650
74
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37422L |
Ras Inhibitory Peptide acetate
Ras Inhibitory Peptide acetate(159088-48-9 Free base) |
Ras | GPCR/G Protein; MAPK |
Ras Inhibitory Peptide acetate 是一种参与 Ras 依赖性信号通路的肽,Ras 在致癌受体引发的人类癌症中起重要作用。 | |||
T16432 |
Pan-RAS-IN-1
|
MAPK; Ras | GPCR/G Protein; MAPK |
Pan-RAS-IN-1是一种广谱的 Ras 抑制剂。Pan-RAS-IN-1破坏 Ras 蛋白及其作用子的相互作用。 | |||
T5469 |
K-Ras-IN-1
|
Raf; Ras | GPCR/G Protein; MAPK |
K-Ras-IN-1 是K-Ras 抑制剂。K-Ras-IN-1 能与 K-Ras (WT)、K-Ras (G12D)、K-Ras (G12V) 和 H-Ras 结合。它对胰腺癌、结肠癌和肺癌的具潜在的研究价值。 | |||
T11738 |
K-Ras G12C-IN-4
|
Ras | GPCR/G Protein; MAPK |
K-Ras G12C-IN-4 是一种 KRAS G12C 共价抑制剂。 | |||
T12692 |
RAS GTPase inhibitor 1
|
Others | Others |
RAS GTPase inhibitor 1 is a inhibitor of RAS GTPase, with anti-tumor activity. | |||
T6556 |
K-Ras(G12C) inhibitor 9
|
Raf | MAPK |
K-Ras(G12C) inhibitor 9 是致癌 K-Ras(G12C) 的变构抑制剂。 | |||
T3725 |
K-Ras(G12C) Inhibitor 6
|
Raf | MAPK |
KRas(G12C) inhibitor 6 是一种变构的,选择性的 K-Ras(G12C)抑制剂。 | |||
T6555 |
K-Ras(G12C) inhibitor 12
|
Apoptosis; Raf; Ras | Apoptosis; GPCR/G Protein; MAPK |
K-Ras(G12C) inhibitor 12是一种K-Ras(G12C)抑制剂,作用于H1792细胞,EC50为0.32 μM。 | |||
T8659 |
K-Ras-PDEδ-IN-1
|
PDE | Metabolism |
K-Ras-PDEδ-IN-1 是新型的 K-Ras-PDEδ 抑制剂,它能够以低纳摩尔Kd8 nM 与 PDEδ 的法尼基结合袋竞争性结合。 | |||
T36642 | RAS/RAS-RAF-IN-1 | ||
RAS/RAS-RAF-IN-1 is a potent RAS and RAS-RAF inhibitor. RAS/RAS-RAF-IN-1 has a KD of 5.0 μμ-15 μμ for cyclophilin A (CYPA) binding affinity. RAS/RAS-RAF-IN-1 has antitumor activity[1]. RAS/RAS-RAF-IN-1 (compound 89; for 4 hours) has an EC50 of 0.5 μμ-5.0 μμ for BRAF-GTP-KRAS-G12C disruption and has an IC50 of 1.0 μμ-10 μμ for pERK inhibition in H358 cells[1]. [1]. Meizhong Jin, et al. Compounds that participate in cooperative binding and uses thereof. WO2020132597A1. | |||
T74698 |
RMC-6236
RAS-IN-2 |
||
RMC-6236(RAS-IN-2 ) 是一种有效的RAS(ON)MULTI 抑制剂,可用于癌症的研究。 | |||
T37422 |
Ras Inhibitory Peptide
|
||
Son of sevenless homolog 1 (Sos1) is a guanine nucleotide exchange factor (GEF) that directs the exchange of Ras-GDP to Ras-GTP by binding to SH3 domains of the growth factor receptor-bound protein 2 (Grb2), leading to the activation of ERK. Ras inhibitory peptide is a synthetic peptide that contains the sequence PVPPR, which corresponds to a region within human Sos1 that interacts with an SH3 domain of Grb2. It specifically blocks the interaction of the GEF with Grb2, preventing an interaction ... | |||
T36641 |
RAS inhibitor Abd-7
|
||
