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T4193TD-198946TD 198946；TD198946
TD-198946, a potent chondrogenic agent, is a thienoindazole derivative.
价 格：￥电议型 号：T4193产 地：中国大陆
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T40686TiazofurinTiazofurin；NSC 286193；Riboxamide
Tiazofurin is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin is anabolized intracellularly to tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH) .
价 格：￥电议型 号：T40686产 地：中国大陆
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T38193Lβ-Endorphin (1-27) (human) acetateβ-Endorphin (1-27) (human) acetate(76622-84-9 Free base)
β-Endorphin (1-27) (human) acetate, existing in the hypophysis cerebri and hypothalamus, exhibits antinociception activity. β-Endorphin (1-27) (human) acetate is an agonist of opioid receptor, showing preferred affinity for μ-opioid receptor and δ-opioid
价 格：￥电议型 号：T38193L产 地：中国大陆
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T36968ARN-21934
ARN-21934 is a potent and selective inhibitor for human topoisomerase II α and topoisomerase II β. ARN-21934(IC50 = 2 μM) inhibits DNA relaxation as compared to the anticancer agent Etoposide (IC50=120 μM).
价 格：￥电议型 号：T36968产 地：中国大陆
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T3539Lu AF21934
Lu AF21934 is a brain-penetrant and selective mGlu4 receptor positive allosteric modulator (IC50: 500 nM, human).
价 格：￥电议型 号：T3539产 地：中国大陆
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T3193Pimelic diphenylamide 106TC-H 106；RGFA-8；Histone Deacetylase Inhibitor VII
Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I HDAC (with IC50 values of 150 nM , 760 nM and 370 nM for HDAC 1, 2, and 3, respectively), showing no activity against class II HDACs.
价 格：￥电议型 号：T3193产 地：中国大陆
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T3180JNJ-42041935HIF-PHD Inhibitor II
JNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and selective inhibitor of PHD enzymes.
价 格：￥电议型 号：T3180产 地：中国大陆
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T2S1193Mogroside III-A1罗汉果苷 III-A1
Mogroside III-A1 is a triterpenoid glycoside from Siraitia grosvenorii Swingle. Mogroside III-A1 a nonsugar sweetener.
价 格：￥电议型 号：T2S1193产 地：中国大陆
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T26193SKLB-163SKLB163；SKLB 163
SKLB-163 acts by downregulating RhoGDI, activating JNK-1 signaling pathway and caspase-3, and reducing phosphorylated Akt and p44/42 MAPK.
价 格：￥电议型 号：T26193产 地：中国大陆
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T22103ML-193ML193；CID 1261822
ML-193 is a potent and selective GPR55 antagonist( IC50 : 221 nM). It shows more than 27-fold selectivity for GPR55 over GPR35, CB1 and CB2, and can improve the motor and the sensorimotor deficits of Parkinson’s disease (PD) rats.
价 格：￥电议型 号：T22103产 地：中国大陆
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T21938AS-041164
AS-041164 is a selective and orally active PI3Kγ isoform inhibitor(IC50 of 70 nM), and shows less activity against PI3Kα, PI3Kβ, and PI3Kδ (IC50s of 240 nM, 1.45 μM, and 1.70 μM, respectively). It has anti-inflammatory effects.
价 格：￥电议型 号：T21938产 地：中国大陆
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T21936M500542,2′-亚甲基双(1,3-环己二酮)
Apoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition.
价 格：￥电议型 号：T21936产 地：中国大陆
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T21935LAMN082 free baseAMN082
AMN082 is a metabotropic glutamate receptor 7 allosteric agonist.
价 格：￥电议型 号：T21935L产 地：中国大陆
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T21674LPKA inhibitor fragment (6-22) amide AcetatePKA inhibitor fragment (6-22) amide Acetate(121932-06-7 F
PKA Inhibitor Fragment (6-22) amide Acetate is a PKA inhibitor with a Ki of 2.8 nM. It can significantly reverse low-level morphine antinociceptive tolerance in mice.
价 格：￥电议型 号：T21674L产 地：中国大陆
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T21193Isoflupredone Acetate
Isoflupredone Acetate is a corticosteroid with the activity of topical anti-inflammatory.
价 格：￥电议型 号：T21193产 地：中国大陆
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T1943ML347LDN 193719
ML347(DN193719) is a highly specific ALK1/2 inhibitor ( IC50: 46/32 nM), and the selectivity for ALK2 is >300-fold than ALK3.
价 格：￥电议型 号：T1943产 地：中国大陆
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T19399L-Ornithine L-aspartateOrnithine Aspartate；L-鸟氨酸 L-天冬氨酸
L-Ornithine L-aspartate lowers blood ammonia concentration and to eliminate symptoms of hepatic encephalopathy associated with liver cirrhosis.
价 格：￥电议型 号：T19399产 地：中国大陆
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T19397L-Methionine sulfoxideL-蛋氨酸亚砜；H-Met(O)-OH
L-Methionine sulfoxide (H-Met(O)-OH) is a metabolite of Methionine. (H-Met(O)-OH) modulates oxidative stress and purinergic signaling parameters, and induces M1/classical macrophage polarization.
价 格：￥电议型 号：T19397产 地：中国大陆
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T1939DMOG二甲基草酰甘氨酸；Dimethyloxaloylglycine；Dimethyloxalylglycine；Dimethyloxallyl Glycine
DMOG, an antagonist of the α-ketoglutarate cofactor, is an inhibitor for HIF prolyl hydroxylase.
价 格：￥电议型 号：T1939产 地：中国大陆
