74
13
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21724L |
Fas C-Terminal Tripeptide Acetate
Fas C-Terminal Tripeptide Acetate (189109-90-8 free base) |
Others; Fatty Acid Synthase | Metabolism; Others |
Fas C-Terminal Tripeptide Acetate 显示出对 Fas/FAP-1 结合的抑制活性。 | |||
T11266L |
FAS-IN-1 Tosylate
|
Fatty Acid Synthase | Metabolism |
FAS-IN-1 Tosylate is an effective fatty acid synthase inhibitor;Has an IC50 of 10 nM. | |||
T11266 |
FASN-IN-4
FAS-IN-1 |
Others | Others |
FAS-IN-1 is a potent inhibitor of Fatty acid synthase (FAS) wtih IC50 of 10 nM. | |||
T80442 |
Fasciculin-II
Fas-2 |
||
Fasciculin-II (Fas-2) 是一种针对 acetylcholinesterase (AChE) 的高效抑制剂。 | |||
T82415 |
Fasciculin-I
FAS-I |
||
Fasciculin-I 是从曼巴蛇的毒液中分离出的化合物。该物质通过抑制乙酰胆碱酯酶(AChE)来发挥其毒性,同时阻碍烟碱乙酰胆碱受体与α-神经毒素以及心脏毒素与细胞膜的相互作用。 | |||
T80584 |
Anti-Mouse Fas Ligand Antibody (MFL3)
|
||
Anti-Mouse Fas Ligand Antibody为针对小鼠Fas Ligand的IgG类抗体抑制剂,由Armenian Hamster产生。 | |||
T8616 |
Fasentin
N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide |
transporter | Metabolism |
Fasentin (N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide) 是葡萄糖摄取抑制剂,可抑制GLUT-1/GLUT-4转运蛋白,优先抑制 GLUT4,IC50为 68 μM。它是死亡受体刺激敏化剂,可敏化细胞对 FAS 诱导的细胞死亡,具有抗血管生成活性。 | |||
T39308 |
Boc-Asp(OMe)-fluoromethyl ketone
Boc-Asp(OMe)-fluoromethyl ketone,Boc-Asp(OMe)-FMK |
Caspase | Apoptosis; Proteases/Proteasome |
Boc-Asp(OMe)-fluoromethyl ketone (Boc-Asp(OMe)-FMK) 是广谱的 caspase 抑制剂,可抑制 Fas 介导的吞噬作用和氧化破裂抑制,但对 IL-8 的趋化活性无影响。 | |||
T10549 |
Bisindolylmaleimide VIII acetate
Ro 31-7549 acetate,Bis VIII acetate |
Apoptosis; PKC | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling |
Bisindolylmaleimide VIII acetate (Ro 31-7549 acetate) 是一种选择性蛋白激酶 C 抑制剂。它促进 Fas 介导的细胞凋亡,并抑制 T 细胞介导的自身免疫性疾病。 | |||
T5045 |
GSK4112
1,1-Dimethylethyl-N-[(4-chlorophenyl)methyl]-N-[(5-nitro-2-thienyl)methyl])glycinate,SR6452 |
Autophagy | Autophagy |
GSK4112 (SR6452) 是一种 Rev-erbα 激动剂,EC50 为 0.4 μM。它也是一种用于核血红素受体 Rev-erbα 的细胞生物学的小分子化学探针。 | |||
T77135 |
Tafasitamab
MOR00208,XmAb5574,Tafasitamab-cxix |
Apoptosis; Immunology/Inflammation related | Apoptosis; Immunology/Inflammation |
Tafasitamab (XmAb5574) 是一种 Fc 修饰的人源化单克隆抗体,靶向人 B 细胞表面抗原 CD19 ,可用于研究弥漫性大B细胞淋巴瘤。 | |||
T11557 |
FASN-IN-3
|
Fatty Acid Synthase | Metabolism |
FASN-IN-3 是脂肪酸合酶抑制剂。 | |||
T0907 |
Sulfasalazine
柳氮磺吡啶,NSC 667219,Azulfidine |
Apoptosis; Ferroptosis; NF-κB; COX; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB |
Sulfasalazine (Azulfidine) 是一种合成的水杨酸衍生物,对含有弹性蛋白的结缔组织具有亲和力,并配制成前药。 | |||
T4640 |
Parimifasor
LYC30937 |
Others | Others |
Parimifasor (LYC30937) 是免疫调节剂,具有抗炎作用。 | |||
