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T25646LB-30057；化合物 T25646PD 172524 free base|||LB-30057 free base|||CI-1028 free base|||PD172524 free base
LB-30057 is used as an oral thrombin inhibitor.
价 格：￥电议型 号：T25646产 地：中国大陆
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T24916UBP646；化合物 T24916UBP-646|||UBP 646；UBP-646|||UBP 646
UBP646 is a GluN1/GluN2 receptors potentiator.
价 格：￥电议型 号：T24916产 地：中国大陆
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T24646PK-3；化合物 T24646CID-20959075|||CID 20959075|||CID20959075；CID-20959075|||CID 20959075|||CID20959075
PK-3 is a cancer cell growth inhibitor. It also has microtubule-binding activity.
价 格：￥电议型 号：T24646产 地：中国大陆
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T2452C646；化合物C646C646
C646 is an inhibitor of histone acetyltransferase p300 (Ki=400 nM), which is competitive and selective, with less effect on other acetyltransferases. C646 acts as an apoptosis inducer and radiosensitizer.
价 格：￥电议型 号：T2452产 地：中国大陆
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T2433NU 7026；化合物NU7026NU7026|||DNA-PK Inhibitor II|||LY293646；NU7026|||DNA-PK Inhibitor II|||LY293646
NU 7026 (DNA-PK Inhibitor II) is an effective DNA-PK inhibitor (IC50: 0.23 μM, in cell-free assays), 60-fold selective for DNA-PK than PI3K and no inhibition against both ATM and ATR.
价 格：￥电议型 号：T2433产 地：中国大陆
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T24302L 646462；化合物 T24302L-646,462|||L-646462|||L646462|||L 646,462|||L646,462；L-646,462|||L-646462|||L646
L 646462 is an antidopaminergic agent.
价 格：￥电议型 号：T24302产 地：中国大陆
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T23646AF 399；化合物 T23646AF399|||AF-399；AF399|||AF-399
AF 399 is a CCR4 antagonist. It reverses the tumor-promoting environment.
价 格：￥电议型 号：T23646产 地：中国大陆
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T23628AD-2646；化合物 T23628AD2646；AD2646
AD-2646 is a new quinoline derivative. It also has similar pharmacological properties to tricyclic antidepressants.
价 格：￥电议型 号：T23628产 地：中国大陆
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T23366SKF 86466 hydrochloride化合物 T23366SKF 86466 hydrochloride
SKF 86466 hydrochloride is an α2-adrenoceptor antagonist.
价 格：￥电议型 号：T23366产 地：中国大陆
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T22646CFM 4；化合物CFM 4CFM-4|||CFM4；CFM-4|||CFM4
CFM 4 is a potent small molecule CARP-1/APC-2 antagonist that prevents CARP-1 from binding to APC-2, contributes to G2M cell cycle arrest, and induces apoptosis, with an IC50 in the range of 10-15 μM.CFM 4 inhibits the growth of drug-resistant human breast cancer cells.
价 格：￥电议型 号：T22646产 地：中国大陆
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T22423SB-200646A；化合物SB-200646ASB-200646A
SB-200646A is an orally active, selective antagonist of 5-HT2B/2C over 5-HT2A receptor with pKi of 7.5, 6.9 and 5.2 for 5-HT2B, 5-HT2C and 5-HT2A, respectively. SB-200646A exerts anxiolytic and electrophysiological properties in vivo.
价 格：￥电议型 号：T22423产 地：中国大陆
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T21646LAR-M 1896 Acetate；化合物AR-M 1896 AcetateAR-M 1896 Acetate (367518-31-8 Free base)；AR-M 1896 Acetate (3
AR-M 1896 Acetate is the selective agonist of GalR2.
价 格：￥电议型 号：T21646L产 地：中国大陆
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T21324R306465；化合物 T21324R-306465|||JNJ 16241199|||R 306465|||JNJ-16241199|||JNJ16241199；R-306465|||JNJ 162
R306465 is a potent inhibitor of HDAC1 and -8 (class I) in vitro. It potently inhibited cell proliferation of all main solid tumour indications, including colon, ovarian, breast, lung and prostate cancer cell lines with IC50 values ranging from 30 to 300 nM.
价 格：￥电议型 号：T21324产 地：中国大陆
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T2084ETP-46464；化合物ETP46464ETP-46464
ETP-46464 is an effective and specific ATR inhibitor (IC50: 25 nM).
价 格：￥电议型 号：T2084产 地：中国大陆
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T20212AI 3-26464；化合物 T20212AI-3-26464|||AI3-26464；AI-3-26464|||AI3-26464
AI 3-26464 is an agent of biochemical.
价 格：￥电议型 号：T20212产 地：中国大陆
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T20091Stearamide；硬脂酰胺Stearic acid amide|||NSC 66462|||NSC66462|||NSC-66462；Stearic acid amide|||NSC 66462|
Stearamide(Stearic acid amide) is a primary fatty acid amide that is cytotoxic and fish toxic and can be used to increase the properties of nanoparticles.
价 格：￥电议型 号：T20091产 地：中国大陆
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T19755Indigo carmine；酸性蓝 74NSC-8646|||NSC 8646|||NSC8646|||Indigotindisulfonate sodium|||Brilliant Indigo；
Indigo carmine (NSC-8646) is an indolesulfonic acid. It is used as a dye in renal function testing for the detection of nitrates and chlorates.
价 格：￥电议型 号：T19755产 地：中国大陆
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T19646Altizide；化合物 T19646CB-8093|||Aldactacine|||P 1779|||CB 8093|||P1779|||P-1779；CB-8093|||Aldactacine||
Altizide is a thiazide diuretic. It is used to treat oedema and hypertension.
价 格：￥电议型 号：T19646产 地：中国大陆
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T18646Pyrene-PEG5-biotin；化合物 T18646Pyrene-PEG5-biotin
Pyrene-PEG5-biotin is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T18646产 地：中国大陆
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T17646Boc-C1-PEG3-C4-OBn；化合物 T17646Boc-C1-PEG3-C4-OBn
Boc-C1-PEG3-C4-OBn (PROTAC Linker 15) is a PEG-based PROTAC linker employed in the synthesis of various PROTACs, including PROTAC SGK3 degrader-1. PROTACs are composed of two distinct ligands connected by a linker; one ligand binds to an E3 ubiquitin ligase, while the other specifically interacts with the target protein. By leveraging the intracellular ubiquitin-proteasome system, PROTACs can selectively degrade target proteins[1].
价 格：￥电议型 号：T17646产 地：中国大陆
