124
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16947 |
SU16f
3-substituted indolin-2-one 16f,SU-16F,SU 16F |
PDGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SU16f (3-substituted indolin-2-one 16f) 是一种有效的,选择性 PDGFRβ 抑制剂,对 PDGFRβ,PDGFR1,PDGFR2 的 IC50 分别为 10 nM,140 nM,2.29 μM。SU16f 抑制 PDGFRβ 受体从而可以阻断胃癌来源的间充质干细胞 (GC-MSC) 条件培养基在胃癌细胞增殖和迁移中的促进作用。 | |||
T19567 | Substituted piperidines-1 | Others | Others |
Substituted piperidines-1 can promote the release of growth hormone in humans and animals. | |||
T34590 |
SD-254
Venlafaxine deuterium-substituted,D9-venlafaxine |
||
SD-254 is a deuterium analog of Effexor, with fewer side effects and a longer half-life. | |||
T39127 |
meso-CF3-BODIPY 2
CF3-substituted Tetramethyl BODIPY,meso-CF3-BODIPY 2 |
||
meso-CF3-BODIPY 2, also known as CF3-substituted Tetramethyl BODIPY, is a fluorescent dye that has an absorption wavelength (λ abs ) of 553 nm and an emission wavelength (λ em ) of 622 nm. This compound is commonly utilized as a labeling reagent and in photodynamic therapy. | |||
T20092 |
Lenacil
634 Hexilure,环草定,Herbicide |
Others | Others |
Lenacil (634 Hexilure) 是选择性尿嘧啶取代的除草剂,用于控制甘蔗,豌豆,苜蓿,苹果,桃子,薄荷和甜菜中的一年生草,阔叶杂草和一些多年生杂草,能够抑制光合作用。 | |||
T4198 |
T.cruzi-IN-1
MDK1088,T.cruzi Inhibitor |
Antibiotic; Parasite | Microbiology/Virology |
T.cruzi-IN-1 (MDK1088) 是一种克氏锥虫抑制剂,IC50为 8 nM。它是一种 4-三氟甲基取代的类似物,有潜力治疗南美锥虫病的急性和慢性阶段。 | |||
T26020 |
R 61837
R-61837,R61837 |
Antiviral | Immunology/Inflammation |
R 61837 是一种新型鼻病毒抑制剂,是一种取代的苯基哒嗪胺,具有抗病毒活性。 | |||
T1629 |
Rifapentine
MDL473,Rifapentina,Rifapentinum,DL 473,利福喷丁,Priftin,Cyclopentylrifampicin |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Rifapentine (Rifapentinum) 是可用于肺结核的抗生素。 | |||
T7075 |
2-Chloronaphthoquinone
2-Chloro-1,4-naphthoquinone,2-氯-1,4-萘醌 |
Others | Others |
2-Chloronaphthoquinone (2-Chloro-1,4-naphthoquinone) 是一种取代的萘醌,用作杀虫剂和杀螨剂。 | |||
T77771 |
Compound 10w
|
Others | Others |
Compound 10w,一种取代吡唑并[1,5-a]嘧啶酰胺化合物,是一种ZSTK474 类似物,对 HeLa细胞显示出抗癌活性。 | |||
T20967 |
Methyltetrazine-Amine
Methyltetrazine amine |
PROTACs | PROTAC |
Methyltetrazine-Amine 是甲基取代的四嗪胺,可用于合成 PROTAC 分子。 | |||
T35048 |
Verofylline
CK 0383,Verofilina,CK-0383,Verofyllinum,CK0383 |
PDE | Metabolism |
Verofylline (Verofyllinum) 是一种可口服的长效多效取代甲基黄嘌呤支气管扩张剂,对 PDE4 具有抑制作用,可用于治疗哮喘疾病研究肥胖症。 | |||
T6109 |
Darapladib
达拉地,SB-480848 |
Phospholipase | Metabolism |
Darapladib (SB-480848) 是脂蛋白相关磷脂酶A2 (Lp-PLA2) 抑制剂,IC50=0.25 nM。 | |||
T8721L |
