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カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
T37979 | N-Desmethyl Pimavanserin | AC-279 | 5-HT Receptor |
N-Desmethyl Pimavanserin (AC-279) is the active metabolite of Pimavanserin, a 5-HT2A receptor inverse agonist, which is used in the treatment of sleep disorders such as insomnia. | |||
T27020L | Isomer-Cilansetron | Others | |
isomer-Cilansetron is an isomer of Cilansetron. | |||
T15270 | Fananserin | RP 62203 | Dopamine Receptor , 5-HT Receptor |
Fananserin is an orally bioavailable and selective antagonist of the 5-HT2 receptor (Ki: 0.37 nM for the rat 5-HT2A receptor). It also is an antagonist of dopamine D4 receptor (Ki: 2.93 nM for the human dopamine D4 recep... | |||
T3467 | Miransertib | ARQ-092,AKT inhibitor 2 | Akt , Parasite |
Miransertib (ARQ-092) is an orally bioavailable, selective, and potent allosteric Akt inhibitor. | |||
T62083 | Camonsertib | ATR inhibitor 4,RP-3500 | ATM/ATR |
Camonsertib (RP-3500) is a selective, orally active ATR kinase inhibitor (ATRi) with an IC50: 1.00 nM in biochemical assays and exhibits potent antitumour effects. Camonsertib is 30 times more selective for ATR than mTOR... | |||
T68141 | Seganserin | 5-HT Receptor | |
Seganserin, a non-selective 5-hydroxytryptamine 2-HT receptor antagonist, reversed the inhibitory effects of fluoxetine and quipazine on luteinizing hormone-induced hyperphagia, depression and nociception, and reversed t... | |||
T3350 | Selonsertib | GS-4997 | Apoptosis , ASK , MAPK |
Selonsertib (GS-4997) is an orally bioavailable inhibitor of apoptosis signal-regulating kinase 1 (ASK1), with potential anti-inflammatory, antineoplastic and anti-fibrotic activities. | |||
T27020 | Cilansetron | KC-9946,KC9946,DU-123265,DU123265 | 5-HT Receptor |
Cilansetron is an effective and selective 5-HT3 receptor antagonist that can be used for related diseases caused by colitis. | |||
T1517 | Benserazide hydrochloride | Benserazide HCl,Serazide,Ro 4-4602 | Dopamine Receptor |
Benserazide hydrochloride (Ro 4-4602) is a peripherally-acting L-amino acid decarboxylase (AAAD) or DOPA decarboxylase inhibitor. | |||
T6615 | Ondansetron | GR-C507/75,GR 38032,GR 38032F,SN 307 | 5-HT Receptor |
Ondansetron (GR 38032) is a serotonin 5-HT3 receptor antagonist used mainly as an antiemetic. | |||
T67914 | Insecticidal agent 364 | mTOR , Autophagy | |
Insecticidal agent 364 is a selective small molecule inhibitor of rapamycin kinase target protein. Insecticidal agent 364 has antitumor activity, and by inhibiting mTOR, Insecticidal agent 364 aims to disrupt signaling p... | |||
T16759 | Ritanserin | R 55667 | Dopamine Receptor , 5-HT Receptor , Adrenergic Receptor , Histamine Receptor |
Ritanserin (R 55667) is a highly effective, relatively selective, long-acting antagonist of 5-HT2 receptor (IC50: 0.9 nM), less active on Histamine H1, Dopamine D2, Adrenergic α1, Adrenergic α2 receptors. | |||
T12477 | Uzansertib phosphate | INCB053914 phosphate | Pim |
Uzansertib phosphate (INCB053914 phosphate) is an orally active, ATP-competitive inhibitor of pan-PIM kinase(PIM1, PIM2, PIM3 with IC50s of 0.24 nM, 30 nM, 0.12 nM , respectively). | |||
T7350 | Nelotanserin | APD125 | 5-HT Receptor |
Nelotanserin (APD125) is a potent 5-HT2A inverse agonist(IC50 : 1.7 nM), a moderately potent 5-HT2C partial inverse agonist t(IC50 :79 nM )and a weak 5-HT2B inverse agonistt(IC50 : 791 nM). | |||