T4276 |
Hydroxyfasudil Hydrochloride
Hydroxyfasudil (HA-1100) HCl,羟基法舒地尔盐酸盐,RHO-激酶抑制剂,HA 1100 hydrochloride |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Hydroxyfasudil Hydrochloride (HA 1100 hydrochloride) 是一种ROCK 抑制剂,对ROCK1和ROCK2的IC50值分别为 0.73 和 0.72 μM。 | |||
T27307L |
Fasnall HCl
Fasnall HCl(929978-58-5 Free base) |
Fatty Acid Synthase | Metabolism |
Fasnall HCl 是一种FASN 选择性抑制剂,通过其辅助因子结合位点起作用。Fasnall HCl 在HER2(+)乳腺癌MMTV-Neu 模型中也显示出强大的抗肿瘤活性,特别是与卡铂联合使用时。 | |||
T4276L |
Hydroxyfasudil
Hydroxy-Fasudil,HA-1100,羟基法舒地尔 |
ROCK; PKA | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Hydroxyfasudil (Hydroxy-Fasudil) 是一种ROCK 抑制剂,对ROCK1和ROCK2的IC50分别为 0.73 和 0.72 μM。 | |||
T1606 |
Fasudil
HA-1077,AT877,法舒地尔 |
ROCK; Serine/threonin kinase; Calcium Channel; PKA; PKC; Autophagy | Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism; Stem Cells; Tyrosine Kinase/Adaptors |
Fasudil (HA-1077) 是一种非特异性 RhoA/ROCK 抑制剂,也是 Ca2+通道拮抗剂和血管扩张剂。它对蛋白激酶有抑制作用,ROCK1 的 Ki 值为 0.33 μM,ROCK2 和 PKA、PKC、PKG 的 IC50值分别 0.158 μM 和 4.58 μM、12.30 μM、1.650 μM。 | |||
T3060 |
Fasudil hydrochloride
Fasudil (HA-1077) HCl,盐酸法舒地尔,HA-1077,Fasudil HCl,HA-1077 hydrochloride,AT-877 |
ROCK; Serine/threonin kinase; Calcium Channel; HIV Protease; PKA; PKC; Autophagy | Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Proteases/Proteasome; Stem Cells; Tyrosine Kinase/Adaptors |
Fasudil hydrochloride (HA-1077) 是一种非特异性RhoA/ROCK 抑制剂,也抑制蛋白激酶,对 ROCK1、PKA、PKC 和 MLCK 的 Ki 值分别为 0.33 μM、1.0 μM、9.3 μM 和 55 μM。 | |||
TP1029 |
Thymalfasin
胸腺法新,Thymosin α1,醋酸胸腺α1 |
Others | Others |
Thymalfasin (Thymosin α1) 是一种免疫调节化合物,可增强 Thl 的免疫应答。 | |||
T11267 |
FASN-IN-1
TVB-2460 |
Fatty Acid Synthase | Metabolism |
FASN- in -1是一种有效的、特异性的脂肪酸合成酶(FASN)抑制剂,是一种专门设计用于靶向和抑制FASN 活性的化合物,是一种参与脂肪酸合成的酶,可抑制FASN 活性可以破坏脂肪酸的产生,并可能影响各种细胞过程。 | |||
T2351 |
Fasiglifam
TAK875 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
Fasiglifam (TAK875) 是一种可口服的选择性GPR40激动剂,EC50值为 72 nM。 | |||
T9099 |
Disperse Fast Yellow 4K
分散黄,Disperse Yellow |
Others | Others |
Disperse Fast Yellow 4K (Disperse Yellow) 是一种用于染料的颜色添加剂。 | |||
T27306 |
Fasidotril
BP 1137,BP1137,BP-1.137,BP1.137,BP-1137,BP 1.137 |
||
Fasidotril is a NEP/ACE inhibitor. Fasidotril was an effective oral antihypertensive agent during chronic treatment in high-renin renovascular rats, normal-renin SHR, and low-renin DOCA-salt hypertensive rats and in patients with essential hypertension. | |||
T37776 | FASN-IN-4 tosylate | ||
FASN-IN-4 tosylate 是高效的脂肪酸合酶 FASN 抑制剂,IC50值为 10 nM。FASN-IN-4 tosylate 还抑制 SARS-CoV-2,EC50为 18.6 nM。 | |||
T27307 |
Fasnall
|
Fatty Acid Synthase | Metabolism |
