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220

抑制剂 & 化合物

21

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T0957	Isradipine PN 200-110,伊拉地平	Calcium Channel; Autophagy	Autophagy; Membrane transporter/Ion channel; Metabolism
	Isradipine (PN 200-110) 是一种二氢吡啶类钙通道阻滞剂，具有抗高血压和血管扩张活性。它是一种具有口服活性的 L 型钙通道阻滞剂，也是一种潜在可行的帕金森病神经保护剂。
T12315	OR-1896	PDE	Metabolism
	OR-1896 is an active long-lived Levosimendan metabolite, is a highly selective inhibitor of phosphodiesterase (PDE) III isoformand a powerful vasodilator.
T67933	BAY-4931	PPAR	DNA Damage/DNA Repair; Metabolism
	BAY-4931 是一种有效的、共价的、选择性的 PPARγ反向激动剂，IC50为 0.17 nM。
T61214	EWP 815	Phosphatase; Hydroxylase	Metabolism
	EWP 815 is a disulfiram analogue that functions as a powerful inhibitor of Ins(1,4) P 2 phosphatase, Ins(1,4,5) P 3 5-phosphatase, and dopamine β-hydroxylase activity [1] [2].
T19774	Methylisothiazolinone KB-838,MI,N-Methylisothiazolin-3-one,甲基异噻唑啉酮,Methylisothiazolinone free base	Antibacterial	Microbiology/Virology
	Methylisothiazolinone (MI) 是合成的杀菌剂和防腐剂，可广泛用于工业和消费产品。它作为化妆品和盥洗用品中的防腐剂。
T9879	Hydroxystilbamidine Oxistilbamidinum,羟芪巴脒,(E)-hydroxystilbamidine,2-Hydroxy-4,4'-diguanylstilbene,Bis(8-hydroxyquinolinium) sulphate	Others	Others
	Hydroxystilbamidine ((E)-hydroxystilbamidine) 是一种能够结合 DNA 和 RNA 的染料，也被发现是细胞核糖核酸酶的强效抑制剂。
T9111	8-Azaadenosine	Adenosine deaminase	Metabolism
	8-Azaadenosine 是 ADAR1抑制剂和是 A-to-I 编辑抑制剂。它可阻断 RNA 编辑并抑制甲状腺癌细胞的增殖、3D 生长、侵袭和迁移。
T24214	Phenamacril JS39919,苯那普利,JS399 19	Myosin; Antifungal	Cytoskeletal Signaling; Microbiology/Virology
	Phenamacril (JS39919) 是一种氰基丙烯酸酯类杀菌剂，对镰刀菌，特别是禾谷镰刀菌有很强的抑制作用。它是一种特异性镰刀菌肌球蛋白 I 抑制剂。
T64347	ALDH1A3-IN-3	Dehydrogenase	Metabolism
	ALDH1A3-IN-3 (化合物 16) 是一种有效的 ALDH1A3 抑制剂，IC50 值为 0.26 μM。ALDH1A3-IN-3 也是 ALDH3A1 的底物。ALDH1A3-IN-3 可用于前列腺癌的研究。
T63166L	(S, R)-LSN 3318839 (S, R)-LSN 3318839(Isomer-2764704-18-7)	Glucagon Receptor	GPCR/G Protein

