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产品数：86101
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TN6738Orthosphenic acidOrthosphenic acid
Orthosphenic acid is a natural product isolated from M. triflora.
价 格：￥电议型 号：TN6738产 地：中国大陆
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TQ0275LysoPC(14:0/0:0)Antispasmodic,Endogenous Metabolite,LysoPC(14:0/0:0),lysophospholipid,Inhibitor,inhi
LysoPC(14:0/0:0) is a lysophospholipid (LyP) and mono-glycerophospholipid.
价 格：￥电议型 号：TQ0275产 地：中国大陆
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T6732WYE-687mTOR,Mammalian target of Rapamycin,WYE-687,Phosphoinositide 3-kinase,WYE687,PI3K,WYE 687,inhi
WYE-687 is an ATP-competitive and selective inhibitor of mTOR with IC50 of 7 nM; blocks mTORC1/pS6K(T389) and mTORC2/P-AKT(S473) but no effect observed on P-AKT(T308). Selectivity for mTOR is greater than PI3Kα (>100-fold) and PI3Kγ (>500-fold).
价 格：￥电议型 号：T6732产 地：中国大陆
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TP1896L1Kisspeptin 234 acetate(1145998-81-7 free base)Kisspeptin 234 acetate(1145998 81 7 free base),Kisspep
kisspeptin receptor (KISS1, GPR54) antagonist; kisspeptin-10 analog. Inhibits kisspeptin-10 stimulation of inositol phosphate (IP) (IC50 = 7 nM) and release of gonadotrophin-releasing hormone (GnRH).
价 格：￥电议型 号：TP1896L1产 地：中国大陆
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T15648KDM5-C70KDM5-C49,Histone Demethylase,JARID1,retinoblastoma,inhibit,KDM5 C70,KDM5-C70,KDM-5-C70,phosp
KDM5-C70 is an ethyl ester derivative of KDM5-C49. KDM5-C70 is an effective, cell-permeable, and pan-KDM5 histone demethylase inhibitor. KDM5-C70 has an antiproliferative effect in myeloma cells, inducing a genome-wide elevation of H3K4me3 levels.
价 格：￥电议型 号：T15648产 地：中国大陆
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T7487LSperact TFA(76901-59-2(free base))Speract TFA(76901 59 2(free base)),Speract TFA(76901592(free base)
Speract TFA is a sea urchin egg peptide that regulates sperm motility, also stimulates sperm mitochondrial metabolism.
价 格：￥电议型 号：T7487L产 地：中国大陆
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T6548IrsogladinePhosphodiesterase (PDE),mAChR,inhibit,Irsogladine,Muscarinic acetylcholine receptor,Inhib
Irsogladine is an anti-gastric ulcer agent that facilitates gap-junctional intercellular communication through M1 muscarininc acetylcholine receptor binding.
价 格：￥电议型 号：T6548产 地：中国大陆
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T9521CHR-6494 TFACHR-6494,inhibit,apoptosis,Haspin Kinase,NRAS mutant melanoma cells,CHR 6494,mitotic cat
CHR-6494 TFA is a potent haspin inhibitor, with an?IC50?of 2 nM. It inhibits histone H3T3 phosphorylation. CHR-6494 TFA induces the?apoptosis?of cancer cells, including melanoma and breast cancer. CHR-6494 TFA can be used in the research of cancer
价 格：￥电议型 号：T9521产 地：中国大陆
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T11106DSP-0565
DSP-0565 exhibits anti-convulsant activity and good safety margin in various models including scPTZ, 6 Hz, MES, and amygdala kindling. DSP-0565 can be used in studies about acting as a broad-spectrum anti-epileptic drug.
价 格：￥电议型 号：T11106产 地：中国大陆
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T8788NaptalamInhibitor,Alanap-1,transport inhibitor,inhibit,Alanap 1,Alanap1,maize,polar auxin,leaf margi
Naptalam is an herbicide.Naptalam is a dicarboxylic acid monoamide which results from addition of one equivalent of 1-naphthylamine to phthalic anhydride. It is a dicarboxylic acid monoamide, a carboxylic acid and a N-(1-naphthyl)carboxamide. It is a conjugate acid of a naptalamate.
