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TP1253Argirelineskin-permeable,BoNTs,inhibit,neurotransmitter,Inhibitor,peptide,Acetyl hexapeptide 3,Argir
Argireline (Acetyl hexapeptide-3) is composed of chains of amino acids known as peptides. Argireline significantly inhibits Ca2+ dependent neurotransmitter release (acetylcholine) at the neuromuscular junction. Argireline has antiwrinkle and anti-aging activity[1][2][3].
价 格：￥电议型 号：TP1253产 地：中国大陆
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T13303Virginiamycin M1
Virginiamycin M1 is a macrocyclic lactone peptide antibiotic and is a member of the streptogramin A group of antibiotics.
价 格：￥电议型 号：T13303产 地：中国大陆
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TP1057LPhe-Met-Arg-Phe Like Peptide acetatePheMetArgPhe Like Peptide acetate,Phe Met Arg Phe Like Peptide a
Phe-Met-Arg-Phe Like Peptide acetate is a FMRF-like peptide from visceral and somatic muscles of the snail Helix aspersa. FMRF (Phe-Met-Arg-Phe) is a neuropeptide peptide consisting of 4 amino acid residues.
价 格：￥电议型 号：TP1057L产 地：中国大陆
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TJS0856Dalbergininhibit,Dalbergin,Inhibitor
1. Dalbergin exhibits similar bone conserving effect against bone-loss as estradiol treatment, it as a therapeutic candidate against postmenopausal osteoporosis. 2. Dalbergin prevents some effects of photoaging and maintain skin integrity by regulating the degradation of the extracellular matrix proteins.
价 格：￥电议型 号：TJS0856产 地：中国大陆
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T7436CilofexorGS9674,Inhibitor,inhibit,NR1H4,FXR,Cilofexor,PSC,GS 9674,oral,NASH,GS-9674,antifibrotic,non
Cilofexor inhibits binding of a synthetic peptide, Cilofexor is a farnesoid X receptor (FXR) agonist.
价 格：￥电议型 号：T7436产 地：中国大陆
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T7570RGD peptide (GRGDNP)inhibit,Integrin,Apoptosis,RGD peptide (GRGDNP),Inhibitor
RGD peptide GRGDNP(2TFA) is a integrin-ligand interactions inhibitor.
价 格：￥电议型 号：T7570产 地：中国大陆
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T6434CCG-50014Regulators of G-protein Signaling,Regulator of G-protein Signaling,RGS Protein,CCG-50014,in
CCG 50014 is a potent and selective inhibitor of RGS4 with IC50 of 30 nM.
价 格：￥电议型 号：T6434产 地：中国大陆
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T7165Basmisanilα subunit-containing GABAA receptors (GABAAα5),RO-5186582,RG-1662,psychiatric disorders,ne
Basmisanil is a negative allosteric modulator/inverse agonist of GABAAα5 receptors.Formulations containing basmisanil are in clinical trials for the treatment of cognitive impairments associated with Down syndrome.
价 格：￥电议型 号：T7165产 地：中国大陆
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TP1931L1[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate[D Arg1,D Phe5,D Trp7,9,Leu11] Substance P acetate
Broad spectrum neuropeptide inverse agonist and antagonist. Potent full inverse agonist for the ghrelin receptor (EC50 = 5.2 nM); diminishes constitutive ghrelin receptor signaling. Also antagonist at tachykinin, bradykinin, CCK and bombesin receptors. Induces apoptosis and inhibits cancer cell growth in vitro.
价 格：￥电议型 号：TP1931L1产 地：中国大陆
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TP1400L[Arg8]-Vasotocin acetate（113-80-4 free base)[Arg8]Vasotocin acetate（113804 free base),[Arg-8]-Vasoto
[Arg8]-Vasotocin acetate is a hormone present in the neurohypophysis of nonmammalian vertebrates that is related to vasopressin and oxytocin.
价 格：￥电议型 号：TP1400L产 地：中国大陆
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TP1459LGly-Arg-Gly-Asp-Ser acetate(96426-21-0 free base)GlyArgGlyAspSer acetate(96426210 free base),Gly Arg
Gly-Arg-Gly-Asp-Ser (GRGDS) acetate is a cell binding protein domain derived from the cell-binding region of fibronectin.
价 格：￥电议型 号：TP1459L产 地：中国大陆
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T35666PRGL493PRGL-493,PRGL493
PRGL493 is an inhibitor of long-chain acyl-CoA synthetase 4 (ACSL4).1It inhibits formation of arachidonoyl-CoA (AA-CoA) from arachidonic acid in, as well as the proliferation and migration of, PC3 and MDA-MB-231 cancer cells when used at a concentration of 50 μM. PRGL493 (5 μM) reduces production of progesterone induced by 8-Br-cyclic AMP (8-Br-cAMP) in MA-10 Leydig tumor cells. It inhibits tumor growth in a PC3 mouse xenograft model when administered at a dose of 0.25 mg/kg.
价 格：￥电议型 号：T35666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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T2344LY 344864migraines,Adrenergic Receptor,BBB penetration,Serotonin Receptor,inhibit,5-HT Receptor,LY-3
LY344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.
价 格：￥电议型 号：T2344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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T6991Nitroprusside disodium dihydrateNitroprusside disodium dihydrate,Autophagy,Inhibitor,decrease,surger
Sodium Nitroprusside Dihydrate is a potent vasodilator working through releasing NO spontaneously in blood.
价 格：￥电议型 号：T6991产 地：中国大陆
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T7045ClonidineClonidine,α2-adrenergic,inhibit,Inhibitor,anesthesia,Adrenergic Receptor,Beta Receptor
Clonidine is a centrally active alpha-adrenergic agonist used predominantly as an antihypertensive agent, usually in combination with other agents. Despite wide-scale use for many years, clonidine has not been linked definitively to either serum aminotransferase elevations or clinically apparent liver injury.
价 格：￥电议型 号：T7045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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TP1696LCGGRGD acetate(1260223-44-6 free base)CGGRGD acetate(1260223446 free base),CGGRGD acetate(1260223 44
CGGRGD acetate is a RGD derivative with cysteine as the n-terminal. CGGRGD was synthesized by solid phase peptide synthesis technology, and amino2-cyanobenzothiazole (2-cyanobenzothiazole) (2-cyanobenzothiazole (CBT) was added on the surface of PCL fiber for ammoniation.
价 格：￥电议型 号：TP1696L产 地：中国大陆
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T16040Mepazinediffuse,B cell,inhibit,large,mucosa associated lymphoid tissue lymphoma translocation gene 1
Mepazine is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM. Mepazine enhances apoptosis and affects the cell viability.
价 格：￥电议型 号：T16040产 地：中国大陆