RAS inhibitor Abd-7 is a powerful compound (Kd=51 nM) that binds to RAS and inhibits the protein-protein interaction (PPI) between RAS and its effectors. By interacting with RAS within cells, RAS inhibitor Abd-7 hinders RAS-effector interactions and suppresses endogenous RAS-dependent signaling. Additionally, RAS inhibitor Abd-7 disrupts the PPI of different mutant KRAS proteins with PI3K, CRAF, RALGDS, as well as NRAS Q61H and HRAS G12V[1]. | |||
T77800 |
Ras inhibitor 134
|
||
T13844 |
PROTAC K-Ras Degrader-1
|
Ras | GPCR/G Protein; MAPK |
PROTAC K-Ras Degrader-1 is potent degrader of K-Ras based PROTAC. | |||
T11735 |
K-Ras G12C-IN-1
|
Phosphatase | Metabolism |
K-Ras G12C-IN-1 is a novel and irreversible inhibitor of mutant K-ras G12C. | |||
T11737 |
K-Ras G12C-IN-3
|
Others | Others |
Heterocyclic compounds as covalent inhibitors of G12C mutant K-Ras protein useful for treating cancers.K-Ras G12C-IN-3 is a novel and irreversible inhibitor of mutant K-ras G12C. | |||
T11736 |
K-Ras G12C-IN-2
|
Others | Others |
K-Ras G12C-IN-2 is a covalent kras g12c inhibitor. | |||
T18056 |
K-Ras ligand-Linker Conjugate 3
|
Others | Others |
K-Ras ligand-Linker Conjugate 3 (Compound 001371) is a chemical compound that consists of a ligand for K-Ras recruiting moiety and a PROTAC linker, responsible for recruiting E3 ligases (e.g., VHL, CRBN, MDM2, and IAP). This compound is essential in the synthesis of PROTAC K-Ras Degrader-1, a potent PROTAC K-Ras degrader that demonstrates a degradation efficacy of ≥70% in SW1573 cells[1]. | |||
T18055 |
K-Ras ligand-Linker Conjugate 2
|
Others | Others |
K-Ras ligand-Linker Conjugate 2 is a chemical compound that includes a ligand for K-Ras and a PROTAC linker. This compound is capable of recruiting E3 ligases like VHL, CRBN, MDM2, and IAP. It is utilized in the synthesis of PROTAC K-Ras Degrader-1, which is a highly effective PROTAC K-Ras degrader with a degradation efficacy of ≥70% in SW1573 cells[1]. | |||
T18057 |
K-Ras ligand-Linker Conjugate 4
|
Others | Others |
K-Ras ligand-Linker Conjugate 4 is a chemical compound that combines a ligand for K-Ras recruiting moiety with a PROTAC linker. This linker is responsible for recruiting E3 ligases such as VHL, CRBN, MDM2, and IAP. The compound has the potential to be used in the synthesis of PROTAC K-Ras Degrader-1, a powerful degrader of K-Ras that has been shown to exhibit a degradation efficacy of ≥70% in SW1573 cells[1]. | |||
T18059 |
K-Ras ligand-Linker Conjugate 6
|
Others | Others |
K-Ras ligand-Linker Conjugate 6 is a chemical compound that combines a ligand for K-Ras recruiting moiety and a PROTAC linker. This compound can recruit E3 ligases, including VHL, CRBN, MDM2, and IAP. K-Ras ligand-Linker Conjugate 6 is particularly useful in the synthesis of PROTAC K-Ras Degrader-1, a highly effective K-Ras degrader that achieves ≥70% degradation efficacy in SW1573 cells[1]. | |||
