845
148
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10775 |
c-Fms-IN-2
|
c-Fms | Tyrosine Kinase/Adaptors |
c-Fms-IN-2 是一种 c-FMS 激酶抑制剂 (IC50 = 24 nM)。 | |||
TNU0810 |
2′-C-Methyl-6-O-methylinosine
2′-C-Methyl-6-O-methylinosine |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2′-C-Methyl-6-O-methylinosine (2′-C-Methyl-6-O-methylinosine) 是一种次黄嘌呤类似物,具有广泛的实物活性,可用于研究多种肿瘤疾病。 | |||
T7215 |
NM107
NM-107,2'-C-甲基胞嘧啶核苷,2'-C-Methylcytidine |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
NM107 (2'-C-Methylcytidine) 是一种具有广谱抗病毒活性的核糖核苷,是丙型肝炎病毒 NS5B 聚合酶的核苷抑制剂,在野生型复制子细胞中的 EC50 为 1.85 μM。 | |||
T67743 |
4-Pyridinecarboxaldehyde, 2-(2-pyridinyl)hydrazone, [C(E)]-
|
Others | Others |
4-Pyridinecarboxaldehyde, 2-(2-pyridinyl)hydrazone, [C(E)]-是混合配体配位聚合物[Zn4(bdc)4(ppmh)2(H2O)]n 的配体。 | |||
T40005 |
Pomalidomide-C2-COOH
|
Others | Others |
Pomalidomide-C2-COOH 是一种合成的 E3 连接酶配体-接头偶联物,它结合了 PROTAC 技术中使用的基于 Pomalidomide 的 CRBN 配体和接头。 | |||
T40020 |
Pomalidomide-C2-acid
|
Others | Others |
Pomalidomide-C2-acid 是 PROTAC 的组成部分。 | |||
T8912 |
5-ETHYL-4,5,6,7-TETRAHYDRO-THIAZOLO[5,4-C]PYRIDIN-2-YLAMINE
5-乙基-4,5,6,7-四氢-噻唑并[5,4-C]吡啶-2-胺 |
PLK | Cell Cycle/Checkpoint |
5-ETHYL-4,5,6,7-TETRAHYDRO-THIAZOLO[5,4-C]PYRIDIN-2-YLAMINE 靶向 PLK1。 | |||
T7761 |
Pomalidomide-C2-NH2 hydrochloride
|
E3 Ligase Ligand-Linker Conjugate; Ligand for E3 Ligase | PROTAC |
Pomalidomide-C2-NH2 hydrochloride 包含基于 Pomalidomide 的 cereblon 配体和 1 个 linker,是合成的 E3 连接酶配体-linker 偶联物。 | |||
T4253 |
Skp2 Inhibitor C1
SKPin C1 |
Others; E1/E2/E3 Enzyme | Others; Ubiquitination |
Skp2 Inhibitor C1 (SKPin C1)(SKPin C1)是Skp2介导p27降解的特异性抑制剂。 | |||
T20889 |
AalphaC
2-Amino-alpha-carboline,Aalpha C,2-氨基-9H-吡啶[2,3-b]吲哚,Aalpha-C |
Others | Others |
AalphaC (2-Amino-alpha-carboline) 是一种潜在的致癌物质。 | |||
T60531 |
2'-C-Methyladenosine
|
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
2'-C-Methyladenosine 是丙型肝炎病毒(HCV)复制的抑制剂,分离自肾棒状杆菌。2'-C-Methyladenosine 抑制 HCV 复制子和 NS5B 催化的 RNA 合成,IC50值分别为 0.3 μM 和 1.9 μM。2'-C-Methyladenosine 还对Leishmania guyanensis (Lgy)和Leishmania braziliensis中的 LRV1有抑制作用。 | |||
T40518 |
C-Peptide 2, rat
|
||
C-Peptide 2, rat, a 31-amino-acid peptide, serves as a constituent in proinsulin. It possesses the ability to hinder glucose-triggered insulin secretion. | |||
T16325 |
NITD008
7-Deaza-2'-C-acetylene-adenosine |
Others | Others |
NITD008 (7-Deaza-2'-C-acetylene-adenosine) 是一种有效的和选择性的腺苷核苷抑制剂,是一种腺苷核苷类似物,具有广谱的抗病毒活性,抑制登革热病毒、动物杯状病毒和寨卡病毒。 | |||
T35653 |
2’-O,4’-C-Methyleneuridine
|
||
2'-O,4'-C-Methyleneuridine (Compound 15a) is a bicyclic nucleoside. [1]. Sharma VK, et al. Chemoenzymatic convergent synthesis of 2'-O,4'-C-methyleneribonucleosides. J Org Chem. 2014 Jul 3;79(13):6336-41. | |||
T8871 |
C/EBPα inducer 1
4(3H)-Quinazolinone, 6-fluoro-2-[(1E)-2-(5-nitro-2-furanyl)ethenyl]-3-phenyl- |
Others | Others |
C/EBPα inducer 1 (4(3H)-Quinazolinone, 6-fluoro-2-[(1E)-2-(5-nitro-2-furanyl)ethenyl]-3-phenyl-) 是一种C/EBPα和骨髓细胞分化的诱导剂。 | |||