T21428 | Mianserin | Lantanon,Lumin,Norval,Lerivon,Depnon | Histamine Receptor |
Mianserin, an H1 receptor reverse agonist, is a psychoactive compound in the tetracyclic antidepressant (TeCA) treatment family. Mianserin has antidepressant, antianxiety, antiemetic, hypotrophic, hypnotic and antihistam... | |||
T6616 | Ondansetron hydrochloride | SN 307,Ondansetron HCl,Emeset,GR 38032 HCl,NSC 665799,Zofran | 5-HT Receptor |
Ondansetron hydrochloride (Zofran) is a serotonin 5-HT3 receptor antagonist, used to prevent nausea and vomiting caused by cancer chemotherapy, and radiation therapy. | |||
T4297 | Flibanserin | BIMT-17BS,Girosa,BIMT-17 | Dopamine Receptor , 5-HT Receptor |
Flibanserin (Girosa) is a serotonergic antidepressant used to treat hypoactive sexual desire disorder. Flibanserin has been associated with a low rate of minor serum aminotransferase elevations during treatment but has n... | |||
T23631 | Adatanserin | WY-50324,WY 50324,WAY SEB 324,WY50324 | 5-HT Receptor |
Adatanserin (WY 50324) is a mixed 5-HT1A receptor partial agonist and a 5-HT2A and 5-HT2C receptor antagonist with potential neuroprotective activity for the study of anxiety and depression. | |||
T9833 | Opiranserin hydrochloride | P2X Receptor , GlyT , 5-HT Receptor | |
Opiranserin (VVZ-149) hydrochloride is a dual antagonist of glycine transporter type 2 (GlyT2) and serotonin receptor 2A (5HT2A), with IC50s of 0.86 and 1.3 μM, respectively. It shows antagonistic activity on rP2X3 (IC50... | |||
T1066L | Ketanserin tartrate | KJK 945 tartrate,KJK-945 tartrate,KJK945 tartrate | 5-HT Receptor , Serotonin Transporter , Adrenergic Receptor |
Ketanserin tartrate (KJK-945 tartrate) is a 5-HT2A receptor and α1-adrenergic receptor antagonist with antihypertensive activity, inhibits serotonin-induced vasoconstriction and platelet activation, and can be used in th... | |||
T6247 | Onvansertib | NMS-P937,NMS-1286937 | Apoptosis , PLK |
Onvansertib (NMS-1286937), an oral, specific Polo-like Kinase 1 (PLK1) inhibitor, is with IC50 of 2 nM. The specificity of NMS-P937 forPLK1 is 5000-fold higher over PLK2/PLK3. | |||
T2076 | Pimavanserin | ACP-103 | 5-HT Receptor |
Pimavanserin (ACP-103)(ACP-103) is an effective and specific 5-HT2A receptor inverse agonist (mean pIC50: 8.7, in the cell-based functional assay). Pimavanserin is an atypical antipsychotic used in the treatment of hallu... | |||
T8451 | Tropanserin | MDL 72422 | 5-HT Receptor |
Tropanserin (MDL 72422) is a 5-hydroxytryptamine receptor antagonist that inhibits 5-HT3 receptor activity.Tropanserin has anxiolytic activity and is used to treat depression and cognitive disorders. | |||
T6946 | Pimavanserin tartrate | ACP-103,ACP-103 tartrate,Nuplazid,Pimavanserin | 5-HT Receptor |
Pimavanserin tartrate (Nuplazid) is an effective and specific serotonin 5-HT2A inverse agonist (pIC50: 8.73), used in the therapy of psychosis associated with Parkinson's disease. | |||
T14968 | Cinanserin hydrochloride | SQ 10643 | Influenza Virus , 5-HT Receptor |
Cinanserin hydrochloride (SQ 10643) is a high affinity antagonist of the 5-HT2 receptor (Ki: 41 nM) and a 3C-like protease inhibitor of severe acute respiratory syndrome coronavirus. | |||
T22243 | Anserine | L-Anserine | Endogenous Metabolite |
