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T12910Sigma-1 receptor antagonist 1；化合物Sigma-1 receptor antagonist 1Sigma-1 receptor antagonist 1
Sigma-1 receptor antagonist 1 is an effective and selective antagonist of sigma-1 receptor. Sigma-1 receptor antagonist 1 exhibits antineuropathic pain activity and can be used in the treatment of neuropathic pain studies.
价 格：￥电议型 号：T12910产 地：中国大陆
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T1291Cisapride；西沙比利Prepulsid|||R 51619|||Pridesia|||Kaudalit|||(±)-Cisaprid|||Kinestase；西沙必利|||西沙比利|||Pre
Cisapride (R 51619) is a serotonin type 4 (5-HT4) receptor agonists are potent prokinetic agents that act on serotonin receptors in the intestine and promote intestinal peristalsis, increase gastric emptying and decrease esophageal reflux.
价 格：￥电议型 号：T1291产 地：中国大陆
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T12909SID 26681509；化合物SID 26681509SID 26681509
SID 26681509 is a selective, reversible and competitive human cathepsin L inhibitor (IC50 of 56 nM).
价 格：￥电议型 号：T12909产 地：中国大陆
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T12907SIAIS178；化合物 T12907SIAIS178
SIAIS178 is a potent and selective degrader of BCR-ABL based on PROTAC technology (IC50 of 24 nM).
价 格：￥电议型 号：T12907产 地：中国大陆
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T12905SI-109；化合物 T12905SI-109
SI-109 is a potent inhibitor of STAT3 SH2 domain (Ki=9 nM),and with antitumor activity.
价 格：￥电议型 号：T12905产 地：中国大陆
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T12904SHR1653；化合物 T12904SHR1653
SHR1653 is a highly potent, selective and brain penetrated antagonist of oxytocin receptor (OTR)(IC50 of 15 nM for hOTR).
价 格：￥电议型 号：T12904产 地：中国大陆
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T12903SHP2 IN-1；化合物 T12903SHP2 IN-1
SHP2 IN-1 is an allergic SHP2 (PTPN11) inhibitor(IC50 : 3 nM).
价 格：￥电议型 号：T12903产 地：中国大陆
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T12902SHMT-IN-1；化合物SHMT-IN-1SHMT-IN-1
SHMT-IN-1 is a potent plasmodial serine hydroxymethyltransferase (SHMT) inhibitor with antitumor activity.
价 格：￥电议型 号：T12902产 地：中国大陆
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T12901SHIP2-IN-1；化合物SHIP2-IN-1SHIP2-IN-1
SHIP2-IN-1 is a potent SHIP2 inhibitor(IC50 : 2 ?M),and used in the research of Alzheimer’s disease.
价 格：￥电议型 号：T12901产 地：中国大陆
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T12900LSetiptiline maleate马来酸司普替林MO-8282|||马来酸司普替林
Setiptiline maleate is an antagonist of serotonin receptor.
价 格：￥电议型 号：T12900L产 地：中国大陆
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T12900Setiptiline司普替林Org-8282|||司普替林
Setiptiline(Org-8282) is an antagonist of serotonin receptor.
价 格：￥电议型 号：T12900产 地：中国大陆
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T1290Oxiconazole nitrate；硝酸奥昔康唑Ro 13-8996；硝酸奥昔康唑|||Ro 13-8996
Oxiconazole nitrate (Ro 13-8996) is the nitrate salt form of oxiconazole, a broad spectrum imidazole derivative with antifungal activity. Although the exact mechanism of action has yet to be fully elucidated, oxiconazole, like other azole antifungals, most likely inhibits the cytochrome P450-dependent demethylation of lanosterol. This prevents the synthesis of ergosterol which is a crucial component of fungal cell membrane. By disrupting fungal cell membrane synthesis and integrity, oxiconazole
价 格：￥电议型 号：T1290产 地：中国大陆
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T12898(+)-SHIN1；化合物 T12898(+)-RZ-2994；(+)-RZ-2994
(+)-SHIN1 ((+)-RZ-2994) is an active (+) enantiomer of SHIN1 [1]. SHIN1 is a human serine hydroxymethyltransferse 1 and 2 (SHMT1/2) inhibitor.
价 格：￥电议型 号：T12898产 地：中国大陆
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T12897LSHIN1；化合物SHIN1RZ-2994；RZ-2994
SHIN1 (RZ-2994) is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.
价 格：￥电议型 号：T12897L产 地：中国大陆
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T12897(-)-SHIN1；化合物 T12897(-)-RZ-2994；(-)-RZ-2994
(-)-SHIN1 ((-)-RZ-2994) is an inactive( ) enantiomer of SHIN1.
价 格：￥电议型 号：T12897产 地：中国大陆
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T12851SB290157 trifluoroacetate；化合物SB290157 trifluoroacetateSB290157 trifluoroacetate
SB290157 trifluoroacetate is a potent and selective antagonist of C3a receptor(IC50 of 200 nM).
价 格：￥电议型 号：T12851产 地：中国大陆
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T1284Megestrol acetate；醋酸甲地孕酮SC10363|||BDH1298；SC10363|||醋酸甲地孕酮|||BDH1298
Megestrol acetate (BDH1298) is a progestogen with actions and uses similar to those of the progestogens in general. Megestrol acetate also has anti-androgenic properties. It is given by mouth in the palliative treatment or as an adjunct to other therapy in endometrial carcinoma and in breast cancer. Megestrol acetate has been approved to treat anorexia and cachexia.
价 格：￥电议型 号：T1284产 地：中国大陆
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T12763Ro 41-3290；化合物 T12763Ro 41-3290
Ro 41-3290 is the desethylated derivative of Ro 41-3696, which is an agonist of nonbenzodiazepine partial at the benzodiazepine receptor.
价 格：￥电议型 号：T12763产 地：中国大陆
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T12729RIPK1-IN-3；化合物 T12729RIPK1-IN-3
RIPK1-IN-3 is a RIPK1 inhibitor, with anti-inflammatory proprieties.
价 格：￥电议型 号：T12729产 地：中国大陆
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T12720Prinoxodan化合物 T12720RGW2938
Prinoxodan is an inhibitor of phosphodiesterase.
价 格：￥电议型 号：T12720产 地：中国大陆
