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T86096-Bromo-3-methyl-1,4-dihydroquinazolin-2-one；6-Bromo-3-methyl-1,4-dihydroquinazolin-2-one6-Bromo-3-m
CHEMBRDG-BB 7118966 is an inhibitor of Bromodomain-containing protein 4 (human).
价 格：￥电议型 号：T8609产 地：中国大陆
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T8579Nav1.8-IN-1；化合物T85795-(4-Chlorophenyl)-N-[[2-(2,2,2-trifluoroethoxy)pyridin-3-yl]methyl]pyridine-3-c
Nav1.8-IN-1 (CHEMBL1270208) is an inhibitor of human NaV1.8
价 格：￥电议型 号：T8579产 地：中国大陆
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T836622,3-dinor-8-iso Prostaglandin F1α；化合物 2,3-dinor-8-iso Prostaglandin F1α2,3-dinor-8-iso PGF1α|||2,3-d
2,3-Dinor-8-iso Prostaglandin F1α (2,3-dinor-8-iso PGF1α), an isoprostane and active metabolite of arachidonic acid deriving its formation from non-enzymatic free radical peroxidation, acts as an active metabolite of the platelet aggregation inhibitor 8-iso PGF2α. This compound exhibits vasoconstrictive properties in isolated porcine retinal and brain microvessels with EC50 values of 12.8 and 18.5 nM, respectively, yet it does not cause contraction in isolated rat aortic rings at a concentration
价 格：￥电议型 号：T83662产 地：中国大陆
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T8356FPL 62064；N-(4-甲氧苯基)-1-苯基-1H-吡唑-3-胺FPL 62064
FPL 62064 is a potent dual inhibitor of 5-lipoxygenase (5-LOX) and COX (IC50 of 3.5 μM and 3.1 μM for RBL-1 cytosolic 5-lipoxygenase and prostaglandin synthetase, respectively).
价 格：￥电议型 号：T8356产 地：中国大陆
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T80502-Methyltetrahydrofuran-3-one；2-甲基四氢呋喃-3-酮2-Methyltetrahydrofuran-3-one
2-Methyltetrahydrofuran-3-one, also known as fema 3373 or tetrahydro-2-methyl-3-furanone, belongs to the class of organic compounds known as furanones.
价 格：￥电议型 号：T8050产 地：中国大陆
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T79013SLMP53-2；化合物 SLMP53-2SLMP53-2
SLMP53-2 is a mutant p53 reactivator that restores the wild-type-like conformation and DNA-binding ability of mutp53-Y220C through enhanced interaction with Hsp70, thereby reinstating p53´s transcriptional activity. This compound induces cell cycle arrest, apoptosis, and endoplasmic reticulum (ER) stress, displaying antitumor activity [1] [2].
价 格：￥电议型 号：T79013产 地：中国大陆
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T77960Thalidomide-5-O-C13-NH2 hydrochloride；化合物 Thalidomide-5-O-C13-NH2 hydrochlorideThalidomide-5-O-C13-N
Thalidomide-5-O-C13-NH2 hydrochloride, a cereblon ligand derived from Thalidomide, facilitates the recruitment of CRBN protein. It is designed to conjugate with a ligand for protein recruitment through a linker, enabling the formation of PROTACs [1].
价 格：￥电议型 号：T77960产 地：中国大陆
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T77936-(4-Methoxyphenyl)-3-pyridazinamine；6-(4-甲氧苯基)哒嗪-3-胺6-(4-Methoxyphenyl)-3-pyridazinamine
6-(4-Methoxyphenyl)-3-pyridazinamine is a GABAA receptor antagonist
价 格：￥电议型 号：T7793产 地：中国大陆
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T777002-Butyl-1,2-benzisothiazolin-3-one；2-丁基-1,2-苯并异噻唑啉-3-酮2-butylbenzo[d]isothiazol-3(2H)-one；2-butylben
2-Butyl-1,2-benzisothiazolin-3-one is an orally available antimicrobial agent with antimicrobial activity commonly used in the pharmaceutical profession and food processing.
价 格：￥电议型 号：T77700产 地：中国大陆
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T75441(8′α,9′β-Dihydroxy)-3-farnesylindole；化合物 (8′α,9′β-Dihydroxy)-3-farnesylindole(8′α,9′β-Dihydroxy)-3-f
(8´α,9´β-Dihydroxy)-3-farnesylindole exhibits significant inhibitory effectiveness (EC 50 9.8 μM) against B. subtilis.
