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T23286S 24795；化合物S24795Catestatin acetate(142211-96-9 free base)|||LNAChR；Catestatin acetate(142211-96-9 f
S 24795 (Catestatin acetate(142211-96-9 free base)) is an α7 nAChR partial agonist. S 24795 improves mnemonic function in aged mice and can be used in studies about aging-related memory disturbances.
价 格：￥电议型 号：T23286产 地：中国大陆
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T23233LRETF-4NA acetate；化合物RETF-4NA acetateRETF-4NA acetate（1160928-63-1 free base）；RETF-4NA acetate（116092
RETF-4NA acetate is a sensitive, specific substrate for chymotrypsin.
价 格：￥电议型 号：T23233L产 地：中国大陆
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T23228(R,S)-Anatabine (tartrate) (2743-90-0 free base)；化合物 T23228(R,S)-Anatabine (tartrate)；(R,S)-Anatabin
Anatabine is a minor tobacco alkaloid with a chemical structural similarity to nicotine. Anatabine is produced in plants of the Solanacea family including tobacco, green tomatoes, peppers, and eggplants. Anatabine is an Aβ inhibitor. (R,S)-Anatabine (tartrate) is preferable to (R,S)-Anatabine for certain applications and formulations.
价 格：￥电议型 号：T23228产 地：中国大陆
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T23215L(R)-3,4-DCPG HCl；(R)-3,4-DCPG 盐酸盐(R)-3,4-DCPG HCl(201730-10-1 Free base)；(R)-3,4-DCPG HCl(201730-10-
(R)-3,4-DCPG HCl is a potent and selective mGlu8a receptor agonist that activates metabotropic glutamate receptors on primary afferent terminals in the neonatal rat spinal cord.
价 格：￥电议型 号：T23215L产 地：中国大陆
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T23210Quinacrine (dihydrochloride hydrate)；化合物 T23210Quinacrine (hydrochloride hydrate) (83-89-6 free base
Quinacrine is a compound that is commonly used as an anti-protozoal agent. It inhibits voltage-dependent sodium channels (IC50: 3.3 μM） and suppresses aldehyde oxidase (IC50: 3.3 μM). Quinacrine prevents misfolding of prion protein (EC50: 0.3 μM). As an effective riboflavin antagonist, quinacrine associates with the riboflavin-binding protein (Ki: 6.7 μM). Voltage-dependent sodium channels play a vital role in action potential initiation and propagation in excitable cells, including muscle, nerv
价 格：￥电议型 号：T23210产 地：中国大陆
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T23204LPSN 375963 hydrochloride（388575-52-8 Free base）；化合物PSN 375963 hydrochloride（388575-52-8 Free base）PS
PSN 375963 hydrochloride, a potent GPR119 agonist, demonstrates EC50 values of 8.4 μM and 7.9 μM for human and mouse GPR119, respectively. Its efficacy is comparable to that of the endogenous agonist oleoylethanolamide (OEA) [1] [2].
价 格：￥电议型 号：T23204L产 地：中国大陆
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T23177PPACK Dihydrochloride (71142-71-7 free base)；化合物 T23177PPACK Dihydrochloride；PPACK Dihydrochloride
PPACK Dihydrochloride is the dihydrochloride form of its active component PPACK (D-Phenylalanyl-L-prolyl-L-arginine chloromethyl ketone), a potent, selective, and irreversible inhibitor of thrombin that inhibits human α-thrombin with inhibition constant (Ki: 0.24 nM).
价 格：￥电议型 号：T23177产 地：中国大陆
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T23149Phenyl-benzothiazole HCl (92-36-4 free base)；化合物 T23149Phenyl-benzothiazole HCl；Phenyl-benzothiazole
An azole for proteomics research
价 格：￥电议型 号：T23149产 地：中国大陆
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T23146PHA 568487 free base；化合物PHA 568487PHA 568487；PHA 568487
The quinuclidine PHA 568487 free base is an agonist of the alpha 7 nicotinic acetylcholine receptor that was designed to mitigate the bioactivation associated with the core scaffold and subsequently remove associated liabilities with in vivo tolerability.
