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T21007m 15；化合物 T210075COB|||5OCB|||D 105；5COB|||5OCB|||D 105
M 15 liquid crystals are a member of the oxycyanobiphenyl family, which exhibits a liquid crystalline phase in the temperature range of 47-67.5℃.
价 格：￥电议型 号：T21007产 地：中国大陆
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T20794Dioctyltin maleate；化合物 T20794TVS 8105|||Thermolite 813|||LIV 1176|||NSC65515|||NSC 65515|||NSC-65515
Dioctyltin maleate is a bioactive chemical.
价 格：￥电议型 号：T20794产 地：中国大陆
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T2070Agerafenib；化合物CEP-32496RXDX-105|||CEP 32496|||CEP-32496|||CEP32496；RXDX-105|||CEP 32496|||CEP-32496|
Agerafenib (CEP32496) is a highly potent inhibitor of BRAF.
价 格：￥电议型 号：T2070产 地：中国大陆
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T20353p-Acetylphenyl acetate；化合物 T20353AI310544|||AI3 10544|||AI3-10544；AI310544|||AI3 10544|||AI3-10544
p-Acetylphenyl acetate is an agent of biochemical.
价 格：￥电议型 号：T20353产 地：中国大陆
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T20345Benzoylacetone；苯甲酰丙酮AI3 10572|||AI3-10572|||AI310572；AI3 10572|||苯甲酰丙酮|||AI3-10572|||AI310572
Benzoylacetone (AI3 10572) exhibits antibacterial activity.
价 格：￥电议型 号：T20345产 地：中国大陆
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T203082-Bromophenetole；化合物 T20308AI3-01058|||AI3 01058|||AI301058；AI3-01058|||AI3 01058|||AI301058
2-Bromophenetole is an agent of biochemical.
价 格：￥电议型 号：T20308产 地：中国大陆
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T19647PNU-105368(S)-5-(氨基甲基)-3-(3-氟-4-吗啉基苯基)-2-唑烷酮PNU105368|||(S)-5-(氨基甲基)-3-(3-氟-4-吗啉基苯基)-2-唑烷酮
PNU-105368 is a bioactive chemical substance that can be used for related research in the field of life sciences.
价 格：￥电议型 号：T19647产 地：中国大陆
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T19264D-Methionine sulfoxide hydrochloride；化合物 T19264D-Methionine sulfoxide hydrochloride (21056-56-4 free
D-methionine sulfoxide hydrochloride is the D-isomer of methionine sulfoxide hydrochloride. Methionine sulfoxide is the oxidation product of methionine. Methionine is a restrictive amino acid in milk or legume proteins and is easily oxidized during storage or processing.
价 格：￥电议型 号：T19264产 地：中国大陆
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T19216BTL-105；化合物 T19216BTL-105
BTL-105, a monobiotinylated Phos-tag derivative, is used for the detection of phosphopeptides and phosphoproteins.
价 格：￥电议型 号：T19216产 地：中国大陆
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T19203Bendamustine D4；化合物 T19203SDX-105 D4；SDX-105 D4
Bendamustine D4 is the deuterium-labeled Bendamustine. Bendamustine is a DNA cross-linking compound with alkylating and antimetabolite properties. Bendamustine causes DNA breaks.
价 格：￥电议型 号：T19203产 地：中国大陆
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T191052-γ-Linolenoyl-1,3-dilinoleoyl-sn-glycerol；化合物 T191052-γ-Linolenoyl-1,3-dilinoleoyl-sn-glycerol
2-γ-Linolenoyl-1,3-dilinoleoyl-sn-glycerol is a triglyceride.
价 格：￥电议型 号：T19105产 地：中国大陆
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T1852Rac-Belinostat；化合物BelinostatNSC726630|||PXD101|||PX-105684；NSC726630|||PXD101|||PX-105684
Rac-Belinostat (PX-105684) is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity. Belinostat targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptosis, promoting cellular differentiation, and inhibiting angiogenesis. This agent may sensitize drug-resistant tumor cells to other antineoplastic agents, possibly through a mechanism involving the down-regulation of thymidylate synthase.
价 格：￥电议型 号：T1852产 地：中国大陆
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T18105m-PEG-NPC (MW 20000)；化合物 T18105m-PEG-NPC (MW 20000)
m-PEG-NPC (MW 20000) 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：T18105产 地：中国大陆
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T17239VU0155069；化合物VU0155069CAY10593；CAY10593
VU0155069 strongly inhibits the invasive migration of several cancer cell lines in transwell assays. VU0155069 is a selective phospholipase D1 inhibitor (IC50: 46 nM in vitro).
价 格：￥电议型 号：T17239产 地：中国大陆
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T17105TM6089；化合物TM6089TM6089
TM6089 is an inhibitor of Prolyl Hydroxylase that stimulates HIF activity without iron chelation, induces angiogenesis, and protects organ against ischemia.
价 格：￥电议型 号：T17105产 地：中国大陆
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T16547PK14105；化合物 T16547PK14105
PK14105 has been evaluated biologically as a potential radioligand for positron emission tomography (PET) studies targeting peripheral benzodiazepine binding sites (PBBS) receptors. When administered to rats with unilaterally lesioned striata, PK14105 was observed to quickly cross the blood-brain barrier, displaying significant radioactivity retention in the lesioned striatum, in contrast to the unlesioned striatum or cerebellar vermis. Additionally, PK14105 has the capability to inhibit recepto
价 格：￥电议型 号：T16547产 地：中国大陆
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T16483PF-05105679；化合物PF-05105679PF-05105679
PF-05105679 is a selective TRPM8 antagonist (IC50 = 103 nM). PF-05105679 can be used in research on cold-related pain.
价 格：￥电议型 号：T16483产 地：中国大陆
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T16443PCS1055 dihydrochloride；化合物 T16443PCS1055 dihydrochloride
PCS1055 dihydrochloride is an effective, selective, and competitive muscarinic M4 receptor antagonist (IC50: 18.1 nM and a Kd: 5.72 nM). PCS1055 dihydrochloride is also a potent AChE inhibitor (IC50 s: 22 nM and 120 nM for electric eel and human AChE, respectively). PCS1055 dihydrochloride inhibits radioligand [3H]-NMS binding to the M4 receptor (Ki: 6.5 nM). PCS1055 dihydrochloride shows >100-fold selectivity over M1-, M3-, and M5-receptors and 30-fold selectivity at the M2 receptor.
价 格：￥电议型 号：T16443产 地：中国大陆
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T16105ML132；化合物 T16105NCGC 00185682；NCGC 00185682
ML132 is an effective and selective inhibitor of caspase 1 (IC50: 0.316 nM).
价 格：￥电议型 号：T16105产 地：中国大陆
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T16032L(Z)-MDL 105519；异构体MDL 105519(Z)-MDL 105519
(Z)-MDL 105519 is an inactive isomer of MDL105519.
价 格：￥电议型 号：T16032L产 地：中国大陆
