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产品数：86101
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T17102Tipifarnib (S enantiomer)；化合物Tipifarnib S entiomerTipifarnib S enantiomer|||(S)-(-)-R-115777|||(S)-T
Tipifarnib S enantiomer ((S)-(-)-R-115777) is the S-enantiomer of Tipifarnib. Tipifarnib is a potent and specific farnesyltransferase inhibitor (IC50: 0.6 nM).
价 格：￥电议型 号：T17102产 地：中国大陆
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T17096Tilapertin；化合物 T17096AMG747；AMG747
Tilapertin is an oral glycine transporter type-1 inhibitor.
价 格：￥电议型 号：T17096产 地：中国大陆
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T17057Tetrahydrocortisol；化合物 T17057Tetrahydrocortisol
The urinary Tetrahydrocortisol/Tetrahydrocortisone ratio decreases with increasing 11β-hydroxysteroid dehydrogenase activity. Tetrahydrocortisol is cortisol metabolite.
价 格：￥电议型 号：T17057产 地：中国大陆
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T17041Tertatolol；化合物 T17041Racemic Tertatolol|||(±)?-?Tertatolol|||dl-?Tertatolol；Racemic Tertatolol|||(±)
Tertatolol is an effective antagonist of beta-adrenoceptor and 5-HT receptors.
价 格：￥电议型 号：T17041产 地：中国大陆
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T1702Nortropinone hydrochloride；去甲托品酮盐酸盐Nortropinone hydrochloride
Nortropinone hydrochloride is used as a pharmaceutical intermediate.
价 格：￥电议型 号：T1702产 地：中国大陆
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T17017TCO-PEG4-NHS ester；化合物TCO-PEG4-NHS esterTCO-PEG4-NHS ester
TCO-PEG4-NHS ester is a PROTAC linker bridge belonging to the PEG class.TCO-PEG4-NHS ester can be used to synthesize a wide range of PROTAC molecules.TCO-PEG4-NHS ester is a cleavable and synthetic ADC that can be used in the synthesis of antibody activated molecule conjugates (ADCs). bridge.
价 格：￥电议型 号：T17017产 地：中国大陆
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T17014TCO-NHS ester化合物TCO-NHS esterTCO-NHS ester|||TCONHS ester|||TCO NHS ester
TCO-NHS ester is a alkyl/ether-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：T17014产 地：中国大陆
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T1701H-ASP-PHE-OH；硫胺杂质BAspartyl-phenylalanine|||Demethylaspartame；Aspartyl-phenylalanine|||硫胺杂质B|||Demeth
H-ASP-PHE-OH (Aspartyl-phenylalanine) is used as pharmaceutical intermediates
价 格：￥电议型 号：T1701产 地：中国大陆
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T16989Tarafenacin D-tartrate；Tarafenacin D-酒石酸盐SVT-40776 D-tartrate；SVT-40776 D-tartrate
Tarafenacin D-tartrate (SVT-40776 D-tartrate) is a selective and potent muscarinic acetylcholine M3 receptor antagonist used in the study of overactive bladder and bronchial disorders.
价 格：￥电议型 号：T16989产 地：中国大陆
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T16978Talaporfin sodium；他拉泊芬钠ME2906|||NPe6|||Mono-L-aspartyl chlorin e6；ME2906|||他拉泊芬钠|||NPe6|||Mono-L-asp
Talaporfin is a photosensitizer used in photodynamic therapy.
价 格：￥电议型 号：T16978产 地：中国大陆
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T16945Streptolydigin；化合物 T16945Portamycin；Portamycin
Streptolydigin inhibits RNA synthesis by binding to RNA polymerase and does not inhibit eukaryotic RNA polymerases. Streptolydigin is a 3-acetyltetramic acid antibiotic and a potent bacterial RNA polymerase inhibitor (Ki: 18 μM and a Kd: 15 μM).
价 格：￥电议型 号：T16945产 地：中国大陆
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T16932SRT 2183；化合物SRT 2183SRT 2183
SRT 2183 is a selective activator of Sirtuin-1 (SIRT1, EC1.5 : 0.36 μM).
价 格：￥电议型 号：T16932产 地：中国大陆
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T16912Sortin1化合物 T16912Sortin1|||Sortin-1
Sortin1, a chemical genetic-hit compound, specifically induces mislocalization of both soluble and membrane-associated vacuolar markers in plants and yeast.
价 格：￥电议型 号：T16912产 地：中国大陆
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T16805RTS-V5；化合物 T16805RTS-V5
RTS-V5 is a dual inhibitor of HDAC/proteasome (IC50s: 6.9, 18, 15, 0.27, 0.53 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, respectively).
价 格：￥电议型 号：T16805产 地：中国大陆
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T16750Rigosertib；瑞格色替ON-01910；ON-01910|||瑞格色替
Rigosertib (ON-01910) is a selective and non-ATP-competitive inhibitor of PLK1 (IC50: 9 nM). Rigosertib is a multi-kinase inhibitor and a selective anti-cancer agent, which induces apoptosis by inhibition of the PI3 kinase/Akt pathway, promotes the phosphorylation of histone H2AX and induces G2/M arrest in the cell cycle.
价 格：￥电议型 号：T16750产 地：中国大陆
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T16727Relacorilant；化合物RelacorilantCORT 125134；CORT 125134
Relacorilant is a selective and orally bioavailable antagonist of glucocorticoid receptor(Ki of 7.2 nM in HepG2 TAT assay, and also shows Kis of 12, 81.2, 210 nM for rat, human and monkey glucocorticoid receptor in cell-based assay, respectively). Relacorilant has the potential for Cushing’s syndrome treatment.
价 格：￥电议型 号：T16727产 地：中国大陆
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T1666LFludrocortisone；氟氢可的松9α-fluorocortisol|||9α-Fludrocortisone|||Florinef|||9α-fluorohydrocortisone|||F
Fludrocortisone (Florinef) is a synthetic corticosteroid with moderate glucocorticoid potency and much greater mineralocorticoid potency. Fludrocortisone can be used to studies on treating low blood pressure.
价 格：￥电议型 号：T1666L产 地：中国大陆
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T16667PROTAC Sirt2 Degrader-1；化合物 T16667PROTAC Sirt2 Degrader-1
PROTAC Sirt2 Degrader-1 is a SirReal-based PROTAC, acts as a Sirt2 degrader, composed of a highly potent and isotype-selective Sirt2 inhibitor, a linker, and a bona fide cereblon ligand for E3 ubiquitin ligase. PROTAC Sirt2 Degrader-1 shows an IC50 of 0.25 μM for Sirt2, with no effect on Sirt1/Sirt3 (IC50s > 100 μM)[1].
价 格：￥电议型 号：T16667产 地：中国大陆
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T1666Fludrocortisone acetate；醋酸氟氢可的松9α-Fluorcortisol acetate|||9α-Fludrocortisone acetate|||9α-fluorocort
Fludrocortisone acetate (9α-Fludrocortisone acetate) , a glucocorticoid-receptor agonist, binds to cytoplasmic receptors, translocates to the nucleus, and subsequently initiates the transcription of glucocorticoid-responsive genes such as lipocortins to inhibit phospholipase A2 (PLA2). Fludrocortisone acetate is the acetate salt of a synthetic fluorinated corticosteroid with anti-inflammatory and antiallergic activities. Inhibition of PLA2 activity prevents the release of arachidonic acid, a pre
价 格：￥电议型 号：T1666产 地：中国大陆