T19637	Aluminum phthalocyanine chloride Phthalocyanine Chloroaluminum,铝酞菁,Chloroaluminum Phthalocyanine	Others	Others
	Aluminum phthalocyanine chloride (Phthalocyanine Chloroaluminum) 是一种强烈的蓝绿色芳香大环化合物，广泛用于染色。
T10213	A-437203 ABT-925,A37203,Lu201640	Dopamine Receptor	GPCR/G Protein; Neuroscience
	A-437203 (Lu201640) 是一种基于1H-pyrimidin-2-one scaﬀold 的、具有选择性的、新型强效的d3受体拮抗剂，对 D2, D3, 和 D4 受体,的Ki 值分别为 71, 1.6 和 6220 nM。
T35528L	TD52 dihydrochloride TD52 dihydrochloride(1798328-24-1 Free base),TD52 2HCl	Others	Others
	TD52 dihydrochloride (TD52 2HCl), a derivative of Erlotinib, is a potent and orally active inhibitor of protein phosphatase 2A (CIP2A). It exhibits strong anti-cancer properties by regulating the CIP2A/PP2A/p-Akt signaling pathway, resulting in the induction of apoptosis in triple-negative breast cancer (TNBC) cells. Mechanistically, TD52 dihydrochloride disrupts the binding of Elk1 to the CIP2A promoter, effectively reducing CIP2A levels. Notably, TD52 dihydrochloride demonstrates powerful anti...
T14513	BBIQ	TLR	Immunology/Inflammation
	BBIQ 是一种有效且选择性的 toll 样受体 7 (TLR7) 激动剂，对人 TLR7 的 EC50 为 59.1 nM。BBIQ 还是一种功能强大的疫苗佐剂，可增强机体的先天免疫应答。
T40465	SAG dihydrochloride	Hedgehog/Smoothened	GPCR/G Protein; Stem Cells
	SAG dihydrochloride 是一种强效的 Smoothened（Smo）受体激动剂（EC 50 =3 nM；K d =59 nM）。SAG dihydrochloride 可激活刺猬信号通路并抵消环丙胺对 Smo 的抑制。
T67835	LKM38
	LKM38是一种新型的重氮烷基胆固醇探针，是一种有前途的胆固醇模拟物。LKM38既能维持抗胆固醇细胞的生长，又能适当地调节关键的胆固醇平衡途径。LKM38可以作为研究胆固醇蛋白相互作用和贩运的有力工具。
T22574L	Angiotensin 1/2 (5-7) acetate	RAAS	Endocrinology/Hormones
	Angiotensin 1/2 (5-7) acetate 是一种具有 H2N-Ile-His-Pro-OH 序列的肽。血管紧张素是一种寡肽，是一种激素和一种强大的双肽原。它来源于前体分子血管紧张素原，一种在肝脏中产生的血清球蛋白。它在肾素-血管紧张素系统中起重要作用。
T21610	Bradykinin (acetate)	Bradykinin Receptor	GPCR/G Protein
	Bradykinin (acetate) 是一种由激肽释放酶-激肽系统产生的活性肽。它是一种炎症介质，也被认为是多种血管和肾功能的神经介质和调节剂。它由血液中的 kallidin 酶促产生，是一种强大的血管扩张剂，可引起平滑肌收缩，并可能介导炎症。它具有作为人血清代谢物和血管扩张剂的作用。它是缓激肽 (2+) 的互变异构体。
T28029	Methylisothiazolinone hydrochloride N-Methylisothiazolin-3-one,MI,2-甲基-4-异噻唑啉-3-酮盐酸盐,KB-838,Methylisothiazolinone HCl
	Methylisothiazolinone is a powerful synthetic biocide and preservative.
T32436	L 1935 Compound l1935,L-1935,Histamine-liberator L 1935,L1935
	L 1935 is a type of powerful histamine-liberator.
T25960	Piperic acid NSC 129538,NSC129538,NSC-129538
	Piperic acid is a powerful antioxidant and has potent antibacterial properties
T34124	Pranolium UM-272,SC-27761,UM 272,SC 27761,SC27761
	Pranolium is a quaternary dimethyl derivative of Propranolol, a well-known powerful betareceptor-blocking agent.
T71443	Amphidinolide D
	Amphidinolide D is a powerful activator of actomyosin ATPase enhances skeletal muscle contraction.
T71140	MDL-27048
	MDL-27048 is a powerful and reversible microtubule inhibitor.
T33590	Nantradol HCl MCV-4161,MCV4161,UM-1159,UM 1159,MCV 4161,UM1159
	Nantradol HCl is a powerful analgesic widely used to investigate the potential therapeutic applications of cannabinoids.
T39753	Etavopivat FT-4202
	Etavopivat is a powerful, specific, orally bioavailable activator of pyruvate kinase (PKR) in red blood cells (RBCs). It exhibits potent properties against sickling.
T38822	D-threo-PPMP
	D-threo-PPMP, a powerful glucosylceramide (GlcCer) synthase inhibitor, effectively impedes karyokinesis and decreases cyst formation.
T25299	Degranol NSC 9698,NSC-9698,NSC9698
	Degranol is a nitrogen mustard derivative alkylating agent utilized as antineoplastic. It causes severe bone marrow depression and is a powerful vesicant.
T30945	Cinolazepam Gerodorm,OX-373
	Cinolazepam is a benzodiazepine derivative drug.It has a powerful sedative effect, so it is mainly used as a hypnotic.
T11107	DSP-1053	Others	Others
	Dsp-1053 is a powerful SERT (Ki=1.02 nM) inhibitor with partial 5-HT1A receptor (Ki=5.05 nM) agonizing activity.
T35661	QTX125
