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T3S1319(+)-Magnoflorine；木兰花碱Escholin|||Magnoflorine|||Thalictrin|||Escholine；Escholin|||Magnoflorine|||Thal
(+)-Magnoflorine (Thalictrin) has sedative and anxiolytic effects, probably mediated by Magnoflorine through a GABAergic mechanism of action. Magnoflorine and Sinomenine have protective effects, are mediated by some mechanism other than prevention of micelle formation or protection of the erythrocyte membrane against osmotic imbalance.
价 格：￥电议型 号：T3S1319产 地：中国大陆
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T3898Schaftoside；夏佛塔苷APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE|||Shaftoside；夏佛塔苷|||APIGENIN-6-GLUCOSIDE-8-ARABIN
Schaftoside (APIGENIN-6-GLUCOSIDE-8-ARABINOSIDE) has antioxidant and anticancer activity.
价 格：￥电议型 号：T3898产 地：中国大陆
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T3897Isoschaftoside；异夏佛塔苷Isoschaftoside
Isoschaftoside is used as an intercrop due to its allelopathic inhibition of parasitism by Striga hermonthica, an obligate parasitic weed that can devastate the maize crop. Isoschaftoside has anti-tumor, antioxidant, and antimicrobial activities, it also possesses strong nematicidal activity against M. incognita.
价 格：￥电议型 号：T3897产 地：中国大陆
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T37408Bischloroanthrabenzoxocinone；BischloroanthrabenzoxocinoneBischloroanthrabenzoxocinone
Bacterial type II fatty acid synthesis (FAS-II) is mediated by a series of enzymes, each of which may be targeted by potential antibiotics. Bischloroanthrabenzoxocinone (BABX) is an inhibitor of FAS-II, blocking fatty acid synthesis in S. aureus and E. coli with IC50 values of 11.4 and 35.3 μg/ml, respectively. It inhibits the growth of S. aureus and permeable E. coli strains with minimum inhibitory concentrations ranging from 0.2-0.4 μg/ml. BABX also displays binding to liver X receptors (LXRs)
价 格：￥电议型 号：T37408产 地：中国大陆
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T3716Rolapitant；罗拉匹坦SCH619734；罗拉吡坦|||SCH619734|||罗拉匹坦
Rolapitant (SCH619734) Hydrochloride is the hydrochloride salt form of rolapitant, an orally bioavailable, centrally-acting, selective, neurokinin 1 receptor (NK1-receptor) antagonist with potential antiemetic activity. Upon oral administration, rolapitant competitively binds to and blocks the activity of the NK1-receptor in the central nervous system, thereby inhibiting the binding of the endogenous ligand, substance P (SP). This may prevent both SP-induced emesis and chemotherapy-induced nause
价 格：￥电议型 号：T3716产 地：中国大陆
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T37042SCH529074；化合物SCH529074SCH 529074；SCH 529074
SCH529074 is a selective activator of p53 (Ki = 1 μM) and can be used in studies about non-small-cell lung carcinoma. SCH529074 restores mutant p53 function and interrupts HDM2-mediated ubiquitination of wild Type p53.
价 格：￥电议型 号：T37042产 地：中国大陆
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T3700SCH900776 (S-isomer)；化合物SCH900776 S-isomerMK-8776 S-isomer|||SCH900776 S-isomer；MK-8776 S-isomer|||S
SCH900776 S-isomer (MK-8776 S-isomer) is an effective, specific and orally bioavailable inhibitor of checkpoint kinase Chk1 (IC50: 3 nM). It also inhibitors Chk2 (IC50: 1500 nM) and cyclin-dependent kinase CDK2 (IC50: 160 nM).
价 格：￥电议型 号：T3700产 地：中国大陆
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T36533SCH 725674；SCH 725674SCH 725674
SCH 725674 is an antifungal macrolide originally isolated from Aspergillus. It inhibits the growth of S. cerevisiae and C. albicans in vitro (MICs = 8 and 32 μg/ml, respectively).
