212
32
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10380 |
AS19
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
AS19 is a potent, selective 5-HT7 receptor agonist (IC50: 0.83 nM; Ki: 0.6 nM). AS19 is selective for 5-HT7 over 5-HT1A, 5-HT1B, 5-HT1D, and 5-HT5A receptors (Kis: 89.7 nM, 490 nM, 6.6 nM and 98.5 nM, respectively). | |||
T23819 |
Braco-19 trihydrochloride
BRAC-O19,BRACO19 hydrochloride,BRACO19 3HCl,BRACO 19,BRACO19 HCl |
Telomerase | DNA Damage/DNA Repair |
Braco-19 trihydrochloride (BRACO19 3HCl) 是一种端粒酶抑制剂,可阻止端粒酶的加帽和催化作用。 Braco-19 trihydrochloride 抑制 HAdV 病毒复制。 | |||
T15655 |
KFM19
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
KFM19 是一种具有强效性和选择性的腺苷受体 (A1-receptor) 拮抗剂(IC50 : 50 nM),可用于研究神经系统疾病。 | |||
T67950 |
S19-1035
|
NADPH | Metabolism |
S19-1035为AKR1C3(aldehyde ketone reductase 1C3)的高效特异性抑制剂,其IC50值为3.04 nM,主要应用于肿瘤研究。 | |||
T8931L |
ICCB-19 hydrochloride
ICCB-19 HCl(750621-52-4 free base) |
Apoptosis; Others; Autophagy; RIP kinase | Apoptosis; Autophagy; NF-κB; Others |
ICCB-19 hydrochloride (ICCB-19 HCl) 是RIPK1激酶活性的间接抑制剂。它是一种 TRADD 抑制剂,可与 TRADD 的 N 端结构域结合,破坏其与 TRADD-C 和 TRAF2 的结合,诱导自噬和长寿命蛋白质的降解。 | |||
T21083 |
TFIIH Modulator-19
TFIIH Modulator19,TFIIH Modulator 19 |
Others | Others |
TFIIH Modulator-19 诱导毛发硫营养不良组 A 蛋白的二聚化以调节 TFIIH 转录活性。 | |||
T10123 |
VEGFR-2-IN-9
KDR-in-4 |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
VEGFR-2-IN-9 (KDR-in-4) 是一种高效的 KDR/VEGFR2 抑制剂(IC50:7 nM),可用于研究乳腺癌。 | |||
T10341 |
Antitumor agent-19
|
Others | Others |
Antitumor agent-19 是一种肿瘤相关巨噬细胞的调节剂,在 RAW 264.7 细胞和 BMDM 细胞中的 EC50 分别为 17.18 μM 和 18.87 μM。 | |||
TP1563 |
Gap19
|
Gap Junction Protein | Cytoskeletal Signaling |
Gap19 是一种衍生自 Cx43 细胞质环九个氨基酸的肽,是选择性连接蛋白 43 半通道阻滞剂。它可以防止 C 末端与 CL 的分子内相互作用,具有保护心肌作用。 | |||
T9998 |
MIND4-19
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
MIND4-19 是一种具有抗肿瘤活性的 SIRT2 抑制剂。 | |||
T36711 |
FM19G11
FM19G11,HIF-1alpha/2alpha Inhibitor |
HIF | Angiogenesis; Chromatin/Epigenetic |
FM19G11 是一种低氧诱导因子 (HIF) α-亚基抑制剂(在低氧诱导的荧光素酶试验中 IC50 为 80 nM)。 | |||
T29017 |
TrxR1-IN-B19
TrxR1INB19,Go Y015,TrxR1 IN B19,Go-Y015 |
Others | Others |
TrxR1-IN-B19 (TrxR1 IN B19) 是一种 TrxR1 抑制剂,通过靶向 TrxR1 和 ROS 介导的 ER 应激激活,通过小分子选择性杀死胃癌细胞。 | |||
T9936 |
ZX-J-19J
N-(2,3-Diphenyl-6-quinoxalinyl)octanamide |
Others | Others |
ZX-J-19J (N-(2,3-Diphenyl-6-quinoxalinyl)octanamide) 是 Cyclophilin J 的抑制剂,对肿瘤细胞生长有显着的抑制作用,与环孢素 A 相当,但比 5-氟尿嘧啶强得多。 | |||
TP2110L |
TAT-Gap19 acetate
|
Gap Junction Protein | Cytoskeletal Signaling |
TAT-Gap19 acetate 是 connexin43 hemichannel (Cx43 HC) 的特异性抑制剂。 它穿过血脑屏障并减轻小鼠的肝纤维化。它不抑制相应的 Cx43 GJC。 | |||
