243
34
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T36832 |
PDE4B-IN-2
A 33 |
PDE | Metabolism |
PDE4B-IN-2 (A 33) 是一种具有口服活性,选择性 PDE4B 抑制剂,IC50 为 15 nM。PDE4B-IN-2 抑制 PDE4D (IC50=1.7 µM)。PDE4B-IN-2 表现出有效的抗炎作用。 | |||
T38404 |
MJ33 lithium salt
|
||
MJ33 is a specific, reversible inhibitor of phospholipase A2 (PLA2) that acts on the active site. It competes with other substrates and hinders the calcium-independent activity of phospholipase A2 (iPLA2) in Prdx6. | |||
T6970 |
RK33
RK-33,RK 33 |
COX | Immunology/Inflammation; Neuroscience |
RK33 (RK 33) 是 DDX3(一种 RNA 解旋酶)的一流小分子抑制剂,可导致 G1 细胞周期停滞,诱导细胞凋亡,并促进 DDX3 过表达细胞的辐射增敏。 | |||
T62929 |
RLX-33
|
ERK; RXFP receptor | GPCR/G Protein; MAPK |
RLX-33 是一种有效的、选择性的、能够透过血脑屏障的松弛素家族肽 3 (RXFP3) 拮抗剂,也能够阻断松弛素 3 (relaxin 3) 诱导的 ERK1/2 磷酸化。RLX-33 作用于 RXFP3、ERK1 和 ERK2 磷酸化的 IC50 分别为 2.36 μM、7.82 μM 和 13.86 μM。RLX-33 可以阻断 RXFP3 选择性激动剂 R3/I5 诱导的大鼠食物摄取增加。RLX-33 能够用于研究代谢综合征。 | |||
T3175 |
LDHA-IN-4
AZ 33,AZ-33,LDHA Inhibitor,AZ33 |
Dehydrogenase | Metabolism |
LDHA-IN-4 (AZ33) 是乳酸脱氢酶 A 选择性抑制剂,IC50=0.5 μM,Kd=0.093 μM。 | |||
T12928 |
SK33
|
Androgen Receptor | Endocrinology/Hormones |
SK33 是一种有效的组织选择性抗雄激素药物,是一种肌醇类似物,能够降低雄激素受体 (AR) 的转录活性。 | |||
T28352 |
PDE9-IN-(S)-C33
(S)-C33 |
PDE | Metabolism |
PDE9-IN-(S)-C33 ((S)-C33) 是一种有效的选择性 PDE9 抑制剂 (IC50 = 11 nM)。 PDE9-IN-(S)-C33 可用于中枢神经系统疾病和糖尿病的相关研究。 | |||
TP1973L |
OXA (17-33) acetate
|
OX Receptor | GPCR/G Protein; Neuroscience |
OXA (17-33) acetate 是一种比 OX2 (EC50 = 187 nM) 更有效的 orexin-1 受体 (OX1, EC50 = 8.29 nM)) 激动剂。 | |||
TP2047L |
CRF (6-33) acetate(120066-38-8 free base)
|
CRFR | GPCR/G Protein |
CRF (6-33) acetate(120066-38-8 free base) 是促肾上腺皮质激素释放因子结合蛋白 (CRFBP) 抑制肽;从 CRFBP 中替换 CRF。在体内抑制肥胖大鼠的体重增加并增加运动活动。 | |||
TP2500 |
Cholecystokinin (26-33) free acid
CCK (26-33) free acid |
cholecystokinin | GPCR/G Protein |
Cholecystokinin (26-33) free acid 是胆囊收缩素 (CCK) 的一部分, 是脊椎动物中枢神经系统中存在的 CCKB 型受体的高选择性配体,可诱导大鼠轻度味觉厌恶条件反射。 | |||
TP1758L |
LCMV gp33-41 acetate
LCMV gp33-41 acetate(151705-84-9 Free base) |
Others | Others |
LCMV gp33-41 acetate 是淋巴细胞性脉络丛脑膜炎病毒的序列,受主要组织相容性复合体 I 类 H-2Db 限制,呈递给细胞毒性 T 淋巴细胞。 | |||
TP1199L |
Urotensin I acetate (83930-33-0 Free base)
|
CRFR | GPCR/G Protein |
Urotensin I acetate 是一种 CRF 样神经肽,可作为 CRF 受体激动剂,对 CHO 细胞中的人 CRF1、人 CRF2 和大鼠 CRF2α 受体的 pEC50 分别为 11.46、9.36 和 9.85,对 CHO 细胞的 Kis 分别为 0.4、1.8 和 5.7 nM hCRF1、rCRF2α 和 mCRF2β 受体分别为。 | |||
T39975 |
MS33
MS33 |
||
