、增强认知效果,并可用于降低血压血糖。 | |||
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。 | |||
T1437 |
D-Panthenol
D-泛醇,D-Pantothenyl alcohol,Ilopan,Dexpanthenol,Pantothenol |
Endogenous Metabolite | Metabolism |
D-Panthenol (D-Pantothenyl alcohol) 是 D-pantothenic acid 和胆碱能剂的酒精类似物。D-Panthenol 作为乙酰化反应所必需的辅酶A的前体,参与乙酰胆碱的合成。虽然 D-Panthenol 作用的确切机制尚不清楚,但它可能增强乙酰胆碱的作用。D-Panthenol 作用于胃肠道,增加下肠蠕动。它也适用于局部皮肤,以缓解瘙痒和促进愈合。 | |||
T3795 |
Corilagin
|
Apoptosis; TLR; Reverse Transcriptase; Antibacterial; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology |
Corilagin 是一种鞣酸,有抑制 RNA 肿瘤病毒逆转录酶的活性。它抑制金黄色葡萄球菌的生长,MIC 为 25 μg/mL。它有抗肿瘤活性,可用于肝癌和卵巢癌。 | |||
T4S0145 |
Corylifol A
Corylinin,补骨脂异黄酮A |
hCE; STAT; UGT | JAK/STAT signaling; Metabolism; Stem Cells |
Corylifol A (Corylinin) 是补骨脂中的一种天然产物,可抑制IL-6 诱导的STAT3激活和磷酸化,IC50值为0.81 μM。 | |||
T4877 |
L-Homocystine
|
Endogenous Metabolite | Metabolism |
L-Homocystine 是一种 L-homocysteine 的氧化物。其中 L-homocysteine 是抗血栓因子、血管舒张损害剂、促炎因子,也是研究心血管疾病发生机制的内质网应激反应的诱导剂。 | |||
T5S0106 |
Peimisine
贝母辛,Ebeiensine |
RAAS; AChR | Endocrinology/Hormones; Neuroscience |
Peimisine (Ebeiensine) 非竞争性拮抗气管平滑肌 M 受体,抑制 Ach 引起的平滑肌收缩。它兴奋 β 受体和拮抗内钙释放,促进一氧化氮释放,可舒张气管平滑肌,有平喘作用。 | |||
T0256 |
Citric acid trilithium salt tetrahydrate
Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate |
Dehydrogenase; GSK-3; HIF/HIF Prolyl-Hydroxylase; Antibacterial; GluR | Chromatin/Epigenetic; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells |
Citric acid trilithium salt tetrahydrate (Lithium citrate tribasic tetrahydrate) 是一种用于治疗精神疾病的药物。它也是一种医药和建筑材料, 可用于氨基酸定量分析时的梯度洗脱。 | |||
TN4974 | Scutebata B | Others | Others |
Scutebata B inhibited NO production efficiently with IC50 values of lower than 50 μM. | |||
TN2193 |
Scutebarbatine W
|
Others | Others |
Scutebarbatine W can inhibit nitric oxide production efficiently with IC50 values of lower than 50 μM, it may have potential effects on the reduction of neuroinflammation. | |||
TN2194 |
Scutebarbatine X
|
Others | Others |
Scutebarbatine X can inhibit nitric oxide production efficiently with IC50 values of lower than 50 μM, it may have potential effects on the reduction of neuroinflammation. | |||
TN3260 |
8(14),15-Isopimaradien-3-ol
|
Calcium Channel; Antifection | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
ent-8(14),15-pimaradien-3beta-ol (8(14),15-Isopimaradien-3-ol) can induce vascular relaxation. It displays high antibacterial activities (MIC values lower than 10 microg /mL for most pathogens). | |||
TN5448 |
Steppogenin
Norartocarpanone |
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Steppogenin exhibits significant tyrosinase inhibition activity, ;it also shows strong mushroom tyrosinase inhibitory activity with IC(50) values lower than 50 microM, more potent than kojic acid (IC(50) = 71.6 microM), a well-known tyrosinase inhibitor. | |||
TN1242 |
3,3'-Di-O-methylellagic acid
3,8-Di-O-methylellagic acid,3,3'-O-二甲基鞣花酸 |
Others; TNF; Antifection | Apoptosis; Microbiology/Virology; Others |
3,3'-Di-O-methylellagic acid reveals moderate antibacterial activity, it also shows strong DPPH radical scavenging activities with SC50 of 123.3 ug/mL. It has a lower capacity of stimulating murine peritoneal macrophages to release nitric oxide and tumoural-alpha necrose factor | |||
T13756 |
Liquiritigenin-7-apiosylglucoside
芹糖新甘草苷,Liquiritigenin-7-O-β-D-glucopyranosyl-(1→2)-β-D-apiofuranoside |
Others | Others |
Liquiritigenin-7-O-β-D-glucopyranosyl-(1→2)-β-D-apiofuranoside is a flavonoid isolated from the roots of Glycyrrhiza, has weaker cytotoxicity against several tumor cells and normal cells. | |||
TMA0127 | Ficusin A | transporter; PPAR | DNA Damage/DNA Repair; Metabolism |
Ficusin has antioxidant, antilipidemic and antidiabetic effects, it can lower the levels of fasting blood glucose, plasma insulin, body weight gain in HFD-STZ induced diabetic rats, and can significantly enhance the PPARγ expression and improve the transl | |||
T82339 |
Gangliotetraose
Gg4 |
||
Gangliotetraose(Gg4)是一种含有GM1及其唾液酸化衍生物的四糖。它能促进分化神经元核内Ca2+的外流,进而降低核内Ca2+浓度。Gg4参与调节神经元的可塑性、修复过程以及大脑中神经营养素的释放。 | |||
T83597 |
(+)-Menthyl acetate
|
||
(+)-Menthyl acetate是一种从Cunila angustifolia Benth精油中分离得到的化学化合物。它对MCF-7细胞株具有较高的选择性,其半抑制浓度(IC50)为34.0 μg/mL,而对SK-Mel-28细胞株的选择性较低,IC50为279.9 μg/mL,并且对A549细胞没有致死作用。 | |||
T79975 |
Dihydrodehydrodiconiferyl alcohol 9-O-α-L-rhamnopyranoside
|
HBV | Microbiology/Virology |
Dihydrodehydrodiconiferyl alcohol 9-O-α-L-rhamnopyranoside(化合物1)是一种具有抗HBV活性的木脂素类化合物。该化合物对HBV表面抗原(HBsAg)的IC50为0.58 mM,而对HBV e抗原(HBeAg)的IC50 > 2.4 mM。其可从八角茴香中提取分离。 | |||
T82031 | Isoguaiacin | ||
Isoguaiacin为一种天然产物,具有复杂的多环化合物结构,广泛应用于生物医药研究领域。 | |||
TN4223 |
Homopterocarpin
|
Antifection | Microbiology/Virology |
Homopterocarpin and Pterocarpus extract offer gastroprotection against indomethacin- induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis, homopterocarpin may be responsible for, or contribute to the antiulcerogenic property |