T40286 |
KRAS G12C inhibitor 19
|
Ras | GPCR/G Protein; MAPK |
KRAS G12C inhibitor 19 是一种有效的 KRAS G12C 抑制剂,在细胞实验中显示出抗肿瘤活性,科抑制肿瘤生长。 | |||
T72022 |
11β-HSD1 inibitor 19
|
||
11β-HSD1 inibitor 19 对 hHSD1 和 mHSD1 显示抑制活性,IC50 为 16 nM 和 10 nM。 | |||
TP1863L |
Glucagon (19-29), human acetate
|
Glucagon Receptor | GPCR/G Protein |
Glucagon (19-29), human acetate 是一种从胰高血糖素加工而来的 COOH 末端片段,是一种有效的胰岛素分泌抑制剂。 | |||
TP1053L |
Protein Kinase C 19-31 acetate
Protein Kinase C 19-31 acetate(121545-65-1 free base),PKC (19-31) acetate |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Protein Kinase C 19-31 acetate(121545-65-1 free base) 是一种蛋白激酶 C (PKC) 的肽抑制剂,源自 PKCa 的假底物调节结构域(残基 19-31),在 25 位用丝氨酸取代野生型丙氨酸作为蛋白激酶 C 底物肽,用于测试蛋白激酶 C 活性。 | |||
T38360 |
NBC 19
|
||
Potent NLRP3 inflammasome inhibitor (IC50 = 60-80 nM). Inhibits nigericin- and ATP-induced IL-1β release. Baldwin et al (2017) Boron-Based Inhibitors of the NLRP3 Inflammasome. Cell Chem.Biol. 24 1321 PMID:28943355 |Redondo-Castro et al (2018) Development of a characterised tool kit for the interrogation of NLRP3 inflammasome-dependent responses. Sci.Rep. 8 5667 PMID:29618797 | |||
T37237 |
(±)19(20)-DiHDTE
|
||
(±)19(20)-DiHDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid . It is formed via cytochrome P450 (CYP) metabolism of DPA via a (±)19(20)-EpDTE intermediate. | |||
T40185 | BTK inhibitor 19 | ||
BTK inhibitor 19 is a highly selective, covalent BTK inhibitor ( IC 50 = 2.7 nM). | |||
T41183 |
Helianorphin-19
|
||
Helianorphin-19 is a high affinity, potent and selective κ-opioid receptor (KOR) agonist (Ki = 25 nM; EC50= 45 nM). Helianorphin-19 exhibits approximately 200-fold selectivity for KOR over μ and δ-opioid receptors.In vivoHelianorphin-19 shows potent peripheral analgesic efficacy in a mouse model of visceral pain without affecting motor coordination/sedation. | |||
T37239 |
(±)19(20)-EpDTE
|
||
(±)19(20)-EpDTE is an oxylipin and an oxidative metabolite of docosapentaenoic acid . It is formed via cytochrome P450 (CYP) metabolism of DPA and can be further metabolized to (±)19(20)-DiHDTE by epoxide hydrolase. | |||
T40991 |
19-Heptatriacontanol
19-Heptatriacontanol,19-Hydroxyheptatriacontane |
||
19-Heptatriacontanol is used to combine macromolecules and small molecules. | |||
T36216 |
19(R)-HETE
|
||