价 格：￥电议型 号：T8788产 地：中国大陆
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T8974ML-211MAGL,ML 211,inhibit,Phospholipase,Monoacylglycerol lipase,ML-211,Inhibitor,ML211
ML-211 is a carbamate-based dual inhibitor of LYPLA1 (IC50 = 17 nM) and the related LYPLA2 (IC50 = 30 nM)
价 格：￥电议型 号：T8974产 地：中国大陆
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T6459CyclosporineCyclosporine
Cyclosporine is a calcineurin phosphatase pathway inhibitor, used as an immunosuppressant drug to prevent rejection in organ transplantation.
价 格：￥电议型 号：T6459产 地：中国大陆
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T8083Pyridoxal 5’-?phosphate monohydrateinhibit,Coenzyme,Pyridoxal phosphate,vitamin B6,PNP,PLP,variant,I
Pyridoxal 5-phosphate monohydrate is an active vitamin B6 metabolite
价 格：￥电议型 号：T8083产 地：中国大陆
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TQ0138K145 hydrochlorideK-145,K 145,ERK,K145 hydrochloride,K145,Sphingosine kinase,anti-proliferative,SphK
K145 hydrochloride is a selective sphk2 inhibitor with substrate competitiveness and oral activity, with IC50 of 4.3 ?M and Ki of 6.4 ?M. K145 hydrochloride can induce apoptosis and has strong antitumor activity.
价 格：￥电议型 号：TQ0138产 地：中国大陆
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T8901YUM70Heat shock proteins,YUM70,HSP,cancer,pancreatic,reticulum,Apoptosis,GRP78,YUM-70,stress-mediate
YUM70 is a potent and selective glucose-regulated protein 78 (GRP78) inhibitor(with an IC50 of 1.5 μM for inhibiting GRP78 ATPase activity of the full-length protein). It induces endoplasmic reticulum (ER) stress-mediated apoptosis in pancreatic cancer.
价 格：￥电议型 号：T8901产 地：中国大陆
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T8506THPP-1PDE10A,SIMA,object,THPP 1,recognition,Phosphodiesterase (PDE),Inhibitor,inhibit,novel,THPP-1,T
THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively).
价 格：￥电议型 号：T8506产 地：中国大陆
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T7879TASP0415914TASP 0415914,inhibit,inflammatory,PKB,stability,TASP0415914,PI3Kγ,oral,Akt,Phosphoinositi
TASP0415914 is an orally potent inhibitor of phosphoinositide 3-kinase γ (PI3Kγ). T
价 格：￥电议型 号：T7879产 地：中国大陆
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T6872L755507HDR,β3-AR,inhibit,L755507,Adrenergic Receptor,Beta Receptor,CRISPR/Cas9,L 755507,Inhibitor,L-
L755507 is an effective, selective agonist of β3-AR（IC50=35 nM）.
价 格：￥电议型 号：T6872产 地：中国大陆
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T9217USP7-IN-8inhibit,USP7,Inhibitor,USP-7-IN-8,Deubiquitinase,DUBs,USP7IN8,anticancer,USP7 IN 8
Benzamide, 4-[6-amino-4-ethyl-5-(4-hydroxyphenyl)-3-pyridinyl]-N-methyl- is a selective ubiquitin-specific protease 7 (USP7) inhibitor with an IC50 of 1.4 μM. USP7-IN-8 has anticancer effects.
价 格：￥电议型 号：T9217产 地：中国大陆
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TN1305EthoxysanguinarinePP2A,colorectal cancer cells,protein phosphatase 2A,Apoptosis,cancerous inhibitor
6-Ethoxydihydrosanguinarine shows human blood acetylcholinesterase (HuAChE) and human plasma butyrylcholinesterase (HuBuChE) inhibitory activity, with IC50 values of 0.83 +/- 0.04 microM and 4.20 +/- 0.19 microM, respectively.
价 格：￥电议型 号：TN1305产 地：中国大陆