MS33 is a highly effective degrader of the WDR5 protein, exhibiting Kd values of 870 nM and 120 nM for VCB and WDR5, respectively. It induces degradation of WDR5 through an E3 ligase VHL-mediated and proteasome-dependent mechanism. MS33 holds promise for furthering research in the field of acute myeloid leukemia. | |||
T38876 | Antibacterial agent 33 | ||
Antibacterial Agent 33, a potent antibacterial compound, effectively decreases the minimum inhibitory concentration (MIC) of Ceftazidime, another antibacterial agent. | |||
T38978 | CYH33 | ||
CYH33 is an orally active, highly selective PI3Kα inhibitor with IC 50 s of 5.9 nM/598 nM/78.7 nM/225 nM against α/β/δ/γ isoform, respectively. CYH33 inhibits phosphorylation of Akt, ERK and induces significant G1 phase arrest in breast cancer cells and non-small cell lung cancer (NSCLC) cells. CYH33 has potent activity against solid tumors. | |||
T38835 |
STK33-IN-1
STK33-IN-1 |
||
STK33-IN-1 (compound 1) is a STK33 inhibitor, with an IC 50 of 7 nM. | |||
T38979 |
CYH33 methanesulfonate
CYH33 methanesulfonate |
||
CYH33 methanesulfonate is a highly selective and orally active inhibitor of PI3Kα, with IC50 values of 5.9 nM, 598 nM, 78.7 nM, and 225 nM against the α, β, δ, and γ isoforms, respectively. This compound effectively inhibits the phosphorylation of Akt and ERK, leading to a significant G1 phase arrest in breast cancer cells and non-small cell lung cancer (NSCLC) cells. Additionally, CYH33 methanesulfonate demonstrates potent activity against solid tumors. | |||
T39677 |
MY33-3
MY33-3 |
||
MY33-3 is a powerful and specific inhibitor of receptor protein tyrosine phosphatase (RPTP)β/ζ, demonstrating an IC50 value of approximately 0.1 μM. Moreover, MY33-3 exhibits inhibitory activity against PTP-1B with an IC50 value of about 0.7 μM. Additionally, MY33-3 has been shown to effectively decrease ethanol consumption and alleviate neuroinflammation and cognitive dysfunction induced by Sevoflurane. | |||
T69377 |
BoNT-IN-33
|
||
BoNT-IN-33 is a potent inhibitor of Botulinum neurotoxin/A light chain (BoNT/A LC). | |||
T82018 | JAK-IN-33 | JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
JAK-IN-33(化合物3(R))为一种JAK抑制剂。 | |||
T78864 |
α-Glucosidase-IN-33
|
Glucosidase | Metabolism |
α-Glucosidase-IN-33 (compound 7c) 是一种有效的α-葡萄糖苷酶抑制剂,IC50值为2.39 μM,主要用于2型糖尿病及高血糖研究。 | |||
T81307 |
RE-33
|
||
RE-33是一种具有穿透血脑屏障能力的镇痛化合物。 | |||
T82204 |
Hexapeptide-33
|
||
Hexapeptide-33为一生物活性肽,报道显示其作为化妆品成分之用。 | |||
T62211 | Antifungal agent 33 | ||