19-HETE is one of the major cytochrome P450 (CYP450) metabolites of arachidonic acid that is released from the kidney in response to angiotensin II. When formed by the CYP2E1 isoform, 19-HETE is composed of 70% and 30% of the (S) and (R) stereoisomers, respectively. Both 19(S)- and 19(R)-HETE are potent vasodilators of renal preglomerular vessels. However, 19(R)-HETE at 1 μM completely blocks 20-HETE-induced vasoconstriction of renal arterioles, whereas 19(S)-HETE remains inactive. | |||
T35850 |
19(S)-HETE
|
||
19-HETE is one of the major cytochrome P450 (CYP450) metabolites of arachidonic acid that is released from the kidney in response to angiotensin II. When formed by the CYP2E1 isoform, 19-HETE is composed of 70% and 30% of the (S) and (R) stereoisomers, respectively. Both 19(S)- and 19(R)-HETE are potent vasodilators of renal preglomerular vessels. 19(S)-HETE stimulates both renal sodium-potassium ATPase and volume absorption in the rabbit proximal straight tubule. | |||
T37238 |
(±)19(20)-EpDPA
|
||
EDHF (endothelium-derived hyperpolarizing factor) is an unidentified mediator released from vascular endothelial cells in response to acetylcholine and bradykinin which is distinct from the NOS- (nitric oxide) and COX-derived (prostacyclin) vasodilators. Cytochrome P450 (CYP450) metabolism of polyunsaturated fatty acids produces epoxides such as (±)14(15)-EpETrE which are prime candidates for the actual active mediator. However, the CYP450 metabolites of eicosapentaenoic acid and docosahexaenoic... | |||
T36217 |
19-hydroxy Cholesterol
|
||
19-hydroxy Cholesterol is formed during metabolic oxidation of cholesterol. It has been used as an internal standard for the quantitative determination of sterols by mass spectroscopic analysis.[1] | |||
T35873 |
C19 Ceramide (d18:1/19:0)
C19 Ceramide (d18:1/19:0) |
||
C19 Ceramide is a naturally occurring ceramide that has been found in J. juncea extracts as well as rat brain and mouse heart.[1],[2],[3] It is elevated in adult and decreased in juvenile whole rat brain extracts by 114 and 37%, respectively, following chronic ethanol exposure.[2] C19 Ceramide is also increased in mouse hearts following administration of angiotensin II.[3] | |||
T35468 |
(±)19(20)-EDP Ethanolamide
|
||
(±)19(20)-EDP ethanolamide is an ω-3 endocannabinoid epoxide and cannabinoid (CB) receptor agonist (EC50s = 108 and 280 nM for CB1 and CB2, respectively). It is produced through direct epoxygenation of docosahexaenoyl ethanolamide by cytochrome P450 (CYP) epoxygenases. (±)19(20)-EDP ethanolamide (25 μM) reduces the viability of 143B metastatic osteosarcoma cells. It decreases the production of IL-6 and increases the production of IL-10 when used at concentrations ranging from 2.5 to 10 μM in BV-... | |||