T32826 |
LNA-Adenosine
LNA-A,LNA Adenosine,2'-O,4'-C-Methyleneadenosine |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
LNA-Adenosine (LNA-A) 是一种核苷类似物,可作为作为腺苷A3受体配体。 | |||
T37102 |
2'-O-Me-C(Bz) Phosphoramidite
|
||
2’-O-Me-C(Bz) Phosphoramidite is a modified phosphoramidite monomer, which can be used for the oligonucleotide synthesis. | |||
TNU0442 |
2’-beta-C-Methyl inosine
2'-C-Methylinosine |
Antiviral; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation |
2’-beta-C-Methyl inosine (2'-C-Methylinosine) 是一种 HCV RNA聚合酶抑制剂,具有抗病毒活性,可用用于研究用于治疗丙型肝炎病毒感染。 | |||
T10654 |
c-Met-IN-2
|
c-Met/HGFR | Tyrosine Kinase/Adaptors |
c-Met-IN-2 is a selective and orally available c-Met inhibitor (IC50: 0.6 nM) with antitumor activity. | |||
TP1051L |
Protein Kinase C Peptide Substrate acetate
Protein Kinase C Peptide Substrate acetate(120253-69-2 free base) |
Others | Others |
Protein Kinase C Peptide Substrate acetate(120253-69-2 free base) 以依赖于第二信使和特定衔接蛋白的方式靶向特定细胞间隔物,以响应激活 g 蛋白偶联受体、酪氨酸激酶受体或酪氨酸激酶偶联受体的细胞外信号。 | |||
T2117 |
PSI-6206
2'-deoxy-2'-fluoro-2'-C-methyluridine,RO 2433,GS-331007 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
PSI-6206 (RO 2433) 是 PSI-6130 的脱氨衍生物,PSI-6206 是一种选择性 HCV RNA 聚合酶抑制剂,低效抑制HCV 复制,EC90为 >100 μM。PSI-6130 是一种有效的选择性 HCV NS5B 聚合酶抑制剂。 | |||
T5349 |
SCR-1481B1
麦他替尼胺丁三醇,c-Met inhibitor 2 |
VEGFR; c-Met/HGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SCR-1481B1 (c-Met inhibitor 2) 能够作用于依赖 Met 激活的癌症,对 VEGFR 具有抑制作用。 | |||
T22489 |
2'-MeCCPA
2-Chloro-N-cyclopentyl-2′-C-methyladenosine |
HCV Protease; Adenosine Receptor | GPCR/G Protein; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
2'-MeCCPA 是一种具有有效性和高选择性的 A1 腺苷受体 (A1AR) 激动剂,对 AR 的 K 值为 1.8 nM。2'-MeCCPA 抑制毛喉素刺激的腺苷酸环化酶活性,IC值为13.1 nM。2'-MeCCPA 具有镇痛活性,可用于研究 HCV 。 | |||
T40518L |
C-Peptide 2, rat acetate
C-Peptide 2, rat acetate (41594-08-5 Free base) |
Others | Others |
C-Peptide 2, rat acetate 是一种可抑制葡萄糖诱导的胰岛素分泌胰岛素原组分,由31个氨基酸残基构成的多肽和醋酸盐组成。 | |||
T10650 | c-Kit-IN-2 | c-Kit | Tyrosine Kinase/Adaptors |
c-Kit-IN-2 is a c-KIT inhibitor (IC50: 82 nM), shows superior antiproliferative activities against all the three GIST cell lines, GIST430, GIST882, and GIST48 (GI50s: 1, 3, and 2 nM). | |||
T9028 |
STING-IN-2
C-170 |
STING | Immunology/Inflammation |
STING-IN-2 (C-170) 是一种 STING 共价抑制剂,可抑制小鼠 STING (mmSTING) 和人类 STING (hsSTING),可用于自身炎症性疾病的研究。 | |||
T39503 |
Hepatitis Virus C NS3 Protease Inhibitor 2
|
||
Hepatitis Virus C NS3 Protease Inhibitor 2 is a peptide inhibitor derived from a product that targets the NS3 protease of the hepatitis C virus (HCV). Its inhibitory activity against the NS3 protease is characterized by a Ki value of 41 nM. | |||
T41069 |
CHO-C-PEG2-C-CHO
CHO-C-PEG2-C-CHO |
||
CHO-C-PEG2-C-CHO is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T0614 |
4-Amino-5-Chloro-2-Methoxybenzoic Acid
甲氧氯普胺杂质C,Metoclopramide EP Impurity C |
