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TN15171-(2,6-dimethoxyphenyl)-3-(4-hydroxyphenyl)propan-1-one1(2,6dimethoxyphenyl)3(4hydroxyphenyl)propan1
Cochinchinenin A is the material basis for the analgesic effect of Dragons Blood.
价 格：￥电议型 号：TN1517产 地：中国大陆
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TN1517LCochinchinenin ACochinchinenin A
Cochinchinenin A is the material basis for the analgesic effect of Dragons Blood.
价 格：￥电议型 号：TN1517L产 地：中国大陆
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T21548PF-4981517
CYP3cide (PF-4981517) is a efficient, specific and time-dependent inhibitor of cytochrome P4503A4 (CYP3A4). The IC 50 values for Midazolam 1’-hydroxylase activity are 0.03 μM, 17 μM, and 71 μM for CYP3A4, CYP3A5, and CYP3A7, respectively. CYP3cide is able to be used to distinguish the contributions of CYP3A4 versus CYP3A5 on drug metabolism [1].
价 格：￥电议型 号：T21548产 地：中国大陆
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T2493PD 151746
PD 151746 is a selective, cell-permeable calpain inhibitor (Ki: 0.26/5.33 μM, μ-Calpain/m-calpain).
价 格：￥电议型 号：T2493产 地：中国大陆
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T2041PD153035SU-5271；AG1517；NSC 669364；ZM 252868
PD153035 hydrochloride is an effective and selective inhibitor of EGFR (Ki/IC50: 5.2/29 pM, in cell-free assays); little inhibitory against FGFR, PGDFR, InsR, CSF-1 and Src.
价 格：￥电议型 号：T2041产 地：中国大陆
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T1761PD153035 hydrochlorideTyrphostin AG 1517；SU 5271；ZM 252868 HCl；PD153035 HCl；ZM 252868；AG 1517
PD153035 hydrochloride (ZM 252868; AG 1517) is a effective and selective inhibitor of EGFR (Ki: 5.2 pM, IC50: 29 pM); few influence against FGFR, PGDFR, InsR, CSF-1, and Src.
价 格：￥电议型 号：T1761产 地：中国大陆
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T15179DTSSP Crosslinker
DTSSP Crosslinker is a cleavable ADC linker and can be used to synthesize antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15179产 地：中国大陆
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T15176DSS Crosslinker
DSS Crosslinker is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).It is a homobifunctional crosslinker that is cell membrane permeable. DSS crosslinker has amine-reactive NHS esters at both ends of an 8-atom (11.4 angs
价 格：￥电议型 号：T15176产 地：中国大陆
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T15175DSP Crosslinker
DSP Crosslinker is a cleavable ADC linker, used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15175产 地：中国大陆
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T15171DSG Crosslinker
DSG Crosslinker is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T15171产 地：中国大陆
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T1517Benserazide hydrochlorideBenserazide HCl；盐酸苄丝肼；Serazide；Ro 4-4602
Benserazide Hydrochloride is a peripherally-acting L-amino acid decarboxylase (AAAD) or DOPA decarboxylase inhibitor.
价 格：￥电议型 号：T1517产 地：中国大陆
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T11517GV-58
GV-58 is a selective N- and P/Q-type Ca2+ channels agonist (EC50: 7.21/8.81 uM for N-type/P-Q-type Ca2+ channel). The inhibitory of GV-58 is 20-fold fewer for CDK kinases activity.
价 格：￥电议型 号：T11517产 地：中国大陆
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T11517GV-58GV-58
GV-58 is a potent, selective N- and P/Q-type Ca2+ channels agonist with EC50 of 7.21/8.81 uM for N-type/P-Q-type Ca2+ channel; 20-fold less potent CDK inhibitor activity. Ca2+ channel agonist In comparison with the parent molecule, (R)-roscovitine, GV-58
价 格：￥电议型 号：T11517产 地：美洲
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T1517Benserazide hydrochlorideBenserazide hydrochloride,Ro 4-4602,Serazide
Benserazide Hydrochloride is a peripherally-acting L-amino acid decarboxylase (AAAD) or DOPA decarboxylase inhibitor.
价 格：￥电议型 号：T1517产 地：美洲
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T15172DSHS00884DSHS00884,SSYA10-001,
DSHS00884 is a potent inhibitor of human papillomavirus E6(IC50: 10 μM).
价 格：￥电议型 号：T15172产 地：美洲
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T15173DSM265DSM265
DSM265 is a long-duration P. falciparum dihydroorotate dehydrogenase inhibitor (IC50: 8.9 nM). DSM265 can also inhibit the growth of Pf3D7 parasites (EC50: 4.3 nM).
价 格：￥电议型 号：T15173产 地：美洲
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T15176DSS CrosslinkerDSS Crosslinker
DSS Crosslinker is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15176产 地：美洲