T39709 |
HPK1-IN-19
HPK1-IN-19 |
||
HPK1-IN-19 is an inhibitor of hematopoietic progenitor kinase 1 (HPK1). | |||
T63125 | Antiviral agent 19 | ||
Antiviral agent 19 (Compound 3) 是一种 Zika 病毒的选择性抑制剂 (EC50: 1.3 μM),具有低细胞毒性。 | |||
T63652 | DHODH-IN-19 | ||
DHODH-IN-19 是 DHODH 的有效抑制剂。其中 DHODH 是一种含铁的黄素依赖性酶,存在于人类线粒体的内膜中,对肿瘤生长具有抑制作用。DHODH-IN-19 对癌症和炎症疾病表现出研究潜力。 | |||
T63837 |
RET-IN-19
|
||
RET-IN-19 是 RET 的有效抑制剂,能够作用于 RET-wt (IC50: 6.8 nM) 和 RET V804M (IC50: 13.51 nM),表现出抗癌效果。RET-IN-19 能够用于研究非小细胞肺癌 (NSCLC)。 | |||
T82126 |
ICMT-IN-19
|
||
ICMT-IN-19 (compound 53)为一种高效ICMT抑制剂,其半抑制浓度(IC50)为0.026 μM。 | |||
T63628 | AChE-IN-19 | ||
AChE-IN-19 是 AChE 的高效抑制剂 (IC50: 0.56 μM),对 Aβ 聚集也表现出抑制作用。AChE-IN-19 表现出神经保护作用,对 SH-SY5Y 细胞几乎没有毒性。AChE-IN-19 能够用于研究阿尔兹海默症。 | |||
T62891 | α-Glucosidase-IN-19 | ||
α-Glucosidase-IN-19 (Compound 6B) 是一种口服具有活力的 α-glucosidase 抑制剂 (IC50: 3.63 μM),具有抗糖尿病作用。 | |||
T80721 | Zndm19 | ||
Zndm19为New Delhi Metallo-β-lactamase-1 (NDM-1)的抑制剂,适用于抗药性细菌感染研究。 | |||
T75067 | Antimalarial agent 19 | Parasite | Microbiology/Virology |
Antimalarial agent 19(compound 6e)是一种活性抗疟疾化合物,对K1型恶性疟原虫和伯氏疟原虫展现出较强的抑制效果,其EC50值分别为0.3 µM和15.3 µM。相较于γ-肝硫平,该化合物具有更好的水溶性、肠道渗透性以及微粒体稳定性。 | |||
T73319 |
BTK-IN-19
|
||
BTK-IN-19 是一种可逆的BTK 抑制剂,IC50<0.001 μM。 | |||
T72330 |
Antibacterial agent 19
|
||
Antibacterial agent 19 是一种有效的抗菌剂。Antibacterial agent 19 对K. pneumoniae,(M-R)S. aureus 和 (M-R,V-R)S. aureus 具有抗菌活性, 其 MIC 值为 0.022, 0.022 和 0.045 mg/mL。 | |||
T125260 |
19-Hydroxypseudovincadifformine
|
||
19-Hydroxypseudovincadifformine 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 T125260。 | |||
T62579 |
HBV-IN-19
|
||
HBV-IN19 对乙型肝炎病毒 (HBV) 感染具有抑制作用。HBV-IN19 能够抑制 HBsAg 分泌和/或产生,可以用于 HBV 感染的研究 (如:慢性 HBV 感染)。 | |||
T62095 | TRK-IN-19 | ||
TRK-IN-19 (Compound I-10 ) 是一种 TRK 的有效抑制剂,对 TRKA、TRKAG595R 的 IC50 值分别为 1.1 nM、5.3 nM。TRK-IN-19 对癌症疾病表现出潜在的研究价值。 | |||
T61257 | Antifungal agent 19 | ||
Antifungal agent 19 显示出强大的抗真菌活性(EC50= 0.72 μM)。 | |||
T80909 | Tyrosinase-IN-19 | Tyrosinase | Proteases/Proteasome |
Tyrosinase-IN-19 是竞争性酪氨酸酶抑制剂,对ROS、ABTS+ 及DPPH 自由基展现显著的抗氧化活性。该化合物通过剂量依赖性方式有效抑制酪氨酸酶表达。 | |||
T80295 |
GLR-19
|
HSV | Microbiology/Virology |
GLR-19 为一种具有抗HIV功能的肽类化合物,亦展现出对HSV-2的抗病毒活性。 | |||
T79692 |
BChE-IN-19
|
||
BChE-IN-19 (Compound 7b) 是一种具有对 BChE 抑制活性(IC50=0.04 μM)的茚酮对位取代衍生物,可改善神经系统胆碱能调控,适用于抗阿尔茨海默病研究。 | |||
T61636 |
ATR-IN-19
|
||
ATR-IN-19 (Compound 15 R-configure) 是一种ATR 抑制剂。 | |||
T63904 |
ATX inhibitor 19
|
||
ATX inhibitor 19 是 ATX 的有效抑制剂 (IC50: 156 nM)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1118 |
Tormentic acid
