193
28
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TD0098 |
Direct Red 80
Sirius Red,天狼猩红,Sirius Red F 3BA,C.I. direct red 80 |
Others | Others |
Direct Red 80 (Sirius Red) 是一种聚偶氮染料,在降解时不会释放联苯胺,比许多传统的直接染料更安全,主要用于胶原蛋白和淀粉样蛋白的染色方法。 | |||
T20033 |
Direct Violet 1
NSC75778,NSC 75778,Airedale Violet ND,NSC-75778,直接青莲N,Direct Violet N,CCRIS 2413 |
SARS-CoV | Microbiology/Virology |
Direct Violet 1 (CCRIS 2413) 是一种偶氮染料,是纺织品染料,也是 SARS-CoV-2 刺突蛋白和 ACE2 抑制剂之间的蛋白质相互作用 ,IC50为 1.47-2.63 µM。 | |||
T2194 |
Direct Blue 1
Pontamine sky blue,滂胺天蓝,Chicago Sky Blue 6B |
GluR | Neuroscience |
Chicago Sky Blue 6B 是免疫荧光组织化学中背景自体荧光的一种复染料。Direct Blue 1 (Pontamine sky blue) 是第一个能够抑制 Aβ 结合的小分子 PrP 配体,在结构上与谷氨酸盐有关,是一种有效且具有竞争性的 VGLUT 抑制剂,不影响质膜转运体。 | |||
T18979 |
Diphenyl Blue
台盼蓝,Direct Blue 14 |
Others | Others |
Diphenyl Blue (Direct Blue 14) 是一种可用作偶氮染料组的参考染料。 | |||
T78234 |
Brilliant Yellow
Direct Yellow 4 |
transporter | Metabolism |
Brilliant Yellow (Direct Yellow 4) 是一种具有有效性和选择性的的 VGLUT 抑制剂,是一种染料,可被光降解。 | |||
T14996 |
Congo Red
刚果红,Direct Red 28 |
Others | Others |
Congo Red (Direct Red 28) 是偶氮染料指示剂,在 pH 3.0的环境下呈紫罗兰色,在 pH5.0的环境下呈红色,常用于组织切片中淀粉样蛋白的测定。 | |||
T19066 |
Thioflavine S
硫磺素,Thioflavin S,Direct Yellow 7 |
Others | Others |
Thioflavine S (Direct Yellow 7) 是荧光组织化学标记物,可用于老年斑块致密核心的标记。 | |||
T0313 |
Evans blue
Direct Blue 53,C.I. 23860,伊文思蓝 |
GluR | Neuroscience |
Evans blue (C.I. 23860) 是一种突触泡谷氨酸吸收的有效抑制剂,同时也是一种AMPA/kainate 受体拮抗剂。 | |||
T20032 |
CI Direct Brown 2
Airedale Brown MD,Brown M,NSC 74701,Direct Brown 2,NSC-74701,NSC74701 |
||
CI Direct Brown 2 is a direct dye. It is soluble in water and ionizable to form colored anions. It also can directly dye cellulose fibers or protein fibers. | |||
T31526 |
Direct Green 6
|
||
Direct Green 6 is a green dye. | |||
T20031 |
C.I. Direct Blue 2
NSC 75779,NSC-75779,Pontamine Diazo Black BHSW,Direct Blue 2,CCRIS 6236,NSC75779 |
||
C.I. Direct Blue 2 is an agent of dye. | |||
T15135 |
Direct Black 38
C.I. 30235,Chlorazol Black E |
Others | Others |
Direct Black 38 is an azo dye.It induces unscheduled DNA synthesis in liver and micronucleus in bone marrow of rats in vivo[1]. | |||
T15135L |
Direct Black 38 free acid
NSC8679,Ferristatin II |
Others | Others |
Ferristatin II (Direct Black 38 free acid) is a polysulphonated dye and promotes the degradation of transferrin receptor-1 in vitro and in vivo. | |||
T20037 |
C.I. Direct Black 17
Azine Fast Black D,CERN prima 17,Telon Fast Black PE,Diazol Black SD |
||
C.I. Direct Black 17 is a compound of dye. | |||
T30665 |
C.I. Direct Red 1, disodium salt
Japanol Fast Red 1,COLUMBIA FAST RED F,Chrome Fast Red F,Neonyl Red 2B,Enianil Fast Red F |
||
C.I. Direct Red 1, disodium salt is a dye. | |||
T30652 |
C.I. 24280
NSC 47753,NSC-47753,Direct Blue 22,Chlorazol Blue RW,NS 47753 |
