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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19257 | Cys modifier 1 | Others | Others |
Cys modifier 1 是一种半胱氨酸选择性蛋白修饰剂。Cys modifier 1 是一种含硝基苯并呋喃嘧啶的荧光羰基丙烯酸衍生物 (λex=465nm,λem539 nm)。 | |||
T32102 | HPG Protein Modifier | ||
HPG protein modifiers or p-hydroxyphenyl glyoxal react with arginine residues, producing an absorbance increase at about 340 nm, and are therefore a good choice for amino acid side chain modification. | |||
TNU1282 | N-(4-Isopropyloxy phenyl)-N-(1H-pyrrol-2-ylmethyl)urea; flavoring agent, flavor modifier | ||
N-(4-Isopropyloxy phenyl)-N-(1H-pyrrol-2-ylmethyl)urea; flavoring agent, flavor modifier 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 TNU1282。 | |||
T13748 |
L-2-Hydroxyglutaric acid disodium
S-2-羟基戊二酸,(S)-2-Hydroxyglutaric acid disodium |
Histone Demethylase; Mitochondrial Metabolism | Chromatin/Epigenetic; Metabolism |
L-2-Hydroxyglutaric acid disodium ((S)-2-Hydroxyglutaric acid disodium) 是一种表观遗传修饰因子,是肾癌中的表观遗传修饰剂和推定的癌代谢物,可用于肾癌的相关研究。它抑制线粒体肌酸激酶活性,Km 和 Ki 分别为 2.52 mM 和11.13 mM。它可抑制组蛋白去甲基化酶,从而促进组蛋白甲基化。 | |||
T12718L |
RG7800
RO6885247 |
Others; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
RG7800 (RO6885247) 是一种 SMN2 拼接修饰剂,有用于治疗脊髓性肌萎缩的研究潜力。 | |||
T25534 |
Indazole-Cl
Indazole Cl |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Indazole-Cl 是一种选择性雌激素受体激动剂和选择性雌激素受体调节剂(SERM)。 | |||
T19335 |
Danegaptide Hydrochloride
GAP-134 (Hydrochloride),ZP 1609 Hydrochloride,(4R)-甘氨酰基-4-(苯甲酰基氨基)-L-脯氨酸盐酸盐 |
Gap Junction Protein | Cytoskeletal Signaling |
Danegaptide Hydrochloride (GAP-134 (Hydrochloride)) 是一种具有口服活性的间隙连接蛋白选择性修饰剂,具有抗心律不齐的作用。 | |||
T64221 |
Linvencorvir
RG7907 |
HBV; Antibiotic | Microbiology/Virology |
Linvencorvir 是一种乙型肝炎病毒(HBV)核心蛋白变构调节剂,用于治疗慢性HBV 感染。 | |||
T5199 |
COH000
|
E1/E2/E3 Enzyme | Ubiquitination |
COH000 是不可逆的泛素样激活酶1 共价变构抑制剂,体外测得对 SUMO 化修饰的IC50=0.2 μM。 | |||
T9493 |
DL-2-AMINOOCTANOIC ACID
|
Others | Others |
DL-2-AMINOOCTANOIC ACID 也称为α-氨基辛酸或α-氨基辛酸,可作为改性剂修饰钠蒙脱石(Na-MMT)粘土。 | |||
T27404 |
GAT107
GAT 107,GAT-107 |
AChR | Neuroscience |
GAT107 是一种新型有效的 α7 烟碱胆碱能受体变构激动剂和调节剂,具有抗炎活性,可逆转小鼠神经疼痛模型中的伤害感受。 | |||
T6482 |
Efaproxiral Sodium
乙丙昔罗钠,RSR13 sodium |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Efaproxiral Sodium (RSR13 sodium) 是血红蛋白 (Hb) 合成变构调节剂,能够减少血红蛋白氧 (O2) 的结合亲和力。 | |||
T0134 |
Imiquimod
咪喹莫特,R 837,S-26308 |
SARS-CoV; TLR; Autophagy; HSV | Autophagy; Immunology/Inflammation; Microbiology/Virology |
Imiquimod (R 837) 是一种免疫反应修饰剂,可作为 toll 样受体7 激动剂。它有抗病毒和抗肿瘤作用,可研究外生殖器、肛周疣、癌症和 COVID-19。 | |||
T16757 |
Risdiplam
RO7034067,RG7916 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Risdiplam (RO7034067) 是一种中枢和外周分布的 SMN2 前 mRNA 剪接修饰剂,可增加运动神经元存活 (SMN) 蛋白水平。 | |||
T34093 |
pNNP
p NNP,p-Nitrophenyl phosphate,p-NNP,Nitrophenylphosphate |
Carbonic Anhydrase | Metabolism |
pNNP (Nitrophenylphosphate) 可用作 PP2C 试验的底物。pNNP 对β-碳酸酐酶和α-碳酸酯脱水酶有抑制作用,对幽门螺杆菌幽门螺杆菌也具有抑制作用。pNNP 是一种活性较弱的组织非特异性碱性磷酸酶调节剂。 | |||
T14348 |
Auristatin E
|
Microtubule Associated | Cytoskeletal Signaling |
Auristatin E 通过阻断微管蛋白的聚合来抑制细胞分裂。它是一种细胞毒性微管蛋白修饰剂,具有强效和选择性抗肿瘤活性。它是一种 MMAE 类似物,是抗体-药物偶联物中的细胞毒素。 | |||
T5521 |
Bropirimine
U-54461,溴匹立明 |
TLR | Immunology/Inflammation |