T18058 |
K-Ras ligand-Linker Conjugate 5
|
Others | Others |
K-Ras ligand-Linker Conjugate 5 is a chemical compound that combines a ligand for the K-Ras recruiting moiety with a PROTAC linker. This linker is responsible for recruiting E3 ligases such as VHL, CRBN, MDM2, and IAP. The K-Ras ligand-Linker Conjugate 5 plays a crucial role in the synthesis of PROTAC K-Ras Degrader-1, a highly potent K-Ras degrader. In SW1573 cells, this degrader exhibits an impressive degradation efficacy of ≥70% [1]. | |||
T18054 | K-Ras ligand-Linker Conjugate 1 | Others | Others |
K-Ras ligand-Linker Conjugate 1 is a chemical compound that includes a ligand for K-Ras and a PROTAC linker, facilitating the recruitment of E3 ligases VHL, CRBN, MDM2, and IAP. It can be utilized in the synthesis of PROTAC K-Ras Degrader-1, a highly effective K-Ras degrader that achieves ≥70% degradation efficacy in SW1573 cells[1]. | |||
T72774 |
Ras modulator-1
|
||
Rasmodulator-1 是Ras 调节剂。 | |||
T1931 |
6H05
K-Ras inhibitor |
Raf; Ras | GPCR/G Protein; MAPK |
6H05 (K-Ras inhibitor) 是致癌突变体 K-Ras(G12C) 的选择性变构抑制剂。 | |||
T1892 |
Kobe2602
|
Raf; Ras | GPCR/G Protein; MAPK |
Kobe2602 是 Ras-Raf 相互作用抑制剂,具有抗癌化疗活性。它抑制 H-Ras·GTP 与 c-Raf-1 RBD 结合的Ki 值为 149 μM。 | |||
T39099 |
G12
Ras 5-17 |
||
G12 (Ras 5-17) is a wild-type Ras peptide composed of amino acids 5-17, specifically KLVVVGAGGVGKS. It can serve as a control in studies focused on mutant Ras peptides, like V12. | |||
T6462 |
Deltarasin
|
PDE; Ras | GPCR/G Protein; MAPK; Metabolism |
Deltarasin 是一种 KRAS-PDEδ 相互作用的小分子抑制剂,与纯化的 PDEδ 结合,Kd 值为 38 nM。 | |||
T4370 |
Resminostat hydrochloride
4SC-201 hydrochloride,RAS2410 hydrochloride |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Resminostat hydrochloride (RAS2410 hydrochloride) 是HDAC1,HHDAC3和HDAC6抑制剂,IC50值分别为 42.5、50.1和71.8 nM,对 HDAC8 的活性较低,IC50值为 877 nM。 | |||
T9407 |
Rasarfin
|
Others; Ras | GPCR/G Protein; MAPK; Others |
Rasarfin 是Ras 和ARF6双抑制剂。 | |||
T2678 |
LB42708
|
Transferase | Metabolism |
LB42708 是一种口服有活力的特异性法尼基转移酶抑制剂。它对H-Ras、N-Ras 和K-Ras4B 的法尼基化均有抑制作用,其IC50分别为 0.8 nM、1.2 nM 和 2.0 nM。 | |||
T1876 |
Kobe0065
|
Apoptosis; Raf; Ras | Apoptosis; GPCR/G Protein; MAPK |
Kobe0065 是一种新型 Ras-Raf 相互作用抑制剂,可完全抑制 H-Ras·GTP 与 c-Raf-1 RBD 的结合,Ki 值为 46±13 μM。 | |||
T60029 |
SOS1-IN-11
|
Raf | MAPK |
SOS1-IN-11 是一种有效的 SOS1 抑制剂 (IC50 = 30 nM)。 | |||
T20759 |
XRP44X
XRP-44-X,XRP 44X,XRP-44X,XRP 44 X |
Ras | GPCR/G Protein; MAPK |
XRP44X (XRP 44X) 是Ras 诱导的转录激活的抑制剂,IC50为 10 nM,通过 FGF-2 抑制 Ras-Erk-1/2 通路激活。它抑制Elk3。它还对微管有影响。 | |||
