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ԱͣԱ
ѻƹ ȼ
(0 -40)ۣ
(41-90)ۣɽǢ̸
(91+ )ۣɳ
ƹԱ5
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עţ ֤
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ҵͣ ֤
עʽ ֤
Ʒ86101
ι۴3847608
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T8277Forsythoside IInhibitor,Forsythoside I,inhibit
Forsythoside I, a caffeoyl phenylethanoid glycoside (CPG), may possess anti-inflammatory activities.
ţT8277 أй½
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T8458CNQX disodiumIonotropic glutamate receptors,inhibit,Inhibitor,startle,non-NMDA,fear-potentiated,kain
CNQX disodium is a competitive non-NMDA receptor antagonist and competitive AMPA/kainate receptor antagonist in neuronal cultures.
ţT8458 أй½
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T7562-Amyloid (31-35)Abeta, Amyloid (31 35),Amyloid (3135),-amyloid peptide,inhibit,Amyloid-,Inhibit
-Amyloid 31-35(TFA) is the shortest sequence of native Amyloid- peptide.
ţT7562 أй½
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T90597Compound 1549Compound 1549
SSR504734 is an orally active, selective and reversible inhibitor of human, rat, and mouse GlyT1 ( IC 50 =18, 15, and 38 nM, respectively). SSR504734 exhibits activity in schizophrenia, anxiety and depression models [1].
ţT90597 أй½
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T16525PhIPPhIP
PhIP is the most abundant generation of heterocyclic amines (HCA), resulted in the cooking of meat. PhIP also has oestrogenic activity that could contribute to its tissue-specific carcinogenicity.
ţT16525 أй½
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TN7215IsochiisanosideIsochiisanoside
Isochiisanoside is a natural product found in the leaves of Acanthopanax chiisanensis NAKAI.
ţTN7215 أй½
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TN71712,4,6-tribromobenzene-1,3,5-triol
2,4,6-tribromobenzene-1,3,5-triol is a marine derived natural products found in Rhabdonia verticillata.
ţTN7171 أй½
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T8402Regorafenib HydrochlorideRaf,PDGFR,Raf kinases,inhibit,Inhibitor,RET,Regorafenib Hydrochloride,Vascu
Regorafenib Hydrochloride is a new oral multikinase inhibitor of angiogenic, stromal and oncogenic receptor tyrosine kinases with potent preclinical antitumor activity
ţT8402 أй½
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T34398RotundifuranRotundifuran
Rotundifuran is extracted from the fruit of Vitex rotundifolia. Rotundifuran inhibits cell cycle progression and induces apoptosis in human myeloid leukemia cells.
ţT34398 أй½
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T8418DCLK1-IN-1DCLK1 IN 1,signaling,PDAC,KRAS,cancer,low,ERK,Inhibitor,selective,DCLK1IN1,inhibit,DCLK-1-
DCLK1-IN-1 is a selective and in vivo-compatible chemical probe of the DCLK1 kinase domain .
ţT8418 أй½
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T124663Sericoside
Sericoside is a triterpenoid with anti-inflammatory activity, can be isolated form Terminalia. Sericoside has a strong lipolytic activity. Sericoside can also reduce skin wrinkles and ameliorating skin texture.
ţT124663 أй½
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TN71495-[(1H-indol-3-yl)methylidene]imidazolidine-2,4-dione
5-[(1H-indol-3-yl)methylidene]imidazolidine-2,4-dione is a marine derived natural products found in Leptopsammia pruvoti.
ţTN7149 أй½
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T9353OXOMEMAZINEhistamine H1-receptor,OXOMEMAZINE,Histamine Receptor,inhibit,phenothiazine,antimuscarinic
Oxomemazine is a phenothiazine-based histamine H1-receptor blocker with pronounced antimuscarinic activity. Oxomemazine is a selective antagonist of mycotoxins M1 receptors, showing high (Ki=84 nM, M1 receptors) and low (Ki=1.65 M, M2 receptors) affinity sites 20 times the difference[1]. Oxomemazine is an antihistamine and anticholinergic agent used in studies related to cough studies[2].
ţT9353 أй½
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TN2315XanthopurpurinXanthopurpurin,Inhibitor,inhibit,Purpuroxanthin
Xanthopurpurin shows antiviral activity. Xanthopurpurin can effectively inhibit rotavirus multiplication by promoting virus-induced apoptosis in MA-104 cells. Xanthopurpurin shows mainly strong inhibition of collagen-induced platelet aggregation.
ţTN2315 أй½
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T28743Seglitide acetate
Seglitide acetate is a selective agonist of sst2 somatostatin receptor.
ţT28743 أй½
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T9782Cytochrome CCytochrome C
Cytochrome C, a protein that belongs to class 1 of the c-type cytochrome family, exerts different functions depending on its cellular localization and the conditions in which it operates.
ţT9782 أй½
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T7126Hydroquinineinhibit,Hydroquinine,Inhibitor
Hydroquinine, is an organic compound and as a cinchona alkaloid closely related to quinine.
ţT7126 أй½
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T6S1683DemethoxycurcuminBacterial,Inhibitor,Autophagy,Demethoxycurcumin,inhibit,Apoptosis
1. Demethoxycurcumin has antioxidant activity. 2. Demethoxycurcumin has anti-inflammatory activity. 3. Demethoxycurcumin has anti-proliferative activity. 4. Demethoxycurcumin has anti-acanthamoebic effect. 5. Demethoxycurcumin is a potential additive natural product in combination with chemotherapeutic agents in drug-resistant cancers. 6. Demethoxycurcumin inhibits energy metabolic and oncogenic signaling pathways through AMPK activation in triple-negative breast cancer cells.
ţT6S1683 أй½