	QTX125, a powerful and highly specific HDAC6 inhibitor, demonstrates exceptional selectivity in comparison to other HDACs, resulting in robust antitumor activity[1].
T68260	Calmidazolium (cation)
	Calmidazolium (cation) is a powerful inhibitor of or red blood cell Ca -ATPase & Ca transport into inside-out red blood cell vesicles; an antagonist of calmodulin.
T28464	p-SCN-Bn-TCMC HCl p-SCN-Bn-TCMC
	p-SCN-Bn-TCMC is a bifunctional chelator, it contains a powerful chelator TCMC and reactive tioisocyante linker. TCMC is a powerful chelator with capability to strongly bind radio-isotopic heavy metal ion, which are widely used for radio-diagnostic/imagin
TP2459	Lysipressin Acetate Lysine pitressin,Lysine vasopressin,Lypressin,Lysopressin,Lysipressin Acetate. L-Lysine vasopressin,Lysine-ADH
	Lysipressin Acetate is an analog of vasopressin, a powerful vasopressin used to regulate blood pressure. Endogenous vasopressin in most mammalian species.
T40943	EMD527040
	EMD527040 is a powerful and highly specific αvβ6 antagonist, exhibiting notable antifibrotic properties. It is suitable for conducting research on carcinoma and liver fibrosis.
T35082	VU6010608 VU-6010608,VU 6010608
	VU6010608 is an effective mGlu7 NAM with excellent CNS permeability and is powerful in electrophysiological studies in blocking long-term enhancement of high-frequency stimuli.
T38914	MPO-IN-3
	MPO-IN-3, a powerful inhibitor of myeloperoxidase (MPO), is described as such in example 191 of WO2013068875A1. MPO, a heme-containing enzyme, is classified under the peroxidase superfamily.
T40841	L-2-Aminooxy-3-phenylpropanoic acid hydrobromide
	L-2-Aminooxy-3-phenylpropanoic acid hydrobromide is a powerful inhibitor of L-phenylalanine ammonia-lyase, an enzyme responsible for catalyzing the conversion of L-phenylalanine to trans-cinnamic acid.
T20778	Epoprostenol U 53217,U 53,217,U-53,217
	Epoprostenol, a prostaglandin, is a powerful vasodilator. It inhibits platelet aggregation.
T61314	DC-CPin7
	DC-CPin7, a powerful inhibitor of the bromodomain of CREB-binding protein (CBP), exhibits an IC50 value of 2.5 μM [1].
T11721L	JDTic dihydrochloride	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	JDTic is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception.
T61310	HIV-1 inhibitor-37
	HIV-1 inhibitor-37 (Compound 83) is a highly powerful HIV-1 inhibitor. It exhibits significant potential for use as an innovative latent HIV-1 reactivating agent [1].
T40642	Chlorpyrifos-oxon
	Chlorpyrifos-oxon, an active metabolite of Chlorpyrifos, is a powerful phosphorylating agent with potent inhibition of AChE activity. It induces cross-linking between tubulin subunits and disrupts microtubule function[4].
T40568	Fmoc-MMAE
	Fmoc-MMAE, a protective group-conjugated variant of monomethyl auristatin E (MMAE), serves as a powerful inhibitor of tubulin. It finds application in the synthesis of antibody-drug conjugates (ADC).
T36901	Pelcitoclax
	Pelcitoclax (APG-1252) is a powerful inhibitor of the Bcl-2 and Bcl-xl proteins, displaying significant antineoplastic and pro-apoptotic properties[1].
T69443	Aminobutane bisphosphonate
	Aminobutane bisphosphonate is a powerful inhibitor of bone resorption. It can potentially be a useful measure for controlling hypercalcemia in patients with carcinoma.
T38779	NS-102
	NS-102 is a powerful and selective antagonist of the kainate receptor (GluK2), as well as a potent antagonist of the GluR6/7 receptor.
T61712	Trk-IN-8
	Trk-IN-8, a powerful TRK inhibitor, demonstrates excellent potency against TRKAa, TRKA(G595R), and TRKC(G623R) with IC50 values of 0.42 nM, 0.89 nM, and 1.5 nM, respectively (WO2021115401A1, compound 3) [1].
T25316	Dexecadotril Retorphan
	Dexecadotril is a powerful and selective neprilysin inhibitor. It behaves as a prodrug of the enantiomer of thiorphan.
T75748	Indolicidin TFA
	Indolicidin TFA 是一种从牛中性粒细胞的细胞质颗粒中纯化的强效抗菌肽。