Fasnall 是一种选择性 FASN 抑制剂,通过其辅因子结合位点起作用。 Fasnall 在 HER2(+) 乳腺癌的 MMTV-Neu 模型中显示出有效的抗肿瘤活性,尤其是与卡铂联合使用时。 | |||
TP2283 |
parathyroid hormone (7-34) [Homo sapiens]/[Macaca fascicularis]
|
Others | Others |
parathyroid hormone (7-34) [Homo sapiens] [Macaca fascicularis] is a peptide with the sequence H2N-LMHNLGKHLNSMERVEWLRKKLQDVHNF-OH, MW= 3474.03. Parathyroid hormone (PTH) is secreted by the chief cells of the parathyroid glands as a polypeptide containing | |||
T61382 |
Fasudil dihydrochloride
|
||
Fasudil dihydrochloride, also known as HA-1077 and AT877, is a nonspecific inhibitor of RhoA/ROCK. It exhibits inhibitory effects on protein kinases, including ROCK1 with a Ki value of 0.33 μM, as well as ROCK2, PKA, PKC, and PKG with IC 50 values of 0.158 μM, 4.58 μM, 12.30 μM, and 1.650 μM, respectively. Additionally, Fasudil dihydrochloride demonstrates potent Ca 2+ channel blocking activity and acts as a vasodilator [1] [2] [3]. | |||
T25405 |
Fasciculic acid B
|
||
Fasciculic acid B is the ester of fasciculol B and 3-hydroxy-3-methylglutaric acid. Fasciculic acid B is calmodulin antagonist from mushroom Naematoloma fasciculare. | |||
T31748 | Fasobegron | ||
Fasobegron is a agonist of β3-adrenoreceptor . | |||
T69954 | Fasoracetam monohydrate | ||
Fasoracetam monohydrate is a small synthetic molecule and a metabotropic glutamate receptor activator, which has previously undergone extensive Phase I-III clinical trials in humans for vascular dementia. | |||
T31749 |
Fast Green free acid
J247.014D |
||
Fast Green free acid is a dye that resists acid once applied. | |||
T68486 |
Fasitibant
|
||
Fasitibant is a potent and selective nonpeptide kinin B2 receptor antagonist. | |||
T31747 |
Fasitibant chloride hydrochloride
Fasitibant chloride (HCl salt),MEN 16132,Fasitibant chloride,MEN-16132,MEN16132 |
||
Fasitibant chloride( MEN16132) is an effective and selective non-peptide antagonist of kinin B2 receptor. | |||
T16954 |
Sulfasymazine
|
Antibacterial | Microbiology/Virology |
Sulfasymazine is a sulfonamide drug. | |||
T125173 |
Fasciculic acid D
|
||
Fasciculic acid D 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 T125173,CAS号为 261638-74-8。 | |||
T64582 | Fasudil hydrochloride semihydrate | ||
Fasudil hydrochloride semihydrate 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 T64582。 | |||
T25406 | Fasciculic acid C | ||
Fasciculic acid C is a calmodulin antagonist isolated from mushroom Naematoloma fasciculare. | |||
T78453 |
Fast Blue B Salt
|
||
Fast Blue B Salt作为染色剂,能溶解黑麦提取物中的脂肪及苯酚化合物和重氮剂。该化合物能够用于黑麦中的烷基间苯二酚半定量分析,并在加入丙酮的情况下形成有色沉淀。 | |||
