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T30092AP-24226；化合物 T3009253D46B0TIH|||UNII-53D46B0TIH|||CHEMBL556874；53D46B0TIH|||UNII-53D46B0TIH|||CHEMBL
AP-24226 is a potent dual Src/ ABL kinase inhibitor.
价 格：￥电议型 号：T30092产 地：中国大陆
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T30035-hydroxytryptophan；5-羟基色氨酸NSC-92523；5-羟基色氨酸|||NSC-92523
5-hydroxytryptophan (NSC-92523) is the immediate precursor in the biosynthesis of SEROTONIN from tryptophan. It is used as an antiepileptic and antidepressant.
价 格：￥电议型 号：T3003产 地：中国大陆
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T2S0837Astragalus Polysacharin；黄芪多糖2-(Chloromethyl)-4-(4-nitrophenyl)thiazole|||89250-26-0；2-(Chloromethyl)
2-(Chloromethyl)-4-(4-nitrophenyl)thiazole is a natural product derived from Astragalus propinquus.2-(Chloromethyl)-4-(4-nitrophenyl)thiazole exhibits anticancer activity. 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole possesses anticancer activity and has been shown to be active in hepatocellular carcinoma (HCC) by inhibiting the M2 polarization of tumor-associated macrophages (TAM).
价 格：￥电议型 号：T2S0837产 地：中国大陆
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T29925Alyssin, (S)-；化合物 T29925Alyssin, (S)-
Alyssin, (S)-, is an analogue of Sulforaphane that has been shown to have cytotoxic effect on CCRF-SB leukemia cells and lymphoblastoid cells.
价 格：￥电议型 号：T29925产 地：中国大陆
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T29670ADR-925；右丙亚胺杂质ICRF198|||ICRF-198|||ADR 925|||ICRF 198|||ADR925；ICRF198|||ICRF-198|||ADR 925|||ICRF 1
ADR-925 (ICRF 198), an active chelated iron metabolite of dexrazoxane, has the ability to protect neonatal rat cardiomyocytes from adriamycin-induced injury.
价 格：￥电议型 号：T29670产 地：中国大陆
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T29534ABT-925 fumarate dihydrate；化合物 T29534ABT 925|||LU201640|||ABT925|||ABT-925|||BSF201640|||DAT201；ABT
ABT-925 is a selective dopamine D3 receptor (DRD3) antagonist with an in vitro affinity approximately 100 times higher for dopamine D3 receptors than for D2 receptors.
价 格：￥电议型 号：T29534产 地：中国大陆
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T29258(R)-N-Desmethyl PK11195；化合物 T29258(R)-N-Desmethyl PK 11195|||(R)-N-Desmethyl PK-11195|||(R)-N Desmet
(R)-N-Desmethyl PK11195 is a precursor for (R)-[N-Methyl-11C-]PK11195.
价 格：￥电议型 号：T29258产 地：中国大陆
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T29257(Maleato)trioxotetralead；化合物 T29257(Maleato)trioxotetralead
(Maleato)trioxotetralead is a bioactive chemical.
价 格：￥电议型 号：T29257产 地：中国大陆
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T29255(E)-4-Undecenal；化合物 T29255(E)-4-Undecenal
(E)-4-Undecenal is a bioactive chemical.
价 格：￥电议型 号：T29255产 地：中国大陆
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T29254MK-0963；化合物 T29254MK-0963
(5Alpha)-23-methyl-4-aza-21-norchol-1-ene-3,20-dione is a bioactive chemical.
价 格：￥电议型 号：T29254产 地：中国大陆
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T29253(4) 2-Methyldecanal；化合物 T292532-Methyldecanal|||2-Methyl-1-decanal|||Decanal, 2-methyl-|||Methyl oct
(4) 2-Methyldecanal is a biochemical.
价 格：￥电议型 号：T29253产 地：中国大陆
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T29251(±)-GC242；化合物 T29251GC242|||(±) GC242；GC242|||(±) GC242
(±)-GC242 is a profluorescent RAMOSUS3 (RMS3) probe with strigalactone-like biological activity.
价 格：￥电议型 号：T29251产 地：中国大陆
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T2925Schisandrin B；五味子乙素gamma-Schisandrin|||Schizandrin B|||Schisandrin B (Sch B)|||Wuweizisu-B；gamma-Sch
Schisandrin B (Schisandrin B (Sch B)) has an antioxidant effect on rodent liver and heart.
价 格：￥电议型 号：T2925产 地：中国大陆
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T29140VU0652925；化合物 T29140VU 0652925|||BMS-3|||VU-0652925|||BMS3|||BMS 3；VU 0652925|||BMS-3|||VU-0652925||
VU0652925 is a PAR4 antagonist. VU0652925 has a P-sel IC50 of 39.2 pM (-pIC50±SEM: 10.41±0.04) and a PAC1 IC50 of 43.0 pM (-pIC50±SEM: 10.4±0.04).
价 格：￥电议型 号：T29140产 地：中国大陆
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T28925TASP0376377；化合物 T28925TASP-0376377|||TASP0376377|||TASP 0376377|||TASP0376377|||TASP-0376377|||TASP-
TASP0376377 is a potent antagonist of CRTH2.
价 格：￥电议型 号：T28925产 地：中国大陆
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T27925LY 88329；化合物 T27925LY-88329|||LY88329；LY-88329|||LY88329
LY 88329 is a narcotic antagonist in the class of phenylpiperidine.
价 格：￥电议型 号：T27925产 地：中国大陆
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T27689JNJ-7925476 HCl；化合物 T27689JNJ-7925476|||JNJ7925476|||JNJ 7925476；JNJ-7925476|||JNJ7925476|||JNJ 7925
JNJ-7925476 HCl is a triple monoamine uptake inhibitor. JNJ-7925476 Salt blocks the dopamine transporter (DAT), norepinephrine transporter (NET) and serotonin transporter (SERT) in the central nervous system. The ED(50) values for JNJ-7925476 occupancy of the DAT, NET and SERT in rat brain were 2.4, 0.09, 0.18 and mg/kg, respectively.
价 格：￥电议型 号：T27689产 地：中国大陆
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T27663JNJ-17029259；化合物 T27663JNJ 17029259；JNJ 17029259
JNJ-17029259 is an orally selective, potent inhibitors of the vascular endothelial growth factor receptor-2 (VEGF-R2).
价 格：￥电议型 号：T27663产 地：中国大陆
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T27003Cheirolin；化合物 T27003BRN1768925|||BRN 1768925|||BRN-1768925；BRN1768925|||BRN 1768925|||BRN-1768925
Cheirolin, an antioxidant and sulfonyl analog of sulforaphane, induces phase II enzyme activity and expression.
价 格：￥电议型 号：T27003产 地：中国大陆
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T26925Butaprost；化合物 T26925Butaprostum|||TR-4979|||(R)-Butaprost；Butaprostum|||TR-4979|||(R)-Butaprost
Butaprost is a chemical compound that functions as a selective agonist for the prostaglandin E receptor (EP2). It exhibits an EC50 of 33 nM and a Ki of 2.4 μM when interacting with the murine EP2 receptor. However, Butaprost demonstrates lower activity against murine EP1, EP3, and EP4 receptors. Furthermore, it effectively attenuates fibrosis by inhibiting the TGF-β/Smad2 signaling pathway [1] [2] [3].
价 格：￥电议型 号：T26925产 地：中国大陆