Bropirimine (U-54461) 是 toll 样受体 7(TLR7)的合成激动剂,可通过 TLR7 介导 IFN-β 的产生抑制破骨细胞前体细胞向破骨细胞分化。它是一种生物反应调节剂,通过诱导淋巴因子起作用,在膀胱和上尿路的原位移行细胞癌中具有抗癌活性。 | |||
T3465 |
Vesnarinone
维司力农,OPC-8212,Arkin,Piteranometozine |
HIV Protease; PDE | Metabolism; Microbiology/Virology; Proteases/Proteasome |
Vesnarinone (Arkin) 是一种喹啉酮衍生物,可抑制磷酸二酯酶III 活性,增加钙通量和减小钾通量。 | |||
TNU0355 |
N6-Methyl-2'-O-methyladenosine
N6,2′-O-Dimethyladenosine |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
N6-Methyl-2'-O-methyladenosine (N6,2′-O-Dimethyladenosine) 是脂肪量和肥胖相关基因 (FTO) 的底物,是一种广泛存在于各种 RNA 分子上的可逆修饰化合物。N6,2′-O-Dimethyladenosine 可用于研究肥胖及其相关疾病。 | |||
T39704 |
KSC-34
|
Others | Others |
KSC-34 是蛋白二硫异构酶 A1(PDIA1)的共价修饰剂,是一种针对 PDIA1 的 a 位点的选择性抑制剂,以时间依赖的方式抑制PDIA1 还原酶活性,可用于研究淀粉样蛋白异常引起的疾病。 | |||
T67883 |
EZH2-IN-15
SHR2554 |
Histone Methyltransferase | Chromatin/Epigenetic |
EZH2-IN-15 是zeste 2组蛋白修饰增强子(EZH2)的特异性抑制剂。EZH2在许多人类癌症中异常过表达,通过调节Treg 活性来控制适应性反应。肿瘤内EZH2的表达也被证明可以控制先天免疫 | |||
T16102 |
ML-792
|
E1/E2/E3 Enzyme | Ubiquitination |
ML-792 是特异性的小泛素样修饰物活化酶抑制剂。ML-792选择性抑制SAE/SUMO1和SAE/SUMO2,IC50分别为 3 和 11 nM,对 NAE/NEDD8 和 UAE/ubiquitin 抑制作用微弱,IC50分别为 32 μM 和 >100 μM。 | |||
T32313 |
JP7
JP-7,JP 7 |
||
JP7 is a hemoglobin allosteric modifier. | |||
T19468 |
Nafocare B1
Methylfurylbutyrolactone |
Others | Others |
Nafocare B1 is a modifier of synthetic immune biological response. | |||
T29260 |
(R)-ß-lysine
R ß lysine,MG1655,R-ß-lysine,(R) ß lysine,MG-1655 |
||
(R) - ß - lysine is a functional modifier of elongation factor P (EF-P). | |||
TP2348 |
Pimelautide
RP 44102,RP44102,RP-44102 |
||
Pimelautide is a biological response modifier medicine. | |||
T31609 |
Eisenin
Pglu-gln-ala,Pyroglutamyl-glutaminyl-alanine |
||
Eisenin shows the activity as a biological response modifier isolated from brown marine algae, Eisenia bicyclis Setchell. | |||
T19159 |
Mal-β-CD
6-O-alpha-D-Maltosyl-beta-cyclodextrin |
Others | Others |
Mal-β-CD is a cellular cholesterol modifier. It can form a soluble inclusion complex with cholesterol. | |||
T22862 | Imiquimod maleate | Others | Others |
Imiquimod maleate is an immune response modifier. It acts as a toll-like receptor 7 agonists and is commonly used topically to treat warts on the skin of the genital and anal areas. | |||
T26122 |
Ropizine
SC13504,Ropizina,SC-13504,SC 13504 |
||
Ropizine is a benzhydryl piperazine that acts as an allosteric modifier to decreases the dissociation rate of [3H]DM so that can be used as an anticonvulsant. | |||
TP1531 |
Guangxitoxin 1E
|
||
Guangxitoxin 1E acts as a gating modifier since it shifts the voltage-dependence of Kv2.1 K+ currents towards depolarized potentials. | |||
T3645 |
Endoxifen E-isomer hydrochloride
E-Endoxifen hydrochloride |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Endoxifen E-isomer hydrochloride (E-Endoxifen hydrochloride) 是 Endoxifen 的 E-异构体,是 Endoxifen Z-isomer 原料中主要的杂质,具有抗雌激素作用。 | |||
T39810 | CEM114 | ||
CEM114 is a potent chemical compound known as a chemical epigenetic modifier (CEM). It functions by employing CRISPR-Cas9 systems to harness endogenous chromatin machinery, thereby exerting its epigenetic modifying effects. | |||
T18319 |
MC-Val-Cit-PAB-Auristatin E
|
Others | Others |
