ҵ
ԱͣԱ
ѻƹ ȼ
(0 -40)ۣ
(41-90)ۣɽǢ̸
(91+ )ۣɳ
ƹԱ5
֤ʱ䣺
עţ ֤
˴ ֤
ҵͣ ֤
עʽ ֤
Ʒ86101
ι۴3874175
-
T8836CY5-SE triethylamine saltoligonucleotides,reactive,dye,amino-groups,inhibit,CY-5-SE triethylamine sa
Fluorolink Cy5 triethanolamine salt is a hydrophilic amine-reactive fluorescent probe. It displays excitation/emission maxima of 646/662 nm, respectively. Cy5-SE-conjugated ligands have been used in the characterization of hematopoietic tumor microenvironments.
ţT8836 أй½
-
T9617RdRP-IN-2RdRP IN 2,RdRPIN2
RdRP-IN-2 is a RNA dependent RNA polymerase (RdRp) inhibitor. It significantly inhibits SARS-CoV-2 RdRp with an IC50 of 41.2 ?M.It also inhibits Feline coronavirus (FIPV) replication.
ţT9617 أй½
-
T8124Sodium benzoateSodium benzoate
Sodium benzoate is a D-Amino Acid Oxidase Inhibitor.Sodium Benzoate is a Food Preservative.
ţT8124 أй½
-
TJS03145,7-Dihydroxy-4-methylcoumarinBacterial,inhibit,Fungal,Inhibitor,5,7Dihydroxy4methylcoumarin,5,7 Dih
5,7-Dihydroxy-4-methylcoumarin inhibits human neutrophil oxidative metabolism and elastase activity. 5,7-Dihydroxy-4-methylcoumarin has in vitro platelet antiaggregatory property. 5,7-Dihydroxy-4-methylcoumarin shows inhibition of the cyclooxygenase pathway.
ţTJS0314 أй½
-
T16704LQuilseconazole Formic acid(1340593-70-5 Free base)
Quilseconazole Formic acid is a selective inhibitor of fungal Cyp51 with potent activities against Cryptococcus neoformans and Cryptococcus gattii.
ţT16704L أй½
-
T9124Laninamivir octanoateH2N2,CS8958,H3N2,inhaled,CS 8958,Laninamivir octanoate,neuraminidase,inhibit,An
Laninamivir octanoate is a long acting influenza neuraminidase (NA) inhibitor which shows superior anti-influenza virus activity.
ţT9124 أй½
-
T7103idalopirdine5-HT Receptor,Serotonin Receptor,Lu AE-58054,idalopirdine,Inhibitor,inhibit,5-hydroxytry
Idalopirdine, a selective 5-HT6 receptor antagonist( Ki : 0.83 nM),as a treatment for Alzheimer´s disease.
ţT7103 أй½
-
T6505Formoterol fumarateinhibit,Formoterol,Beta Receptor,Inhibitor,Formoterol fumarate,Adrenergic Recepto
Formoterol Hemifumarate, an effective, specific and long-acting 2-adrenoceptor agonist, is utilized in the treatment of chronic obstructive pulmonary disease(COPD) and asthma.
ţT6505 أй½
-
TQ0011PF-06869206inhibit,PF-06869206,Na+ channels,Sodium Channel,Na channels,PF 06869206,Inhibitor,PF06869
PF-06869206 is an oral selective inhibitor of the sodium-phosphate cotransporter NaPi2a (SLC34A1, IC50: 380 nM).
ţTQ0011 أй½
-
TN1634Euphorbia factor L7bEuphorbia factor L7b,Inhibitor,inhibit,Euphorbia factor L-7b
Euphorbia factor L7b,a natural product obtained from the herbs of Euphorbia pekinensis Rupr.
ţTN1634 أй½
-
TN6457N-trans-caffeoyltyramine
N-trans-caffeoyltyramine is a modulator of inflammatory responses and can be used in studies about treatment for chronic inflammatory diseases.
ţTN6457 أй½
-
TQ01951,5-AnhydrosorbitolInhibitor,Endogenous Metabolite,1,5 Anhydrosorbitol,1,5Anhydrosorbitol,inhibit,1,
1,5-Anhydrosorbitol is a validated marker of short-term glycemic control. This substance is derived mainly from food.
ţTQ0195 أй½
-
T9040Aurora kinase inhibitor-2inhibit,Aurora-A,Aurora kinase inhibitor2,Aurora Kinase,ATP-competitive,Aur
Aurora Kinase Inhibitor II is a cell-permeable anilinoquinazoline that inhibit the activity of Aurora A (IC50 = 0.39 M).
ţT9040 أй½
-
T9031MCU-i4C2C12,Inhibitor,mitochondrial,MCU-i-4,Mitochondrial Metabolism,MCU-i4,MCUi4,Ca2+,uptake,inhibi
MCU-i4 is a novel negative modulator of the MCU, binding MICU1 and impairing muscle cell growth.
ţT9031 أй½
-
T12902SHMT-IN-1SHMT IN 1,SHMTIN1
SHMT-IN-1 is a potent plasmodial serine hydroxymethyltransferase (SHMT) inhibitor with antitumor activity.
ţT12902 أй½
-
T6S0654IsocorynoxeineIsocorynoxeine,inhibit,5-HT Receptor,5-hydroxytryptamine Receptor,Serotonin Receptor,I
1. Isocorynoxeine shows the effects of lowering blood pressure, vasodilatation, and protection against ischemia-induced neuronal damage. 2. Isocorynoxeine exhibits a significant neuroprotective effect against glutamate-induced HT22 cell death at the maximum concentration.
ţT6S0654 أй½
-
TN1569DeoxylapacholDeoxylapachol,Fungal,inhibit,Inhibitor
Deoxylapachol has anti-wood rot activity, it can inhibit the brown rot fungi Gloeophyllum sepiarium CBS 353.74 and Gloeophyllum trabeum CBS 318.50 and the white rot fungi Merulius tremellosus CBS 280.73 and Phlebia brevispora CBS 509.92. It also can induce fungal cell wall stress.
ţTN1569 أй½
-
T19206-Lactamase-IN-1
-Lactamase-IN-1 is a -Lactamase inhibitor and targets the infection of Neisseria gonorrhoeae.
ţT19206 أй½