2Α,19Α-二羟基熊果酸,委陵菜酸 |
Immunology/Inflammation related | Immunology/Inflammation |
Tormentic acid 是一种分离自 Rosa rugosa 中的三萜,具有抗炎、降血脂和抗动脉粥样硬化活性。 | |||
TN1198 |
19-Hydroxybufalin
|
Others | Others |
19-Hydroxybufalin 是蟾二烯羟酸内酯,能够阻碍上皮间质转化,抑制 PC3 细胞的迁移和侵袭。 | |||
TN2237 |
Steviol-19-O-glucoside
Steviol-19-O-Glucoside,甜菊醇-19-葡萄糖苷 |
Others | Others |
Steviol-19-O-glucoside 是甜叶菊 Stevia rebuadiana 中甜菊糖苷生物合成途径的天然产物。 | |||
T35609 |
19-O-Acetylchaetoglobosin A
|
||
19-O-Acetylchaetoglobosin A is a fungal metabolite originally isolated fromC. globosumthat has actin polymerization inhibitory and cytotoxic activities.1,2It inhibits actin polymerization in a cell-free assay when used at a concentration of 2 μM.219-O-Acetylchaetoglobosin A (3.2, 10, and 32 μg/ml) is cytotoxic to HeLa cervical cancer cells.1 1.Umeda, M., Ohtsubo, K., Saito, M., et al.Cytotoxicity of new cytochalasans from Chaetomium globosumExperientia31(4)435-438(1975) 2.Sekita, S., Yoshihira, ... | |||
T35483 |
19,20-Epoxycytochalasin D
|
||
19,20-Epoxycytochalasin D is a fungal metabolite that has been found in the endophytic fungus Nemania sp. UM10M. It is active against the chloroquine-sensitive and -resistant strains of P. falciparum (MIC = 0.4 ng/ml for both) without inducing cytotoxicity in Vero cells. It is cytotoxic to BT-549, LLC-PK11, and P388 cells (IC50s = 7.84, 8.4, and 0.16 µM, respectively) but not SK-MEL, KB, or SKOV3 cells up to a concentration of 10 µM. | |||
T83578 |
(19R,23E)-5b,19-Epoxy19-ethoxycucurbita-6,23-diene-3b,25-diol
|
||
(19R,23E)-5b,19-Epoxy19-ethoxycucurbita-6,23-diene-3b,25-diol 是一种葫芦烷型三萜。该化合物在 MTT 法检测中对癌细胞系 MCF-7、HepG2、Du145、Colon205 以及 HL-60 均未表现出抑制效果。 | |||
TN1199 |
19-Oxocinobufagin
|
Others | Others |
19-Oxocinobufagin is a natural product from Bufo bufo gargarizans Cantor. | |||
T83435 |
19-Hydroxy-10-deacetylbaccatin III
|
||
19-Hydroxy-10-deacetylbaccatin III (compound 13) 是紫杉烷类化合物,显示出潜在的抗肿瘤作用。在 A498 和 NCI-H226 细胞系中,此化合物表现出轻微的细胞毒性效应。研究指出,当浓度为 30 μg/mL 时,19-Hydroxy-10-deacetylbaccatin III 对 A498 细胞和 NCI-H226 细胞的抑制率为 16.6% 和 32%。 | |||
TN1200 |
19-Oxocinobufotalin
|
Others | Others |
19-Oxocinobufotalin 3-adipoylarginine ester shows significant inhibition effect against human hepatocellular carcinoma cell line SMMC-7721 in vitro. | |||
T83458 | 12E,14-Trien-19-oic acid | ||
12E,14-Trien-19-oic acid 为一类二萜,源自不丹药用植物 shug chher。该化合物在血小板聚集研究中有应用。 | |||
TN3941 | ent-17-Hydroxykaur-15-en-19-oic acid | Others | Others |
ent-17-Hydroxykaur-15-en-19-oic acid 是从香树叶中发现的天然化合物,对人前列腺细胞的IC50为17.63microg/mL。 | |||
TN1178 |