MC-Val-Cit-PAB-Auristatin E is an antibody-drug conjugate (ADC) linker compound featuring Auristatin E, a potent cytotoxic tubulin modifier, connected through the MC-Val-Cit-PAB linker, exhibiting significant antitumor activity. | |||
T19941 |
MBS Crosslinker
MBS protein crosslinker |
||
MBS crosslinker is a non-cleavable, water-insoluble, heterobifunctional protein crosslinking reagent. The MBS protein crosslinker extended spacer arm analog is SMPB crosslinker SATA Protein Modifier can be used to add sulfhydryl groups to proteins or pept | |||
T19336 |
Danegaptide
ZP 1609,GAP-134 |
Others | Others |
Danegaptide (GAP-134), has been identified as a potent and selective second generation gap junction modifier with oral bioavailability.a small modified dipeptide. | |||
T37646 |
HB007
|
||
HB007 is a potent degrader of small ubiquitin-related modifier 1 (SUMO1). It mediates the ubiquitination and subsequent degradation of SUMO1, leading to a decrease in tumor growth in vivo. HB007 is a valuable tool for investigating brain, breast, colon, and lung cancers[1][2]. | |||
T74483 | Aminobenzenesulfonic auristatin E | ||
AminobenzenesulfonicauristatinE 是抗体偶联活性分子的一部分。AminobenzenesulfonicauristatinE 由细胞毒性微管蛋白修饰剂 AuristatinE 和 ADC linkerAminobenzenesulfonic 连接而成,具有抗肿瘤活性。 | |||
T80437 |
μ-TRTX-Hd1a
|
Sodium Channel | Membrane transporter/Ion channel |
μ-TRTX-Hd1a为特异性NaV 1.7抑制剂,源自蜘蛛毒液。该化合物作为门控修饰剂,通过与人NaV 1.7通道域II中S3b-S4桨基序互作,实现抑制功能。 | |||
T74484 | Aminobenzenesulfonic auristatin E TFA | ||
AminobenzenesulfonicauristatinE TFA,作为一种抗体偶联药物(Antibody-Drug Conjugate, ADC)的活性成分,该化合物通过Aminobenzenesulfonic和细胞毒性微管蛋白修饰剂AuristatinE的连接构建而成,展现出对肿瘤的抗性活性。 | |||
T22091 |
Imiquimod hydrochloride
|
||
Imiquimod hydrochloride (R 837 hydrochloride)是一种免疫反应调节剂,是一种选择性的 toll 样受体 7 (TLR7) 激动剂。Imiquimod hydrochloride 在体内表现出抗病毒和抗肿瘤作用。Imiquimod hydrochloride 可用于外生殖器、肛周疣、癌症和 COVID-19 的研究。 | |||
T5499 |
gardiquimod TFA salt
|
||
Gardiquimod diTFA,咪唑啉类似物TLR7/8激动剂,可特异性抑制巨噬细胞和活化外周血单个核细胞(PBMCs)的HIV-1感染。在浓度低于10 μM时,该化合物特异性激活TLR7。 | |||
T75855 |
Phrixotoxin 3 TFA
|
||
Phrixotoxin 3 TFA 是一种高效的电压门控钠通道阻滞剂,对NaV1.2、NaV1.3、NaV1.4、NaV1.1及NaV1.5的IC50值分别为0.6、42、72、288和610 nM。该化合物通过改变门控动力学的去极化并阻断钠电流的内向流,调控电压门控钠通道,表现出类似典型门控修饰毒素的作用机制。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5043 |
Lentinan
|
Others | Others |
Lentinan 是一种 β-葡聚糖,从香菇中提取获得。它在日本已被批准用作胃癌的生物反应调节剂。 | |||
T20868 |
Isophthalic acid
Acide isophtalique |
||
Isophthalic acid is an intermediate for a modifier of polyethylene terephthalate for bottles, gel coats, high solids paints, resins for coatings, and high-performance unsaturated polyesters. | |||
T39614 | Mogroside VI A | ||
Mogroside VI A is a saccharide compound, an isomer of Mogroside VI, that has been extracted from the Luo Han Guo plant. It possesses inherent sweetness properties. Mogroside VI A holds potential for application in sweetener and taste modifier studies. | |||
T13749 |
L-2-Hydroxyglutaric acid
(S)-2-Hydroxyglutaric acid |
Others | Others |
L-2-Hydroxyglutaric acid, an epigenetic modifier and potential oncometabolite in renal cancer, impedes mitochondrial creatine kinase (Mi-CK) activity, exhibiting Km and Ki values of 2.52 mM and 11.13 mM, respectively. Additionally, it obstructs histone demethylases, thereby encouraging histone methylation. |