Antifungal agent 33 (compound 4e) 是一种有效的抗真菌剂。Antifungal agent 33 对白念珠菌具有明显的抗真菌作用 (MIC: 16 μg/ml)。Antifungal agent 33 能够较强的抑制羊毛甾醇 14α-去甲基化酶 (CYP51) (IC50: 0.19 μg/ml)。 | |||
T63264 |
EGFR-IN-33
|
||
EGFR-IN-33 是一种丙烯酰胺衍生物,是低毒副作用的抗肿瘤药物,是 EGFR 的有效抑制剂。其中表皮生长因子受体 (EGFR) 的过度表达和突变已被证实会导致细胞无节制的生长,并与大多数癌症疾病,尤其是 NSCLC 的进展有关。EGFR-IN-33 表现出 EGFR 突变相关疾病的研究潜力。 | |||
T78917 | Tubulin inhibitor 33 | ||
Tubulin inhibitor 33为一种抗微管蛋白聚合化合物,其抑制作用表现为剂量依赖性,具有9.05 μM的IC50。该化合物不仅具备抗肿瘤活性,还能诱导细胞凋亡(apoptosis),在抗肿瘤研究领域有应用潜力。 | |||
T83044 | Antimalarial agent 33 | Parasite | Microbiology/Virology |
Antimalarial agent 33 (compound 5g) 显示针对红细胞期和肝期疟原虫的抗活性,特别是对 K1 恶性疟原虫株,其EC50为1.1 μM。Antimalarial agent 33 还展示出提升的微粒体稳定性(T1/2=29分钟),并且对原代肝细胞未表现出明显的细胞毒效应。 | |||
T82110 |
ICMT-IN-33
|
||
"ICMT-IN-33 (化合物73)为一种有效ICMT抑制剂,具有0.46 μM的半抑制浓度(IC50)。" | |||
T78754 |
COX-2-IN-33
|
COX | Immunology/Inflammation; Neuroscience |
COX-2-IN-33(化合物5f)作为一种COX-2抑制剂(IC50=45.5 nM),同样具备潜在抗炎作用。该化合物能抑制促炎细胞因子的生成,同时确保胃部安全。 | |||
T81286 |
RG33 Peptide
|
||
"RG33 Peptide 是抗 2 型糖尿病 (T2D) 的化合物,它显著增强了胰岛素抵抗小鼠的葡萄糖清除效率。此外,该肽还能高效溶解脂质囊泡,并在培养的巨噬细胞中促进胆固醇排泄。RG33 Peptide 主要用于 2 型糖尿病的研究领域。" | |||
T83022 |
Antiproliferative agent-33
|
||
Antiproliferative agent-33 (Compound 2g) 为抗增殖、抗真菌及抗菌化合物,可抑制MDA-MB-231细胞增殖(IC50为16.38 μM),并对革兰氏阴性菌具有生长抑制作用,S. faecalis的MIC值达到8 μg/mL。 | |||
T61429 | HDAC-IN-33 | ||
HDAC-IN-33 is a highly potent HDAC inhibitor, effectively inhibiting HDAC1, HDAC2, and HDAC6 with IC50 values of 24, 46, and 47 nM, respectively. This compound demonstrates significant antiproliferation activity against tumor cells and exhibits remarkable in vivo antitumor efficacy. Additionally, HDAC-IN-33 initiates the activation of antitumor immunity [1]. | |||
T82995 | Antiviral agent 33 | ||
Antiviralagent 33(化合物 1c)作为一种抗双链 DNA (dsDNA) 病毒的抑制剂,针对 VACV 和 AdV5 表现出的IC50值分别是 0.0790 µM 和 0.1572 µM,同时展现了潜在的口服给药能力。 | |||
T83078 | Anticancer agent 33 | ||
Anticanceragent 33 (compound 3) 为Squamocin与Bullatacin衍生物,展现出有效的抗癌特性。本化合物对4T1乳腺癌细胞系(包括A549、HeLa、HepG2和MCF-7细胞)的生长抑制作用显著,其IC50范围为1.9-5.4 µM。 | |||
T63566 |
HCV-IN-33
|
||
HCV-IN-33 (Compound (S)-3i) 是 HCV 进入抑制剂。 | |||
T83892 |
33-BCRP Inhibitor
33-Breast Cancer Resistance Protein Inhibitor |
||
33-BCRP抑制剂是一种乳腺癌耐药蛋白(BCRP)的抑制剂。它使得对米托蒽醌耐药的H460/MX20肺癌细胞对米托蒽醌诱导的细胞死亡更加敏感,无论是单独使用还是与UV辐射联合使用。33-BCRP抑制剂还能够增强表达P-糖蛋白(P-gp,亦称为多药耐药蛋白MDR)的KB-C2表皮癌细胞对秋水仙碱诱导的细胞死亡的敏感性。当使用5 µM浓度时,它能增加米托蒽醌在H460/MX20细胞中的细胞内积累。 | |||
T73149 | HPK1-IN-33 | ||
HPK1-IN-33(化合物21)是造血祖细胞激酶1(HPK1)的高效抑制剂,其Ki值为1.7 µM。此化合物在Jurkat WT细胞中抑制IL-2产生的EC50为286 nM,而在Jurkat HPK1 KO细胞中的EC50则大于10000 nM。 | |||
