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T16267Naminidil化合物 T16267BMS 234303-01
Naminidil is an opener of cyanoguanidine KATP.
价 格：￥电议型 号：T16267产 地：中国大陆
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T16266NAMI-A；化合物NAMI-ANAMI-A
NAMI-A is a ruthenium-based compound with selective activity against tumor metastasis.NAMI-A inhibits cancer cell adhesion and migration.
价 格：￥电议型 号：T16266产 地：中国大陆
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T16265Naluzotan；那鲁佐坦PRX 00023；PRX 00023
Naluzotan（PRX 00023） is a novel and potent 5-HT1A agonist with IC50 and Ki values of approximately 20 nM and 5.1 nM, respectively.Naluzotan is a potent hERG K+ channel blocker with an IC50 value of 3800 nM.Naluzotan exhibits anxiolytic activity and can be used to study depression.
价 格：￥电议型 号：T16265产 地：中国大陆
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T16264Nagilactone B；竹柏内酯 BNagilactone B
Nagilactone B is extracted from the root bark of Podocarpus nagi and it also is a liver X receptor (LXR) agonist.
价 格：￥电议型 号：T16264产 地：中国大陆
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T16263N6-Cyclopentyladenosine；N6-环戊基腺苷酸UK-80882|||CPA；UK-80882|||CPA
N6-Cyclopentyladenosine (CPA) is a selective agonist of the adenosine A1 receptor and can be used to mimic the action of the adenosine A1 receptor, with Ki´s of 2.3 nM, 790 nM, and 43 nM for human A1, A2A, and A3 receptors, respectively.N6-Cyclopentyladenosine (CPA) can be used to modulate cellular signaling and neurotransmission and other biological processes. Cyclopentyladenosine (CPA) is used to regulate cell signaling, neurotransmitter release and other biological processes.
价 格：￥电议型 号：T16263产 地：中国大陆
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T16262N33-TEG-COOH；化合物 T1626214-Azido-3,6,9,12-tetraoxatetradecanoic acid|||N3-TEG-COOH；14-Azido-3,6,9,12-
N33-TEG-COOH 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：T16262产 地：中国大陆
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T16261N3-PEG8-CH2COOH；化合物 T16261N3-PEG8-CH2COOH
N3-PEG8-CH2COOH 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：T16261产 地：中国大陆
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T16260N3-PEG4-C2-Pfp ester；化合物 T16260N3-PEG4-C2-Pfp ester
N3-PEG4-C2-Pfp ester is a four-unit polyethylene glycol linker, noncleavable in nature, specifically employed in the fabrication of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16260产 地：中国大陆
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T1626Prostaglandin E1；前列地尔PGE1|||Alprostadil；前列地尔|||PGE1|||列腺素E1|||Alprostadil
Prostaglandin E1 (Alprostadil) is the naturally occurring prostaglandin E1 (PGE1) which displays a variety of pharmacologic actions. Prostaglandin E1 is a potent vasodilator agent that increases peripheral blood flow, inhibits platelet aggregation, and induces bronchodilation. Used in the treatment of erectile dysfunction, this agent produces corporal smooth muscle relaxation by binding to PGE receptors, resulting in the activation of adenylate cyclase and the subsequent accumulation of 3´
价 格：￥电议型 号：T1626产 地：中国大陆
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T16259N3-PEG4-C2-NHS ester；化合物 T16259N3-PEG4-C2-NHS ester
N3-PEG4-C2-NHS ester is a four-unit polyethylene glycol (PEG) linker that is noncleavable, serving as a crucial component in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16259产 地：中国大陆
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T16258N3-PEG3-CH2CH2COOH；化合物 T16258N3-PEG3-CH2CH2COOH
N3-PEG3-CH2CH2COOH, a PEG-based PROTAC linker, is utilized in the synthesis of BI-3663, BI-4216, and BI-0319. Additionally, Azido-PEG3-acid, a non-cleavable 3-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16258产 地：中国大陆
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T16257N3-PEG3-CH2CH2-Boc；化合物 T16257N3-PEG3-CH2CH2-Boc
N3-PEG3-CH2CH2-Boc is a cleavable 3 unit polyethylene glycol (PEG) ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1]. This compound also functions as a PEG- and alkyl/ether-based PROteolysis TArgeting Chimera (PROTAC) linker, suitable for the construction of PROTAC molecules[2].
价 格：￥电议型 号：T16257产 地：中国大陆
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T16256N3-PEG3-C2-PFP ester；化合物 T16256N3-PEG3-C2-PFP ester
N3-PEG3-C2-PFP ester is a 3-unit polyethylene glycol (PEG) linker devoid of cleavable bonds. It is commonly employed in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16256产 地：中国大陆
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T16255N3-PEG3-C2-NHS ester；化合物 T16255N3-PEG3-C2-NHS ester
N3-PEG3-C2-NHS ester is a noncleavable trifunctional polyethylene glycol (PEG) linker, designed for the conjugation of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16255产 地：中国大陆
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T16254N3-PEG2-C2-PFP ester；化合物 T16254N3-PEG2-C2-PFP ester
The N3-PEG2-C2-PFP ester, a nonclaevable 2-unit polyethylene glycol (PEG) linker, is commonly employed in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16254产 地：中国大陆
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T16253N3-PEG2-C2-NHS ester；化合物 T16253N3-PEG2-C2-NHS ester
N3-PEG2-C2-NHS ester is a two-unit PEG linker, noncleavable in nature, specifically designed for the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T16253产 地：中国大陆
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T16252N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl)；化合物 T16252N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl
N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl) is a polyethylene glycol (PEG) derivative specifically designed as a linker for PROTAC synthesis [1].
价 格：￥电议型 号：T16252产 地：中国大陆
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T16251N-Succinimidyl-S-acetylthioacetate；N-丁二酸，S-乙酰基巯基乙二醇酯SATA；SATA|||N-丁二酸，S-乙酰基巯基乙二醇酯
N-Succinimidyl-S-acetylthioacetate (SATA) is a protein modification agent that introduces thiol-groups into protein molecules and adds sulfhydryl groups in a protected form to proteins and other amine-containing molecules for later reaction with sulfhydryl reactive crosslinkers such as Sulfo-SMCC, Sulfo-MBS, etc.
价 格：￥电议型 号：T16251产 地：中国大陆
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T16250N-Succinimidyl 3-(Bromoacetamido)propionate；化合物 T162503-(2-Bromoacetamido)propanoic acid NHS ester；3
N-Succinimidyl 3-(Bromoacetamido)propionate is a PEG-based PROTAC linker employed in the synthesis of PROTACs and antibody-drug conjugates (ADCs) [1, 2]. It acts as a cleavable ADC linker, facilitating the conjugation of drugs to antibodies for targeted delivery [2].
价 格：￥电议型 号：T16250产 地：中国大陆
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T1625Lomefloxacin hydrochloride；盐酸洛美沙星Lomefloxacin HCl|||Okacyn|||Maxaquin；Lomefloxacin HCl|||盐酸洛美沙星|||Ok
Lomefloxacin hydrochloride (Okacyn) inhibits DNA gyrase, a type II topoisomerase involved in the induction or relaxation of supercoiling during DNA replication. This inhibition leads to a decrease in DNA synthesis during bacterial replication, resulting in cell growth inhibition and eventually cell lysis. Lomefloxacin Hydrochloride is the hydrochloride salt form of lomefloxacin, a synthetic broad-spectrum fluoroquinolone with antibacterial activity.
价 格：￥电议型 号：T1625产 地：中国大陆