Others | Others |
4-Amino-5-Chloro-2-Methoxybenzoic Acid (Metoclopramide EP Impurity C) 是一种Metoclopramide 代谢物。 | |||
T8005 |
Cardiogenol C hydrochloride
2-[[2-[(4-甲氧基苯基)氨基]-4-嘧啶基]氨基]乙醇盐酸盐,Cardiogenol C HCl,Cardiogenol C |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
Cardiogenol C hydrochloride (Cardiogenol C) 是一种细胞渗透性嘧啶诱导剂,能够促使 ESCs 分化为心肌细胞。在有限的可塑性范围内,它可以对已经沿袭的祖细胞类型产生心肌生成效应,是一种心肌生成试剂,在动物模型中可以用作细胞移植研究中提高心脏修复的工具。 | |||
T29504 |
A(2)C
A2C,A 2C,A-2C |
||
A(2)C is a biochemical. | |||
T9013 |
Autogramin-2
tert-butyl 2-(4-isopropoxybenzamido)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate |
Autophagy | Autophagy |
Autogramin-2 (tert-butyl 2-(4-isopropoxybenzamido)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate) 有效抑制由饥饿诱导的自噬,IC50为 0.27 μM。它也抑制 Rapamycin,通过抑制 mTORC1 诱导的自噬,IC50为 0.14 μM。 | |||
T13194 |
CSF1R-IN-2
|
c-Fms; c-Met/HGFR; Src | Angiogenesis; Tyrosine Kinase/Adaptors |
CSF1R-IN-2 是一种口服具有活力的、有效的 SRC,MET 和 c-FMS 抑制剂,它们的 IC50 值分别为 0.12 nM,0.14 nM 和 0.76 nM。 | |||
T19784 |
DBT
NSC701994,4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole,NSC 701994,NSC-701994 |
Others | Others |
DBT (NSC-701994) 是一种远红/近红外荧光探针,用于肿瘤相关蛋白的特异性体外和体内成像。 | |||
T33467 |
MOMIPP
|
PI3K | PI3K/Akt/mTOR signaling |
MOMIPP 是一种 PIKfyve 抑制剂,是一种巨胞饮作用的诱导剂,可穿过血脑屏障 (BBB)。 | |||
T38237 |
2′-O-Methylcytidine
|
Nucleoside Antimetabolite/Analog; HCV Protease | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
2'-O-Methylcytidine 是 2'-代核苷,可抑制 HCV 复制。 它在体外抑制 NS5B 催化的 RNA 合成,其抑制方式是与底物核苷三磷酸竞争。 | |||
T21870 |
C-021
4-Quinazolinamine, 2-[1,4'-bipiperidin]-1'-yl-N-cycloheptyl-6,7-dimethoxy- |
CCR | Immunology/Inflammation; Microbiology/Virology |
C 021 dihydrochloride 是一种 CC 趋化因子受体 4 (CCR4) 拮抗剂,抑制人和小鼠的功能趋化性,IC50分别为 140 和 39 nM。C-021 (4-Quinazolinamine, 2-[1,4'-bipiperidin]-1'-yl-N-cycloheptyl-6,7-dimethoxy-) 可有效阻止人 CCL22 衍生的 [35S]GTPγS 与受体结合,IC50为 18 nM。 | |||
T38279 |
C2-8
C2-8 |
||
C2-8 is an inhibitor of polyglutamine (polyQ) aggregation (IC50s = 25 and 0.05 μM for recombinant HDQ51 and in PC12 cells, respectively). It also inhibits polyQ aggregation in organotypic hippocampal slice cultures isolated from R6/2 transgenic mice and reduces neurodegeneration in a dose-dependent manner in a Drosophila model of Huntington's disease. C2-8 (100 and 200 mg/kg) reduces huntingtin aggregate size, reduces neuronal atrophy, and improves motor performance in a rotarod test in the R6/2... | |||
T9939 |
JMJD6 inhibitor WL12
2H-1-Benzopyran-2-one, 3-(3H-imidazo[4,5-c]pyridin-2-yl)-6-methyl-,ZINC6733033 |
Others | Others |
JMJD6 inhibitor WL12 (ZINC6733033) 是一种JMJD6 抑制剂,能够抑制JMJD6依赖的癌细胞增殖,包括宫颈癌细胞和肝癌细胞,为研究JMJD6在癌症发展中的生物学功能提供了一个小分子探针。 | |||
T39392L |
C-Type Natriuretic Peptide (CNP) (1-22), human acetate
C-Type Natriuretic Peptide (CNP) (1-22), human acetate(1966153-17-2 Free base) |
Others | Others |
C-Type Natriuretic Peptide (CNP) (1-22), human acetate 是一种利钠肽受体 B (NPR-B) 的激动剂,一种内皮衍生的松弛剂和生长抑制因子。 C-Type Natriuretic Peptide (CNP) (1-22), human acetate 抑制由组胺和 5-HT 或直接由毛喉素刺激的 cAMP 合成。 | |||
