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T36630MRTX9768 hydrochloride；MRTX9768 hydrochlorideMRTX9768 hydrochloride
MRTX9768 hydrochloride is a potent, orally active PRMT5 inhibitor. MRTX9768 hydrochloride is a synthetic lethal-based inhibitor binding the PRMT5-MTA complex[1].
价 格：￥电议型 号：T36630产 地：中国大陆
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T365954-epi-Chlortetracycline (hydrochloride)；4-epi-Chlortetracycline (hydrochloride)4-epi-Chlortetracycli
Chlortetracycline is an analog of tetracycline , a broad spectrum antibiotic. In addition to its actions against microorganisms, chlortetracycline suppresses inflammation by inhibiting neutrophil action and other aspects of the innate immune response. 4-epi-Chlortetracycline is an epimer of chlortetracycline.
价 格：￥电议型 号：T36595产 地：中国大陆
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T3659Zorifertinib；化合物AZD3759AZD3759；AZD3759
Zorifertinib (AZD3759) is an orally active, effective and central nervous system-penetrant EGFR inhibitor. The IC50 values were 0.2, 0.3 and 0.2 nM for EGFR L858R mutant, TK wild-type, and Exon 19Del enzymes, respectively.
价 格：￥电议型 号：T3659产 地：中国大陆
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T36373Urocortin II (mouse) (trifluoroacetate salt)；Urocortin II (mouse) (trifluoroacetate salt)Urocortin I
Urocortin II is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin III , frog sauvagine, and piscine urotensin I.
价 格：￥电议型 号：T36373产 地：中国大陆
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T3634Osimertinib mesylate；奥希替尼甲磺酸盐Mereletinib mesylate|||AZD-9291 mesylate；甲磺酸奥希替尼|||Mereletinib mesylate
Osimertinib mesylate (Mereletinib mesylate) is an irreversible and mutant selective EGFR inhibitor (IC50s: 12/1 nM for EGFR(L858R) and EGFR(L858R/T790M)).
价 格：￥电议型 号：T3634产 地：中国大陆
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T36314Wortmannin-Rapamycin Conjugate；Wortmannin-Rapamycin ConjugateWortmannin-Rapamycin Conjugate
Phosphoinositide 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) act synergistically in promoting cancer. Wortmannin is a potent inhibitor of PI3K enzymes, while rapamycin blocks mTOR Complex 1 TORC1. Wortmannin-rapamycin conjugate consists of analogs of 17-hydroxy wortmannin and rapamycin conjugated via a prodrug linker. Hydrolysis of the prodrug linker in vivo releases the inhibitors. The wortmannin-rapamycin conjugate inhibits the growth of HT-29 colon tumors and A498 renal tumors in
价 格：￥电议型 号：T36314产 地：中国大陆
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T36287Pirtobrutinib；化合物PirtobrutinibPirtobrutinib
Pirtobrutinib (LOXO-305) is an advanced BTK inhibitor that displays high selectivity and operates through a non-covalent mechanism. This compound effectively inhibits various BTK C481 substitution mutations, leading to tumor regression in BTK-dependent lymphoma tumors in mouse xenograft models. Furthermore, Pirtobrutinib exhibits remarkable selectivity for BTK, with more than a 300-fold difference compared to 370 other kinases tested. Notably, at a concentration of 1 μM, Pirtobrutinib demonstrat
价 格：￥电议型 号：T36287产 地：中国大陆
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T361343,4,6-Tri-O-benzyl-β-D-Mannopyranose 1,2-(methyl orthoacetate)；3,4,6-Tri-O-benzyl-β-D-Mannopyranose
3,4,6-Tri-O-benzyl-β-D-mannopyranose 1,2-(methyl orthoacetate) is a synthetic intermediate used in glycosylation reactions. Typically, the methyl orthoester protecting group is first removed by mild acid hydrolysis, producing a glycosyl donor. Removal of the O-benzyl protecting groups is performed late in the synthesis.
价 格：￥电议型 号：T36134产 地：中国大陆
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T36029Desertomycin A；Desertomycin ADesertomycin A
Desertomycin A is fungal metabolite and the major component of the desertomycin antibiotic complex that has been found in S. flavofungini.
价 格：￥电议型 号：T36029产 地：中国大陆
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T36006Olmesartan medoxomil impurity C；Olmesartan medoxomil impurity COlmesartan medoxomil impurity C
Olmesartan medoxomil impurity C is an impurity of Olmesartan medoxomil, a potent and selective angiotensin AT1 receptor inhibitor with an IC50 of 66.2 μM.