T7772 |
Fast Green FCF
C.I. 42053,固绿 FCF,Food green 3,FD&C Green No. 3 |
Others | Others |
Fast Green FCF (FD&C Green No. 3) 是海绿色三芳基甲烷食用染料,最大吸收在625nm 处,将在电泳过程中的蛋白质染色,。 | |||
T79416 |
FASN-IN-6
|
||
FASN-IN-6(Compound 44)作为脂肪酸生物合成(FAB)抑制剂表现出高效性。该化合物具备抗菌作用,针对金黄色葡萄球菌ATCC 25923及粪肠球菌ATCC 29212的最小抑菌浓度(MIC)分别为1 μg/mL与4 μg/mL。 | |||
T25404 |
Fasciculic acid A
|
||
Fasciculic acid A is a calmodulin antagonist isolated from mushroom Naematoloma fasciculare. | |||
T60483 |
Fasedienol
|
||
Fasedienol 是一种犁鼻器 (VON) 的神经化学刺激剂,可缓解焦虑和经前综合症。 | |||
T61319 |
Onfasprodil
|
||
Onfasprodil, a negative allosteric modulator of NR2B, has been identified as a potential compound for researching Alzheimer's disease. This compound, in combination with a GABA receptor regulator.[1] | |||
T28039 |
Milfasartan
LR-B081,LRB-081,LR-B-081,LRB 081,LR-B 081 |
||
Milfasartan is a potent, selective antagonist of AT1 receptor with oral activity. It markedly lowers the blood-pressure in conscious renal and spontaneously hypertensive rats. | |||
T33889 |
Passitrifasciatin
|
||
Passitrifasciatin is a cyclopentanoid cyanohydrin glycoside isolated from Passiflora trifasciata. | |||
T31746 | Fasciculol A | ||
Fasciculol A is a terpenoid. | |||
T74332 | Rifasutenizol | ||
Rifasutenizol (TNP-2198)为一种有效的口服生物利用度高的双靶向抗菌剂,对微需氧菌和厌氧菌病原体展现出强大的活性。 | |||
T76901 | Afasevikumab | ||
Afasevikumab (RG 7624; RO 5553110; NI-1401) 是一种全人单克隆 IgG1κ 抗体,可中和 IL-17A 和 IL-17F。Afasevikumab 具有抗炎活性。 | |||
T62925 |
FASN-IN-5
|
||
FASN-IN-5 (example 11) 是一种 FASN 抑制剂,能够用于 TH17 或 CSF1 介导的疾病或障碍(如癌症、免疫障碍、肥胖症)的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21936 |
M50054
2,2′-亚甲基双(1,3-环己二酮) |
Caspase | Apoptosis; Proteases/Proteasome |
M50054 是一种有效的细胞凋亡抑制剂,可用于研究抗 Fas 抗体引起的肝炎和化疗引起的脱发。它抑制 Etoposide 诱导的 U937 细胞 caspase-3 活化,IC50为 79 μg/mL。 | |||
T5S0246 |
Pseudoprotodioscin
山药 |
Others; Fatty Acid Synthase | Metabolism; Others |
Pseudoprotodioscin 是一种呋喃葡糖苷,抑制SREBP1/2和microRNA 33a/b 水平,降低胆固醇和甘油三酯合成相关的基因表达。 | |||
T27305 |
Fascaplysin chloride
NSC622398,NSC 622398,Fascaplysin,NSC-622398 |
||
Fascaplysin is a cyclin D kinase 4/ cyclin D1 inhibitor (IC50 = 0.35 μM). Fascaplysin induces caspase mediated crosstalk between autophagy and apoptosis through the inhibition of PI3K/AKT/mTOR signaling cascade in human leukemia HL-60 cells. | |||
TJS0387 |
Desoxyrhaponticin
去氧土大黄苷,Deoxyrhapontin,脱氧土大黄苷,Deoxyrhaponticin |
Apoptosis; Fatty Acid Synthase | Apoptosis; Metabolism |
Desoxyrhaponticin (Deoxyrhaponticin) 是来自西藏营养食品唐古特大黄中的一种二苯乙烯苷。它是脂肪酸合成酶抑制剂,抑制细胞内 FAS 活性,下调人乳腺癌 MCF-7细胞中 FAS 的表达。它是控制糖尿病餐后高血糖的潜在药物。 | |||