I-37 free base( 2359690-13-2(free base))
|
Raf | MAPK |
I-37 free base( 2359690-13-2(free base)) 是一种新型苄氨基取代的吡啶并嘧啶酮,可作为 SOS1 抑制剂。 | |||
T5448 |
Clanfenur
|
Others | Others |
Clanfenur 属于一类新的取代苯甲酰苯基脲。该药物在体外和体内均显示出抗肿瘤活性。 | |||
T6581 |
Methyclothiazide
Duretic,Enduron,甲氯噻嗪,Aquatensen |
Others; Carbonic Anhydrase | Metabolism; Others |
Methyclothiazide (Aquatensen) 是一种具有口服活性的利尿剂,也是一种降压剂。它能够拮抗体外的电压依赖性钙通道的 (VDCC) 活性,也可以抑制内源性血管收缩刺激导致的血管反应。 | |||
T6047 |
Ralimetinib dimesylate
LY2228820 dimesylate,Ralimetinib,LY2228820,Ralimetinib Mesylate |
Apoptosis; p38 MAPK; Autophagy | Apoptosis; Autophagy; MAPK |
Ralimetinib dimesylate (LY2228820 dimesylate) 是一种选择性,ATP 竞争性的 p38 MAPK α/β抑制剂,IC50分别为5.3 和 3.2 nM。 | |||
T63736 |
Bafrekalant
|
Others | Others |
Bafrekalant 是一种二氮杂双环取代的咪唑并[1,2-a]嘧啶衍生物。Bafrekalant 可用于研究阻塞性和中枢性睡眠呼吸暂停和打鼾等与睡眠相关的呼吸障碍类疾病。 | |||
T78556 |
Antidepressant agent 5
|
Others | Others |
Antidepressant agent 5 是一种具有抗抑郁活性的 7-取代四氢异喹啉衍生物。Antidepressant agent 5 在研究抑郁症方面和木兰花碱作用效果类似,可用于预防和治疗抑郁症疾病。 | |||
T1021 |
(R)-Lansoprazole
Dexlansoprazole,右旋兰索拉唑,T 168390,TAK 390,R-(+)-Lansoprazole |
Proton pump | Membrane transporter/Ion channel |
(R)-Lansoprazole (T 168390) 是Lansoprazole 的R 型异构体。Lansoprazole 是口服有效的质子泵抑制剂,能抑制胃酸生成。Lansoprazole 是中性鞘磷脂酶(N-SMase)的抑制剂(外泌体抑制剂),能透过血脑屏障。 | |||
T0314 |
Hexylresorcinol
己雷锁辛,4-己基间苯二酚,4-Hexylresorcinol |
Apoptosis; Tyrosinase; Antibacterial; Parasite | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Hexylresorcinol (4-Hexylresorcinol) 是在植物中发现的一种天然产物,具有抗菌、驱虫、防腐和抗肿瘤活性。它是一种可逆、非竞争性的 α-葡萄糖苷酶抑制剂,有抗 DNA 氧化损伤的保护作用。它可诱导鳞癌细胞凋亡。 | |||
T21729 |
(±)-Lisofylline
|
Others | Others |
(±)-Lisofylline 是一种对映异构体特异性、烷基取代的甲基黄嘌呤,在下调白细胞活化方面具有特异性和有效的活性。它是一种抗炎剂。 | |||
T19415 |
Medronic acid
亚甲基二磷酸,Methylenediphosphonic acid |
Others | Others |
Medronic acid (Methylenediphosphonic acid) 是一种亚甲基取代的二膦酸盐。它对骨基质中的羟基磷灰石晶体的表面具有亲和力,并且可粘附在其表面。它能够在类骨质矿化的位点累积,可以在骨成像中与放射性同位素复合使用。 | |||
T22363 |
Methyl 3-aminopyrazine-2-carboxylate
|
Others | Others |
Methyl 3-aminopyrazine-2-carboxylate 是一种吡嗪,在 2 位被甲氧基羰基和 3 位氨基取代。它是吡嗪、甲酯和芳香胺的成员。 3-氨基吡嗪-2-羧酸甲酯可用于化学合成。 | |||
T8613 |
1-Ethyl-6-aminouracil
6-AMINO-1-ETHYL-1H-PYRIMIDINE-2,4-DIONE,1-乙基-6-氨基脲嘧啶 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
1-Ethyl-6-aminouracil (6-AMINO-1-ETHYL-1H-PYRIMIDINE-2,4-DIONE) 是合成一系列新的取代黄嘌呤的中间体,这些黄嘌呤对人腺苷 A2B 受体具有高亲和力和选择性。 | |||
T24807 |
S-Methylglutathione
Glutathione S-methyl ester,Glutathione ester,S-Methyl glutathione |
