123
14
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5210 |
BAI1
|
Apoptosis; BCL | Apoptosis |
BAI1 是一种选择性凋亡因子BAX 变构抑制剂。它结合 BAX 并变构抑制其激活,具有潜力研究 BAX 依赖性细胞死亡介导的疾病。 | |||
T2199 |
Myclobutanil
Systhane,腈菌唑 |
Antifungal | Microbiology/Virology |
Myclobutanil (Systhane) 是康唑类抗真菌剂,可用作农药。 | |||
T24212 |
XX-650-23
XX65023,XX 650 23 |
Apoptosis; Epigenetic Reader Domain | Apoptosis; Chromatin/Epigenetic |
XX-650-23 是一种小分子 CREB 抑制剂,阻断 CREB 与其所需的共激活因子 CBP(CREB 结合蛋白)之间的关键相互作用,诱导AML细胞凋亡和细胞周期停滞,可用于研究急性髓系白血病 (AML)。 | |||
T3940 |
CID5721353
BCL6 inhibitor |
Apoptosis; BCL | Apoptosis |
CID5721353 (BCL6 inhibitor) 是一种 B 细胞淋巴瘤 6 抑制剂,IC50为 212 μM,Ki 值为 147 μM。它可在体内外破坏 BCL6/辅助阻遏物复合物,并显示与 BTB 沟内的关键位点结合。 | |||
T4647 |
M2I-1
M2I 1 |
Others | Others |
M2I-1 是Mad2抑制剂,靶向的 Mad2 与 Cdc20 的结合,该结合是纺锤体装配检查点内必不可少的蛋白-蛋白相互作用。 | |||
T6904 |
Necrosulfonamide
(E)-Necrosulfonamide |
MLK | MAPK |
Necrosulfonamide ((E)-Necrosulfonamide) 是一种坏死性凋亡抑制剂,通过选择性靶向(MLKL),可阻止 MLKL-RIP1-RIP3 坏死小体复合体与其下游效应子相互作用。MLKL 是诱导坏死过程中 RIP3 的重要底物。 | |||
T6386 |
Ampicillin sodium
氨苄西林钠,Domicillin,D-(-)-α-Aminobenzylpenicillin sodium salt,Penialmen,Citteral |
Antibacterial; Antibiotic | Microbiology/Virology |
Ampicillin sodium (Domicillin) 是Ampicillin 的钠盐形式,是Ampicillin 的广谱半合成衍生物。它通过与青霉素结合蛋白结合来抑制细菌细胞壁的合成,从而抑制肽聚糖的合成,肽聚糖是细菌细胞壁的关键成分。 | |||
T1433 |
Ritodrine hydrochloride
DU21220,盐酸利托君,Ritodrine HCl,NSC 291565 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ritodrine hydrochloride (NSC 291565) 是一种 β-2肾上腺素受体激动剂。 | |||
T2170 |
SKF-96365 hydrochloride
1-[2-(4-甲氧基)-2-[3-(4-甲氧基苯基)丙氧基]乙基]咪唑,SKF96365 |
Apoptosis; Potassium Channel; Calcium Channel; TRP/TRPV Channel; Autophagy | Apoptosis; Autophagy; Membrane transporter/Ion channel; Metabolism |
SKF-96365 hydrochloride (SKF96365) 是store-operated Ca2+entry 抑制剂,也是TRP channel 阻滞剂。它显著抑制豚鼠离体心脏 hERG、hKCNQ1/hKCNE1、hKir2.1 和 hKv4.3 电流,延长QTc 间期。它通过诱导结直肠癌细胞的细胞周期阻滞和凋亡起抗肿瘤作用。 | |||
T9574 |
PF-07304814
Lufotrelvir,卢夫特韦 |
||
Lufotrelvir (PF-07304814) 是 PF-00835231 的磷酸盐前药,是一种有效的3CLpro 蛋白酶 (Mpro) 抑制剂,具有 抗SARS-CoV-2 病毒活性。Lufotrelvir 结合并抑制 SARS-CoV-2 3CLpro 活性,Ki 为 174nM。Lufotrelvir 是一种很有前途的单一抗病毒试剂,也可用于与针对冠状病毒生命周期其他关键阶段的其他抗病毒试剂的联合研究。 | |||
T4013 |
SGC2085 HCl
|
Histone Methyltransferase | Chromatin/Epigenetic |
SGC2085 HCl 是一种有效的选择性辅激活剂相关的精氨酸甲基转移酶 1 (CARM1) 抑制剂,IC50 为 50 nM,选择性比其他 PRMT 高出数倍。 CARM1 是结直肠癌中 Wnt/β-catenin 转录和肿瘤转化的重要正调节因子,也是雌激素刺激的乳腺癌生长的关键因素,其耗竭导致体内髓性白血病细胞增殖减少。 | |||
T14134 |
Afabicin
AFN-1720,Debio 1450 |
Antibacterial | Microbiology/Virology |
Afabicin is the prodrug of Debio1452. Debio1452 is an inhibitor FabI, an enzyme critical to fatty acid biosynthesis in staphylococci. | |||
T28808 |
SLUPP-417
SLUPP417 |
||
SLUPP-417 is an efflux pump inhibitor (EPI) by interacting with the membrane fusion protein AcrA, a critical component of the AcrAB-TolC efflux pump in Escherichia coli. | |||
T34458 |
Ryanodol
|
||
Ryanodol is a complex diterpenoid that modulates intracellular calcium-ion release at ryanodine receptors, ion channels critical for skeletal and cardiac muscle excitation-contraction coupling and synaptic transmission. | |||