T40224 |
2',3'-cGAMP-C2-PPA
2',3'-cGAMP-C2-PPA |
||
2',3'-cGAMP-C2-PPA (45) is a cyclic di-nucleotide that acts as a STING agonist (US20210015941A1). It is a drug-linker conjugate for antibody-drug conjugates (ADC) used in the targeted treatment of cancer. | |||
T39582 |
2',3'-cGAMP-C2-SH
2',3'-cGAMP-C2-SH |
||
2', 3'-cGAMP-C2-SH is a ADC cytotoxin. | |||
T2242 |
Wnt-C59
4-(2-甲基-4-吡啶基)-N-[4-(3-吡啶基)苯基]苯乙酰胺,C59 |
Wnt/beta-catenin; Porcupine | Cytoskeletal Signaling; Stem Cells |
Wnt-C59 (C59) 是一种高效的、口服具有活力的PORCN 抑制剂(IC50:74 pM)。 | |||
T36671 | C2 Phytoceramide (t18:0/2:0) | ||
C2 Phytoceramide is a bioactive semisynthetic sphingolipid that inhibits formyl peptide-induced oxidant release (IC50 = 0.38 μM) in suspended polymorphonuclear cells. It increases COX-2 protein levels 15-fold through ERK signaling. It induces death of keratinocytes (20% viability) with an ED50 value of 30 μM, the same concentration at which 35% of cells in a TUNEL assay are apoptotic. C2 Phytoceramide also has antiproliferative effects in CHO cells, with greater than 80% cytotoxicity achieved at... | |||
T39597 |
diABZI-C2-NH2
diABZI-C2-NH2 |
||
DiABZI-C2-NH2, a STING agonist with a primary amine functionality, is an active analogue. | |||
T50001 |
Tinoridine
ethyl 2-amino-6-benzyl-4H,5H,6H,7H-thieno[2,3-c]pyridine-3-carboxylate,替诺立定 |
P450 | Metabolism |
Tinoridine 通过抑制环氧合酶-2(COX-2)的产生来发挥作用,具有抗炎、抗过敏和抗凝血等活性。 | |||
T36230 |
C2 Ceramide (d14:1/2:0)
C2 Ceramide (d14:1/2:0) |
||
C2 Ceramide (d14:1/2:0) is a bioactive sphingolipid. Dietary administration of C2 ceramide (d14:1/2:0) (100 μM) induces lipotoxic cardiomyopathy via increasing diastolic and systolic diameter as well as reducing fractional shortening and the number of normal cardiac contractile events in Drosophila. | |||
T40726 |
Azide-C2-Azide
Azide-C2-Azide |
||
Azide-C2-Azide is a cleavable linker vital in ADC synthesis. Azide-C2-Azide joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness. | |||
T38011 |
C2 Adamantanyl Globotriaosylceramide (d18:1/2:0)
|
||
C2 Adamantanyl globotriaosylceramide (AdaGb3) is a bioactive sphingolipid and water-soluble form of globotriaosylceramide that contains an adamantanyl group in place of the fatty acyl chain. It inhibits Vero toxin binding to globotriaosylceramide in an ELISA assay when used at a concentration of 10 μM. AdaGb3 decreases cell surface expression of P-glycoprotein (P-gp) and reduces efflux of rhodamine 123 in MDCK cells. It also increases apical-to-basal transport of vinblastine in human intestinal ... | |||
T37440 |
C2 Adamantanyl Galactosylceramide (d18:1/2:0)
|
||
