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T28475Pyrazoloacridine；化合物PyrazoloacridinePD-115934|||NSC 366140|||NSC-366140|||PD 115,934|||PD 115934；PD-
Pyrazoloacridine (PD 115934) is a nucleic acid binding agent that inhibits the activity of topo I and II with an IC50 of 1.25 μM in K562 cells. Pyrazoloacridine shows anti-cancer activity.
价 格：￥电议型 号：T28475产 地：中国大陆
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T28344PD159790；化合物 T28344PD-159790|||PD 159790；PD-159790|||PD 159790
PD159790 is an selective inhibitor of ECE-1.
价 格：￥电议型 号：T28344产 地：中国大陆
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T28159Nerisopam；化合物NerisopamEGIS-6775|||GYKI 52322|||GYKI52322|||EGIS6775|||GYKI-52322；EGIS-6775|||GYKI 52
Nerisopam is an agonist of gamma-aminobutyric acid (GABA) receptor.
价 格：￥电议型 号：T28159产 地：中国大陆
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T28134NC00075159；化合物 T28134NC 00075159|||NC-00075159；NC 00075159|||NC-00075159
NC00075159 is an opener of human KCNQ4 (Kv7.4) potassium channel.
价 格：￥电议型 号：T28134产 地：中国大陆
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T27723LKDM5-C49 HCl；KDM5-C49醋酸盐KDM5-C49 HCl(1596348-16-1 Free base)|||KDOAM-20 hydrochloride；KDM5-C49 H
KDM5-C49 HCl (KDOAM-20 hydrochloride) is a potent and selective inhibitor of KDM5 demethylase. KDM5-C49 HCL(1596348-16-1 Free base) is a candidate compound for the treatment of cancer.
价 格：￥电议型 号：T27723L产 地：中国大陆
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T26697AX15910；化合物 T26697AX-15910|||AX 15910；AX-15910|||AX 15910
AX15910 is a potent inhibitor of BRD4 and ERK5.
价 格：￥电议型 号：T26697产 地：中国大陆
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T26159Rubiflavin；化合物 T26159B17476|||B 17476|||B-17476；B17476|||B 17476|||B-17476
Rubiflavin is an antitumor antibiotic belonging to the pluramycin family.
价 格：￥电议型 号：T26159产 地：中国大陆
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T25159Bisnafide；化合物 T25159DMP 840；DMP 840
Bisnafide is a Naphthalimide Analogue that acts as a DNA intercalator and topo II inhibitor. It is also an antiangiogenic agent that can normalize tumor vessels and promote the delivery of cytotoxic agents to tumor sites.
价 格：￥电议型 号：T25159产 地：中国大陆
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T24772SCH-351591；化合物 T24772SCH351591|||SCH 351591|||D4396|||D 4396|||D-4396；SCH351591|||SCH 351591|||D4396
SCH-351591 is an orally active inhibitor of phosphodiesterase 4.
价 格：￥电议型 号：T24772产 地：中国大陆
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T2435LEPZ011989 HCl(1598383-40-4 Free base)；化合物 EPZ011989 HClEPZ-011989 TFA|||EPZ011989 TFA salt|||EPZ 011
EPZ011989 is a highly potent and selective oral EZH2 inhibitor with Ki value <3 nM.
价 格：￥电议型 号：T2435L产 地：中国大陆
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T24159IHR-1；化合物IHR-1IHR 1；IHR 1
IHR-1 is a Potent Smo antagonist (IC50 = 7.6 nM). Selectively inhibits Hedgehog signaling over Wnt and Notch signaling pathways. Blocks Smo accumulation in primary cilium in vitro.
价 格：￥电议型 号：T24159产 地：中国大陆
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T23900Clothiapine；氯噻平S-805C|||HF2159|||HF 2159|||HF-2159|||LW 2159；S-805C|||HF2159|||HF 2159|||HF-2159|||L
Clothiapine (HF 2159) is an atypical antipsychotic agent with potent anti 5-hydroxytryptaminergic and serotonergic activity, which has been used in the study of schizophrenia.
价 格：￥电议型 号：T23900产 地：中国大陆
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T23879Chartreusin；化合物 T23879NSC5159|||NSC 5159|||NSC-5159；NSC5159|||NSC 5159|||NSC-5159
Chartreusin is an antibiotic. It also has anticancer activity.
价 格：￥电议型 号：T23879产 地：中国大陆
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T23744Antibiotic Z-1159-2；化合物 T23744Z-1159-2；Z-1159-2
Antibiotic Z-1159-2 is an agent of biochemical.
价 格：￥电议型 号：T23744产 地：中国大陆
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T23743Antibiotic Z-1159-1；化合物 T23743Z-1159-1；Z-1159-1
Antibiotic Z-1159-1 is an agent of biochemical.
价 格：￥电议型 号：T23743产 地：中国大陆
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T23479LTT-232 TFA（147159-51-1 free base）；化合物TT-232 TFATT-232 TFA（147159-51-1 free base）
TT2-32 TFA induces a biphasic activation of phosphotyrosine phosphatase activity in human colon tumor cell line, SW620
价 格：￥电议型 号：T23479L产 地：中国大陆
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T23159Pimobendan hydrochloride；盐酸匹莫苯丹Pimobendan hydrochloride
Pimobendan hydrochloride is a selective inhibitor of PDE3 (IC50: 0.32 μM).
价 格：￥电议型 号：T23159产 地：中国大陆
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T22159TCS HDAC6 20b；化合物 T22159TCS HDAC6 20b
TCS HDAC6 20b is a HDAC6 -selective inhibitor that blocks the growth of estrogen receptor α-positive breast cancer MCF-7 cells [1].
价 格：￥电议型 号：T22159产 地：中国大陆
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T21872CCT018159；化合物CCT018159CCT018159
CCT018159 is a 3,4-diarylpyrazole resorcinol, an ATP-competitive HSP90ATPase inhibitor that inhibits human Hsp90β and yeast Hsp90 with IC50s of 3.2 and 6.6 μM, respectively.CCT018159 inhibits key endothelial and tumor cell functions associated with invasion and angiogenesis. CCT018159 caused cellular inhibition associated with G1 phase block and induced apoptosis.
价 格：￥电议型 号：T21872产 地：中国大陆
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T21598LG3335 Acetate；化合物G3335 AcetateG3335 Acetate (36099-95-3 free base)；G3335 Acetate (36099-95-3 free ba
G3335 Acetate was discovered to be a novel PPARgamma antagonist.
价 格：￥电议型 号：T21598L产 地：中国大陆