11,15-Dihydroxy-16-kauren-19-oic acid
|
Others | Others |
11,15-Dihydroxy-16-kauren-19-oic acid is a natural product | |||
T83570 |
(23E)-5b,19-epoxycucurbita-6,23,25(26)-triene-3b-ol
|
||
(23E)-5b,19-epoxycucurbita-6,23,25(26)-triene-3b-ol,一种葫芦烷三萜,可从苦瓜籽中提取。 | |||
TN1401 |
Arjunetin
|
Others | Others |
Arjunetin, an insect feeding-deterrent and growth inhibitor, shows antioxidant and anti-inflammatory activities. | |||
TN3651 |
Cichoriin
|
Others | Others |
Cichoriin 对SARS-CoV-2有明显活性,是治疗重症COVID-19的潜在候选物质。 | |||
T8070 |
Nonadecanoic acid
|
Others | Others |
Nonadecanoic acid 是19 C 长的饱和脂肪酸,是白蚁防御时分泌的主要物质。 | |||
T0194 |
Chloroquine phosphate
Chloroquine diphosphate,Aralen phosphate,磷酸氯喹,Chingamin phosphate |
SARS-CoV; TLR; HIV Protease; Antibiotic; Parasite; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Chloroquine phosphate (Aralen phosphate) 是广泛用于疟疾和类风湿性关节炎的抗疟疾和抗炎剂。它是autophagy 和toll-like receptors 抑制剂,有效抑制SARS-CoV-2(COVID-19) 感染 (EC50=1.13 μM)。 | |||
T3921 |
Punicalagin
安石榴甙,安石榴苷 |
SARS-CoV; HBV | Microbiology/Virology |
Punicalagin 是一种在石榴中发现的主要鞣花单宁,是可逆且非竞争性的3CLpro 抑制剂,有抗氧化、抗炎和抗癌作用。它有潜力研究 COVID-19 。 | |||
TN3948 |
ent-3Beta-Angeloyloxykaur-16-en-19-oic acid
|
Others | Others |
ent-3Beta-Angeloyloxykaur-16-en-19-oic acid是一种天然产物,属于菊科蟛蜞菊属,其产品编号为 TN3948,CAS号为 74635-61-3。ent-3Beta-Angeloyloxykaur-16-en-19-oic acid可用作对照参考。 | |||
TN3939 |
ent-16beta,17-dihydroxy-9(11)-kauren-19-oic acid
|
Others | Others |
ent-16beta,17-dihydroxy-9(11)-kauren-19-oic acid是一种天然产物,属于菊科苍耳属,其产品编号为 TN3939,CAS号为 55483-24-4。ent-16beta,17-dihydroxy-9(11)-kauren-19-oic acid可用作对照参考。 | |||
TN6493 | 19-O-beta-D-carboxyglucopyranosyl-12-O-beta-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene | ||
19-O-beta-D-carboxyglucopyranosyl-12-O-beta-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene是一种天然产物,属于松科松属,其产品编号为 TN6493,CAS号为 1011714-20-7。19-O-beta-D-carboxyglucopyranosyl-12-O-beta-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene可用作对照参考。 | |||
TN2757 |
2-Epitormentic acid
|
Others | Others |
2-Epitormentic acid是一种天然产物,属于蔷薇科委陵菜属,其产品编号为 TN2757,CAS号为 119725-19-8。2-Epitormentic acid可用作对照参考。 | |||
TN2700 | 2,3-dihydrosciadopitysin | Others | Others |
2,3-dihydrosciadopitysin是一种天然产物,属于罗汉松科罗汉松属,其产品编号为 TN2700,CAS号为 34421-19-7。2,3-dihydrosciadopitysin可用作对照参考。 | |||
TN2486 | 1-(3,4-Dimethoxyphenyl)propane-1,2-diol | Others | Others |
β-Aflatrem是一种天然产物,属于金粟兰科金粟兰属,其产品编号为 TN2486,CAS号为 20133-19-1。β-Aflatrem可用作对照参考。 | |||
TN3254 |
7alpha-Hydroxystigmasterol
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Others | Others |