Anserine (L-Anserine) is a dipeptide containing β-alanine and histidine, which can be found in the skeletal muscle and brain of mammals and birds. Anserine is not cleaved by serum carnosinase and act as biochemical buffe... | |||
T1066 | Ketanserin | R41468,Ketanserin tartrate,Ketanserinum | Potassium Channel , 5-HT Receptor , Autophagy |
Ketanserin (Ketanserinum) is a quinazoline derivative and serotonin (5-hydroxytryptamine, 5HT) receptor subtype 2 (5-HTR2) antagonist with potential antihypertensive and antiplatelet activities. Following administration,... | |||
T1180 | Blonanserin | AD-5423 | Dopamine Receptor , Sigma receptor , 5-HT Receptor , Adrenergic Receptor |
Blonanserin (AD-5423) is an atypical antipsychotic approved in Japan in January, 2008. Relative to many other antipsychotics, blonanserin has an improved tolerability profile, lacking side effects such as extrapyramidal ... | |||
T29645 | Adatanserin hydrochloride | WY50324 hydrochloride | 5-HT Receptor |
Adatanserin hydrochloride (WY50324 hydrochloride) is a novel 5-HT(1A)/5-HT(2) receptor ligand with potential neuroprotective effects and inhibition of ischemic efflux of endogenous amino acids, which can be used in the s... | |||
T23445 | Anxiolytic/nonsedative agent-1 | TCS 1205 | GABA Receptor |
Anxiolytic/nonsedative agent-1 (TCS 1205) is a potent and selective GABAA agonist. Anxiolytic/nonsedative agent-1 shows appreciable affinity for the BzR in bovine brain membranes with Kis of 14, 121, 239 nM for α1β2γ2, α... | |||
T76774 | Ponsegromab | PF 06946860 | TGF-beta/Smad |
Ponsegromab (PF 06946860) is a selective and effective humanized anti-GDF15 antibody inhibitor. Ponsegromab has anti-cachexic activity by binding to GDF15 to prevent its binding to GFRAL, thus disrupting GDF15/GFRAL medi... | |||
T22964 | Glemanserin | MDL11939 | 5-HT Receptor |
Glemanserin (MDL11939) is a specific 5-HT2A antagonist with Ki values of 0.54 nM, 2.5 nM and 2.89 nM for rabbit, human and rat 5-HT2A. | |||
T5389 | Volinanserin | M 100907,MDL100907 | 5-HT Receptor |
Volinanserin (MDL100907) (MDL 100907) is a potent and selective antagonist of the serotonin receptor 5-HT2 (Ki: 0.36 nM) and shows 300-fold selectivity for 5-HT2 receptor over 5-HT1c, alpha-1 adrenergic and sigma recepto... | |||
T11217 | Eplivanserin | SR-46349 | 5-HT Receptor |
T1478 | Ondansetron hydrochloride dihydrate | SN 307,NSC 665799,GR 38032,Ondansetron hydrochloride | 5-HT Receptor |
Ondansetron hydrochloride dihydrate (GR 38032) is a competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, a... | |||
T15552 | Iferanserin | S-MPEC | 5-HT Receptor |
Iferanserin (S-MPEC) is a selective antagonist of the 5-HT receptor (serotonin receptor) with an affinity for 5-HT2A receptors. Iferanserin has the potential for internal hemorrhoid disease treatment. | |||
T16399 | Opiranserin | P2X Receptor , GlyT , 5-HT Receptor | |
Opiranserin is a development as an injectable agent for the treatment of postoperative pain. Opiranserin is a non-opioid and non-NSAID analgesic candidate and is a dual antagonist of glycine transporter type 2 (GlyT2) an... | |||
T83106 | Anselamimab | ||
Anselamimab (CAEL-101), a humanized IgG1-κ anti-amyloid fibrils antibody, specifically targets serum amyloid A1 (SAA1) [1] [2]. | |||
T34918 | Trelanserin | SL650472,SL-650472,SL 650472 | |
Trelanserin (SL-650472) is an antagonist of the serotonin receptor. | |||
T32164 | Insect repellent M 3535 | ||
Insect repellent M 3535 is a bug repellant. | |||