T83757 |
RG33 TFA
|
||
RG33是一种33个氨基酸的合成肽,与apolipoprotein A1 (ApoA1)的C-末端域中两个Y类螺旋的209-219和220-241氨基酸相对应。它能溶解含有1,2-dimyristoyl-sn-glycero-3-PC (DMPC)的多层囊泡(MLVs),形成重组HDL。与脂质结合的RG33在J774巨噬细胞中诱导胆固醇外流。RG33 (12 mg/kg)可降低胰岛素抵抗性小鼠的血糖水平。 | |||
T62116 |
ALK5-IN-33
|
||
ALK5-IN-33 (Compound EX-10) 是一种口服具有活性的、选择性的 ALK-5 抑制剂 (IC50≤10 nM)。 | |||
T81555 |
Pancreastatin (33-49), porcine
|
||
Pancreastatin (33-49), porcine,一种来自猪胰腺的肽片段,体外显示出抑制胰岛素的活性,并增强葡萄糖启动作用。 | |||
T37206 |
CCK (27-33) (non-sulfated)
|
||
CCK (27-33) is a C-terminal fragment of CCK , a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. Non-sulfated CCK (27-33) inhibits binding of [3H]naloxone in rat cerebellum membranes (IC50 = 4 uM) and inhibits electrically-stimulated contraction of isolated guinea pig ileum (IC50 = 17 uM), an effect that can be reversed by naloxone. Unlike sulfated CCK (27-33), the non-sulfated form does not reduce exploratory behavior in m... | |||
T80203 |
Diaminopropionoyl tripeptide-33
|
Tyrosinase | Proteases/Proteasome |
Diaminopropionoyl tripeptide-33为生物活性肽,能保护皮肤细胞不受UVA引发的DNA损伤,已报道在化妆品成分中应用。 | |||
T63111 | Tubulin polymerization-IN-33 | ||
Tubulin polymerization-IN-33 是一种 [1,2] 恶唑洛异吲哚微管蛋白聚合的抑制剂,能够较好的抗 NCI 系列癌细胞的增殖。 | |||
T78819 |
VEGFR-2-IN-33
|
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
VEGFR-2-IN-33(Compound 4d)为一种有效的VEGFR抑制剂,其IC50值为61.04 nM。该化合物在抑制HepG2细胞增殖方面表现出更高的效力,IC50仅为4.31 nM,因此常用于肝细胞癌(HCC)研究领域。 | |||
T39569 |
Gp100 (25-33), mouse
Mgp100 (25-33),Gp100 (25-33), mouse |
||
Gp100 (25-33) corresponds to residues 25 to 33 of the mouse self/tumor antigen glycoprotein (mgp100), which is an enzyme responsible for pigment synthesis. This epitope fragment is found in both normal melanocytes and melanoma cells. | |||
T63323 |
PI3K-IN-33
|
||
PI3K-IN-33 是高度选择性的 PI3K 抑制剂,能够作用于 PI3K-α (IC50: 11.73 μM),PI3K-β (IC50: 6.09 μM) 和 PI3K-δ (IC50: 11.18 μM)。PI3K-IN-33 能够将细胞周期阻滞在 G2/M 期,并可以诱导细胞凋亡,能够用于研究白血病。 | |||
T72202 |
Anti-inflammatory agent 33
|
||
Anti-inflammatory agent 33,一种有效的p38α抑制剂,抑制NO产生,并抑制LPS诱导的iNOS、COX-2、p-p38α、p-MK2蛋白表达,具有抗炎活性。 | |||
T75766 |
GP(33-41) TFA
|
||
GP(33-41) TFA 是一种由 9 个氨基酸残基组成的多肽,它是淋巴细胞性脉络丛脑膜炎病毒 GP1 抗原决定基中的序列。GP(33-41) TFA 能够上调 RMA-S (Db Kb) 细胞表面 H-2Db 分子,SC50值为 344 nM。 | |||
T75922 |
OXA(17-33) TFA
|
||
OXA(17-33) TFA,一种高效且选择性的orexin-1 receptor (OX1)激动剂,其对OX1 (EC50=8.29 nM) 的选择性是对OX2 (187 nM) 的23倍。 | |||
T63694 |
SARS-CoV-2-IN-33
|
||