Glyoxalase | Proteases/Proteasome |
S-Methylglutathione (S-Methyl glutathione) 是一种 S 取代的谷胱甘肽,是一种转移酶A催化的1-氯-2,4-二硝基苯偶联物的抑制剂,也是一种 XOCl 清除剂。S-Methylglutathione 抑制乙二醛酶 1 (glyoxalase 1) ,诱导水螅触手球形成。 | |||
T8746L |
I-49 free base
Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-6-(tetrahydro-2H-pyran-4-yl)-,I-49 |
Raf | MAPK |
I-49 free base (Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-6-(tetrahydro-2H-pyran-4-yl)-) 是一种新型苄氨基取代的吡啶并嘧啶酮,可作为 SOS1 抑制剂。 | |||
T64322 |
4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester
|
Others | Others |
4-(9H-fluoren-9-ylmethoxycarbonylamino)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester 是一种取代的哌啶衍生物,在有机合成中被广泛用作形成肽和拟肽分子的连接体,被广泛应用于肽合成和肽模拟,也用于合成药物、生物聚合物和其他有机分子。 | |||
T67955 |
Ensaculin
Anseculin |
||
Ensaculin (Anseculin) 是一种用哌嗪部分取代的新型苯并吡喃酮,在正常和人工遗忘啮齿动物的被动和条件回避范式中显示出记忆增强作用。它在NMDA 毒性模型中表现出神经保护活性,在原代培养的大鼠脑细胞中表现出神经营养作用。Ensaculin 可用于治疗痴呆。 | |||
T1756 |
Ilaprazole sodium
IY-81149 sodium,艾普拉唑钠 |
Proton pump; TOPK | MAPK; Membrane transporter/Ion channel |
Ilaprazole sodium (IY-81149 sodium) 是一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制 H+/K+-ATPase,在兔壁细胞制剂中的 IC50为 6 μM。它也是一种有效的 T 细胞起源蛋白激酶(TOPK)抑制剂,用于胃溃疡的研究。 | |||
T6929 |
Pantoprazole sodium
Pantecta,泮托拉唑钠盐,SKF96022 sodium,SKF96022 (sodium),BY1023 (sodium),泮托拉唑钠,BY-1023 sodium,Pantoloc |
Apoptosis; Others; Proton pump; HIF; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; Others |
Pantoprazole sodium (Pantecta) 是一种具有口服活性的质子泵抑制剂,是一种取代的苯并咪唑,是H+/K+-ATPase 抑制剂,IC50为 6.8 μM。它可以改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。它联合阿霉素可显著增加肿瘤生长延迟。 | |||
T3157 |
COH29
RNR Inhibitor COH29 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
COH29 (RNR Inhibitor COH29) 是一种口服可用的芳香族取代噻唑,是人类核糖核苷酸还原酶 (RNR) 的抑制剂,具有潜在的抗肿瘤活性。它抑制核糖核苷酸还原酶的IC50为 16 μM。 | |||
T12781 |
RV01
|
Others | Others |
RV01 是一种新型的白藜芦醇喹啉取代类似物,可抑制 DNA 损伤,降低乙醇诱导的乙醛脱氢酶 (ALDH2) 的 mRNA 表达,具有清除羟自由基的活性。RV01 降低 iNOS 的表达,具有抗神经炎症作用。RV01降低肿瘤坏死因子-a (TNF-a)和白细胞介素-6 (IL-6) mRNA 水平和分泌,抑制lps 诱导的ROS 生成和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶活化,降低toll 样受体4 (TLR4)的蛋白表达,抑制lps 诱导的丝裂原活化蛋白激酶(MAPK)和核转录因子-кB (NF-кB)信号通路的激活。 | |||
T34132 |
Primapterin
L-Erythro-7-isobiopterin,7-Isobiopterin |
||
Primapterin, 7-Substituted pterins, is a new type of mammalian pteridines. | |||
TP2409 |
SP-346 nonapeptide
H-Val-Ser-Gln-Asn-Tyr-Pip-Ile-Val-Gln-NH2 |
||
SP-346 nonapeptide is a pipecolic acid substituted nonapeptide. | |||
T25095 |
Antibiotic LB 10517