价 格：￥电议型 号：T36533产 地：中国大陆
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T36532SCH 38519；SCH 38519SCH 38519
SCH 38519 is an isochromanequinone fungal metabolite originally isolated from Thermomonospora. It inhibits aggregation induced by thrombin , as well as inhibits serotonin secretion in human platelets (IC50s = 68 and 61 μg/ml, respectively). It inhibits the growth of various Gram-negative and Gram-positive bacteria (mean MICs = 122.1 and 0.92 μg/ml, respectively).
价 格：￥电议型 号：T36532产 地：中国大陆
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T36418O-Desmethyl-N-deschlorobenzoyl Indomethacin；O-Desmethyl-N-deschlorobenzoyl IndomethacinO-Desmethyl-N
O-Desmethyl-N-deschlorobenzoyl indomethacin is a metabolite of the non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor indomethacin .1It is formed from indomethacin in isolated rabbit hepatocytes. O-Desmethyl-N-deschlorobenzoyl indomethacin (600 μM) decreases the viability of HL-60 leukemia cells when cultured with glucose oxidase.2It has also been used in the synthesis of prostaglandin D2receptor antagonists.3
价 格：￥电议型 号：T36418产 地：中国大陆
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T3580FIPI；化合物FIPI5-Fluoro-2-indolyl deschlorohalopemide；5-Fluoro-2-indolyl deschlorohalopemide
FIPI (5-Fluoro-2-indolyl deschlorohalopemide) is a derivative of halopemide which potently inhibits both PLD1 (IC50 = 25 nM) and PLD2 (IC50 = 20 nM); prevents PLD regulation of F-actin cytoskeleton reorganization, cell spreading, and chemotaxis.
价 格：￥电议型 号：T3580产 地：中国大陆
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T35339Mometasone Furoate HydrateMometasone Furoate HydrateSCH 32088 hydrate|||Mometasone Furoate Hydrate
Mometasone Furoate (SCH 32088) Hydrate 是一种具有抗炎活性的合成糖皮质激素。
价 格：￥电议型 号：T35339产 地：中国大陆
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T34951Trimopam；化合物 T34951Sch12679|||Sch 2679|||Sch-12679；Sch12679|||Sch 2679|||Sch-12679
Trimopam is a dopamine receptor agonist of the benzazepine group.
价 格：￥电议型 号：T34951产 地：中国大陆
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T34580Schweinine；化合物 T34580Schweinine
Schweinine is a macrocylic alkaloid isolated from the whole plant of Schweinfurthia papilionacea.
价 格：￥电议型 号：T34580产 地：中国大陆
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T34579Schumanniofoside；化合物 T34579Schumanniofoside
Schumanniofoside is a chromone alkaloidal glycoside isolated from the stem bark of Schumanniophyton magnificum.
价 格：￥电议型 号：T34579产 地：中国大陆
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T34577Schkuhriolide；化合物 T34577Schkuhriolide
Schkuhriolide is a melampolide.
价 格：￥电议型 号：T34577产 地：中国大陆
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T34576Schizozygine；化合物 T34576Schizozygine
Schizozygine is an alkaloid isolated from Schizozygia caffaeoides.
价 格：￥电议型 号：T34576产 地：中国大陆
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T34575Schizokinen；化合物 T34575Schizokinen
Schizokinen is a citrate-containing dihydroxamate and a siderophore produced by Bacillus megaterium and Anabaena sp.
价 格：￥电议型 号：T34575产 地：中国大陆
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T34574Schisandronic acid；化合物 T34574Schizandronic acid|||Ganwuweizic acid；Schizandronic acid|||Ganwuweizic
Schisandronic acid is a triterpenoid acid isolated from the stems of Schisandra propinqua.
价 格：￥电议型 号：T34574产 地：中国大陆
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T34573SCH-900271；化合物SCH-900271SCH 900271；SCH 900271
SCH-900271 is a potent nicotinic acid receptor for the treatment of dyslipidaemia and is commonly used in the study of mixed hyperlipidaemia and primary hypercholesterolaemia.
价 格：￥电议型 号：T34573产 地：中国大陆
