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T1582LNaproxen sodium；萘普生钠Miranax|||Anaprox|||RS-3650|||Naprelan；Miranax|||Anaprox|||RS-3650|||Naprelan|||
Naproxen sodium (Anaprox) is a COX inhibitor for COX-1 and COX-2 with analgesic and antipyretic properties.
价 格：￥电议型 号：T1582L产 地：中国大陆
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T15714LAS-31180；化合物 T15714LAS-31180
LAS-31180 is a phosphodiesterase 3 inhibitor. It also has positive inotropic and vasodilator properties.
价 格：￥电议型 号：T15714产 地：中国大陆
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T1564Cisplatin顺铂cis-Diaminodichloroplatinum|||CDDP|||顺铂
Cisplatin (CDDP) is a DNA cross-linking agent. Cisplatin has antitumor activity and inhibits DNA synthesis by forming DNA adducts in cancer cells. Cisplatin also activates iron death and induces autophagy.
价 格：￥电议型 号：T1564产 地：中国大陆
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T15580Inolitazone dihydrochloride化合物 T15580RS5444 dihydrochloride|||CS-7017 dihydrochloride|||Efatutazone
Inolitazone dihydrochloride is an effective, high-affinity PPARγ agonist; its biological activity is dependent on PPARγ (IC50:0.8 nM) to inhibit cell growth. Inolitazone dihydrochloride enhances the role of cell cycle kinase inhibitor p21 WAF1/CIP1.
价 格：￥电议型 号：T15580产 地：中国大陆
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T1558Resveratrol；白藜芦醇trans-Resveratrol|||SRT 501；白藜芦醇|||trans-Resveratrol|||SRT 501
Resveratrol (SRT 501) is a polyphenolic natural product, a plant antitoxin with antioxidant and chemopreventive activities. Resveratrol has a wide range of targets including COX, SIRT, LOC, etc. Resveratrol induces autophagy and apoptosis.
价 格：￥电议型 号：T1558产 地：中国大陆
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T15552Iferanserin；化合物 T15552S-MPEC；S-MPEC
Iferanserin (S-MPEC) is a selective antagonist of the 5-HT receptor (serotonin receptor) with an affinity for 5-HT2A receptors. Iferanserin has the potential for internal hemorrhoid disease treatment.
价 格：￥电议型 号：T15552产 地：中国大陆
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T15527Hydroxy-PEG3-SS-PEG3-alcohol；化合物 T15527Hydroxy-PEG3-SS-PEG3-alcohol
Hydroxy-PEG3-SS-PEG3-alcohol is a 6 unit polyethylene glycol (PEG) linker that can be cleaved. It is commonly employed in the synthesis of antibody-drug conjugates (ADCs) [1].
价 格：￥电议型 号：T15527产 地：中国大陆
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T15504HS-PEG6-CH2CH2-Boc；化合物 T15504HS-PEG6-CH2CH2-Boc
HS-PEG6-CH2CH2-Boc 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：T15504产 地：中国大陆
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T15457LH-Lys-Trp-Lys-OH acetate；化合物 H-Lys-Trp-Lys-OH acetateH-Lys-Trp-Lys-OH acetate(38579-27-0 free base)；
H-Lys-Trp-Lys-OH acetate is a peptide with antibacterial and antiviral activities.
价 格：￥电议型 号：T15457L产 地：中国大陆
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T15457H-Lys-Trp-Lys-OH；化合物 T15457H-Lys-Trp-Lys-OH
H-Lys-Trp-Lys-OH is a small molecule peptide that shows antibacterial and antiviral activities.
价 格：￥电议型 号：T15457产 地：中国大陆
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T1545Levamlodipine；左旋氨氯地平(S)-Amlodipine|||S-amlodipine；左旋氨氯地平|||(S)-Amlodipine|||S-amlodipine
Levamlodipine (S-amlodipine) belongs to the dihydropyridine group of calcium channel blockers. Levamlodipine, also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. The names S-amlodipine and levamlodipine may be used interchangeably as both substances are the same, however, with differing nomenclature. As a racemic mixture, amlodipine contains (R) and (S)-amlodipine isomers, but only (S)-amlodipine as the active moiet
价 格：￥电议型 号：T1545产 地：中国大陆
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T15420GS-9901；化合物 GS-9901GS-9901
GS-9901 is a selective, orally active and potent PI3Kδ inhibitor (IC50: 1 nM) for the study of non-Hodgkin´s lymphoma and chronic lymphocytic leukemia.
价 格：￥电议型 号：T15420产 地：中国大陆
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T15418GS-6201；化合物GS-6201CVT-6883；CVT-6883
GS-6201 (CVT-6883) is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors with a Ki of 22 nM.
价 格：￥电议型 号：T15418产 地：中国大陆
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T15370GANT 58；化合物GANT 58NSC 75503；4,44乔,4乔(2,3,4,5-Thiophentetrayl)tetrakis-pyridine|||NSC 75503
GANT 58 (NSC-75503) is a potent antagonist of Gli. Which inhibits GLI1-induced transcription (IC50: 5 μM).
价 格：￥电议型 号：T15370产 地：中国大陆
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T15342Fosravuconazole；化合物 T15342E-1224|||BMS-379224；E-1224|||BMS-379224
Fosravuconazole is a ravuconazole prodrug. It has antifungal activity.
价 格：￥电议型 号：T15342产 地：中国大陆
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T15336Fonadelpar；化合物 T15336SJP0035|||Fonadelpar|||SJP-0035|||NPS005|||SJP 0035|||NPS-005|||NPS-005|||Fonad
Fonadelpar is an agonist of PPARδ. It also is used in the research of neuroparalytic keratopathy.
价 格：￥电议型 号：T15336产 地：中国大陆
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T15312Fmoc-NH-ethyl-SS-propionic NHS ester；化合物 T15312Fmoc-NH-ethyl-SS-propionic NHS ester
Fmoc-NH-ethyl-SS-propionic NHS ester is a cleavable linker for antibody-drug conjugates (ADCs)[1]. It is employed in the synthesis of ADCs, facilitating the covalent attachment of drugs to antibodies through the formation of stable amide bonds.
价 格：￥电议型 号：T15312产 地：中国大陆
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T15311Fmoc-NH-ethyl-SS-propionic acid；化合物 T15311Fmoc-NH-ethyl-SS-propionic acid
Fmoc-NH-ethyl-SS-propionic acid is a cleavable linker compound utilized for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15311产 地：中国大陆
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T1530Mitiglinide calcium hydrate；米格列奈钙KAD-1229 calcium hydrate|||Mitiglinide calcium|||S-21403 calcium hy
Mitiglinide calcium hydrate (S-21403 calcium hydrate) is a drug for the treatment of type 2 diabetes. Mitiglinide is thought to stimulate insulin secretion by closing the ATP-sensitive K(+) K(ATP) channels in pancreatic beta-cells. Mitiglinide belongs to the meglitinide class of blood glucose-lowering drugs and is currently co-marketed in Japan by Kissei and Takeda.
价 格：￥电议型 号：T1530产 地：中国大陆
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T15295Fluorescein-PEG6-bis-NHS ester；化合物 T15295Fluorescein-PEG6-bis-NHS ester
Fluorescein-PEG6-bis-NHS ester is a polyethylene glycol (PEG)-based linker used for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T15295产 地：中国大陆