T9986 | (E/Z)-ZINC09659342 | Rho | Cell Cycle/Checkpoint |
(E/Z)-ZINC09659342 是 Lbc-RhoA 相互作用的抑制剂。 | |||
T5597 |
ZT-12-037-01
|
Serine Protease; Ras | GPCR/G Protein; MAPK; Proteases/Proteasome |
ZT-12-037-01 是一种 ATP 竞争性 STK19 抑制剂,对 STK19 (WT) 和 STK19 (D89N) 的 IC50 值分别为 23.96 和 27.94 nM | |||
T10375 |
ARS-1323
|
Ras | GPCR/G Protein; MAPK |
ARS-1323 是 ARS-1620 的消旋体。ARS-1323 是突变型K-Ras G12C 的新型抑制剂。 | |||
T2267 |
BQU57
|
GTPase; Ras | GPCR/G Protein; MAPK |
BQU57 能够选择性抑制 Ral,且对 Ral 的选择性高于 Ras、Rho,能够作用于 H2122(IC50:2.0 μM)和 H358(IC50:1.3 μM)。 | |||
T10376 |
ARS-1630
|
Ras | GPCR/G Protein; MAPK |
ARS-1630 是一种突变型 K-ras G12C 抑制剂。 它是 ARS-1620 的活性较低的对映异构体。 | |||
T6634 |
RBC8
|
GTPase; Ras | GPCR/G Protein; MAPK |
RBC8是一种特异性 GTP 酶 RalA/RalB 抑制剂,通过抑制 Ral 与其效应物 RALBP1 的结合,对 GTP 酶 RhoA 和 Ras 没有抑制作用。 | |||
T7609 |
ARS-1620
|
Ras | GPCR/G Protein; MAPK |
ARS-1620 是 K-RASG12C 的共价抑制剂,具有理想的药代动力学。 | |||
T3553 |
Y16
|
Rho; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
Y16 是一种 G 蛋白偶联的 Rho GEFs 抑制剂,与 Rhosin/G04 协同作用,抑制 LARG-RhoA 相互作用、RhoA 激活和 RhoA 介导的信号传导功能。它是 LARG 的特异性抑制剂,Kd 值为 76 nM。 | |||
T5418 |
BAY-293
|
Raf; Ras | GPCR/G Protein; MAPK |
BAY-293 是化学探针,是一种有效的细胞活性 SOS1 抑制剂,可破坏 KRAS-SOS1 相互作用,IC50为 21 nM。 | |||
T39738 |
ASP2453
|
Ras | GPCR/G Protein; MAPK |
ASP2453是选择性的KRAS G12C 共价抑制剂,抑制Son of Sevenless 介导的KRAS G12C 和Raf 之间的相互作用,IC50为40 nM。 | |||
T10533 |
BI-2852
|
Ras | GPCR/G Protein; MAPK |
BI-2852 是具有纳摩尔亲和力的开关 I/II 口袋(SI/II-口袋)的 KRAS 抑制剂,可抑制 KRAS 突变细胞的下游信号传导和抗增殖作用。 | |||
T38050 |
CP-609754
|
Transferase | Metabolism |
CP-609754 是高效的、可逆的法尼基转移酶抑制剂,对重组人 H-Ras 和重组 K-Ras 法尼基化的 IC50分别为 0.57 ng/mL 和 46 ng/mL。CP-609754有潜在的抗癌作用。 | |||
T8006 |
Oncrasin-1
1-(4-氯苄基)-1H-吲哚-3-甲醛 |
Apoptosis; Raf; Ras | Apoptosis; GPCR/G Protein; MAPK |
Oncrasin 1 是一种有效的抗癌抑制剂,可在低或亚微摩尔浓度下杀死具有 K-Ras 突变的各种人类肺癌细胞。 | |||
T16021 |
MBQ-167
|
CDK; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
MBQ-167 是一种 Rac/Cdc42 的双重抑制剂,在 MDA-MB-231 细胞中,Rac 1/2/3 和 Cdc42 的 IC50 分别为 103 nM 和 78 nM。 | |||
T14004 |
1A-116
|
Rho | Cell Cycle/Checkpoint |
1A-116 是 Rac1的抑制剂,对几种类型的癌症具有抗肿瘤和抗转移作用,如乳腺癌。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S1261 |
Methylophiopogonanone B
|
Ras | GPCR/G Protein; MAPK |
Methylophiopogonanone B 是一种高异二氢黄酮,提取自麦冬的根,抗氧化能力强,它通过 Rho 信号传导途径及增加 GTP-Rho 发挥效果。它能够重组肌动蛋白细胞骨架,使细胞形态(如树突收缩、应力纤维形成)发生变化。 | |||
T5S0777 |
Phellodendrine chloride
|
Others | Others |
Phellodendrine chloride 是一种Phellodendron amurense 中的生物碱。它通过巨胞饮抑制营养物质的吸收,进而抑制 KRAS 突变的胰腺癌细胞的增殖。 | |||
T5368 |
Eicosapentaenoic Acid
|
Histone Demethylase; Others; Endogenous Metabolite | Chromatin/Epigenetic; Metabolism; Others |