||
C.I. 24280 is a dye. | |||
T11064 |
DMT1 blocker 2
|
Others | Others |
DMT1 blocker 2 是一种二价金属转运蛋白 1 的直接抑制剂(IC50:0.83 μM)。它可以阻断体内肠细胞的铁摄取。 | |||
T23820 |
BRD32048
BRD-32048,BRD 32048 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BRD32048 可以与与 ETV1直接结合,KD 为 17.1 μM。BRD32048调节 ETV1 介导的转录活性和 ETV1 驱动的癌细胞侵袭。 BRD32048可以抑制 ETV1 乙酰化并促进其降解。 | |||
T20034 |
Solaminrot 4B
Direct Red 81,Airedale Red KD,Solar Red B,Pryamoi krasnyi svetoprochnyi 2S,Fastusol Red 4BA-CF,C.I. 28160 |
||
Solaminrot 4B is an agent of dye. | |||
T19862 |
Voxilaprevir
维昔普维,伏西瑞韦 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Voxilaprevir 是丙型肝炎病毒非结构蛋白 3/4A 蛋白酶的抑制剂,具有抗病毒活性。它抑制基因型 1b 和 3a 野生型 NS3 蛋白酶的 Ki 值分别为 0.038 nM 和 0.066 nM。 | |||
T16156 |
MT 63-78
|
Apoptosis; AMPK; mTOR | Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
MT 63-78 是一种有效的直接AMPK 激活剂,EC50为 25 μM。它诱导细胞有丝分裂阻滞和细胞凋亡,通过抑制脂肪生成和mTORC1途径来阻止前列腺癌的生长,具有抗肿瘤作用。 | |||
T25702 |
Levovirin
ICN 17261,L-Ribavirin,ICN-17261,ICN17261 |
||
Levovirin is a monocyclic L-nucleosides with type 1 cytokine-inducing activity. Levovirin is the L-enantiomer of Ribavirin. Levovirin has similar immunomodulatory activity but does not have direct antiviral activity or hemolytic anemia. | |||
T2453 |
BAM7
|
BCL | Apoptosis |
BAM7 是一种促凋亡 Bax 的直接和特异性激活剂,IC50为 3.3 μM。 | |||
T6775 |
BAY 41-2272
|
Guanylate cyclase | GPCR/G Protein |
BAY 41-2272 是一种直接且不依赖一氧化氮的可溶性鸟苷酸环化酶刺激剂。 | |||
T0504 |
Cyclandelate
安脉生,BS 572,环扁桃酯,3,5,5-Trimethylcyclohexyl mandelate |
Acyltransferase | Metabolism |
Cyclandelate (BS 572) 是直接作用的平滑肌松弛剂,用于扩张血管。 | |||
T31806 |
Flovagatran
TGN 255 |
Thrombin | Proteases/Proteasome |
Flovagatran (TGN 255) 是一种具有口服活性和有效性的凝血酶和肠外直接因子 II 抑制剂。Flovagatran 可用于研究静脉血栓栓塞。 | |||
T7298 |
FT011
|
Others | Others |
FT011 是抗纤维化剂,能够抑制胶原蛋白 I 和 III 的 mRNA 表达,减少胶原蛋白合成。 | |||
TD0069 |
5-ROX, SE
5-羧基-X-罗丹明 SE |
Others | Others |
5-ROX, SE ([5-Carboxy-X-rhodamine, succinimidyl ester] *Single isomer*) 是一种标记试剂,用于制备电荷修饰的染料标记的双脱氧核苷酸三磷酸 (ddNTP) 以“直接加载”DNA 测序。 | |||
T0324 |
Isoxsuprine hydrochloride
Duvadilan,Isolait,盐酸异克舒令,盐酸苯氧丙酚胺 |
Adrenergic Receptor; iGluR | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Isoxsuprine hydrochloride (Isolait) 是 β 肾上腺素受体激动剂和NMDA 受体拮抗剂,对子宫肌层和胎盘的 β 肾上腺素受体的Ki 值分别为 13.65 和 3.48 μM。 | |||
T14017 |
2-NBDG
2-(N-7-硝基-2,1,3-苯并恶二唑-4-氨基)-2-脱氧-D-葡萄糖 |
Others | Others |
2-NBDG 是一种荧光指示剂 (λex=467 nm,λem=542 nm),是一种荧光 D-葡萄糖类似物,可用于监测活细胞中的葡萄糖吸收。 | |||
T67778 |
dCeMM1
|
Molecular Glues | PROTAC |
dCeMM1 是 RBM39 分子胶降解剂,可以降低 WT KBM7 细胞中 RBM39 水平的表达。dCeMM1 活性发挥通过重定向 CRL4DCAF15 连接酶进行。 | |||
T41302 |
Itaconate-alkyne
ITalk |
Others | Others |
Itaconate-alkyne (ITalk) 是一种生物正交探针,用于对炎症性巨噬细胞中的衣康酸进行定量和位点特异性化学蛋白质组学分析,并能够对其直接靶标进行生化评估和蛋白质组学分析。 | |||
T28972 |
Tiaramide hydrochloride
FK-1160,NTA-194,FK 1160,FK1160,tiaramide |