T10046 |
16,16-Dimethyl prostaglandin E2
16,16-dimethyl PGE2 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
16,16-Dimethyl prostaglandin E2 is an orally active vertebrate Hematopoietic stem cells homeostasis critical regulator. It can act through EP2/EP4 and has an interaction with the Wnt pathway. | |||
T68291 |
APSR-IN-8
|
||
APSR-IN-8 is a first-in-class inhibitor of APS reductase (APSR), which is a critical enzyme in the assimilation of sulfate for the biosynthesis of cysteine and other essential sulfur-containing molecules. | |||
T38614 |
TLR7 agonist 3
|
||
TLR7 agonist 3 (Compound 2), a potent activator of toll-like receptor 7 (TLR7), plays a critical role in initiating immune responses, positioning it as a promising target for immunomodulator development. | |||
T75410 | Ganglioside sialidase (AuSialidase S) | ||
Ganglioside sialidase (AuSialidase S)为一种内源性代谢物,与神经元分化过程有关,涉及神经突生长。 | |||
T40781 |
Geranylgeranyl pyrophosphate
|
||
Geranylgeranyl pyrophosphate, a key metabolite in protein geranylgeranylation, serves as the universal precursor for diterpenoids, such as Paclitaxel. Its role in cancer research stems from this critical function. | |||
T28807 |
SLUPP-225
SLUPP 225 |
||
SLUPP-225 is an efflux pump inhibitor (EPI) by interacting with the membrane fusion protein AcrA, a critical component of the AcrAB-TolC efflux pump in Escherichia coli. | |||
T73107 | RAD51-IN-4 | ||
RAD51-IN-4 是一种有效的RAD51抑制剂。RAD51是一种真核生物基因。RAD51-IN-4 具有研究线粒体缺陷病症的潜力。 | |||
T80055 |
Beta-glucuronidase (bovine liver)
|
||
Beta-glucuronidase是一种关键溶酶体酶,主要功能是参与糖胺聚糖中含有葡萄糖醛酸成分的降解过程。 | |||
T27068 |
CPI098
CPI-098,CPI 098 |
||
CPI098 is a potent and selective inhibitors for the bromodomains of CREBBP/EP300. CREBBP/EP300 bromodomains play a critical role in regulatory T cell biology. T cell recruitment to tumors is a major mechanism of immune evasion by cancer cells. | |||
T18618 |
Bis-NH2-C1-PEG3
PROTAC Linker 24 |
Others | Others |
Bis-NH2-C1-PEG3 (PROTAC Linker 24) is a polyethylene glycol (PEG)-based linker compound utilized in the synthesis of PROTACs. This compound serves as a critical component in constructing PROTAC molecules, facilitating the targeted degradation of specific proteins[1]. | |||
T7459 |
Abametapir
5 5'-二甲基-2,2-联吡啶,HA-44,BRN 0123183 |
MMP; Others; Parasite | Microbiology/Virology; Others; Proteases/Proteasome |
Abametapir (BRN 0123183) 是一种金属蛋白酶抑制剂,能够靶向对卵孵化和虱子发育至关重要的金属蛋白酶。 | |||
T16592 |
Propargyl-PEG1-SS-PEG1-propargyl
|
Others | Others |
Propargyl-PEG1-SS-PEG1-propargyl refers to a cleavable di-functional polyethylene glycol (PEG) linker composed of two units. This specific linker is employed in the synthesis of antibody-drug conjugates (ADCs), where it plays a critical role in linking the antibody to the drug. [1] | |||
T18630 |
Tos-PEG3-NH-Boc
PROTAC Linker 9 |
Others | Others |
Tos-PEG3-NH-Boc (PROTAC Linker 9) is a PEG-based linker utilized for the synthesis of PROTACs. It plays a critical role in facilitating the connection between a target protein and an E3 ubiquitin ligase, ultimately leading to the degradation of the target protein. | |||
