TN3695Coniine hydrochlorideConiine hydrochloride

Coniine hydrochloride, a polyketide-derived alkaloid, is poisonous to humans and animals. It is a nicotinic acetylcholine receptor antagonist, which leads to inhibition of the nervous system.

价 格：￥电议型 号：TN3695产 地：中国大陆

T38776LP-922056cortical,Pectinacetylesterase,thickness,orally,femur,inhibit,Wnt,lipase,bone,LP-922056,Notu

LP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.

价 格：￥电议型 号：T38776产 地：中国大陆

TP1994LM871 acetateM871 acetate,M-871 acetate(908844-75-7 Free base)

M871 acetate is a selective galanin GAL2 receptor antagonist (Ki values are 13.1 and 420 nM at GAL2 and GAL1 receptors, respectively).It blocks pronociceptive effects of GAL2 agonists including AR-M1896.

价 格：￥电议型 号：TP1994L产 地：中国大陆

T6588Mitoxantroneleukaemia,NSC301739,PKC,MCF-7,NSC 301739,lymphocytes,Topoisomerase,Mitoxantrone,HL60 cel

Mitoxantrone is an anthracenedione antibiotic with antineoplastic activity. Mitoxantrone intercalates into and crosslinks DNA, thereby disrupting DNA and RNA replication. This agent also binds to topoisomerase II, resulting in DNA strand breaks and inhibition of DNA repair. Mitoxantrone is less cardiotoxic compared to doxorubicin.

价 格：￥电议型 号：T6588产 地：中国大陆

T9146ms48107Inhibitor,GPR68,GPCR,MS 48107,ms48107,brain-penetrant,BBB,inhibit,5-HT2B,MS-48107,bioavailabl

MS48107 is a potent and selective positive allosteric modulator of G protein-coupled receptor 68 (GPR68). It is selective for GPR68 over the closely related proton GPCRs, neurotransmitter transporters, and hERG ion channels. It can readily cross the blood-brain barrier (BBB) in mice.

价 格：￥电议型 号：T9146产 地：中国大陆

T30855CGP77675

CGP77675 is a potent and selective inhibitor of Src family kinase with IC50s of 5-20 and 40 nM for the phosphorylation of peptide substrates and autophosphorylation of purified Src. CGP77675 exhibits anticancer activity.

价 格：￥电议型 号：T30855产 地：中国大陆

TN71275,6-Epoxyergosterol5,6Epoxyergosterol,5,6 Epoxyergosterol

5,6-Epoxyergosterol is derived from the endophytic fungus Phyllosticta capitalensis.

价 格：￥电议型 号：TN7127产 地：中国大陆

TN1599Eburicoic acid

Eburicoic acid exhibits anti-inflammatory and antioxidant activity thereby protecting the liver from CCl4-induced hepatic damage and can be used in studies about anti-liver cancer.

价 格：￥电议型 号：TN1599产 地：中国大陆

T26520ABP688ABP688

ABP688 is a non-competitive and selective mGluR5 antagonist(Ki = 1.7 nM). ABP688 can be used as a PET tracer for clinical imaging.

价 格：￥电议型 号：T26520产 地：中国大陆

T60052BMS-905BMS905,BMS 905

BMS-905 is a potent dual inhibitors of TLR7 and TLR8 with good selectivity against TLR9 and other family members. BMS-905 can be used in studies about the treatment of diseases such as psoriasis, arthritis, and lupus.

价 格：￥电议型 号：T60052产 地：中国大陆

TMA05362-Acetylbenzoic acid2 Acetylbenzoic acid,2Acetylbenzoic acid

2-Acetylbenzoic acid is more potent than 2-propionyloxybenzoic acid in inhibiting platelet function and platelet prostaglandin (PG) synthesis although the potencies of these agents were comparable in inhibiting prostacyclin (PGI2) synthesis.

价 格：￥电议型 号：TMA0536产 地：中国大陆

T7415DKM 2-93E1 activating enzyme,Ubiquitin activating enzyme,E1/E2/E3 Enzyme,Inhibitor,DKM 2-93,Ubiquiti

DKM 2-93 is a relatively selective inhibitor of UBA5(IC50 : 430 μM).

价 格：￥电议型 号：T7415产 地：中国大陆

T8505SC-236SC-236,gastric,PPAR,cancer,ischemia,Liver,inhibit,allodynia,Inhibitor,fibrogenesis,neuroprotec

Sc 236 is an orally active and selective inhibitor of COX-2 (IC50 of 0.005 μM and 17.8 μM for COX-2 and COX-1, respectively).

价 格：￥电议型 号：T8505产 地：中国大陆

Fr14395Compound Fr14395Compound Fr14395

价 格：￥电议型 号：Fr14395产 地：中国大陆

T93325-Pyrimidinecarboxamide, 2-[[(1R,2S)-2-aminocyclohexyl]amino]-4-[[3-(2H-1,2,3-triazol-2-yl)phenyl]am

5-Pyrimidinecarboxamide, 2-[[(1R,2S)-2-a is a chemical compound.

价 格：￥电议型 号：T9332产 地：中国大陆

T15767LLY-283LLY283,LLY 283

LLY-283 is a potent, selective and oral protein arginine methyltransferase 5 (PRMT5) inhibitor, with an IC50 of 22 nM and a Kd of 6 nM for PRMT5:MEP50 complex, and shows antitumor activity.

价 格：￥电议型 号：T15767产 地：中国大陆

TP1760LAMARA peptide acetate(163560-19-8 free base)AMARA peptide acetate(163560 19 8 free base),AMARA pep

AMARA peptide acetate is a substrate for SIK and AMPK.AMARA peptide is a minimal substrate of several members of the protein kinases family. It consists of the phosphorylation site for AMP-activated Protein Kinase (AMPK).

价 格：￥电议型 号：TP1760L产 地：中国大陆

TP1053LProtein Kinase C 19-31 acetateProtein Kinase C 19 31 acetate,Protein Kinase C 1931 acetate

Protein Kinase C 19-31 acetate, a peptide inhibitor of protein kinase C (PKC), derived from the pseudo-substrate regulatory domain of PKCa (residues 19-31) with a serine at position 25 replacing the wild-type alanine, is used as protein kinase C substrate peptide for testing the protein kinase C activity.

价 格：￥电议型 号：TP1053L产 地：中国大陆

T9225Vebicorvirantiviral,Inhibitor,Vebicorvir,inhibit,Hepatitis B virus,HBV,CHB,DBT

Vebicorvir is a first-generation hepatitis B virus (HBV) core protein inhibitor, has demonstrated effective antiviral activity.

价 格：￥电议型 号：T9225产 地：中国大陆

T9050AG-270inhibit,Inhibitor,cancer,Low,solid,AG-270,SAM,pancreatic,lymphoma,tumor,AG 270,toxicity,AG270

AG-270 is an allosteric and orally active inhibitor of MAT2A.

价 格：￥电议型 号：T9050产 地：中国大陆