Others | Others |
Tiaramide hydrochloride (FK-1160) 是一种抗炎药,可抑制肥大细胞释放的介质的作用,并具有直接的平滑肌松弛特性。 | |||
T9208 |
1,3,6,8-Tetrahydroxynaphthalene
T4HN,1,3,6,8-THN,naphthalene-1,3,6,8-tetrol |
Others | Others |
1,3,6,8-Tetrahydroxynaphthalene (T4HN) 是一种独特的对称聚酮起源化合物,是 DHN 黑色素不可缺少的前体。 | |||
T10174 |
5-R-Rivaroxaban
|
Factor Xa | Metabolism |
5-R-Rivaroxaban 是一种 Rivaroxaban 的 R 型对映体。其中 Rivaroxaban 是选择性的Factor Xa(FXa) 抑制剂。 | |||
T15639 |
K-756
|
PARP; Wnt/beta-catenin | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Stem Cells |
K-756 是一种直接的 tankyrase(TNKS) 选择性抑制剂,对 TNKS1和 TNKS2的 ADP-核糖基化活性有抑制作用,IC50分别为 31 和 36 nM。 | |||
T1299 |
3-Pyridinemethanol
烟醇,Nicotinyl alcohol,Roniacol |
Others | Others |
3-Pyridinemethanol (Roniacol) 是一种具有降胆固醇作用的吡啶衍生物。 | |||
T14932 |
Ceruletide
Cerulein,Caerulein,雨蛙素,FI-6934 |
cholecystokinin | GPCR/G Protein |
Ceruletide (Caerulein) 是一种十肽,是一种安全有效的胆囊收缩剂,是一种胆囊收缩素受体激动剂,对胆囊肌肉和胆管有直接的痉挛性作用。 | |||
TP1724L |
PUMA BH3 acetate
PUMA BH3 acetate(PUMA BH3 Free base) |
BCL | Apoptosis |
PUMA BH3 acetate (PUMA BH3 Free base) 是一种 p53 凋亡阳性调节因子 (PUMA) BH3 结构域多肽,可作为 Bak 的直接激活剂,Kd 为 26 nM。 | |||
T14034 |
3CAI
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
3CAI 是特异性的AKT1和AKT2抑制剂。 | |||
T5133 |
Dabigatran Etexilate Mesylate
甲磺酸达比加群酯,BIBR 1048MS,Dabigatran etexilate methanesulfonate |
Thrombin | Proteases/Proteasome |
Dabigatran Etexilate Mesylate (BIBR 1048MS) 是一种口服具有活性的 Dabigatran 前药,具有抗凝作用,能够预防心房颤动引起的静脉血栓栓塞和中风。 | |||
T8404 |
Kasugamycin hydrochloride hydrate
Ksg (hydrochloride hydrate),春雷霉素盐酸盐一水合物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Kasugamycin hydrochloride hydrate (Ksg (hydrochloride hydrate)) 是一种能结合 30s 和 70s 核糖体,但不能结合 50s 亚基的抗生素。它模拟 mRNA 核苷酸破坏 tRNA 结合并抑制典型翻译起始。 | |||
T5383 |
D3-βArr
NCGC00379308 |
TSH Receptor | GPCR/G Protein |
D3-βArr (NCGC00379308) 是一种促甲状腺激素受体正变构调节剂,通过直接激活促甲状腺激素受体启动 β-Arr 1 的易位,EC50为 11.6 μM。它还可增强促甲状腺激素介导的体外成骨细胞分化。 | |||
T8408 |
GKT136901
AK120765 |
NADPH-oxidase; NADPH | Immunology/Inflammation; Metabolism |
GKT136901 (AK120765) 是选择性的和具有口服活性的 NADPH 氧化酶 NOX-1/4抑制剂,Ki 分别为 160 和 165 nM。它具有抗炎症活性。它也是一种选择性和直接的过氧亚硝酸清除剂。它可用于糖尿病肾病,中风和神经退行性疾病的研究。 | |||
T14577 |
Biotin-DADOO
EZ-Link Amine-PEO2-Biotin,Biotinyl-3,6-dioxaoctanediamine |
Others | Others |
Biotin-DADOO (Biotinyl-3,6-dioxaoctanediamine) 是生物素酰化试剂,能够与雌二醇结合,形成生物素-雌二醇共轭化合物,进而利用酶免疫测定法测定血浆雌二醇的浓度。 | |||
T3570 |
SU4312
SU 4312,NSC 86429 |
VEGFR; PDGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
NSC-86429 是一种 (Z)-SU4312 (SU 4312) 和 (E)-SU4312 的外消旋体。其中(Z)-SU4312 能够抑制 PDGFR 和 FLK-1。(E)-SU4312 能够抑制 PDGFR, FLK-1, EGFR, HER-2, 和 IGF-1R。 | |||
T2186 |
Tris(2,2,2-trifluoroethyl) borate
SL 75212,硼酸三酯(2,2,2-三氟乙基) |
Others | Others |
Tris(2,2,2-trifluoroethyl) borate (SL 75212) 主要用于缩合反应。它已被证明可以促进羧酸和胺直接形成酰胺,以及胺或酰胺与羰基化合物形成亚胺。 | |||
