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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T2777 | Ginsenoside Rg1 | Sanchinoside C1,Panaxoside Rg1,Sanchinoside Rg1,Panaxoside A,Ginsenoside A2 | Apoptosis , Beta Amyloid , NF-κB |
Ginsenoside Rg1 (Panaxoside Rg1) is a class of steroid glycosides, and triterpene saponins found exclusively in the plant genus Panax (ginseng). It improves spatial learning and increase hippocampal synaptophysin level i... | |||
T71600 | Benazoline oxalate salt | ||
Benazoline oxalate salt is a pharmacological active compound that inhibits casein kinase Iε (CKIε) or CKIδ phosphorylation of the PER2 protein. | |||
T4253 | Skp2 Inhibitor C1 | SKPin C1 | Others , E1/E2/E3 Enzyme |
Skp2 Inhibitor C1 (SKPin C1)(SKPin C1) is a specific small molecule inhibitor of Skp2-mediated p27 degradation. | |||
T76702 | Sutimlimab | Complement System | |
Sutimlimab is a novel monoclonal antibody targeting complement protein C1. Sutimlimab is commonly used as a C1 inhibitor to treat cold agglutina-associated hemolysis. | |||
T18494 | NH2-PEG6-C1-Boc | H2N-PEG6-CH2COOtBu | Others , PROTAC Linker |
NH2-PEG6-C1-Boc (H2N-PEG6-CH2COOtBu) is a PEG-based PROTAC linker. NH2-PEG6-C1-Boc can be used in the synthesis of PROTACs. | |||
T17352 | Acid-C1-PEG5-Boc | Others , PROTAC Linker | |
Acid-C1-PEG5-Boc is a PEG-based PROTAC linker that can be used in PROTAC synthesis. | |||
T18560 | Propargyl-C1-NHS ester | 4-Pentynoic Acid Succinimidyl Ester | Others |
Propargyl-C1-NHS ester (4-Pentynoic Acid Succinimidyl Ester) is a nonclaevable linker used for antibody-drug-conjugation (ADC). | |||
T19503 | Papain | Others , Cysteine Protease | |
Papain is a cysteine protease of the peptidase C1 family. Papain is used in food, pharmaceutical, textile, and cosmetic industries. | |||
T21275 | Azoxystrobin | HSDB 7017,ICI-A 5504,Bankit,ICIA-5504,Amistar | Antifungal |
Azoxystrobin (Bankit) is a broad-spectrum fungicide. Azoxystrobin induces ROS production, cell apoptosis and mitochondrial respiration by blocking electron transfer between cytochromes b and c1. | |||
TN2103 | PROCYANIDIN C1 | Apoptosis | |
Procyanidin C1 is a natural product, with anti-inflammatory effects, and induces apoptosis. | |||
T18479 | NH-bis(C1-Boc) | Others | |
NH-bis(C1-Boc)is a uncleavable linker. NH-bis can be used for antibody-drug conjugates (ADC). | |||
T11205 | Ent-Ezetimibe | ent-SCH 58235 | Others |
Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator.ent-Ezetimibe (ent-SCH 58235) (ent-SCH 58235) is the RRS-enantiomer of Ezetimibe. Ezetimibe is a potent cholesterol absorption inhib... | |||
T0437 | Inosine | INO 495,NSC 20262 | ROS , Endogenous Metabolite , Adenosine Receptor |
Inosine (NSC-20262) is a purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It has immunomodulatory, neuroprotective, and analgesic properties. | |||
T4758 | 2'-Deoxycytidine | Cytosine deoxyribonucleoside,2'-Deoxycytidine monohydrate,2(1H)-Pyrimidinone,Cytosine deoxyriboside,Deoxyribose cytidine,Deoxycytidine | Endogenous Metabolite |
2'-Deoxycytidine (Deoxyribose cytidine) is one of the principal nucleosides of DNA composed of cytosine and deoxyribose. A nucleoside consists of only a pentose sugar linked to a purine or pyrimidine base, without a phos... | |||
T25313 | Detoxin C1 | Detoxin calpha1 | |
Detoxin C1 is a selective blasticidin S antagonist. | |||
T29081 | UTA1inh-C1 | UTA1-inh-C1,UTA1(inh)-C1 | |
UTA1inh-C1 is a novel inhibitor of kidney urea transporter UT-A1. | |||
T69393 | SID-7977382 | ||
SID-7977382 is a complement factor C1 inhibitor. | |||
T39177 | Bromoacetamide-PEG3-C1-acid | Bromoacetamide-PEG3-C1-acid | |
Bromoacetamide-PEG3-C1-acid is a PEG-based PROTAC linker utilized for PROTAC synthesis. | |||
TP2439 | Sarasinoside C1 | Sarasinoside-C1 | |
Sarasinoside C1 is a norlanostane-triterpenoid oligoglycoside from the Palauan marine sponge Asteropus sarasinosum. | |||
T17384 | Ald-Ph-amido-PEG3-C1-Boc | Others | |
Ald-Ph-amido-PEG3-C1-Boc is a polyethylene glycol (PEG) linker specific to antibody-drug conjugates (ADC). |