C2 Adamantanyl Galactosylceramide (d18:1/2:0) (AdaGalCer) is a bioactive sphingolipid. It reduces globotriaosylceramide 3 synthesis from exogenous lactosylceramide in microsomes. AdaGalCer stimulates recombinant glucocerebrosidase activity in a pH-dependent manner. It activates glucocerebrosidase to decrease glucosylceramide accumulation in fibroblasts and lymphoblasts isolated from patients with Gaucher and Fabry disease, respectively. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1661 |
Ganoderic acid C2
灵芝酸 C2 |
Reductase; Histamine Receptor; Immunology/Inflammation related | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Ganoderic acid C2 是分离自灵芝的一种三萜化合物, 具有潜在的抗肿瘤生物活性,以及抗组胺、抗衰老和细胞毒性作用。它对rat lens aldose reductase 具有很高的抑制活性,IC50为 3.8 µM。 | |||
T13851 |
Pseudolaric Acid C2
|
Others | Others |
Pseudolaric Acid C2 是一种从 Pseudolarix kaempferi 二萜酸,是大鼠口服和静脉注射后血浆、尿液、胆汁和粪便中 Pseudolaric acid B 的特异性代谢产物。 | |||
TN2373 |
(E/Z)-Ginkgolic acid C17:2
Ginkgolic Acid C17:2 |
Dehydrogenase | Metabolism |
(E/Z)-Ginkgolic acid C17:2 (Ginkgolic Acid C17:2) 是一种可从银杏中提取的天然产物,可靶向人二氢乳清酸脱氢酶 (DHODH). | |||
T7607 |
PSI-6130
R 1656,2'-去氧-2'-氟-2'-C-甲基胞苷 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
PSI-6130 (R 1656) 是高效选择性 HCV NS5B 聚合酶抑制剂,抑制 HCV 复制,IC50值为 0.6 μM。 | |||
TN2379 |
2-C-Methyl-D-erythritol
|
Others | Others |
2-C-Methyl-D-erythritol is a natural product from the fruit of Carum ajowan | |||
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。 | |||
TN1949 |
Moracin C
桑辛素 C,5-(6-羟基-2-苯并呋喃基)-2-(3-甲基-2-丁烯基)-1,3-苯二醇 |
ROS; NO Synthase | Immunology/Inflammation |
Moracin C 是一种发现于Morus mesozygia、Morus alba var. multicaulis 中的天然化合物,是一种抗炎剂。Moracin C 可抑制细胞中的一氧化氮(NO)释放和LPS 激活的活性氧(ROS)。 | |||
TN7180 |
2-Pyrimidinamine, 4-(5-bromo-1H-indol-3-yl)-
4-(5-溴-1H-吲哚-3-基)嘧啶-2-胺,Meridianin C |
Others | Others |
2-Pyrimidinamine, 4-(5-bromo-1H-indol-3-yl)- (Meridianin C)是一种海洋来源的天然产物,存在于Aplidium meridianum。 | |||
TN6772 |
Malabaricone C
|
Others | Others |
Malabaricone C 是天然的鞘磷脂合成酶抑制剂,对 SMS 1 和 SMS 2 的IC50分别为 3 和 1.5 μM。 | |||
T3671 |
Vitexin-2"-O-rhamnoside
牡荆素鼠李糖苷,牡荆素-2-O-鼠李糖苷,2''-O-Rhamnosylvitexin,Vitexin-2-O-rhaMnoside,Vitexin-2''-O-rhamnoside,Apigenin-8-C-glucoside |
Others | Others |
Vitexin-2"-O-rhamnoside (Apigenin-8-C-glucoside) 是一种黄酮苷类化合物,存在于Cratagus pinnatifidaBge 中,对 H2O2介导的氧化应激损伤具有保护作用,可用于研究心血管系统疾病。 | |||
TN2499 |
2'-O-Methylbroussonin C
1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxy-3-prenylphenyl)propane |
Others | Others |
2'-O-Methylbroussonin 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 TN2499,CAS号为 376362-03-7。 | |||
T22644 |
C2 Ceramide
Ceramide |
Others | Others |
A potent modulator of cell proliferation and differentiation. | |||
T3919 |
Ginsenoside Rb2
Ginsenoside C,人参皂苷 Rb2,人参皂苷Rb2 |
GPR; Others; Influenza Virus; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism; Microbiology/Virology; Others |
Ginsenoside Rb2 (Ginsenoside C) 是人参提取物中的一种主要生物活性成分,具有抗病毒活性,可上调 GPR120 基因表达。 | |||
TN1195 |
17-Hydroxy sprengerinin C
17-羟基麦冬皂苷C |
BCL; Others; Caspase | Apoptosis; Others; Proteases/Proteasome |
17-Hydroxy sprengerinin C 是从黄精的根茎中分离得到的一种糖苷化合物,具有更强的抗癌活性。17-Hydroxy sprengerinin C 降低 Blc-2 和 pro-caspase3 的表达并增加 Bax 的产生。 | |||
