T8933JNJ-63576253 free baseJNJ 63576253 free base,resistant,TRC 253,JNJ63576253,TRC-253,CRPC,JNJ63576253

JNJ-63576253 is a potent and orally active full antagonist of androgen receptor (AR), with IC50s of 37 and 54 nM for F877L mutant AR and wild-type AR in LNCaP cells. JNJ-63576253 can be used for the research of castration-resistant prostate cancer (CRPC).

价 格：￥电议型 号：T8933产 地：中国大陆

Fr14145Compound Fr14145Compound Fr14145

价 格：￥电议型 号：Fr14145产 地：中国大陆

Fr13755Compound Fr13755Compound Fr13755

价 格：￥电议型 号：Fr13755产 地：中国大陆

TQ0228DerazantinibARQ 087,Derazantinib,Fibroblast growth factor receptor,inhibit,FGFR,ARQ087,Inhibitor

Derazantinib (ARQ-087) is an ATP competitive tyrosine kinase inhibitor. It exhibits potent activity against FGFR1/FGFR2/FGFR3 chondrocytes (IC50s: 4.5 nM/1.8 nM/4.5 nM).

价 格：￥电议型 号：TQ0228产 地：中国大陆

T8742G5-7antiangiogenic,inhibit,Apoptosis,JAK,Glioma,G-5-7,cycle,G5 7,phase,G57,STAT3,cell,Inhibitor,EGFR

JAK2 inhibitor G5-7 is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for glioma study

价 格：￥电议型 号：T8742产 地：中国大陆

T8934(6R)-FR054inhibit,ERS,(6R)-FR054,Inhibitor,(6R) FR054,Apoptosis,TNBC,(6R)-FR-054,cancer,breast,(6R)F

FR054 is an inhibitor of the Hexosamine Biosynthetic Pathway (HBP) enzyme PGM3, with a remarkable anti-breast cancer effect.

价 格：￥电议型 号：T8934产 地：中国大陆

TP1911LCALP3 acetate(261969-05-5 free base)CALP-3 acetate(261969-05-5 free base),CALP3 acetate(261969055 fr

CALP3 acetate is a potent Ca2+ channel blocker that activates EF hand motifs of Ca2+-binding proteins. CALP3 acetate can functionally mimic increased [Ca2+]i by modulating the activity of Calmodulin (CaM), Ca2+ channels and pumps.

价 格：￥电议型 号：TP1911L产 地：中国大陆

TP2323LDeslorelin acetate(57773-65-6 free base)Deslorelin acetate(57773656 free base),Deslorelin acetate(57

Deslorelin acetate is a gonadotropin releasing hormone super-agonist (GnRH agonist)

价 格：￥电议型 号：TP2323L产 地：中国大陆

T7768RGX-104RGX 104,inhibit,LXR,RGX-104,Liver X receptor,RGX104,Inhibitor

RGX-104 free Acid is an agonist of potent liver-X nuclear hormone receptor (LXR)

价 格：￥电议型 号：T7768产 地：中国大陆

TP1019LUrechistachykinin I acetate(149097-03-0 free base)Urechistachykinin I acetate(149097 03 0 free base)

Urechistachykinin I (Uru-TK I) acetate is an invertebrate kalinin-related peptide (TRPs) isolated from thylakoid nematodes.

价 格：￥电议型 号：TP1019L产 地：中国大陆

T60108PDGFR Tyrosine Kinase Inhibitor III

PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].

价 格：￥电议型 号：T60108产 地：中国大陆

TN2376Fructo-oligosaccharide DP8/GF7inhibit,Fructo oligosaccharide DP8/GF7,Fructooligosaccharide DP8/GF7,F

Fructo-oligosaccharide DP8 / GF7 belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=8). Fructo-oligosaccharides (FOS) are composed of 7 fructose units linked by (2→1)-β-glycosidic bonds and having a single D-glucosyl unit at the non-reducing end.

价 格：￥电议型 号：TN2376产 地：中国大陆

T7101Tyrphostin AG30HER1,ErbB-1,Inhibitor,EGFR,Tyrphostin AG30,Epidermal growth factor receptor,Tyrphosti

Tyrphostin AG30 (AG30) is a potent protein tyrosine kinases (PTK) inhibitor.

价 格：￥电议型 号：T7101产 地：中国大陆

T7127DC260126stress,DC260126,DC-260126,FFAR,Inhibitor,insulin,inhibit,secretion,Apoptosis,DC 260126,Free

DC260126 is a small-molecule antagonist of FFA1 (GPR40)

价 格：￥电议型 号：T7127产 地：中国大陆

T7665[Leu5]-Enkephalin TFA(58822-25-6(free bas))[Leu5] Enkephalin TFA(58822 25 6(free bas)),[Leu-5]-Enkep

[Leu5]-Enkephalin is the most potent δ-receptor ago

价 格：￥电议型 号：T7665产 地：中国大陆

TP1895L1KYL acetate(676657-00-4 free base)KYL acetate(676657 00 4 free base),KYL acetate(676657004 free base

EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM); inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). Prevents AβO induced synaptic damage, dendritic spine loss and prevents the blocking of LTP in hippocampal CA3-CA1 transmissions. Exhibits a long half life in cell culture media (8 and 12 hours in PC3 and C2C12 media respectively). Neuroprotective.

价 格：￥电议型 号：TP1895L1产 地：中国大陆

T6836FIIN-2inhibit,FGFR,FIIN2,FIIN 2,Fibroblast growth factor receptor,Inhibitor,FIIN-2

FIIN-2, an irreversible, pan-FGFR inhibitor, inhibits FGFR1/2/3/4 with IC50 of 3.09 nM, 4.3 nM, 27 nM and 45.3 nM, respectively.

价 格：￥电议型 号：T6836产 地：中国大陆

T12262L1NPS ALX Compound 4a hydrochloride(1:1)NPSALXCompound4ahydrochloride(299433106Freebase)

NPS ALX Compound 4a hydrochloride(1:1) is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM.

价 格：￥电议型 号：T12262L1产 地：中国大陆

TP1862L[Sar9] Substance P acetate(77128-75-7 free base)[Sar9] Substance P acetate(77128 75 7 free base),[Sa

[Sar9]-Substance P acetate is one of NK-1 receptor agonist. The action of SP on progesterone metabolism was mimicked by the rNK1-specific agonist [Sar-9,Met(O2)11]-SP.

价 格：￥电议型 号：TP1862L产 地：中国大陆

T17098TilfrinibTilfrinib

Tilfrinib is an effective and selective inhibitor of breast tumor kinase(Brk, IC50 = 3.15 nM) which displays anti-proliferative and anti-tumor activities.

价 格：￥电议型 号：T17098产 地：中国大陆