T71347 | Galdansetron | ||
Galdansetron is a serotonin antagonist. | |||
T124935 | Fonsecin | ||
Fonsecin is a useful organic compound for research related to life sciences. The catalog number is T124935 and the CAS number is 3748-39-8. | |||
T9901A-011 | Lunsekimig | SAR443765 | |
Lunsekimig (SAR443765) is an IL-13/TSLP bis-antibody that links a nano-antibody targeting IL-13 and a variable region of the heavy chain (VHH) targeting TSLP for use in asthma research. | |||
T68311 | Ritanserin tartrate | ||
Ritanserin tartrateis is a selective and potent serotonin-2 antagonist. | |||
T11295 | Flibanserin-d4 | BIMT-17BS D4,BIMT-17 D4,Flibanserin D4 | Others |
Flibanserin, a compound identified as BIMT-17, acts as a complete agonist at the serotonin 5-HT1A receptor, with a binding affinity (Ki) of 1 nM, while functioning as an antagonist at the 5-HT2A receptor with a 49 nM aff... | |||
T82066 | Insecticidal agent 1 | ||
Insecticidal agent 1 exhibits greater insecticidal potency than both obacunone and toosendanin. | |||
T80855 | Vonsetamig | ||
Vonsetamig, a humanized immunoglobulin G4-kappa monoclonal antibody, targets both TNFRSF17 and CD3E. It serves as an antineoplastic agent. | |||
T69905 | Iferanserin HCl | ||
Iferanserin HCl is a selective serotonin receptor antagonist. | |||
T1517L | Benserazide | Ro-44602,Ro44602,Ro 44602,Serazide | |
Benserazide is an inhibitor of dopa decarboxylase. It is often given with levodopa in the treatment of Parkinson's to prevent the conversion of levodopa to dopamine in the periphery, thereby increasing the amount that re... | |||
T1180L | Blonanserin HCl | AD 5423,AD5423,AD-5423,Blonanserin | |
Blonanserin is an antagonist of dopamine-D2 and serotonin-S2. |
カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
TN1096 | Ginsenoside Ra1 | Others , Tyrosine Kinases | |
Ginsenoside Ra1 is a component from ginseng. Ginsenoside Ra1 shows significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R). | |||
TN2296 | Vinaginsenoside R4 | Others | |
Vinaginsenoside R4 was isolated from the leaves of hydroponically grown ginseng. It inhibits melanin biosynthesis and enhances pigmentation in zebrafish without any cytotoxic effects on melan-a cells. It may have potenti... | |||
T3915 | Ginsenoside Ro | Chikusetsusaponin 5,Polysciasaponin P3,Chikusetsusaponin V | Calcium Channel , Reductase , Prostaglandin Receptor |
Ginsenoside Ro (Chikusetsusaponin V) can reduce TXA2 production, weakly reduce COX-1 and TXAS activities, and has antiplatelet effects as a Ca2+ antagonist with an IC50 of 155 μM. | |||
T2822 | Ginsenoside Rb1 | Gypenoside Ⅲ,Gypenoside III | ATPase , Mitophagy , IRAK , NF-κB , Autophagy , HSV |
Ginsenoside Rb1 (Gypenoside Ⅲ) is part of a class of steroid glycosides; may have properties that inhibit or prevent the growth of tumors. | |||
T2959 | Ginsenoside Rh2 | 20(S)-Rh2,20S-Ginsenoside Rh2,20(S)-Ginsenoside Rh2 | Apoptosis , EGFR , Caspase , Endogenous Metabolite |
Ginsenoside Rh2 (20(S)-Ginsenoside Rh2), an extract of red Panax ginseng, is a potent anti-inflammatory and anticancer drug. | |||
T0783 | Mianserin hydrochloride | Mianserin HCl,Org GB 94,ORG GB-94 HCl | Dopamine Receptor , 5-HT Receptor , Opioid Receptor , Adrenergic Receptor , Histamine Receptor |
Mianserin hydrochloride (Org GB 94) is a tetracyclic compound with antidepressant effects. it apparently blocks alpha-adrenergic, histamine H1, and some types of serotonin receptors. It may cause drowsiness and hematolog... | |||
