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T4987NSC 42196葡庚糖酸钙水合物；Calcium glucoheptonate；Calcium α-D-heptagluconate hydrate
Calcium glucoheptonate is the calcium salt of (2xi)-D-gluco-heptonic acid. It is used as a calcium supplement for treatment of hypocalcemia.
价 格：￥电议型 号：T4987产 地：中国大陆
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T4968KHS 101
KHS101 is a novel inhibitor of transforming acidic coiled-coil protein 3 (TACC3). It is a selective inducer of neuronal differentiation.
价 格：￥电议型 号：T4968产 地：中国大陆
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T4967NPS-2143 hydrochloride2-氯-6-[(2R)-3-[[1,1-二甲基-2-(2-萘基)乙基]氨基]-2-羟基丙氧基]苯腈盐酸盐；NPS-2143 HCL
NPS-2143 is a selective potent calcium ion-sensing receptor antagonist.
价 格：￥电议型 号：T4967产 地：中国大陆
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T4966Ufenamate氟芬那酸丁酯；氟灭酸丁酯；Flufenamic acid butyl ester；Butyl flufenamate
Ufenamate is an anthranilic acid-based anti-inflammatory drug developed for skin diseases
价 格：￥电议型 号：T4966产 地：中国大陆
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T4965TCS-OX2-29
TCS-OX2-29 is a potent and selective OX2 receptor antagonist (IC50: 40 nM). It displays >250-fold selectivity for OX2 over OX1.
价 格：￥电议型 号：T4965产 地：中国大陆
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T4964steviolbiosideCCRIS-6025；菊双糖甙；甜菊双糖苷
Steviolbioside is a natural sweetener, it presents notable inhibition on human hepatocarcinoma cell Hep3B, human breast cancer cell MDA-MB-231 and human pancreatic cancer cell BxPC-3, thus, steviolbioside could be a potential remedy for human breast cance
价 格：￥电议型 号：T4964产 地：中国大陆
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T4963HigenamineDemethyl-Coclaurine；去甲乌药碱
Higenamine is a novel α1 -adrenoceptor antagonist.
价 格：￥电议型 号：T4963产 地：中国大陆
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T4960VASICINE
Vasicine is oxytocic and abortifacient agents.Vasicine, a potential natural cholinesterase inhibitor, has been in development for treatment of Alzheimer´s disease. Vasicine can regulate the inflammatory reaction, have great potentials to develop safe medi
价 格：￥电议型 号：T4960产 地：中国大陆
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T4896D-LyxoseD-(-)-Lyxose；来苏糖
D-(-)-Lyxose is used as a chiral building block.
价 格：￥电议型 号：T4896产 地：中国大陆
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T4783JNJ0966
JNJ0966 is a highly selective MMP-9 zymogen inhibitor (IC50: 440 nM).
价 格：￥电议型 号：T4783产 地：中国大陆
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T4696BMS202 hydrochloride (1675203-84-5(free base))PD-1/PD-L1 inhibitor 2 hydrochloride
PD-1/PD-L1 inhibitor 2 is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50: 18 nM). Biophysical studies demonstrate that BMS202 binds directly to PD-L1. Binding of BMS202 promotes PD-L1 dimerisation and blocks the PD-L1/ PD1 interaction.
价 格：￥电议型 号：T4696产 地：中国大陆
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T4613Arg-Gly-Asp TFA (99896-85-2(free base))RGD；RGD Trifluoroacetate
RGD Trifluoroacetate is a tripeptide that effectively triggers cell adhesion, addresses certain cell lines and elicits specific cell responses; binds to integrins.
价 格：￥电议型 号：T4613产 地：中国大陆
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T45964-IBP
4-IBP is a selective σ1 agonist with a high level of affinity for the σ1 receptor (Ki = 1.7 nM) and a moderate affinity for the σ2 receptor (Ki = 25.2 nM) .
价 格：￥电议型 号：T4596产 地：中国大陆
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T4496LM22B-10LM22B10；LM22B 10
LM22B-10 is an activator of TrkB/TrkC neurotrophin receptor and can induce TrkB, TrkC, ERK and AKT activation in vitro and in vivo.
价 格：￥电议型 号：T4496产 地：中国大陆
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T4418GSK2879552 2HCl (1401966-69-5(free base))
GSK2879552 is an orally available, irreversible inhibitor of lysine specific demethylase 1 (LSD1), with potential antineoplastic activity.
价 格：￥电议型 号：T4418产 地：中国大陆
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T4396Officinalisinin I
Officinalisinin I can effectively reduce the blood glucose and protect nerve injuryin diabetic mice.
价 格：￥电议型 号：T4396产 地：中国大陆
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T4343A-196A196；A 196
A-196 is a potent and selective inhibitor of SUV420 h1 and SUV420 h2 with IC50 values of 0.025 and 0.144 μM, respectively; more than 100-fold selective over other histone methyltransferases and non-epigenetic targets.
价 格：￥电议型 号：T4343产 地：中国大陆
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T4324PQ401 hydrochloride (196868-63-0(free base))
PQ401 inhibits autophosphorylation of IGF-1R domain with IC50 of <1 μM.
价 格：￥电议型 号：T4324产 地：中国大陆
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T4308F1063-0967
F1063-0967 is a Dual-specificity phosphatase 26 (DUSP26) inhibitor with an IC50 of 11.62 μM.
价 格：￥电议型 号：T4308产 地：中国大陆
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T4298JNJ-47965567JNJ-479655
JNJ-47965567 is a selective antagonist of the purinergic receptor P2X subtype 7 (P2X7), a ligand-gated ion channel(with pKis of 7.9 and 8.7 for human and rat P2X7, respectively).
价 格：￥电议型 号：T4298产 地：中国大陆