TN3301 |
8beta-(2-Hydroxy-2-methyl-3-oxobutyryloxy)glucozaluzanin C
|
Others | Others |
8beta-(2-Hydroxy-2-methyl-3-oxobutyryloxy)glucozaluzanin 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 TN3301,CAS号为 93395-31-4。 | |||
TQ0054 |
Purpureaside C
|
Others | Others |
Purpureaside C 是一种酚类糖苷类,具有显着的促炎、免疫调节和抗菌作用。 | |||
TN2750 |
2-C-Methyl-D-erythrono-1,4-lactone
|
Others | Others |
(-)-2-C-Methyl-D-erythrono-1,4-lactone is inactive alone, but elicits oviposition behavior when mixes with other fractions. | |||
T11848 |
Licorice glycoside C2
甘草苷 C2 |
Others | Others |
Licorice glycoside C2 is a oleanane-type triterpene oligoglycoside isolated from Glycyrrhiza uralensis. | |||
T3810 |
Saikosaponin B2
柴胡皂苷 B2,柴胡皂甙 B2 |
Others; HCV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Saikosaponin B2 是从柴胡根中分离得到的一种活性成分,可抑制 HCV 病毒感染的侵入,有抗癌作用。 | |||
T2873 |
Ginsenoside Rg2
Chikusetsusaponin I,Panaxoside Rg2,人参皂苷Rg2,Prosapogenin C2,(20S)Ginsenoside Rg2,人参皂苷 Rg2 |
Beta Amyloid; GSK-3; NF-κB | Neuroscience; NF-κB; PI3K/Akt/mTOR signaling; Stem Cells |
Ginsenoside Rg2 (Chikusetsusaponin I) 是一种人参的主要活性成分。它能够降低Aβ1-42积聚,抑制脂多糖介导的VCAM-1和ICAM-1表达的增加。 | |||
TN7108 |
Urolithin C
|
Apoptosis; Calcium Channel; Reactive Oxygen Species; IGF-1R; Endogenous Metabolite | Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB; Tyrosine Kinase/Adaptors |
Urolithin C 属于多酚类,是鞣花酸的肠道微生物代谢产物,具有胰岛素分泌的葡萄糖依赖性激活活性。Urolithin C 是 L 型 Ca2+通道开放剂,可增强 Ca2+的流入。它通过线粒体介导的途径诱导细胞凋亡,并刺激活性氧的形成。 | |||
TN6785 |
Dihydrocatalpol
(2S,3R,4S,5S,6R)-2-[[(1aS,1bS,2S,5aR,6S,6aS)-6-hydroxy-1a-(hydroxymethyl)-2,4,5,5a,6,6a-hexahydro-1bH-oxireno[5,6]cyclopenta[1,3-c]pyran-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol |
Others | Others |
Dihydrocatalpol ((2S,3R,4S,5S,6R)-2-[[(1aS,1bS,2S,5aR,6S,6aS)-6-hydroxy-1a-(hydroxymethyl)-2,4,5,5a,6,6a-hexahydro-1bH-oxireno[5,6]cyclopenta[1,3-c]pyran-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol) 是一种从地黄中提取的天然产物。 | |||
TN6837 |
Syringopicroside
2-(4-hydroxyphenyl)ethyl (1S,4aS,7R)-7-methyl-6-oxo-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate |
Others | Others |
Syringopicroside (2-(4-hydroxyphenyl)ethyl (1S,4aS,7R)-7-methyl-6-oxo-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate) 是一种来自 Syringa oblata Lindl (S. oblata) 的具有抗菌活性的天然药物。 | |||
T6S0052 |
Chelerythrine
Toddalin,Broussonpapyrine,白屈菜红碱,Cheleritrine |
Apoptosis; BCL; PKC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling |
Chelerythrine (Broussonpapyrine) 是一种天然生物碱,为有效、选择性的 Ca2+/磷脂依赖性PKC 拮抗剂,IC50值为 0.7 μM。它具有抗肿瘤、抗糖尿病、抗炎的活性。它抑制BclXL-Bak BH3肽结合,IC50为 1.5 μM,并从 BclXL 取代了 Bax。它诱导细胞凋亡和自噬。 | |||
T13108 |
Pamufetinib
H2OL3Q4XRD,4-(2-Fluoro-4-(3-(2-phenylacetyl)thioureido)phenoxy)-7-methoxy-N-methylquinoline-6-carboxamide,TAS-115 |
VEGFR; c-Met/HGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Pamufetinib (TAS-115) 是VEGFR 和c-Met/HGFR 抑制剂,能够抑制 rVEGFR2 (IC50:30 nM)和 rMET (IC50:32 nM)的活性。 | |||