T74122 | Deoxythymidine-5'-triphosphate sodium hydrate | ||
Deoxythymidine-5'-triphosphate (dTTP) sodium hydrate 是四种核苷三磷酸之一,可以合成 DNA。 | |||
T68755 | NZ-28 | ||
NZ28, also known as NSC134754, is potent HSF1 inhibitor, which induced inhibition of HSF1, SP1 and NF-κB triggers the loss of the natural killer cell-activating ligands MICA/B on human tumor cells. Heat-shock transcription factor HSF1 has a critical role in human epidermal growth factor receptor-2-induced cellular transformation and tumorigenesis. | |||
T69830 |
GSK2239633
|
||
GSK2239633 is a potent CC-chemokine receptor 4 antagonist with pIC50 of 7.9. The CC-chemokine receptor 4 (CCR4) is thought potentially to play a critical role in asthma pathogenesis due to its ability to recruit type 2 T-helper lymphocytes to the inflamed airways. Therefore, CCR4 provides an excellent target for anti-inflammatory therapy. | |||
TD0053 |
Fluo-3, pentapotassium salt
|
||
Calcium measurement is critical for numerous biological investigations. Fluorescent probes that show spectral responses upon binding calcium have enabled researchers to investigate changes in intracellular free calcium concentrations by using fluorescence microscopy, flow cytometry, fluorescence spectroscopy and fluorescence microplate readers. Fluo-3, pentapotassium salt is most commonly used among the visible light-excitable calcium indicators. | |||
T18268 | Mal-PEG1-Val-Cit-PABC-OH | Others | Others |
Mal-PEG1-Val-Cit-PABC-OH is a 1 unit polyethylene glycol (PEG) ADC linker that possesses cleavable properties. This linker, commonly utilized in the synthesis of antibody-drug conjugates (ADCs), serves as a critical component facilitating the conjugation of drugs to antibodies[1]. | |||
T40456 |
8-Bromoadenosine 5'-triphosphate tetrasodium
8-Br-ATP tetrasodium,8-Bromoadenosine 5'-triphosphate tetrasodium |
||
8-Bromoadenosine 5'-triphosphate tetrasodium (8-Br-ATP tetrasodium) is a tetrasodium ATP analogue, serving as a vital element for energy storage and metabolic processes in living organisms. ATP, a central component in vivo, plays a critical role in these functions. | |||
T82589 |
Delpacibart
|
||
Delpacibart为针对TFRC的人源化小鼠IgG1κ抗体,TFRC作为关键膜蛋白负责调控细胞铁元素转运。 | |||
T25749 |
L-NIL dihydrochloride
L-NIL HCl,N-Iminoethyl-L-lysine dihydrochloride |
||
L-NIL HCl is a relatively selective iNOS inhibitor (IC50s: 0.4-3.3, 8-38, and 17-92 µM for iNOS, eNOS, and nNOS). L-NIL effectively inhibits iNOS both in vitro and in vivo. L-NIL has been used to demonstrate a critical role for iNOS in the immune response | |||
TD0052 |
Fluo-3, pentasodium salt
|
||
Calcium measurement is critical for numerous biological investigations. Fluorescent probes that show spectral responses upon binding calcium have enabled researchers to investigate changes in intracellular free calcium concentrations by using fluorescence microscopy, flow cytometry, fluorescence spectroscopy and fluorescence microplate readers. Fluo-3, pentasodium salt is most commonly used among the visible light-excitable calcium indicators. | |||