Eicosapentaenoic Acid 是一种 ω-3 脂肪酸。 | |||
TQ0165 |
Arglabin
阿格拉宾,(+)-Arglabin |
NOD-like Receptor (NLR); Transferase; NOD; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Arglabin ((+)-Arglabin) 是从青蒿中分离出的一种天然产物,是一种 NLRP3 炎性体抑制剂,具有抗动脉粥样硬化和抗癌作用。 | |||
TN1413 |
Atranorin
荔枝素,巴美灵,荔枝素 |
Endogenous Metabolite; NO Synthase; Ras | GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism |
Atranorin 是地衣的次生代谢产物,具有显着的抗伤害、抗炎和氧化还原活性,对 H(2)O(2) 诱导的氧化应激下的细胞具有细胞保护作用。 | |||
T7131 |
Antineoplaston A10
3-苯基乙酰氨基-2,6-哌啶二酮,NSC-648539 |
Apoptosis; Endogenous Metabolite; Ras | Apoptosis; GPCR/G Protein; MAPK; Metabolism |
Antineoplaston A10 (NSC-648539) 是存在于人体内的一种天然产物,可研究胶质瘤、淋巴瘤、星形细胞瘤和乳腺癌,是一种 Ras 抑制剂。 | |||
T8244 |
Raspberry ketone glucoside
覆盆子酮葡糖苷,树莓苷,覆盆子酮葡萄糖甙 |
Others | Others |
Raspberry ketone glucoside 是一种山莓果实中的天然产物。它能够抑制黑色素的合成。 | |||
T41372 |
(22S,23S)-Homobrassinolide
油菜素内酯,SSHB |
Others | Others |
(22S,23S)-Homobrassinolide (SSHB) 在各种植物生物测定试验中均能诱导植物生长。 | |||
T15753 |
Licraside
Licuraside |
Tyrosinase | Proteases/Proteasome |
Licraside 是一种酪氨酸酶抑制剂,对单酚酶的 IC50 为 0.072 mM,可用于抗褐变和脱色剂的研究。 | |||
T4S1114 |
Dryocrassin ABBA
东北贯众素,Dryocrassin |
Influenza Virus; Antibacterial | Microbiology/Virology |
Dryocrassin ABBA (Dryocrassin) 是一种从苦参中提取的黄酮类天然产物,具有抗病毒和抗菌活性。它抑制树突状细胞的免疫刺激功能,延长同种异体皮肤移植成活率。 | |||
T3345 |
Hederasaponin B
常春藤皂苷B,Eleutheroside M,刺五加叶中,Hederacoside B |
Others; Virus Protease | Microbiology/Virology; Others |
Hederasaponin B (Hederacoside B) 是从Hedera helix 中分离的,有广谱抗病毒活性。 | |||
TN7077 |
Sinocrassoside C1
|
Others | Others |
Sinocrassoside C1 是中国景天(景天科)全植物的甲醇提取物。 | |||
T7132 |
(Rac)-Brassinazole
BRASSINAZOLE,3-(4-氯苯基)-1-甲基-1-苯基-2-(1,2,4-三唑-1-基)-1-丙醇,(Rac)-芸苔素唑 |
P450 | Metabolism |
(Rac)-Brassinazole 是三唑型化合物,是油菜素甾醇 (BR) 生物合成抑制剂。它能够增强 CYP90B 在 BR 生物合成中的抑制作用。 | |||
T2S0633 |
Raspberry ketone
Oxyphenalon,Rasketone,Aloenin,4-(4-Hydroxyphenyl)-2-butanone,p-Hydroxybenzyl acetone,Frambinone,覆盆子酮 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Raspberry ketone (p-Hydroxybenzyl acetone) 是覆盆子中主要的芳香族天然产物,主要用作化妆品的香料和食品增味剂,也可作 PPAR-α激动剂。 | |||
T3151 |
Brassinolide
Brassin lactone,24-Epibrassinolide,芸苔素内酯 |
Apoptosis; Others | Apoptosis; Others |
Brassinolide (Brassin lactone) 是一种植物生长调节剂,可调节植物细胞伸长。 | |||
T4373 |
Brassinin
BSN,芸苔宁 |
Antifungal | Microbiology/Virology |
Brassinin (BSN) 是一种从 B. campestris 中分离出来的植物抗毒素,具有抗癌、化学预防、抗增殖和抗真菌活性。 | |||
TQ0160 |
Hydrastine
北美黄连碱,(-)-β-Hydrastine,(1R,9S)-β-Hydrastine |
Others | Others |
Hydrastine ((-)-β-Hydrastine) 是一种天然生物碱,存在于Hydrastis canadensis 和Ranunculaceae 家族其他植物。 | |||
T3S1892 |
Crassicauline A
粗茎乌头碱甲,Crassicauline I |
Others | Others |