化合物

Cat.No: T0957

Synonym: PN 200-110,伊拉地平

Target: Calcium Channel, Autophagy

Cat.No: T12315

Target: PDE

Cat.No: T67933

Target: PPAR

Cat.No: T61214

Target: Phosphatase, Hydroxylase

Methylisothiazolinone

Cat.No: T19774

Synonym: KB-838,MI,N-Methylisothiazolin-3-one,甲基异噻唑啉酮,Methylisothiazolinone free base

Target: Antibacterial

Hydroxystilbamidine

Cat.No: T9879

Synonym: Oxistilbamidinum,羟芪巴脒,(E)-hydroxystilbamidine,2-Hydroxy-4,4'-diguanylstilbene,Bis(8-hydroxyquinolinium) sulphate

Target: Others

Cat.No: T9111

Target: Adenosine deaminase

Cat.No: T24214

Synonym: JS39919,苯那普利,JS399 19

Target: Myosin, Antifungal

Cat.No: T64347

Target: Dehydrogenase

(S, R)-LSN 3318839

Cat.No: T63166L

Synonym: (S, R)-LSN 3318839(Isomer-2764704-18-7)

Target: Glucagon Receptor

Aluminum phthalocyanine chloride

Cat.No: T19637

Synonym: Phthalocyanine Chloroaluminum,铝酞菁,Chloroaluminum Phthalocyanine

Target: Others

Cat.No: T10213

Synonym: ABT-925,A37203,Lu201640

Target: Dopamine Receptor

TD52 dihydrochloride

Cat.No: T35528L

Synonym: TD52 dihydrochloride(1798328-24-1 Free base),TD52 2HCl

Target: Others

Cat.No: T14513

Target: TLR

SAG dihydrochloride

Cat.No: T40465

Target: Hedgehog/Smoothened

Cat.No: T67835

Angiotensin 1/2 (5-7) acetate

Cat.No: T22574L

Target: RAAS

Bradykinin (acetate)

Cat.No: T21610

Target: Bradykinin Receptor

Methylisothiazolinone hydrochloride

Cat.No: T28029

Synonym: N-Methylisothiazolin-3-one,MI,2-甲基-4-异噻唑啉-3-酮盐酸盐,KB-838,Methylisothiazolinone HCl