T4704 | L-Anserine nitrate | L-Anserine nitrate salt | Others , Endogenous Metabolite |
L-Anserine nitrate (L-Anserine nitrate salt) is a dipeptide found in most animal tissues. In model systems it is a potent Antioxidant and scavener of hydroxyl radicals. The compound inhibits nonenzymatic protein glycatio... | |||
T6S1495 | Ginsenoside Rk3 | Others , NF-κB | |
1. Ginsenoside Rk3 and Rh4 could have a role in treating inflammatory diseases. 2. Ginsenoside Rk3 is often used as a major ingredient of the compound preparation for ischemic heart diseases. | |||
T3920 | Pseudoginsenoside F11 | Ginsenoside A1 | Others , Endogenous Metabolite |
Pseudoginsenoside F11 (Ginsenoside A1) is a component of Panax quinquefolium (American ginseng) which main pharmacological activities are positive inotropic effect on isolated heart function, good therapeutic effect on m... | |||
T3402 | 20(S)-Ginsenoside Rg3 | 20(S)-Ginsenoside-Rg3,Rg3,20S-Ginsenoside Rg3,Ginsenoside Rg3,S-Ginsenoside Rg3 | EGFR , Beta Amyloid , Potassium Channel , NF-κB , COX , Sodium Channel , Endogenous Metabolite |
20(S)-Ginsenoside Rg3 (Rg3) possess an ability to inhibit the lung metastasis of tumor cells via inhibition of the adhesion and invasion of tumor cells. It inhibits the proliferation of human umbilical vein endothelial c... | |||
T2878 | Ginsenoside Rd | Panaxoside Rd,Sanchinoside Rd,Gypenoside VIII | P450 , Calcium Channel , NF-κB , COX , Endogenous Metabolite |
Ginsenoside Rd (Gypenoside VIII) may have properties that inhibit or prevent the growth of tumors. | |||
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... | |||
T3830 | 20(R)-Ginsenoside Rg2 | 20R-Ginsenoside Rg2 | IL Receptor |
20(R)-Ginsenoside Rg2 (20R-Ginsenoside Rg2) is a compound with anti-oxidant and anti-apoptosis. | |||
T3918 | Ginsenoside Rb3 | Gypenoside IV | NF-κB , COX , NO Synthase |
Ginsenoside Rb3 (Gypenoside IV) is a natural triterpenoid saponin, exhibiting inhibition effect on TNFα-induced NF-κB transcriptional activity. It also inhibits the induction of COX-2 and iNOS mRNA. | |||
T4S1518 | Pseudoginsenoside RT1 | Others | |
Pseudoginsenoside RT1, isolated from the fruit of Randia siamensis, exhibits acute ichthyotoxic activity. Pseudoginsenoside RT1 can cause a decrease in blood pressure, an increase in heart rate and an increase in spontan... | |||
TN1686 | Ginsenoside Rg4 | Antibacterial | |
Ginsenoside Rg4 is a natural product | |||
T3S1591 | Notoginsenoside Fc | Others , Autophagy | |
1. Notoginsenoside Fc has perfect anti-platelet aggregatory effect. | |||
TN7110 | Ginsenoside Rs2 | Others | |
Ginsenoside Rs2 is a natural product isolated from the leaves of Panax japonicus var.. | |||
T3916 | Ginsenoside F2 | Apoptosis , Endogenous Metabolite , Autophagy | |
Ginsenoside F2 has antiproliferative activity against breast cancer stem cells (CSCs). It induces apoptosis in breast CSCs by activating the intrinsic apoptotic pathway and mitochondrial dysfunction. | |||
T3401 | Ginsenoside F1 | 20(S)-Ginsenoside F1 | P450 , Endogenous Metabolite |
Ginsenoside F1 (20(S)-Ginsenoside F1) is an enzymatically modified derivative of ginsenoside Rg1, showing competitive inhibition of the activity of CYP3A4 and a weaker inhibition of the activity of CYP2D6. | |||
T6S1485 | Ginsenoside Rh4 | Others | |