T17265 |
Ximelagatran
EXANTA,H 376-95,H37695,希美加群,H 376/95,H-37695,H 37695 |
Thrombin | Proteases/Proteasome |
Ximelagatran (H 376-95) 是一种口服活性凝血酶抑制剂,可选择性的、竞争性的抑制游离和凝块结合的凝血酶。它是一种抗凝药物,具有快速起效的抗凝作用,可预测的,剂量依赖性的药代动力学和药效学。 | |||
T5122 |
Alofanib
RPT835 |
Apoptosis; FGFR | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Alofanib (RPT835) 是一种高效和选择性的成纤维细胞生长因子受体2的变构抑制剂,具有抗癌和抗血管生成活性。 | |||
T11994 |
Melagatran
|
Thrombin | Proteases/Proteasome |
Melagatran 是一种直接作用且可口服的凝血酶抑制剂。Melagatran 专一性抑制凝血酶,但不影响凝血级联中的其他酶或纤溶酶。Melagatran不依赖内源性辅因子发挥其抗凝血酶效果,可缓解内毒素血症的有害影响。因此,Melagatran作为预防动脉闭塞的策略显示出前景。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1064 |
Norepinephrine bitartrate monohydrate
酒石酸去甲肾上腺素,Levophed,Noradrenaline bitartrate monohydrate,降肾上腺素 |
Endogenous Metabolite; Adrenergic Receptor; Autophagy | Autophagy; GPCR/G Protein; Metabolism; Neuroscience |
Norepinephrine bitartrate monohydrate (Levophed) 是一种β1-选择性的肾上腺素能受体激动剂,EC50为 5.37 μM。 | |||
T9155 |
Fumagillol
|
Others; Antibacterial | Microbiology/Virology; Others |
Fumagillol 是有效的血管生成抑制剂 TNP-470 和 fumagillin 的直接前体。Fumagillin 作为一种抗菌药物,是选择性有效血管生成抑制剂。 | |||
T4S1983 |
Periplogenin
5-beta-Hydroxydigitoxigenin,Desoxostrophanthidin,杠柳苷元 |
Others | Others |
Periplogenin (Desoxostrophanthidin) 是一种天然呋喃香豆素,存在于白芷根中,可以诱导脂肪细胞分化,具有高抗银屑病作用。 | |||
THS1455 |
DihydroarteMisinic acid
双氢青蒿酸,Dihydro-Artmisinic Acid,二氢青蒿酸 |
Ferroptosis; Parasite | Apoptosis; Microbiology/Virology |
DihydroarteMisinic acid (Dihydro-Artmisinic Acid) 是青蒿的天然产物,是青蒿素的主要直接前体,青蒿素是一种广泛用于治疗疟疾的药草。 | |||
T2A2497 |
L-Glutamic acid
谷氨酸,(S)-Glutamic acid,glutamic acid,(+)-L-Glutamic acid,Aciglut,L-谷氨酸,glutacid,Glutaminol |
Apoptosis; Ferroptosis; Endogenous Metabolite; iGluR | Apoptosis; Membrane transporter/Ion channel; Metabolism; Neuroscience |
L-Glutamic acid (Glutaminol) 作为一种兴奋性氨基酸神经递质,为谷氨酸盐受体所有亚型的激动剂,对多巴胺从神经末梢释放的过程有激动作用。 | |||
T5714 |
5-O-Demethylnobiletin
5-DEMETHYLNOBILETIN,去甲基川陈皮素 |
Leukotriene Receptor; Lipoxygenase | GPCR/G Protein; Metabolism |
5-O-Demethylnobiletin (5-DEMETHYLNOBILETIN) 是从黄芪中分离出的多甲氧基黄酮,具有抗炎活性,可通过直接抑制 5-LOX 发挥作用,IC50为 0.1 μM。 | |||
TN2031 |
γ-Terpinene
Moslene,p-Mentha-1,4-diene,Crithmene |
Antioxidant | oxidation-reduction |
γ-Terpinene (p-Mentha-1,4-diene) 是一种单萜化合物,具有高抗氧化属性,适合口服。它展示了直接的自由基清除能力,并且已知是一种有效的抗痛剂。 | |||
TN1733 |
Hesperetin 7-O-glucoside
|
Anti-infection; Antibacterial; HMG-CoA Reductase | Metabolism; Microbiology/Virology |
Hesperetin 7-O-glucoside 是通过 Hesperidin 的酶促转化产生的一种人 HMG-CoA 还原酶抑制剂,具有降压作用,可抑制幽门螺杆菌的生长。 | |||
T4S1616 |
Sanggenon D
桑根酮D,Sanggenone D |
NOS; COX; GABA Receptor | Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Sanggenone D represents a new scaffold of positive GABAA receptor modulators, it also inhibits COX-2 activity (IC 50 = 73-100 μM). Sanggenone D has anti-inflammatory activity, it can inhibit NO production from lipopolysaccharide (LPS)-induced RAW 264.7 ce | |||