LB 10517,LB10517,Antibiotic LB10517,LB-10517,Antibiotic LB-10517 |
||
Antibiotic LB 10517 is a catechol-substituted cephalosporin with a broad spectrum of antibacterial. | |||
T34412 |
RS 49676
RS49676,RS-49676 |
||
RS 49676 is an N-substituted imidazole. | |||
T69064 |
Clavulanic Acid Methyl Ester
|
||
Clavulanic Acid Methyl Ester is a substituted Clavulanic acid and β-lactamase inhibitor. | |||
T30522 |
BMS-422461
BMS422461,BMS 422461 |
||
BMS-422461 is a prodrug of the novel fluoro-substituted camptothecin analog, BMS-286309. | |||
T30881 |
Chir 4531
Chir4531,Chir-4531 |
||
Chir 4531 is a N-(substituted)glycine peptoid trimer. | |||
T33813 |
Ophthalmic acid
|
||
Ophthalmic acid is a glutathione analog in which cysteine is substituted by L-aminobutyrate. | |||
T33556 |
N,N-Diethylphenethylamine
Phenethylamine, N,N-diethyl-,J381.711C,N-Phenethyldiethylamine,Diethyl(phenethyl)amine |
||
N, N-dimethyl phenylethylamine (N, N-DMPEA) is a substituted phenylethylamine used as a flavouring agent. | |||
T71590 | AHR-5645B fumarate | ||
AHR-5645B fumarate is a substituted benzamide that has been shown to inhibit 3H-spiperone binding to bovine anterior pituitary membranes. | |||
T20715 |
Bromacil
Bromax,Uragan,Hyvar X bromacil,Cynogan,Urox B,Ureabor |
||
Bromacil, a substituted uracil herbicide used worldwide, is not readily biodegradable and therefore has consequences to the environment. | |||
TNU1411 | 2,6-Bis(4-morpholinyl)-9-b-D-ribofuranosyl-9H-purine | ||
Nucleoside Derivatives –6-Subtituted nucleosides;2-Substituted nucleosides | |||
T69174 | AHR-5645B free base | ||
AHR-5645B free base is a substituted benzamide which has been shown to inhibit 3H-spiperone binding to bovine anterior pituitary membranes. | |||
T34434 |
RU 45196
RU45196,RU-45196 |
||
RU 45196 is an 11 beta-substituted 19-norsteroid of the estra-4,10-diene series. | |||
TNU0520 |
N6,N6-Dimethyl-xylo-adenosine
|
||
N6,N6-Dimethyl-xylo-adenosine is a Nucleoside Derivative - Xylo-nucleoside;6-Substituted purine nucleoside. | |||
T69597 | Befiperide HCl | ||
Befiperide, also known as DU-29325, is a substituted piperazine that has agonist activity at serotonin1 receptors. | |||
T25542 |
Isamfazone
Isamfazona,Isamfazonum |
||
Isamfazone is utilized in the chemical and pharmacological studies on substituted pyridazones, the discovery of novel anti-inflammatory agents by aligning screening. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6723 |