7alpha-Hydroxystigmasterol是一种天然产物,属于菊科苍耳属,其产品编号为 TN3254,CAS号为 64998-19-2。7alpha-Hydroxystigmasterol可用作对照参考。 | |||
T75670 | Lacto-N-fucopentaose II | ||
Lacto-N-fucopentaose II (LNFP II)作为人Lewis血型决定因子的半抗原,其单唾液神经节苷/糖脂以及唾液酰衍生物CA 19-9,都是胆胰恶性肿瘤中的分子肿瘤标记物(TM)。 | |||
TN3269 |
8,9-Didehydro-7-hydroxydolichodial
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Others | Others |
8,9-Didehydro-7-hydroxydolichodial是一种天然产物,属于败酱科败酱属,其产品编号为 TN3269,CAS号为 97856-19-4。8,9-Didehydro-7-hydroxydolichodial可用作对照参考。 | |||
TN1194 | 16beta,17-Dihydroxy-ent-kaurane-19-oic acid | HIV Protease | Microbiology/Virology; Proteases/Proteasome |
16beta,17-Dihydroxy-ent-kaurane-19-oic acid as an anti-HIV principle, it showed significant activity against HIV replication in H9 lymphocyte cells with an EC50 value of 0.8 microgram/mL. It also possesses the activities of decompression and blood viscosi | |||
TN5637 |
5-(Z-Heptadec-8-enyl)resorcinol
5-(8-Heptadecenyl)-1,3-benzenediol |
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5-(Z-Heptadec-8-enyl)resorcinol是一种天然产物,属于紫金牛科紫金牛属,其产品编号为 TN5637,CAS号为 52483-19-9。5-(Z-Heptadec-8-enyl)resorcinol可用作对照参考。 | |||
T38262 |
Sphingosine (d14:1)
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Sphingosine (d14:1) is a bioactive sphingolipid that has been found in B. mori (silkworm), P. clarkii (crayfish), and A. aurita (jellyfish) extracts. It increases the germination rate of N. rileyi, an entomopathogenic fungus, with an EC50 value of 10.2 nM. Sphingosine (d14:1) inhibits protein kinase C (PKC) in vitro (IC50 = 7.3 mol%) as well as superoxide generation induced by phorbol 12-myristate 13-acetate in neutrophils and reduces growth of CHO cells (IC50s = 19 and 8 μM, respectively). | |||
T72581 |
SARS-CoV MPro-IN-2
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SARS-CoVMPro-IN-2 是一种有效的SARS-CoV-2 Mpro 抑制剂,IC50sub>值为 72.07 nM。病毒的主要蛋白酶 Mpro 作为加工病毒多蛋白的主要酶,有助于 SARS-CoV-2 在宿主细胞中的复制和转录,并已被定性为药物发现的有吸引力的靶点。SARS-CoVMPro-IN-2 具有研究 COVID-19 的潜力。 | |||
T38069 |
Aquastatin A
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Aquastatin A is a fungal metabolite originally isolated fromF. aquaeductuumthat has diverse biological activities.1It is active againstS. aureus(MIC = 32 μg/ml) and inhibits enoyl-acyl carrier protein reductase (Fabl; IC50= 3.2 μM) andS. aureusfatty acid synthesis (IC50= 3.5 μM).2Aquastatin A also inhibits the Na+/K+-ATPase and H+/K+-ATPase (IC50s = 7.1 and 6.2 μM, respectively), as well as protein tyrosine phosphatase 1B (PTP1B; IC50= 0.19 μM).1,3 1.Hamano, K., Kinoshita-Okami, M., Minagawa, K.... |