SARS-CoV-2-IN-33 是 COVID-19 抑制剂。ARS-CoV-2-IN-3 对 COVID-19 主要蛋白酶 (Mpro) (PDB ID:6LU7) 表现出较好的结合亲和力 (-8.0 Kcal/mole)。SARS-CoV-2-IN-33 对癌细胞表现出较好的抗增殖效果。SSARS-CoV-2-IN-33 能够用于研究癌症和 COVID-19。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19124 |
3-Oxocholic acid
3-Ketocholic acid |
Endogenous Metabolite | Metabolism |
3-Oxocholic acid(3-Ketocholic acid) 是胆汁酸的代谢产物,也是产气荚膜梭菌在肠道中由胆汁降解的主要产物。33-Oxocholic acid 是一种主要存在于哺乳动物的胆汁中类固醇酸。 | |||
T1626 |
Prostaglandin E1
前列地尔,PGE1,列腺素E1,Alprostadil |
Endogenous Metabolite; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism |
Prostaglandin E1 (Alprostadil) 是一种前列腺素受体配体,对小鼠 EP1、EP2、EP3、EP4和 IP 的 Ki 值分别为 36、10、1.1、2.1 和 33 nM。它诱导血管舒张并抑制血小板聚集,可作为血管扩张剂用于外周血管疾病的研究。 | |||
TN6076 |
Delbonine
14-O-Acetyldeltatsine,14-O-乙酰基德尔塔生 |
||
Delbonine 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 TN6076,CAS号为 95066-33-4。 | |||
TMS1460 |
Qingyangshengenin A
|
Others | Others |
Qingyangshengenin A 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 TMS1460,CAS号为 106644-33-1。 | |||
TN6022 | Stephavanine | ||
Stephavanine 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 TN6022,CAS号为 33116-33-5。 | |||
TN6781 |
SarMentine
|
||
SarMentine 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 TN6781,CAS号为 78910-33-5。 | |||
T75570 | Justicidin C | ||
Justicidin C 是一种抗病毒木脂素,对水泡性口炎病毒展现了较强的抗病毒活性,同时在兔肺细胞(RL-33)中显示较低的细胞毒性。 | |||
TN6189 | Koenigine | ||
Koenigine 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 TN6189,CAS号为 28513-33-9。 | |||
TN6643 | Bruceantinol B | ||
Bruceantinol B 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 TN6643,CAS号为 1822332-33-1。 | |||
TN4095 |
gamma-Diasarone
|
Others | Others |
gamma-Diasarone 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 TN4095,CAS号为 80434-33-9。 | |||
TN6354 |
Trigochinin C
|
||
Trigochinin 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 TN6354,CAS号为 1210299-33-4。 | |||
TMA0343 |
Mellein
|
Others | Others |
Mellein是一种天然产物,属于番荔枝科哥纳香属,其产品编号为 TMA0343,CAS号为 480-33-1。Mellein可用作对照参考。 | |||
TN5868 |
8-Hydroxythymol
p-Cymene-3,8-diol,8-羟基百里香酚 |
||
8-Hydroxythymol 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 TN5868,CAS号为 4478-33-5。 | |||
TN6236 | Taraxinic acid | ||
Taraxinic acid 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 TN6236,CAS号为 75911-33-0。 | |||
TN3640 | Chlorantholide A | Others | Others |
Chlorantholide A 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 TN3640,CAS号为 1372558-33-2。 | |||
TN3398 | Alstolenine | Others | Others |