价 格：￥电议型 号：T75441产 地：中国大陆
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T75417alpha-1,3-Galactosyltransferase (a1,3GalT)；化合物 alpha-1,3-Galactosyltransferase (a1,3GalT)alpha-1,3-G
Alpha-1,3-Galactosyltransferase (a1,3GalT) (GGTA1) catalyzes the synthesis of the α-gal epitope by transferring a galactose (Gal) molecule in an α1-3 linkage from a uridyl-diphosphate (UDP) donor to the N-acetyllactosamine (Galβ1,4GlcNAc-R) on glycoproteins. This enzyme is essential for the production of the α-galactose (α-Gal) epitope, a biomolecule prevalent in most mammalian species [1].
价 格：￥电议型 号：T75417产 地：中国大陆
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T74554Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH；化合物 Tazemetostat de(methylene morpholine)-O-C3-O
Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH (Compound 21b), an EZH2 degrader, is employed in lymphoma research [1].
价 格：￥电议型 号：T74554产 地：中国大陆
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T71998673-A；化合物 673-A673-A
673-A is an aldehyde dehydrogenase (ALDH1A) inhibitor that depletes CD133+ cancer stem cells (CSC) in ovarian cancer cell lines. 673-A triggers necroptosis in ovarian CSCs and induces expression of mitochondrial uncoupling proteins (UCP). 673-A also overcomes chemotherapy resistance in vivo.
价 格：￥电议型 号：T71998产 地：中国大陆
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T7138FB23-2；化合物FB23-2FB23-2
FB23-2 is a potent and selective mRNA N6-methyladenosine (m6A) demethylase FTO inhibitor(IC50 : 2.6 μM).
价 格：￥电议型 号：T7138产 地：中国大陆
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T70470Lisomer-CM 352；CM 352异构体isomer-1542205-83-3；isomer-1542205-83-3
isomer-CM 352 is a metalase inhibitor that can be used to slow brain damage.
价 格：￥电议型 号：T70470L产 地：中国大陆
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T69486BMD4503-2；化合物 BMD4503-2BMD4503-2
BMD4503-2 is an LRP5/6-sclerostin interaction inhibitor. BMD4503-2 recovers the downregulated activity of the Wnt/β-catenin signaling pathway by competitively binding to the LRP5/6-sclerostin complex.
价 格：￥电议型 号：T69486产 地：中国大陆
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T69316DA 3003-2；化合物 DA-3003-2NSC663285；NSC663285
DA 3003-2, a selectively potent Cdc25 inhibitor, exhibits antiproliferative activity and holds potential for prostate cancer research. It induces cell cycle arrest at the G2/M phase and increases the expression of P-tyr 15 Cdc2.
价 格：￥电议型 号：T69316产 地：中国大陆
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T67647(2R,3R)-2-Amino-3-hydroxybutanoic acid；化合物 (2R,3R)-2-Amino-3-hydroxybutanoic acid(2R,3R)-2-Amino-3-h
(2R,3R)-2-Amino-3-hydroxybutanoic acid is a natural product for research related to life sciences. The catalog number is T67647 and the CAS number is 24830-94-2.
价 格：￥电议型 号：T67647产 地：中国大陆
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T67603(S)-2-(Cbz-amino)-3-phenyl-1-propanol；化合物 (S)-2-(Cbz-amino)-3-phenyl-1-propanol(S)-2-(Cbz-amino)-3-p
(S)-2-(Cbz-amino)-3-phenyl-1-propanol is a useful organic compound for research related to life sciences. The catalog number is T67603 and the CAS number is 6372-14-1.
价 格：￥电议型 号：T67603产 地：中国大陆
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T67456Argatroban Related Compound A；化合物 (2R,4R)-4-Methyl-1-((S)-2-(3-methylquinoline-8-sulfonamido)-5-(3-n
(2R,4R)-4-Methyl-1-((S)-2-(3-methylquinoline-8-sulfonamido)-5-(3-nitroguanidino)pentanoyl)piperidine-2-carboxylic acid is a useful organic compound for research related to life sciences and the catalog number is T67456.
价 格：￥电议型 号：T67456产 地：中国大陆
