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T26259Tenovin-D3；化合物 T26259TenovinD3；TenovinD3
Tenovin-D3 is a sirtuin SirT2 inhibitor. It acts by increasing p21 (CDKN1A) expression in a p53-independent manner.
价 格：￥电议型 号：T26259产 地：中国大陆
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T26207Spirgetine；化合物 T26207Spirgetin|||LD3598|||Espirgetina|||LD 3598|||L-3598；Spirgetin|||LD3598|||Espirg
Spirgetine is an adrenergic compound that can be used for research related to the life sciences.
价 格：￥电议型 号：T26207产 地：中国大陆
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T25919Paraflutizide；化合物 T25919LD3612|||LD 3612|||Paraflutizida|||LD-3612；LD3612|||LD 3612|||Paraflutizida|
Paraflutizide is a thiazide analog antihypertensive.
价 格：￥电议型 号：T25919产 地：中国大陆
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T25912Oxypyrronium bromide；化合物 T25912L.D. 3055|||Immetropan|||LD 3055|||LD3055|||LD-3055；L.D. 3055|||Immet
Oxypyrronium bromide is an anticholinergic and spasmolytic agent containing quaternary ammonium. In animal models it inhibited gastric motility, hypotension induced by vagus stimulation or intravenation of acetylcholine; salivation induced by chorda tympani nerve stimulation, and contraction elicited by preganglionic cervical sympathetic nerve stimulation.
价 格：￥电议型 号：T25912产 地：中国大陆
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T25276Crilvastatin；克伐他汀PMD387|||PMD 387|||PMD-387；PMD387|||PMD 387|||PMD-387
Crilvastatin (PMD 387) is a novel non-competitive hydroxymethylglutaryl coenzyme A reductase inhibitor with cholesterol-lowering activity that inhibits cholesterol uptake in rats with hereditary hypercholesterolemia.
价 格：￥电议型 号：T25276产 地：中国大陆
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T25267Cmpd 339509；化合物 T25267Cmpd339509|||Cmpd-339509；Cmpd339509|||Cmpd-339509
Cmpd 339509 is a DprE1 inhibitor. DprE1 is an epimerase required for cell wall biosynthesis.
价 格：￥电议型 号：T25267产 地：中国大陆
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T24920UCD38B HCl；化合物 T24920UCD38B hydrochloride|||UCD 38 B hydrochloride|||UCD-38-B HCl|||UCD-38-B Hydroch
UCD38B HCl is a cell-permeable intracellular uPA inhibitor that acts by killing proliferative and non-proliferative high-grade glioma cells by programmed necrosis.
价 格：￥电议型 号：T24920产 地：中国大陆
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T24725ROCK-IN-D3；化合物 T24725ROCK inhibitor D3|||ROCK-inhibitor-D3；ROCK inhibitor D3|||ROCK-inhibitor-D3
ROCK-IN-D3 is an effective and selective inhibitor of ROCK.
价 格：￥电议型 号：T24725产 地：中国大陆
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T24693QD325；化合物 T24693QD 325|||QD-325；QD 325|||QD-325
QD325 is a potent redox modulator for the Treatment of Pancreatic Ductal Adenocarcinoma. Nascent RNA sequencing following treatments with QD325 revealed induction of stress responses in the nucleus, endoplasmic reticulum, and mitochondria of pancreatic cancer cells.
价 格：￥电议型 号：T24693产 地：中国大陆
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T24603PD-34799-SA；化合物 T24603PD 34799-SA|||PD34799-SA；PD 34799-SA|||PD34799-SA
PD-34799-SA is an effective inhibitor of vasoconstrictor responses to sympathetic nerve stimulation.
价 格：￥电议型 号：T24603产 地：中国大陆
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T24545NPD-340；化合物 T24545NPD340；NPD340
NPD-340 is an effective TbrPDEB1 inhibitor.
价 格：￥电议型 号：T24545产 地：中国大陆
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T23950Dacomitinib metabolite M2；化合物 T23950Dacomitinib cysteine conjugate|||UNII-SOA52D3NLL；Dacomitinib cys
Dacomitinib metabolite M2 is also known as Dacomitinib cysteine conjugate. Dacomitinib inhibits both the wild-type (WT) EGFR and EGFR T790M.
价 格：￥电议型 号：T23950产 地：中国大陆
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T23934D36；化合物 T23934D 36|||D-36；D 36|||D-36
D36 is an androgen receptor allosteric antagonist. It also has inverse agonist properties.
价 格：￥电议型 号：T23934产 地：中国大陆
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T23820BRD32048；化合物BRD32048BRD-32048|||BRD 32048；BRD-32048|||BRD 32048
BRD32048 is a top candidate ETV1 perturbagen. BRD32048 inhibits p300-dependent acetylation of ETV1, thereby promoting its degradation.
价 格：￥电议型 号：T23820产 地：中国大陆
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T23783Benzoxonium chloride；化合物 T23783Bradophen|||Bialcol|||D 301|||D301|||Cohortan；Bradophen|||Bialcol|||D
Benzoxonium chloride, The topical treatment of anthroponotic cutaneous leishmaniasis with the tincture of thioxolone plus benzoxonium chloride (Thio-Ben) along with cryotherapy.
价 格：￥电议型 号：T23783产 地：中国大陆
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T22298CPD3615-A5；化合物CPD3615-A5CPD3615-A5
CPD3615-A5 is an active chemical.
价 格：￥电议型 号：T22298产 地：中国大陆
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T21097Decamethyltetrasiloxane；化合物 T21097Tetrasiloxane, decamethyl-|||decamethyl-tetrasiloxan|||D3780；Tetra
Decamethyltetrasiloxane, a non-cyclic silicone oligomer, is used in the methylation of mercury(II) salts. It is transformed by a specific microflora. In the natural environment, it is degraded by mechanisms similar to other organic compounds.
价 格：￥电议型 号：T21097产 地：中国大陆
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T19710Ciglitazone；环格列酮Ciglitazona|||U 63287|||ADD3878|||ADD-3878|||U-63287|||ADD 3878；Ciglitazona|||U 6328
Ciglitazone (ADD 3878) is a potent and selective PPARγ agonist (EC50: 3 μM) and oral hypoglycemic agent. Ciglitazone inhibits proliferation and differentiation of th17 cells, decreases insulin levels, vascular endothelial growth factor production and blood pressure, and induces cell cycle arrest in gastric cancer cells. Selegiline induces apoptosis in opossum kidney epithelial cells and activates nuclear translocation of p38 MAPK and apoptosis-inducing factor (AIF). Ciglitazone exhibits hypoglyc
价 格：￥电议型 号：T19710产 地：中国大陆
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T1967AZD-3463；化合物AZD3463ALK/IGF1R inhibitor；ALK/IGF1R inhibitor
AZD-3463 (ALK/IGF1R inhibitor) , an orally bioavailable ALK inhibitor (Ki: 0.75 nM), can inhibit IGF1R with equivalent potency.
价 格：￥电议型 号：T1967产 地：中国大陆
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T19610(24S)-24,25-Dihydroxyvitamin D3；化合物 T19610(24S)-24,25-Dihydroxycholecalciferol；(24S)-24,25-Dihydroxy
(24S)-24,25-Dihydroxyvitamin D3 undergoes various levels of hydroxylation to form active vitamin D3 analogs.
价 格：￥电议型 号：T19610产 地：中国大陆