Crassicauline A (Crassicauline I) 是一种乌头根中具有生物活性的生物碱。它对赤拟谷盗成虫具有拒食剂作用,其 EC50=1134.5 ppm。 | |||
T5514 |
Epibrassinolide
24-Epibrassinolide,B1105,表油菜素内酯,BP55 |
Apoptosis | Apoptosis |
Epibrassinolide (BP55) 是一种广泛存在的植物生长激素,具有缓解植物重金属和农药胁迫潜力。它在各种癌细胞中是一种潜在的凋亡诱导剂。 | |||
TN3051 | 4-Methoxyglucobrassicin | Others | Others |
4-Methoxyglucobrassicin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3051,CAS号为 83327-21-3。 | |||
TN4925 | Rubiprasin B | Others | Others |
Rubiprasin B is a natural product from Rubia cordifolia var. pratensis. | |||
TN4924 | Rubiprasin A | Others | Others |
Rubiprasin A is a natural product from Rubia cordifolia var. pratensis. | |||
TN6191 |
Murrastinine C
|
||
Murrastinine C 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6191,CAS号为 20105-20-8。 | |||
T28415 |
Picrasidine N
Picrasidine-N,PicrasidineN |
||
Picrasidine N is a naturally occurring dimeric alkaloid and a PPARβ/δ agonist. | |||
T1607 |
Hydrastinine hydrochloride
北美黄连碱分碱盐酸盐,北美黄连碱分碱 |
Others | Others |
Hydrastinine hydrochloride 是金印草中的一种主要生物碱成分,可用作止血剂。 | |||
TN2597 |
12-Hydroxy-6-epi-albrassitriol
|
Others | Others |
12-Hydroxy-6-epi-albrassitriol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2597,CAS号为 178330-78-4。 | |||
T24638 | Picrasidine M | ||
Picrasidine M is a PARP-1 inhibitor. | |||
TN3270 | (R)-3β-Hydroxy steroid sulfotransferase-IN-11 | Others | Others |
TN6651 | Picrasidine Q | ||
Picrasidine Q has the capacity of anti-cell transformation and anti-cancer, it might be a chemopreventive and chemotherapeutic agent by direct targeting FGFR2 and inhibiting cell proliferation of ESCC cells. | |||
TN4785 | Picrasidine I | NF-κB; ROS; MAPK | Immunology/Inflammation; MAPK; NF-κB |
Picrasidine I has antiosteoclastogenic effect by inhibiting inflammation induced activation of MAPKs, NF-κB and ROS generation followed by suppressing the gene expression of c-Fos and NFATc1 in osteoclast precursors. | |||
T82822 | Brassicanate A sulfoxide | ||
Brassicanate A sulfoxide 表现出除草效果,它能抑制植物中必需氨基酸的生物合成路径。该化合物通过结合并抑制多种酶的活性来发挥其作用,包括二羟酸脱水酶 (DHAD)、羟甲基丙酮酸双加氧酶 (HPPD)、乙酰乳酸合酶 (ALS)、PYL家族蛋白及转运抑制剂响应 1 (TIR1)。Brassicanate A sulfoxide 可以从甘蓝 (Brassica oleracea) 中提取获得。 | |||
TN5387 |
Grasshopper ketone
|
ERK; p38 MAPK; NO Synthase; JNK | Immunology/Inflammation; MAPK |
Grasshopper ketone 是从褐藻马尾藻中分离的化合物,是 RAW 264.7 细胞中 LPS 诱导的 NO 产生的有效抑制剂,通过抑制 MAPK(ERK,JNK 和 p38)和 NF-κB p65磷酸化来诱导抗炎作用。 | |||
TN3593 |
Carasiphenol C
|
Others | Others |
Carasiphenol C is a natural product from Carex humilis Leyss. | |||
TN3591 |
Carasinol B
|
Others | Others |
Carasinol B is a natural product from Carex humilis Leyss. | |||
TN4787 |
Picrasin B
|