Alstolenine是一种天然产物,属于夹竹桃科鸡骨常山属,其产品编号为 TN3398,CAS号为 85769-33-1。Alstolenine可用作对照参考。 | |||
TN4378 | Kanshone H | Others | Others |
Kanshone H 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 TN4378,CAS号为 1445952-33-9。 | |||
TN2782 |
2''-O-Acetylsprengerinin C
|
Others | Others |
2''-O-Acetylsprengerinin 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 TN2782,CAS号为 1220707-33-4。 | |||
TN4553 |
Methyl pseudolarate A
|
Others | Others |
Methyl pseudolarate A是一种天然产物,属于松科金钱松属,其产品编号为 TN4553,CAS号为 82508-33-6。Methyl pseudolarate A可用作对照参考。 | |||
TN5689 |
2-(2,4-Dihydroxybenzoyl)benzoic acid
Monosodium salt form |
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2-(2,4-Dihydroxybenzoyl)benzoic acid 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 TN5689,CAS号为 2513-33-9。 | |||
TN1306 | 6-Feruloylcatalpol | Others | Others |
6-Feruloylcatalpol是一种天然产物,属于车前科胡黄连属,其产品编号为 TN1306,CAS号为 770721-33-0。6-Feruloylcatalpol可用作对照参考。 | |||
T31135 |
Cycloechinulin
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Cycloechinulin is a diketopiperazine fungal metabolite originally isolated from A. ochraceus. It reduces weight gain of corn earworms by 33% compared to controls when used at a dose of 100 ppm in the diet. | |||
TN2981 | 3-Phenyl-1,2-dihydroacenaphthylene-1,2-diol | Others | Others |
3-Phenyl-1,2-dihydroacenaphthylene-1,2-diol 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 TN2981,CAS号为 193892-33-0。 | |||
TN6610 |
Cyanidin-3-O-sambubioside-5-O-glucoside chloride
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Cyanidin-3-O-sambubioside-5-O-glucoside chloride 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 TN6610,CAS号为 53925-33-0。 | |||
TN4688 | O-Methylpallidine | Others | Others |
O-Methylpallidine是一种天然产物,属于番荔枝科索木属,其产品编号为 TN4688,CAS号为 27510-33-4。O-Methylpallidine可用作对照参考。 | |||
TN5586 | 14-Deoxy-12-hydroxyandrographolide | ||
14-Deoxy-12-hydroxyandrographolide是一种天然产物,属于爵床科穿心莲属,其产品编号为 TN5586,CAS号为 219721-33-2。14-Deoxy-12-hydroxyandrographolide可用作对照参考。 | |||
T35910 |
Petromurin C
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Petromurin C is a bis-indolyl benzenoid fungal metabolite originally isolated from the ascostromata of P. muricatus. It is cytotoxic to NS-1 mouse myeloma cells (IC50 = 33 μg/ml) and has activity against T. foetus in vitro (IC50 = 100 μg/ml). | |||
TN5399 | 4α,8β-Dihydroxy-3α-(2-hydroxy-3-acetoxy-2-methylbutyryloxy)eudesm-7(11)-en-12,8α-olide | ||
