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T10872CP-96021 hydrochloride；化合物 T10872CP-96021 hydrochloride
CP-96021 hydrochloride is a potent and orally active antagonist of leukotriene D4 (LTD4)/platelet activating factor receptor (Kis: 34 nM and 37 nM).
价 格：￥电议型 号：T10872产 地：中国大陆
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T10860Col003；化合物Col003Col003
Col003 is a selective and potent inhibitor of Hsp47 and competitively binds to the collagen-binding site on Hsp47 (IC50: 1.8 μM). It can be used for the investigation of fibrosis.
价 格：￥电议型 号：T10860产 地：中国大陆
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T10760Ceramides Mixture神经酰胺混合物神经酰胺混合物|||神经酰胺
Ceramides Mixture, an endogenous ceramide, consists of hydroxy and non-hydroxy fatty acid-containing ceramides. It is involved in the regulation of cell cycle arrest, growth inhibition, and modulation of telomerase activity.
价 格：￥电议型 号：T10760产 地：中国大陆
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T10759CEP-28122 mesylate salt (1022958-60-6 free base)；化合物CEP-28122 mesylate saltCEP-28122 mesylate salt；C
CEP-28122 mesylate salt (1022958-60-6 free base) is a highly selective orally active ALK inhibitor (IC50: 1.9 nM in an enzyme-based TRF assay).
价 格：￥电议型 号：T10759产 地：中国大陆
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T10749Cebranopadol ((1α,4α)stereoisomer)；化合物 T10749GRT6005 (1α,4α)stereoisomer；GRT6005 (1α,4α)stereoisomer
Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol which is a potent ORL-1 agonist.
价 格：￥电议型 号：T10749产 地：中国大陆
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T10732Tematropium；化合物TematropiumCDDD3602|||Tematropium metilsulfate|||HGP6；CDDD3602|||Tematropium metilsul
Tematropium (CDDD3602) possesses anticholinergic effects and can be used in neurological studies.
价 格：￥电议型 号：T10732产 地：中国大陆
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T10683Carmoxirole hydrochloride；卡莫昔罗EMD 45609 hydrochloride；EMD 45609 hydrochloride|||卡莫昔罗
Carmoxirole hydrochloride (EMD 45609 hydrochloride) is a selective dopamine D2 receptor agonist with antihypertensive activity in vivo.
价 格：￥电议型 号：T10683产 地：中国大陆
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T10660L2CAL-130 Racemate；化合物 T10660L2CAL-130 Racemate
CAL-130 Racemate is the racemate of CAL-130. CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660L2产 地：中国大陆
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T10660LCAL-130 Hydrochloride；化合物 T10660LCAL-130 Hydrochloride
CAL-130 Hydrochloride is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660L产 地：中国大陆
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T10660CAL-130；化合物 T10660CAL-130
CAL-130 is a PI3Kδ and PI3Kγ inhibitor (IC50s: 1.3 and 6.1 nM).
价 格：￥电议型 号：T10660产 地：中国大陆
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T10609Brevetoxin-3；化合物 T10609PbTx-3；PbTx-3
Brevetoxin-3 (PbTx-3) is a potent allosteric voltage-gated Na+ channel activator. Brevetoxin-3 has a high affinity to site 5 of the voltage-sensitive Na+ channels, inhibits the inactivation of Na+ channels.
价 格：￥电议型 号：T10609产 地：中国大陆
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T10608BRD5648；化合物BRD5648(R)-BRD0705；(R)-BRD0705
BRD5648 ((R)-BRD0705) is an inactive (R)-enantiomer of BRD0705. BRD0705 is a GSK3α inhibitor (IC50: 66 nM; Kd: 4.8 μM) and can be used in acute myeloid leukemia (AML) studies.
价 格：￥电议型 号：T10608产 地：中国大陆
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T10607BRD5631；化合物 T10607BRD5631
BRD5631 is an autophagy enhancer, enhances autophagy through an mTOR-independent pathway. BRD5631 affects several cellular disease phenotypes previously linked to autophagy, including protein aggregation, cell survival, bacterial replication, and inflammatory cytokine production. BRD5631 can serve as a valuable tool for studying the role of autophagy in the context of cellular homeostasis and disease. [1].
价 格：￥电议型 号：T10607产 地：中国大陆
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T10606BRD0705；化合物BRD0705BRD0705
BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor (IC50: 66 nM; Kd: 4.8 μM). BRD0705 displays increased selectivity for GSK3α (8-fold) versus GSK3β (IC50: 515 nM).
价 格：￥电议型 号：T10606产 地：中国大陆
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T10605BRD-K98645985；化合物 T10605BRD-K98645985
BRD-K98645985 is a BAF transcriptional repression inhibitor (EC50: ~2.37 μM). It binds ARID1A-specific BAF complexes, potently reverses HIV-1 latency and prevents nucleosomal positioning.
价 格：￥电议型 号：T10605产 地：中国大陆
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T10604BRD-IN-3；化合物 T10604BRD-IN-3
BRD-IN-3 is a highly potent PCAF bromodomain (BRD) inhibitor (IC50: 7 nM). It also exhibits activity against GCN5 and FALZ.
价 格：￥电议型 号：T10604产 地：中国大陆
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T10603BRD-6929；化合物BRD-6929BRD-6929
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: ?1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1.5 nM) [2]. BRD-6929 potentiates the efficacy of gnidimacrin (a PKC Agonist) against latent HIV-1. BRD-6929 can be used for mood-related behavioral model research[3].
价 格：￥电议型 号：T10603产 地：中国大陆
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T10602LBRD 4354；化合物BRD 4354BRD 4354
BRD 4354 is an inhibitor of HDAC5 and HDAC9. For HDAC5 and HDAC9, the IC50s values are 0.85 and 1.88 μM, respectively.
价 格：￥电议型 号：T10602L产 地：中国大陆
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T10602BRD 4354 ditrifluoroacetate；化合物 T10602BRD 4354 ditrifluoroacetate (315698-07-8 free base)；BRD 4354 d
BRD 4354 (ditrifluoroacetate) is a moderately potent inhibitor of HDAC5 and HDAC9 (IC50s: 0.85 and 1.88 μM).
价 格：￥电议型 号：T10602产 地：中国大陆
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T10601BRCA1-IN-2；BRCA1 抑制剂2BRCA1-IN-2
BRCA1-IN-2 is a cell membrane-crossing BRCA1 protein-protein interaction (PPI) inhibitor with antitumor activity that acts by disrupting the interaction of BRCA1 (BRCT)2 with proteins.
价 格：￥电议型 号：T10601产 地：中国大陆