价 格：￥电议型 号：T23146产 地：中国大陆
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T23077LNovokinin acetate；化合物Novokinin acetateNovokinin acetate (358738-77-9 free base)；Novokinin acetate (3
Novokinin acetate exhibited an affinity for the AT2 receptor with Ki of 7 nM, and its antihypertensive and vasorelaxing activities were blocked by PD123319, an AT2 receptor antagonist.
价 格：￥电议型 号：T23077L产 地：中国大陆
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T23038LNα-Methylhistamine FA；Methylhistamine 甲酸盐Nα-Methylhistamine FA（673-50-7 Free base)；Nα-Methylhistamin
Nα-Methylhistamine FA is a histamine H3 receptor agonist
价 格：￥电议型 号：T23038L产 地：中国大陆
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T23030MS023 (hydrochloride) (1831110-54-3 free base)；化合物 T23030MS023 (hydrochloride)；MS023 (hydrochloride)
MS023 is a type I PRMT inhibitor (IC50: 20, 119, 83, 8, and 8 nM for PRMT1, 3, 4, 6, and 8, respectively).
价 格：￥电议型 号：T23030产 地：中国大陆
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T23028MRT67307 HCl (1190378-57-4 free base)；化合物 T23028MRT67307 HCl；MRT67307 HCl
MRT67307 is an inhibitor for TBK1, IKKε , MARK1-4 and NUAK1 with IC50 value of 19, 160, 27-52 and 230nM , respectively [1]. It is an inhibitor for ULK1and ULK2 with IC50 value of 45 and 38nM, respectively [2]. Also, it is a salt inducible kinase (SIK) inhibitor with IC50 value of 250, 67 and 430nM for SIK1, SIK2 and SIK3, respectively.
SIKs prevent the formation of regulatory macrophages and their inhibition induces increasing in some markers of regulatory macrophages, such as IL-10 and oth价 格：￥电议型 号：T23028产 地：中国大陆
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T23008LMMPIP hydrochloride；化合物MMPIP hydrochlorideMMPIP hydrochloride (479077-02-6 Free base)；MMPIP hydrochl
MMPIP hydrochloride is a selective antagonist of allosteric mGluR7. MMPIP hydrochloride can be used in research on the roles of mGluR7 on central nervous system functions.
价 格：￥电议型 号：T23008L产 地：中国大陆
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T22957LY2606368 HCl (1234015-52-1 free base)；化合物 T22957LY2606368 HCl；LY2606368 HCl
LY2606368 HCl is a selective ATP competitive inhibitor of checkpoint kinase 1 (IC50: 1.5nM in SW1990 cells).
价 格：￥电议型 号：T22957产 地：中国大陆
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T22932LLPYFD-NH2 acetate；化合物LPYFD-NH2 acetateLPYFD-NH2 acetate (700361-48-4 free base)；LPYFD-NH2 acetate (7
LPYFD-NH2 acetate shows some inhibitory effect on the aggregation of Abeta(1-42).
价 格：￥电议型 号：T22932L产 地：中国大陆
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T22890KHS 101 hydrochloride (1262770-73-9 free base)；化合物 T22890KHS 101 hydrochloride；KHS 101 hydrochloride
KHS 101 hydrochloride is a neuronal differentiation inducer
价 格：￥电议型 号：T22890产 地：中国大陆
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T22820GSK J5 HCl (1394854-51-3 free base)；化合物 T22820GSK J5 HCl；GSK J5 HCl
GSK J5 HCl is the hydrochloride form of GSK J5. GSK J5 is an inactive isomer of GSK J4 and a cell-permeable ester derivative of inactive control GSK J2.
价 格：￥电议型 号：T22820产 地：中国大陆
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T22811LGR 94800 acetate；化合物GR 94800 acetateGR 94800 acetate (141636-65-9 free base)；GR 94800 acetate (14163
GR 94800 acetate is a potent and selective neurokinin 2(NK-2) antagonist.
价 格：￥电议型 号：T22811L产 地：中国大陆
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T22804GPP 78 hydrochloride (1202580-59-3 free base)；化合物 T22804GPP 78 hydrochloride；GPP 78 hydrochloride
NAMPT inhibitor
价 格：￥电议型 号：T22804产 地：中国大陆