4α,8β-Dihydroxy-3α-(2-hydroxy-3-acetoxy-2-methylbutyryloxy)eudesm-7(11)-en-12,8α-olide 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 TN5399,CAS号为 1442989-33-4。 | |||
TN2874 | 3,4-Dihydro-2,2-dimethyl-2H-naphtho[1,2-b]pyran | Others | Others |
3,4-Dihydro-2,2-dimethyl-2H-naphtho_1,2-b_pyran是一种天然产物,属于茜草科拉拉藤属,其产品编号为 TN2874,CAS号为 16274-33-2。3,4-Dihydro-2,2-dimethyl-2H-naphtho_1,2-b_pyran可用作对照参考。 | |||
TN2479 | 1,2,3,10-Tetramethoxy-9-(2-hydroxy-4,5-dimethoxybenzyloxy)oxoaporphine | Others | Others |
1,2,3,10-Tetramethoxy-9-(2-hydroxy-4,5-dimethoxybenzyloxy)oxoaporphine是一种天然产物,属于莲叶桐科莲叶桐属,其产品编号为 TN2479,CAS号为 872729-33-4。1,2,3,10-Tetramethoxy-9-(2-hydroxy-4,5-dimethoxybenzyloxy)oxoaporphine可用作对照参考。 | |||
T36992 |
Monocerin
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Monocerin is a fungal metabolite that has been found inF. larvarumand has diverse biological activities.1,2,3It is active against the bacteriaE. coliandB. megaterium, the phytopathogenic fungusM. violaceum, and the algaC. fuscain an agar diffusion assay when used at a concentration of 50 μg/disc.1Monocerin (17.5 μg/ml) induces mortality in adultC. erythrocephala.2It reduces root elongation in pre-germinatedS. halepenseseeds when used at a concentration of 33 ppm.3 1.Zhang, W., Krohn, K., Draeger... | |||
T38243 | Hygrolidin | ||
Hygrolidin is a macrocyclic lactone originally isolated from S. hygroscopicus. It inhibits proliferation of a variety of cancer cell lines, including DLD-1 colon cancer, LNCaP prostate cancer, and K562 leukemia cells (IC50s = 2.9, 5.2, and 33 ng/ml, respectively). Hygrolidin induces the expression and levels of p21 in DLD-1 cells, but not WI-38 fibroblasts, and leads to cell accumulation in the G1 and S phases without inducing apoptosis. It has antiparasitic activity against T. cruzi, L. donovan... | |||
T80950 |
Tricetin 7-O-glucoside
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Tricetin 7-O-glucoside (compound 33)为一种黄酮类单-O-糖苷。 | |||
T37451 |
Stachybotrysin B
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Stachybotrysin B is a fungal metabolite originally isolated from S. chartarum and has antiviral and anticancer activities.1,2 It has antiviral activity against HIV in SupT1 cells (IC50 = 19.2 μM).1 Stachybotrysin B is cytotoxic to K562, HeLa, and HL-60 cells (IC50s = 21.72, 39.63, and 18.5 μM, respectively).2 |1. Zhao, J., Feng, J., Tan, Z., et al. Stachybotrysins A-G, phenylspirodrimane derivatives from the fungus Stachybotrys chartarum. J. Nat. Prod. 80(6), 1819-1826 (2017).|2. Ma, X.-h., Zhen... |