TD0054 |
Fluo-3, pentaammonium salt
|
||
Calcium measurement is critical for numerous biological investigations. Fluorescent probes that show spectral responses upon binding calcium have enabled researchers to investigate changes in intracellular free calcium concentrations by using fluorescence microscopy, flow cytometry, fluorescence spectroscopy and fluorescence microplate readers. Fluo-3, pentaammonium salt is most commonly used among the visible light-excitable calcium indicators. | |||
T60363 | Nitrefazole | ||
Nitrefazole 是一种4-nitroimidazole 衍生物,对醛脱氢酶(ALDH)具有强烈而持久的抑制作用,醛脱氢酶是一种参与酒精代谢的酶。 | |||
T81578 |
p60c-src substrate II, phosphorylated
|
||
p60c-src substrate II, phosphorylated 是磷酸化的五肽,为 p60c-src substrate II 的磷酸化形式。其代表了蛋白质翻译后修饰的一种,对生物调控具有重要作用。 | |||
T78356 |
Fructosyl amino acid oxidase
|
||
Fructosyl amino acid oxidase是测量糖化蛋白的重要试剂,特别是用于评估糖尿病指标糖化血红蛋白A1c。 | |||
T74435 | Alicaforsen sodium | ||
Alicaforsen sodium为20个碱基长度的反义寡核苷酸,主要通过抑制ICAM-1的产生发挥作用,ICAM-1作为关键粘附分子,参与白细胞向炎症部位的迁移和转运。 | |||
T80397 |
Darobactin
|
Antibiotic | Microbiology/Virology |
Darobactin为一种有效的抗生素,其针对多种重要革兰氏阴性病原体展现出显著的抑制作用,无论是在体外实验还是动物感染模型中均有证实。 | |||
T37715 |
Galactosylcerebrosides (bovine)
|
||
Galactosylcerebrosides (SGal-CB) 在髓鞘形成的早期阶段可由周围神经系统 (PNS) 中的 Schwann 细胞 (SC) 表达,在鞘中的持续存在对于长期维持其结构完整性至关重要。 | |||
T82123 |
ICMT-IN-21
|
||
ICMT-IN-21(化合物6ag)是一种具有8.8 μM IC50值的ICMT抑制剂,属于磺胺修饰法尼基半胱氨酸(SMFC)。该化合物以其特有的法尼基和羧酸基序列对ICMT活性起抑制作用。 | |||
T74318 |
18:0 EPC chloride
|
||
18:0 EPC chloride为合成阳离子磷脂,(在临界协同浓度2.34-2.93 μM)可显著增强丁香酚对大肠杆菌的灭活效能。 | |||
T36365 |
KAPA (hydrochloride)
KAPA (hydrochloride),7-keto-8-Aminopelargomic Acid |
||
Biotin is a growth factor that plays an important role in numerous reactions that are critical to microorganisms, plants, and animals. Biotin has a strong affinity for the protein avidin, a trait that has been utilized for many assay reporter applications. KAPA is a key intermediate in the biotin biosynthetic pathway.[1] | |||
T75971 |
γ-1-Melanocyte Stimulating Hormone (MSH), amide
|
||
γ-1-Melanocyte Stimulating Hormone (MSH), amide为含11个氨基酸的多肽,主要通过激活黑皮质素受体3 (MC3-R) 调节钠 (Na+) 平衡及血压。 | |||
T80189 |
Hainantoxin-IV
HNTX-IV |
Sodium Channel | Membrane transporter/Ion channel |
Hainantoxin-IV是针对河豚毒素敏感(TTX-S)电压门控钠通道的特异性拮抗剂。该化合物以His28和Lys32为主要残基与靶标结合,并采用了抑制剂胱氨酸结基序。 | |||
T82403 |
Fibronectin Type III Connecting Segment Fragment 1-25
|
||
Fibronectin Type III Connecting Segment Fragment 1-25,一种多肽,主要作用于黑色素瘤细胞的粘附,并在鸡的周围神经系统发育中扮演关键角色。 | |||
T61554 | CSF1R-IN-13 | ||
CSF1R-IN-13 is a powerful CSF1R inhibitor with potential applications in researching cancer diseases [1]. CSF1R, also known as colony stimulating factor 1 receptor, is a critical growth factor that regulates various cell types, including bone marrow progenitor cells, monocytes, macrophages, and giants [1]. CSF1R-IN-13 shows promise in furthering our understanding of cancer-related disorders (WO2019134661A1, compound 32) [1]. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4912 |