T13815 |
Penicillic acid
|
Apoptosis; Caspase; Antibacterial; Antibiotic | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Penicillic acid, a polyketide mycotoxin, synthesized by various species of Aspergillus and Penicillium, acts as an inhibitor of Fas ligand-induced apoptosis by impeding self-processing of caspase-8. Additionally, in vitro studies have shown that Penicillic acid displays cytotoxic properties in rat alveolar macrophages. | |||
TQ0260 |
Cerulenin
|
Antibiotic; Antifungal; Fatty Acid Synthase | Metabolism; Microbiology/Virology |
Cerulenin 是广泛使用的天然脂肪酸合成酶抑制剂。它是由真菌Cephalosporium caeruleus 产生的。它抑制拓扑异构酶I 催化活性并增强 SN-38 诱导的细胞凋亡。它具有抗真菌和抗肿瘤活性。 | |||
T4S0290 |
Araloside A
Chikusetsusaponin IV,竹节参皂苷IV |
RAAS; Fas/FasL | Apoptosis; Endocrinology/Hormones |
Araloside A (Chikusetsusaponin IV) 是竹节参中的一种成分,对肾素renin 具有低抑制活性(IC50:77.4 μM)。 | |||
T3S1775 |
Tectochrysin
NSC 80687,Techtochrysine,Techtochrysin,柚木柯因 |
NF-κB; STAT | JAK/STAT signaling; NF-κB; Stem Cells |
Tectochrysin (Techtochrysine) 是Alpinia oxyphylla 的主要黄酮类化合物之一,能够抑制NF-κB 活性。 | |||
T2854 |
Phillyrin
Forsythin,连翘苷 |
P450; Influenza Virus; AMPK | Chromatin/Epigenetic; Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Phillyrin (Forsythin) 是从连翘中分离出来的一种天然产物,具有抗甲型流感病毒的活性,以及抗菌和消炎作用。 | |||
TN1365 |
Albaspidin AP
|
Fatty Acid Synthase | Metabolism |
Albaspidin-AP, -PP, -PB inhibit Fatty acid synthase (FAS) with IC50 values ranging from 23.1+/-1.4 to 71.7+/-3.9 microM, they could be considered to be a promising class of FAS inhibitors, and FAS is emerging as a potential therapeutic target to treat can | |||
TN4496 |
Marginatoxin
|
Caspase; Fas/FasL | Apoptosis; Proteases/Proteasome |
Marginatoxin may be a promising chemopreventive agent for treating hepatocellular carcinoma, it induces human hepatoma BEL-7402 cells apoptosis in vitro and in vivo via activation of Fas/FasL-mediated apoptotic pathway. | |||
TN1532 | Crenulatin | BCL; Caspase | Apoptosis; Proteases/Proteasome |
Crenulatin has dual- direction effects on apoptosis of cerebral microvascular endothelial cells, inhibitive effect in 25 mg/L and stimulative effect in 100 mg/L group, respectively; the mechanism is related to the alterations of Fas/Bcl-2 expression and caspase-3 activity. | |||
TMA0918 |
Neochamaejasmine A
|
Caspase | Apoptosis; Proteases/Proteasome |
Neochamaejasmin A can inhibit cellular (3)H-thymidine incorporation (IC 50 12.5 microg/mL) and subsequent proliferation of human prostate cancer LNCaP cells, it blocks cell cycle progression at the G1 phase by activating the p21 protein and ultimately pro |