1. Ginsenoside Rh4 could be safely used as adjuvant with low or non-haemolytic effect. 2. Ginsenoside Rh4 has cytotoxic activity and its aglycone against cancer cell lines. | |||
T6S1487 | Ginsenoside Rg5 | NF-κB , COX , IGF-1R | |
1. Ginsenoside Rg5 could be a beneficial agent for the treatment of Alzheimer's disease. 2. Ginsenoside Rg5 suppresses LPS-induced nitric oxide (NO) production and proinflammatory TNF-α secretion. 3. Ginsenoside Rg5 can ... | |||
T3849 | Kinsenoside | (+)-Kinsenoside | Apoptosis , Nrf2 |
Kinsenoside ((+)-Kinsenoside) shows significant antihepatotoxic, and anti-inflammatory activities. Kinsenoside could be useful for repairing beta cells in pancreatic islet injury as well as improving its function, it cou... | |||
T6S1587 | Notoginsenoside R2 | 20(S)-Notoginsenoside R2,Ginsenoside Ng-R2 | Others , Nrf2 |
Notoginsenoside R2 (20(S)-Notoginsenoside R2) has neuroprotection against 6-OHDA-induced neurotoxicity, is associated with Notoginsenoside R2-mediated P90RSK and Nrf2 activation through MEK1/2-ERK1/2 pathways. | |||
T2S0223 | Isosinensetin | 6-Demethoxynobiletin | Antioxidant , HIV Protease , Antibacterial , P-gp |
1. Isosinensetin (6-Demethoxynobiletin) shows antioxidant and HIV-1 protease inhibiting activities. | |||
T11398 | Ginsenoside Ra3 | Others | |
Ginsenoside Ra3 is a natural product isolated from Panax ginseng, has anti-cancer activity. | |||
T3S1589 | Notoginsenoside Fa | Others | |
1. Notoginsenosides Fa and R4 show significant neurite outgrowth enhancing activities in human neuroblastoma SK-N-SH cells. | |||
TN1684 | Ginsenoside F5 | Apoptosis | |
Ginsenoside F5 is a natural product from Panax ginseng C. A. Mey, remarkably inhibits the growth of HL-60 cells by the apoptosis pathway | |||
T3793 | (20R)-Ginsenoside Rh1 | 20(R)-Ginsenoside Rh1 | Others |
(20R)-Ginsenoside Rh1 (20(R)-Ginsenoside Rh1) can inhibit the thrombin-induced conversion of fibrinogen to fibrin. | |||
T5761 | Notoginsenoside Ft1 | Others , HIF/HIF Prolyl-Hydroxylase | |
Notoginsenoside Ft1 is a saponin originally isolated from P. notoginseng with diverse biological activities | |||
TN6930 | 5-Desmethylsinensetin | Others | |
5-Desmethylsinensetin is a natural product. | |||
TN1997 | Notoginsenoside FP2 | Others | |
Notoginsenoside FP2 is a natural product isolated from the fruit pedicels of Panax notoginseng and can be used in studies about the treatment of cardiovascular diseases. | |||
T13626 | Cottonseed oil | Others | |
Cottonseed oil, a cooking oil extracted from the seeds of cotton plants, has been considered the most insecticidal of vegetable oils. | |||
T2872 | Ginsenoside Re | Ginsenoside B2,Panaxoside Re,Chikusetsusaponin Ivc,Sanchinoside Re | Beta Amyloid , NF-κB , Endogenous Metabolite , JNK |
Ginsenoside Re (Ginsenoside B2) may have properties that inhibit or prevent the growth of tumors. | |||
T2720 | Ginsenoside Rc | Panaxoside Rc | Others , TNF , GABA Receptor , Interleukin |
Ginsenoside Rc (Panaxoside Rc) is one of the ginsenosides from Panax ginseng, inhibits the expression of TNF-α and IL-1β. | |||
TQ0199 | Ginsenoside Rh3 | Antioxidant , Nrf2 , Antifungal | |
Ginsenoside Rh3 is a natural product extracted from Ginseng C. A. Mey.Ginsenoside Rh3 has antifungal and antioxidant activities and induces Nrf2 activation in human retinal cells. | |||
TN2100 | Pratensein | Others , NF-κB | |