T3419 |
Chelerythrine chloride
白屈菜红碱,盐酸白屈菜红碱 |
Apoptosis; BCL; PKC; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling |
Chelerythrine chloride 是一种可渗透细胞的蛋白激酶 C 抑制剂,对磷酸盐受体具有竞争性,而对 ATP 是非竞争性的。它诱导细胞凋亡和自噬。 | |||
T7792 |
Hispidin
6-[(1E)-2-(3,4-二羟基苯基)乙烯基]-4-羟基-2H-吡喃-2-酮 |
Endogenous Metabolite; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism |
Hispidin 是来自裂蹄木层孔菌的酚类天然产物,是一种 PKC 抑制剂,具有很强的抗氧化、抗癌、抗糖尿病和抗痴呆作用。 | |||
T8301 |
Amaranth
Acid Red 27,酸性红 27 |
Others | Others |
Amaranth (Acid Red 27) 是一种阴离子染料, 可应用到天然和合成纤维、皮革、纸张及苯酚-甲醛树脂。它是一种暗红色至紫色的偶氮染料,可用作食品染料和化妆品。 | |||
T2185 |
L-Ascorbic acid 2-phosphate trisodium
L-抗坏血酸-2-磷酸三钠盐(维生素C),L-Ascorbic acid 2-phosphate trisodium salt,Sodium L-ascorbyl-2-phosphate,Sodium ascorbyl phosphate,2-Phospho-L-ascorbic acid trisodium salt,Sodium ascorbyl monophosphate,L-抗坏血酸-2-磷酸三钠盐 |
Reactive Oxygen Species; c-Met/HGFR; Endogenous Metabolite | Immunology/Inflammation; Metabolism; NF-κB; Tyrosine Kinase/Adaptors |
L-Ascorbic acid 2-phosphate trisodium (Sodium ascorbyl phosphate) 是长效的维生素 C 衍生物,能够刺激胶原蛋白的表达和形成。Sodium L-ascorbyl-2-phosphate 提高成骨细胞分化过程中 hASC 中的碱性磷酸酶活性和 runx2A 的表达,因此,能够促进人脂肪干细胞的成骨分化。 | |||
T6S1529 |
Cynarin
Cyclohexanecarboxylic acid, 1,3-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1R,3R,4S,5R)-,Cynarine,1,5-Dicaffeoylquinic acid,洋蓟素,金银花 |
Antioxidant; Antiviral; Influenza Virus; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction |
Cynarin (1,5-Dicaffeoylquinic acid) 是一种抗窒息剂,具有抗氧化、抗组胺和抗病毒等多种生物活性。 | |||
TN5525 |
Orientin 2''-O-rhamnoside
2''-O-Rhamnosylorientin,Luteolin 8-C-neohesperidoside |
||
Orientin 2''-O-rhamnoside 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 TN5525,CAS号为 81398-30-3。 | |||
TN5698 |
8-Glucosyl-5,7-dihydroxy-2-isopropylchromone
5,7-Dihydroxy-2-isopropylchromone 8-C-glucoside |
||
8-Glucosyl-5,7-dihydroxy-2-isopropylchromone 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 TN5698,CAS号为 188785-44-6。 | |||
T83150 |
Ajugasterone C 2-acetate
|
||
Ajugasterone C 2-acetate,一种可从Cyanotis arachnoidea分离得到的蜕皮类固醇。 | |||
T82799 |
C-2′-Decoumaroylaloeresin G
|
||
C-2′-Decoumaroylaloeresin G (化合物8)为一种色酮糖苷,源自芦荟属植物。 | |||
TN3265 |
Yuehgesin C
8-(3-Ethoxy-2-hydroxy-3-methylbutyl)-7-methoxycoumarin |
Others | Others |
Yuehgesin 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 TN3265,CAS号为 125072-68-6。 | |||
T2764 |
(S)-10-Hydroxycamptothecin
10-羟喜树碱,10-羟基喜树碱,10-Hydroxycamptothecin,10-HCPT |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
(S)-10-Hydroxycamptothecin (10-HCPT) 是一种从喜树中分离的 DNA 拓扑异构酶 I 抑制剂。它显著诱导细胞凋亡,可研究肝癌、胃癌、结肠癌和白血病。 | |||
T5736 |
1,3-Dicaffeoylquinic acid
CYNARIN,1,3-二咖啡酰奎宁酸,Cyclohexanecarboxylic acid, 1,3-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1S,3R,4R,5R)-,1,3-O-Dicaffeoylquinic acid,1,5-Dicaffeoylquinic acid |
Reactive Oxygen Species; Akt; PI3K | Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; NF-κB; PI3K/Akt/mTOR signaling |