Jatrorrhizine chloride
盐酸药根碱,Yatrorhizine chloride,Neprotine chloride |
Others; 5-HT Receptor; OCT; Antibacterial; AChE | GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Others |
Jatrorrhizine chloride (Neprotine chloride) 是从黄连中分离得到的生物碱,具有神经保护、抗菌、抗氧化和抗疟原虫活性。它通过抑制摄取2转运蛋白的活性减少血清素和去甲肾上腺素的摄取。它是具有口服活性的乙酰胆碱酯酶抑制剂。 | |||
T3909 |
Pulsatilla saponin D
白头翁皂苷D,Hederacolchiside A,SB365 |
Apoptosis; Others | Apoptosis; Others |
Pulsatilla saponin D (Hederacolchiside A) 是从朝鲜白头翁根部分离得到的一种天然产物,具有抗癌活性。 | |||
T5S0527 |
Rhodojaponin III
闹羊花素 Ⅲ,闹羊花毒素III |
Others | Others |
Rhodojaponin III 是二萜类化合物,提取于Rhododendron molle 叶子,具有抗炎作用。 | |||
T19316 |
Ethyl oleate
|
Others | Others |
Ethyl oleate 是由油酸和乙醇的缩合形成的脂肪酸酯。它是纳米结构脂质载体 (NLC) 中的液体脂质成分。其中 NLC 是一种口服有活性的反式阿魏酸的给药载体。 | |||
T36585 |
Isodeoxycholic Acid
isoDCA |
Chloride channel; Antibacterial | Membrane transporter/Ion channel; Microbiology/Virology |
Isodeoxycholic Acid 是一种胆汁酸,由肠道细菌通过脱氧胆酸的表聚作用形成。Isodeoxycholic acid 的临界胶束浓度高于二氯苯甲醚,这表明它的去污活性降低了,而且在抑制七种肠道共生细菌生长方面的活性低于二氯苯甲醚。Isodeoxycholic Acid(0.1%)能抑制几种艰难梭菌菌株在牛磺胆酸诱导下的孢子萌发,并能降低艰难梭菌培养上清对 Vero 细胞的细胞毒性。在高脂饮食诱发肥胖的大鼠模型中,血浆中的Isodeoxycholic acid 水平比正常饮食的大鼠低。 | |||
T3S0027 |
Picropodophyllotoxin
AXL 1717,Picropodophyllin,苦鬼臼毒素 |
IGF-1R | Tyrosine Kinase/Adaptors |
Picropodophyllotoxin (AXL 1717) 是一种环木脂素生物碱,存在于五月树(Podophyllum peltatum) 中,是一种具有潜在抗肿瘤活性的胰岛素样生长因子 1 受体 (IGF1R) 的小分子抑制剂。它特异性抑制 IGF1R 的活性并下调细胞表达,而不干扰其他生长因子受体的活性,例如胰岛素受体、表皮生长因子、血小板衍生生长因子、成纤维细胞生长因子和肥大/干细胞生长因子 (KIT) )。该药剂在抑制肿瘤细胞增殖和诱导肿瘤细胞凋亡方面显示出有效的活性。 IGF1R 是一种在多种人类癌症中过度表达的受体酪氨酸激酶,在多种癌细胞的生长和存活中起关键作用。 | |||
T3794 |
Pentagalloylglucose
Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖 |
Influenza Virus | Microbiology/Virology |
1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中,具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。 | |||
T82636 | Cyclosporin U | ||
Cyclosporin U (SMP0V32C6L)为一种细胞免疫抑制剂,关键用于防止移植器官的排斥反应。 | |||
TN2655 |
17alpha-Neriifolin
|
Others | Others |
17alpha-Neriifolin and 17alpha-Deacetyltanghinin have little anti-proliferative activity, indicating that the 17beta configuration is critical for the anti-proliferative activity of these compounds. | |||
T80020 |
UDP-3-O-acyl-GlcNAc diammonium
UDP-3-O-(3-hydroxytetradecanoyl)-N-acetylglucosamine diammonium |
Endogenous Metabolite | Metabolism |
UDP-3-O-acyl-GlcNAc diammonium 是一种E. coli代谢产物,涉及3-deoxy-D-manno-octulosonate (KDO) 生物合成途径。 | |||
T74191 |
Tanshinol borneol ester
|
||
Tanshinol borneol ester 是一种血管生成刺激剂,通过 Akt 和 MAPK 信号通路促进血管生成的多个关键步骤。Tanshinol borneol ester 具有抗缺血和抗动脉粥样硬化作用。 | |||
T73812 |
Phosphatidylinositol 4,5-bisphosphate
|
||
Phosphatidylinositol 4,5-bisphosphate(L-alpha-Phosphatidylinositol-4,5-bisphosphate)为细胞膜磷脂成分,主要作为磷脂酶C(PLC)与磷酸肌醇3-激酶(PI3K)的底物,充当重要信使。 | |||
T73073 |
PTP1B-IN-21
|
||
PTP1B-IN-21 是蛋白酪氨酸磷酸酶 1B (PTP1B) 的选择性抑制剂 (IC50=1.56 μM),抑制力超出高度同源 T 细胞蛋白酪氨酸磷酸酶 (TCPTP;IC50>100 μM),PTP1B 是抑制 2 型糖尿病的重要靶点。 | |||
T4448 | NADP | ||
NADP,也称为烟酰胺腺嘌呤二核苷酸磷酸,是各种代谢过程中电子转移所必需的重要氧化还原辅因子。 它在促进细胞能量产生和维持细胞内氧化还原平衡方面发挥着关键作用。 |