TWS1977 |
Kamebakaurin
尾叶香茶菜丙素,Kamebakaurine |
NF-κB | NF-κB |
Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物,是一种NF-κB 的抑制剂,能够抑制 p50 的 DNA 结合活性。 | |||
T5074 |
Cholesteryl palmitate
|
Others; Endogenous Metabolite | Metabolism; Others |
Cholesteryl palmitate 是一种慢性间质性肺炎的有用预后生物标志物。 | |||
T4716 |
Pyrrole-2-carboxylic acid
吡咯-2-羧酸,2-Pyrrolecarboxylic acid,Minaline |
Endogenous Metabolite | Metabolism |
Pyrrole-2-carboxylic acid (Minaline) 是一种天然生物碱类,从海洋细菌Pelomonas puraquaesp. Nov 中分离得到。 | |||
T3S0013 |
Ethyl trans-caffeate
咖啡酸乙酯,Ethyl caffeate,Caffeic Acid Ethyl Ester |
Others | Others |
Ethyl trans-caffeate (Caffeic Acid Ethyl Ester) 具有抗炎作用。 它是一种有前途的天然化合物,未来在慢性肝病中的应用。它是一种有效的化学预防化合物,可防止因太阳紫外线照射引起的皮肤癌变。它是与人胰腺α-淀粉酶复合的代表性抑制剂的高分辨率结构。 它强烈抑制 JB6 Cl41细胞的肿瘤转化,无毒性。 PI3K、ERK1/2 和 p38 激酶活性在体外通过与 HOEC 直接结合而受到抑制。 | |||
TN3872 |
Diosbulbin D
山药 |
ROS | Immunology/Inflammation |
Diosbulbin D shows direct toxic effect on hepatocytes, the mechanism could be associated with oxidative stress. | |||
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. | |||
TMA0291 | Dehydroglyasperin D | GSK-3; p38 MAPK; ROS; Akt; COX; PI3K; DNA/RNA Synthesis; Prostaglandin Receptor; JNK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells |
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet o... | |||
T15255 |
Etilevodopa
Levodopa ethyl ester,L-DOPA ethyl ester |
Others | Others |
Etilevodopa is an ethyl-ester prodrug of Levodopa which is used for the treatment of Parkinson's disease (PD). It is rapidly hydrolyzed to Levodopa and ethanol by nonspecific esterases in the gastrointestinal tract. Levodopa is the direct precursor of dop | |||
TN5235 |
Vinorine
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Others | Others |
Vinorine is a direct biosynthetic precursor along the complex pathway to the monoterpenoid indole alkaloid ajmaline, an antiarrhythmic drug from the Indian medicinal plant Rauvolfia serpentina. | |||
T83426 |
1-Oxomicrostegiol
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1-Oxomicrostegiol,一种二萜类化合物,源自Salvia viridis L. cvar根部,为viroxocin的直接前体。 | |||
T15467 |
Helenalin
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Others | Others |
Helenalin is a selective inhibitor of transcription factor NF-κB by direct targeting of p65. It is an anti-inflammatory sesquiterpene lactone compound with alkylating activity. Through its ability to target the cysteine sulfhydryl groups in the p65 subunit of NF-κB, helenalin effectively inhibits its DNA binding. | |||
TN4654 | Niazirin | Others | Others |
The Moringa oleifera extract(including niaziridin and Niazirin) can successfully attenuate the development of pulmonary hypertension via direct vasodilatation and a potential increase in antioxidant activity. | |||