1,3-Dicaffeoylquinic acid (CYNARIN) 是一种咖啡酰奎宁酸衍生物,具有抗氧化、自由基清除作用。 | |||
T4069 |
Fatsiaside C
2)-alpha-L-arabinopyranoside'>Oleanolic acid-3-O-beta-D-glucopyranosyl (1->2)-alpha-L-arabinopyranoside |
Others | Others |
Fatsiaside 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 T4069,CAS号为 60213-69-6。 | |||
T81397 |
Procyanidin C2
Procyanidine C2 |
||
Procyanidin C2,源自Fagopyrum dibotrys (D. Don) Hara,为酚苷类化合物。 | |||
T79941 |
Antimycin A2c
|
Apoptosis | Apoptosis |
Anticanceragent 141(compound AE)是一种针对HPV感染宫颈癌具有抑制作用的抗霉素生物碱。该化合物能够抑制宫颈癌HeLa细胞的增殖并导致细胞周期在S期停滞。Anticanceragent 141破坏线粒体功能,诱导caspase依赖性细胞凋亡,并激活ROS介导的泛素依赖性蛋白酶体系统,进而引起E6/E7癌蛋白的降解。 | |||
T2851 |
Daphnetin
7,8-Dihydroxycoumarin,Daphnetol,瑞香素 |
EGFR; PKA; PKC; Parasite; Autophagy | Angiogenesis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Daphnetin (7,8-Dihydroxycoumarin) 是从 Genus Daphne 中分离得到的香豆素衍生物,有抗氧化、抗炎、抗疟疾和解热作用,可用于凝血功能障碍、类风湿性关节炎等疾病的相关研究。 | |||
T7060 |
Amantadine
1-Aminoadamantane,1-金刚烷胺,金刚烷胺,1-Adamantanamine,1-Adamantylamine |
Others | Others |
Amantadine (1-Aminoadamantane) 是抗病毒药物,也是是 NMDA 型谷氨酸受体的弱拮抗剂,能促进高多巴胺的释放,并阻断多巴胺的再摄取。 | |||
T81363 |
Pseudolaric acid C2-O-β-D-glucoside
|
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Pseudolaric acid C2-O-β-D-glucoside, 一种天然产物,来源于Pseudolarix kaempferi,并通过分离提取得到。 | |||
TN1201 |
25(S)-Ruscogenin-1-O-α-L-rhamnopyranosyl (1→2)-β-D-xylopyranoside
25(S)-鲁斯可皂苷元-1-O-Α-L-吡喃鼠李糖基-(1→2)-Β-D-吡喃木糖苷,山麦冬皂苷C,(1beta,3beta,25S)-3-Hydroxyspirost-5-en-1-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-xylopyranoside |
Others | Others |
(1beta,3beta,25S)-3-Hydroxyspirost-5-en-1-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-xylopyranoside is a natural product | |||
TN1321 |
6'-O-Cinnamoyl harpagide
6'-O-Cinnamoylharpagide,(1S,4AS,5R,7S,7AR)-1,4A,5,6,7,7A-六氢-4A,5,7-三羟基-7-甲基环戊二烯并[C]吡喃-1-基 BETA-D-吡喃葡萄糖苷 6-[(2E)-3-苯基-2-丙烯酸酯],6'-O-肉桂酰基哈巴苷,6'-O-肉桂酰哈巴苷 |
Others | Others |
6'-O-Cinnamoylharpagide has anti-inflammatory activity. | |||
TN1488 |
Chrysin 6-C-glucoside 8-C-arabinoside
|
Others | Others |
Chrysin 6-C-glucoside 8-C-arabinoside 是α±-葡萄糖苷酶抑制剂,α±-葡萄糖苷酶抑制剂广泛用于2型糖尿病的治疗。 | |||
TN1487 |
Chrysin 6-C-arabinoside 8-C-glucoside
|
Others | Others |
Chrysin 6-C-arabinoside 8-C-glucoside 是α±-葡萄糖苷酶抑制剂,α±-葡萄糖苷酶抑制剂广泛用于2型糖尿病的治疗。 | |||
T1192 |
Protoporphyrin IX
PPIX,原卟啉,原卟啉IX |
Others; Endogenous Metabolite | Metabolism; Others |
Protoporphyrin IX (PPIX) 是一种四吡咯,是血红素、细胞色素 c 和叶绿素的代谢前体。 | |||
TN1977 |
Neochamaejasmine B
新狼毒素B |
Antifection | Microbiology/Virology |
Neochamaejasmin B 是一种提取自Stellera chamaejasme L.的双黄酮化合物。它在 C-2/C-3 和 C-2″/C-3″ 位置具有顺反几何结构。 | |||
T2S1158 |
4,5-Dicaffeoylquinic acid
3,4-Dicaffeoylquinic acid,异绿原酸C(4,5),Isochlorogenic acid C |
Others; HBV; Endogenous Metabolite | Metabolism; Microbiology/Virology; Others |
4,5-Dicaffeoylquinic acid (Isochlorogenic acid C) 是一种天然产物,有抗病毒、抗肝毒性活性。 | |||
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