Pratensein as a novel transcriptional up-regulator of scavenger receptor class B type I in HepG2 cells. | |||
T3919 | Ginsenoside Rb2 | Ginsenoside C | GPR , Others , Influenza Virus , Endogenous Metabolite |
Ginsenoside Rb2 (Ginsenoside C) found in species of Panax, upregulating GPR120 gene expression. | |||
T2932 | Ginsenoside Rh1 | Sanchinoside B2,Prosapogenin A2,20(S)-Ginsenoside Rh1,Sanchinoside Rh1 | IL Receptor , TNF , Endogenous Metabolite , PPAR , Interleukin |
Ginsenoside Rh1 (Sanchinoside B2) , one of the main constituents of Panax ginseng, exhibits anti-inflammatory effect. | |||
TN2802 | 20-O-Glucoginsenoside Rf | Others | |
20-O-Glucoginsenoside Rf is a natural product extracted from Panax ginseng C. A. Mey. | |||
T3813 | 20(R)-Ginsenoside Rh2 | (20R)Ginsenoside Rh2,Ginsenoside Rh2 | Apoptosis , MMP , HSV |
20(R)-Ginsenoside Rh2 (Ginsenoside Rh2) is a minor stereoisomer of ginsenoside Rh2, possesses matrix metalloproteinase inhibitory. | |||
TN2245 | Sunset Yellow FCF | Food Yellow 3,Orange Yellow S,Sunset yellow,CI 15985 | Androgen Receptor |
Sunset Yellow FCF (Sunset yellow) is an orange azo dye with pH-dependent absorbance.Sunset Yellow FCF is used in food, cosmetics and pharmaceuticals.It is used as a colorant food additive in many food products.They may b... | |||
T5S1590 | Notoginsenoside Fe | Notoginseng triterpenes,Ginsenoside Mb | Others |
Notoginsenoside Fe (Ginsenoside Mb) is a natural compound found in Panax japlcus var. | |||
T2873 | Ginsenoside Rg2 | Chikusetsusaponin I,Panaxoside Rg2,Prosapogenin C2,(20S)Ginsenoside Rg2 | Beta Amyloid , GSK-3 , NF-κB |
Ginsenoside Rg2 (Chikusetsusaponin I) is one of the major active components of ginseng, act as an NF-κB inhibitor. | |||
T2961 | Notoginsenoside R1 | Sanqi glucoside R1,Sanchinoside R1 | Apoptosis , ERK , Beta Amyloid |
Notoginsenoside R1 (Sanchinoside R1) has been shown to exhibit antioxidant, antiapoptotic, anti-inflammatory, and immune-stimulatory properties. | |||
T4S0227 | Sinensetin | Pedalitin permethyl ether | TNF , PGE Synthase |
Sinensetin (Pedalitin permethyl ether) is a methylated flavone found in certain citrus fruits. pocess potent antiangiogenesis and anti-inflammatory, sinensetin enhances adipogenesis and lipolysis. | |||
T6S1500 | Ginsenoside Rf | Ginsenoside-Rf,Panaxoside Rf | Calcium Channel , Endogenous Metabolite |
Ginsenoside Rf (Panaxoside Rf) is a trace component of ginseng root. Ginsenoside Rf inhibits N-type Ca2+ channel. | |||
T3812 | (20R)-Ginsenoside Rg3 | 20(R)-Ginsenoside Rg3,(20R)Ginsenoside Rg3,20(R)-Propanaxadiol | Others |
(20R)-Ginsenoside Rg3 (20(R)-Propanaxadiol) is a compound with anti-aging and antifatigue activities. | |||
TN1094 | Ginsenoside Rg6 | Apoptosis , NF-κB | |
Ginsenoside Rg6 can inhibit JK cell proliferation in human lymphocytoma and induce its apoptosis, the mechanism may through mitochondrial dysfunction and an increase of Bax expression and decrease of Bcl-2 expression. | |||
T4S1519 | Pseudoginsenoside RT5 | Others | |
1. Pseudoginsenoside RT5 has anti-epilepsy, anti-depressant activity by promoting nerve growth and improve cognitive ability. 2. Pseudoginsenoside RT5 has anti-bacterial, anti-tumor and anti-malaria activities. | |||
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カタログ番号 | 製品名 | Species | Expression System |
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TMPY-02646 | NSE/ENO2 Protein, Human, Recombinant (His) | Human | E. coli |