Voglibose
AO 128,伏格列波糖,Glustat,Basen |
Glucosidase | Metabolism |
Voglibose (Glustat) 是一种 valiolamine 的衍生物,可抑制α-葡萄糖苷酶活性,可作用于高血糖症等。 | |||
T4760 |
KSD 2405
3-羟基苯甲醇,3-Hydroxybenzyl alcohol |
Others; Endogenous Metabolite | Metabolism; Others |
KSD 2405 (3-Hydroxybenzyl alcohol) 是内源性代谢产物的一种。 | |||
T5037 |
Midecamycin
Antibiotic SF-837,Turimycin P3,Medecamycin A1,Rubimycin,麦迪霉素,Platenomycin B1,Espinomycin A |
Antibacterial; Antibiotic | Microbiology/Virology |
Midecamycin (Medecamycin A1) 是乙酰氧基取代的大环内酯类抗生素,对革兰氏阳性和阴性菌有效。 | |||
T5569 |
3-Amino-4-methylpentanoic acid
DL-Homovaline,3-氨基-4-甲基戊酸,DL-beta-leucine,beta-Aminoisocaproic acid,beta-Leucine |
Endogenous Metabolite | Metabolism |
3-Amino-4-methylpentanoic acid (DL-Homovaline) 是 L-亮氨酸的异构体,是 β 氨基酸,通过亮氨酸 2,3-氨基变位酶在人体中由 L-亮氨酸代谢天然产生。 | |||
T4513 |
Vanillyl butyl ether
4-(Butoxymethyl)-2-methoxyphenol,香兰醇丁醚,Butyl vanillyl ether,香草醇丁醚 |
Others | Others |
Vanillyl butyl ether (Butyl vanillyl ether) 是香草特有风味和香气的来源。它是辣椒素类似物,对人体有感官刺激作用。它是环保且无毒的物质。它是烷氧基取代的苄基衍生物,主要用作调味剂。 | |||
T6569 |
Mimosine
Leucenine,NSC 69188,含羞草素,Leucenol,L-Mimosine |
Others | Others |
Mimosine (Leucenol) 是一种酪氨酸类似物,具有抗癌和抗炎等活性。它可通过其强大的铁结合活性作为抗氧化剂,是一种 Fe(III) 螯合剂。它作用于人类白血病细胞,通过金属离子螯合、线粒体激活和诱导活性氧产生来诱导细胞凋亡。 | |||
T4768 |
Diethyl oxalpropionate
草酰丙酸二乙酯,HYL 2-METHYL-3-OXOSUCCINATE |
Others; Endogenous Metabolite | Metabolism; Others |
Diethyl oxalpropionate (HYL 2-METHYL-3-OXOSUCCINATE) 是一种合成 PDMMLA 的中间体。其中 PDMMLA 的衍生物可用于纳米粒子的合成和研究。 | |||
T2S1907 |
Coniferaldehyde
Ferulaldehyde,Ferulyl aldehyde,4-HYDROXY-3-METHOXYCINNAMALDEHYDE,松柏醛,Coniferyl aldehyde,松柏醛;4-羟基-3-甲氧基肉桂醛 |
Apoptosis; Antioxidant | Apoptosis; oxidation-reduction |
Coniferaldehyde (Ferulaldehyde) 是一种血红素加氧酶-1 的有效诱导剂,具有抗炎作用。在 RAW264.7 巨噬细胞中,它通过 PKCα/βII/Nrf-2/HO-1 依赖性途径来抑制 LPS 诱导的细胞凋亡。 | |||
T3929 |
Kaurenoic acid
Kauren-19-Oic Acid,异贝壳杉烯酸,kaurenoate,kaur-16-en-18-oic acid |
Others | Others |
Kaurenoic acid (kaurenoate) 是一种二萜,来源于 Sphagneticola trilobata 中,可以抑制细胞因子的产生和激活 NO–cyclic GMP–PKG–ATP- 敏感型钾通道信号通路,并抑制炎症疼痛。 | |||
T3339 |
Sophoridine
5-Epidihydrosophocarpine,槐定碱,Dihydro-5-episophocarpine |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
Sophoridine (Dihydro-5-episophocarpine) 是一种从豆科植物槐豆斜生植物的叶子中分离出来的喹喔啉生物碱。它是胰腺癌的候选药物,诱导细胞凋亡。 | |||
TN4784 |
Picraline
|
SGLT | GPCR/G Protein |
A series of a hydroxy substituted derivatives 21-28 at C-17 of the Picraline-type alkaloids have been derived as having potent SGLT inhibitory activity. |