Others | Others |
Picrasin B shows a significant clastogenic activity in cell cultures of Don lung cells of Chinese hamster. | |||
TN3592 | Carasinol D | Others | Others |
Carasinol D is a natural product from Carex humilis Leyss. | |||
TN4636 | Neoglucobrassicin | Others | Others |
Neoglucobrassicin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4636,CAS号为 5187-84-8。 | |||
T27281 |
Eritoran Tetrasodium
B 1287,E 5564,B-1287,E5564,B1287,E-5564 |
||
Eritoran Tetrasodium, a TLR4 receptor antagonist, is used potentially for the treatment of type 2 diabetes. | |||
T2S0799 | Noroxyhydrastinine | Tyrosinase | Proteases/Proteasome |
Noroxyhydrastinine exhibits potent melanogenesis-inhibitory activities, it inhibits melanogenesis, at least in part, by inhibiting the expression of protein levels of tyrosinase, TRP-1, and TRP-2 in α-MSH-stimulated B16 melanoma cells. | |||
T13082 |
Tarasaponin VI
|
Others | Others |
Tarasaponin VI 是从 Aralia elata 中分离出来的,对乙醇吸收具有有效的抑制活性。 | |||
T75767 |
Parasin I TFA
|
||
Parasin I (TFA) 是一种含有19个氨基酸残基的多肽,源自鲶鱼皮肤中分离出的组蛋白H2A,具备抗菌功能。 | |||
T21577 |
Narasin (sodium salt)
Naracin sodium salt,naransin sodium,海南霉素,HainanMycin |
NF-κB | NF-κB |
Narasin (sodium salt) (HainanMycin) 通过神经胶质瘤细胞中的 ER 应激诱导肿瘤坏死因子相关凋亡诱导配体 (TRAIL) 介导的细胞凋亡,并通过抑制 IκBα 的磷酸化来抑制 NF-κB 信号传导。 | |||
TN4441 |
Linderaspirone A
|
Others | Others |
Linderaspirone A shows significant activity against glucosamine-inducedinsulin resistance. | |||
T40758 |
Hydrastinine
|
||
Hydrastinine, a key alkaloid component found in Hydrastis canadensis (goldenseal), serves as an effective hemostatic agent. | |||
T82304 |
Glucobrassicanapin potassium
4-Pentenylglucosinolate potassium |
||
Glucobrassicanapin (4-Pentenylglucosinolate) potassium 是脂肪族硫代葡萄糖苷类化合物,主要存在于白菜等蔬菜作物中。 | |||
TN3373 | Albrassitriol | Others | Others |
Albrassitriol is a natural product from the cultures of the fungus Penicillium sp. | |||
TN1796 |
Brassicin
油菜,Isorhamnetin 7-O-glucoside |
Others | Others |
Isorhamnetin 7-O-glucoside has antioxidant activity, it showed the peroxynitrite and DPPH scavenging activities with IC50 values of 2.07 /- 0.17 and 13.3 microM, respectively. | |||
TN3163 | 6-epi-Albrassitriol | Others | Others |
6-epi-Albrassitriol is a natural product from A spergillussp. | |||
TN3717 | Crassanine | Others | Others |
Crassanine 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3717,CAS号为 16790-92-4。 | |||
T25596 | Lactiflorasyne | ||
Lactiflorasyne is a bioactive chemical from Artemisia lactiflora Wall that contains an ester group, a spiro system and two triple bonds. | |||
------------------------ 更多 ------------------------ |