The combination of silencing ENO2 and 2-deoxyglucose (2-DG) synergistically inhibited leukemia cell survival. ENO2 may be a biological marker for monitoring chemotherapeutic efficacy and relapse in ALL. Reduced ENO2 expr... | |||
TMPH-03617 | Miraculin Protein, Synsepalum dulcificum, Recombinant (His) | Synsepalum dulcificum | P. pastoris (Yeast) |
Miraculin has the property of modifying a sour taste into a sweet taste. This alteration of taste perception persists for many minutes. Miraculin Protein, Synsepalum dulcificum, Recombinant (His) is expressed in yeast wi... | |||
TMPH-03094 | Phl p 5b Protein, Phleum pratense, Recombinant (His & SUMO) | Phleum pratense | E. coli |
Has ribonuclease activity. May be involved in host-pathogen interactions. Phl p 5b Protein, Phleum pratense, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecul... | |||
TMPH-03616 | Miraculin Protein, Synsepalum dulcificum, Recombinant (E. coli, His) | Synsepalum dulcificum | E. coli |
Miraculin has the property of modifying a sour taste into a sweet taste. This alteration of taste perception persists for many minutes. Miraculin Protein, Synsepalum dulcificum, Recombinant (E. coli, His) is expressed in... | |||
TMPH-03627 | Beta-mammal/insect toxin Ts1 Protein, Tityus serrulatus, Recombinant (E. coli, His & Myc) | Tityus serrulatus | E. coli |
Beta-mammal/insect toxin Ts1 Protein, Tityus serrulatus, Recombinant (E. coli, His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 14.3 kDa and the accessio... | |||
TMPY-06149 | Phl p 5 Protein, Phleum pratense, Recombinant (His) | Phleum pratense | HEK293 Cells |
Phl p 5 Protein, Phleum pratense, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 30.9 kDa and the accession number is Q40960-1. | |||
TMPY-06016 | Phl p 5 Protein, Phleum pratense, Recombinant | Phleum pratense | E. coli |
Phl p 5 Protein, Phleum pratense, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 28.7 kDa and the accession number is Q40960-1. | |||
TMPH-03626 | Beta-mammal/insect toxin Ts1 Protein, Tityus serrulatus, Recombinant (His & Myc) | Tityus serrulatus | Baculovirus Insect Cells |
Beta-mammal/insect toxin Ts1 Protein, Tityus serrulatus, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 10.8 kDa and the accession number i... | |||
TMPH-03093 | Phl p 5a Protein, Phleum pratense, Recombinant (His & SUMO) | Phleum pratense | E. coli |
N/A. Phl p 5a Protein, Phleum pratense, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 44.5 kDa and the accession number is Q40962. | |||
TMPY-06015 | Phl p 2 Protein, Phleum pratense, Recombinant (His) | Phleum pratense | HEK293 Cells |
Phl p 2 Protein, Phleum pratense, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 13.1 kDa and the accession number is P43214-1. | |||
TMPH-03095 | Phl p 6 Protein, Phleum pratense, Recombinant (His & Myc) | Phleum pratense | E. coli |
Phl p 6 Protein, Phleum pratense, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 19.2 kDa and the accession number is P43215. | |||
TMPH-03096 | Profilin 2 Protein, Phleum pratense, Recombinant (His & Myc) | Phleum pratense | E. coli |
Binds to actin and affects the structure of the cytoskeleton. At high concentrations, profilin prevents the polymerization of actin, whereas it enhances it at low concentrations. By binding to PIP2, it inhibits the forma... |