TMA0627 | Taxiresinol | TNF | Apoptosis |
Taxiresinol shows anticancer, antinociceptive, and antiallergic activities, it shows inhibitory activity on induced histamine release from the human basophilic cell line, KU812. Taxiresinol can protect the hepatocytes from apoptosis via an inhibition of TNF- alpha production by activated macrophages and a direct inhibition of apoptosis induced by TNF- alpha in D-GalN/LPS-treated mice. | |||
TMA1130 |
2,4-Dihydroxyphenylacetic acid
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Others | Others |
2,4-Dihydroxyphenylacetic acid is a functional moiety in the toxin molecule and the biological action of spider toxin is explained by direct interaction with an Fe-S center which is known to play an important role for the glutamate binding. | |||
TN4308 |
Isolupalbigenin
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Antifection | Microbiology/Virology |
Isolupalbigenin shows promising cytotoxic effects toward HL-60 cells (IC50 4.3 ± 0.7 to 18.0 ± 1.7 uM), it also shows in vitro inhibitory activity toward human glyoxalase I. Isolupalbigenin shows two different antibacterial activities against MRSA: direct growth inhibition and intensification of methicillin sensitivity, it could lead to the development of compounds for new approaches against MRSA infection. | |||
TN4334 | Isotaxiresinol | TNF | Apoptosis |
Isotaxiresinol prevents d-GalN/LPS-induced hepatic injury by inhibiting hepatocyte apoptosis through the blocking of TNF-alpha and IFN-gamma production by activated macrophages and direct inhibition of the apoptosis induced by TNF-alpha. Isotaxiresinol ma | |||
TN2169 |
Saikogenin D
柴胡皂甙元 D,皂苷元 D |
IL Receptor; Calcium Channel; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Saikogenin D possesses a dual effect: an inhibition of A23187-induced PGE2 production without a direct inhibition of cyclooxygenase activity; and an elevation of [Ca2+]i that is attributed to Ca2+ release from intracellular stores. Saikogenin D has immuno | |||
T73856 |
Anagyrine hydrochloride
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Anagyrine ((-)-Anagyrine) hydrochloride 是一种存在于Lupinus albus 中的喹啉类生物碱。Anagyrine hydrochloride 可与毒蕈碱和烟碱乙酰胆碱受体 (AChR) 结合,IC50值分别为 132 和 2096 µM。Anagyrine hydrochloride 是一种有效的nAChR 脱敏剂,Anagyrine hydrochloride 可以直接脱敏nAChR,不需要代谢。 | |||
T78467 |
trans-10-Heptadecenoic acid
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trans-10-Heptadecenoic acid 是一种能在特定酶作用下参与生物合成与代谢过程的反式脂肪酸。在 2,4-二烯酰基-CoA 还原酶与 Delta3,Delta2-烯酰基-CoA 异构酶催化下,trans-10-Heptadecenoic acid 可合成聚羟基链烷酸酯。当缺乏 2,4-二烯酰基-CoA 还原酶时,该化合物则经由多功能酶 (MFE) 中的烯酰辅酶 A 水合酶 II 进行降解。此外,trans-10-Heptadecenoic acid 能通过还原酶依赖性与直接 MFE 依赖性途径引起细胞内的碳外流。 |