价 格：￥电议型 号：T36006产 地：中国大陆
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T359504-Epianhydrochlortetracycline (hydrochloride)；4-Epianhydrochlortetracycline (hydrochloride)4-Epianhy
4-Epianhydrochlortetracycline (hydrochloride) can be used in related research in the field of life sciences. Its product number is T35950 and CAS number is 158018-53-2.
价 格：￥电议型 号：T35950产 地：中国大陆
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T35876Chlorthalidone Impurity G；Chlorthalidone Impurity GChlorthalidone Impurity G
Chlorthalidone impurity G is a potential impurity found in commercial preparations of chlorthalidone that has moderate antihypertensive effects. Chlorthalidone is a thiazide-like diuretic that inhibits the Na+/Cl- cotransporter in the distal convoluted tubule of the kidney, which prevents reabsorption of sodium and chloride leading to a reduction in plasma volume and cardiac output. It also inhibits carbonic anhydrase (CA), including the isoforms CAVB, VII, IX, XII, and XIII (Kis = 2.8-23 nM) an
价 格：￥电议型 号：T35876产 地：中国大陆
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T35844(R)-Pirtobrutinib；(R)-Pirtobrutinib(R)-Pirtobrutinib
(R)-Pirtobrutinib ((R)-LOXO-305) is a less active enantiomer of Pirtobrutinib, and Pirtobrutinib is a highly selective and non-covalent next generation BTK inhibitor. Pirtobrutinib (LOXO-305) effectively inhibits diverse BTK C481 substitution mutations[1].
价 格：￥电议型 号：T35844产 地：中国大陆
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T35830Dehydro Olmesartan；Dehydro OlmesartanDehydro Olmesartan
Dehydro Olmesartan, deriving from Olmesartan, acts as an angiotensin II receptor (AT1R) antagonist and exhibits potential for the study of high blood pressure [1][2].
价 格：￥电议型 号：T35830产 地：中国大陆
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T35814Urocortin III (human) (trifluoroacetate salt)；Urocortin III (human) (trifluoroacetate salt)Urocortin
Urocortin III is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin II , frog sauvagine, and piscine urotensin I.
价 格：￥电议型 号：T35814产 地：中国大陆
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T35745Marcfortine AMarcfortine AMarcfortine A
Marcfortine A is an indole alkaloid originally isolated from P. roqueforti. It has nematocidal activity against the parasitic nematode H. contortus (LD99 = 0.06 μg/ml) and inhibits motility of adult worms (EC50 = 2 μM)., Marcfortine A eliminates H. contortus, T. colubriformis, and O. ostertagi from experimentally infected jirds (ED95s = 0.33, 0.11, and 2.5 mg/animal, respectively). It dose-dependently inhibits nicotine-induced calcium mobilization in SH-SY5Y and TE-671 cells expressing α3 subuni
价 格：￥电议型 号：T35745产 地：中国大陆
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T357254-hydroxy Valsartan；4-hydroxy Valsartan4-hydroxy Valsartan
4-hydroxy Valsartan is a major metabolite of the angiotensin II type 1 (AT1) receptor antagonist valsartan . It reduces platelet aggregation induced by epinephrine and collagen but not ADP in human whole blood.
价 格：￥电议型 号：T35725产 地：中国大陆
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T35663Cortistatin-29 (rat) (trifluoroacetate salt)；Cortistatin-29 (rat) (trifluoroacetate salt)Cortistatin
Cortistatin-29 is a neuropeptide that is structurally similar to somatostatin-28. It is produced by cleavage of preprocortistatin to procortistatin, which is cleaved at dibasic amino acids to form cortistatin-29 and cortistatin-14 as well as other partial cleavage products. Cortistatin mRNA is expressed in the human brain and in interneurons of the rat hippocampus and cerebral cortex. Cortistatin-29 binds to somatostatin (SST) receptors with IC50 values of 2.8, 7.1, 0.2, 3, and 13.7 nM for SST1-
价 格：￥电议型 号：T35663产 地：中国大陆
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T35662Cortistatin-29 (1-13) (rat) (trifluoroacetate salt)；Cortistatin-29 (1-13) (rat) (trifluoroacetate sa
Cortistatin-29 (1-13) is a neuropeptide and cleavage product of cortistatin-29 , which is a cleavage product of procortistatin. Cortistatin-29 (1-13) corresponds to the first 13 amino acids of cortistatin-29.
价 格：￥电议型 号：T35662产 地：中国大陆
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T35642Tritylolmesartan Medoxomil；Tritylolmesartan MedoxomilTritylolmesartan Medoxomil
Tritylolmesartan medoxomil is an intermediate in the synthesis of olmesartan medoxomil , a prodrug form of the angiotensin II receptor 1 (AT1) antagonist olmesartan .1
价 格：￥电议型 号：T35642产 地：中国大陆