Cat.No: T32436

Synonym: Compound l1935,L-1935,Histamine-liberator L 1935,L1935

Cat.No: T25960

Synonym: NSC 129538,NSC129538,NSC-129538

Cat.No: T34124

Synonym: UM-272,SC-27761,UM 272,SC 27761,SC27761

Amphidinolide D

Cat.No: T71443

Cat.No: T71140

Cat.No: T33590

Synonym: MCV-4161,MCV4161,UM-1159,UM 1159,MCV 4161,UM1159

Cat.No: T39753

Synonym: FT-4202

Cat.No: T38822

Cat.No: T25299

Synonym: NSC 9698,NSC-9698,NSC9698

Cat.No: T30945

Synonym: Gerodorm,OX-373

Cat.No: T11107

Target: Others

Cat.No: T35661

Calmidazolium (cation)

Cat.No: T68260

p-SCN-Bn-TCMC HCl

Cat.No: T28464

Synonym: p-SCN-Bn-TCMC

Lysipressin Acetate

Cat.No: TP2459

Synonym: Lysine pitressin,Lysine vasopressin,Lypressin,Lysopressin,Lysipressin Acetate. L-Lysine vasopressin,Lysine-ADH

Cat.No: T40943

Cat.No: T35082

Synonym: VU-6010608,VU 6010608

Cat.No: T38914

L-2-Aminooxy-3-phenylpropanoic acid hydrobromide

Cat.No: T40841

Cat.No: T20778

Synonym: U 53217,U 53,217,U-53,217

Cat.No: T61314

JDTic dihydrochloride

Cat.No: T11721L

Target: JAK

HIV-1 inhibitor-37

Cat.No: T61310

Chlorpyrifos-oxon

Cat.No: T40642

Cat.No: T40568

Cat.No: T36901

Aminobutane bisphosphonate

Cat.No: T69443

Cat.No: T38779

Cat.No: T61712

Cat.No: T25316

Synonym: Retorphan

Indolicidin TFA

Cat.No: T75748

Cat. No.	Product Name	Target	Signaling Pathways
TP1180	Dolastatin 10 尾海兔素10,NSC 376128,DLS 10	Microtubule Associated	Cytoskeletal Signaling
	Dolastatin 10 (DLS 10) 是一种多肽，可以抑制微管蛋白聚合，显示除抗有丝分裂的活性。
T5297	3-Indolepropionic acid Indolepropionic acid,IPA,indole-3-propionic acid,吲哚-3-丙酸	Antioxidant; Reactive Oxygen Species; Endogenous Metabolite	Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction
	3-Indolepropionic acid (Indolepropionic acid) 是强效的抗氧化剂，具有研究阿尔兹海默症的潜能。
T3749	Pyrogallol 连苯三酚,Piral,焦榈酚,1,2,3-trihydroxybenzene	Apoptosis; Others; Endogenous Metabolite; Antifungal	Apoptosis; Metabolism; Microbiology/Virology; Others
	Pyrogallol (Piral) 是一种通过加热没食子酸制备的强还原剂，能产生自由基。它是一种具有抗真菌和抗牛皮癣活性的多酚。
T0965	Histamine Ergamine,组胺	5-HT Receptor; Endogenous Metabolite; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience
	Histamine (Ergamine) 是通过组胺的酶促脱羧衍生的胺。它是一种强大的胃分泌兴奋剂、支气管平滑肌的收缩剂、血管扩张剂以及中枢作用的神经递质。
S00015	Tea polyphenol	Apoptosis; Others; Autophagy	Apoptosis; Autophagy; Others
	Tea polyphenol 也称为绿茶提取物，是茶中天然存在的酚类化合物，具有抗癌、抗氧化、抑制细胞增殖、诱导细胞凋亡、延缓细胞周期和调节致癌物代谢等生物活性。
T6534	Histamine dihydrochloride 组胺二盐酸盐,peremin,Ceplene,Histamine 2HCl	Endogenous Metabolite; Histamine Receptor	GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience
	Histamine dihydrochloride (Ceplene) 是 Histamine 的二盐酸形式。Histamine 是一种有机氮化合物，是一种强效的胃分泌兴奋剂，支气管平滑肌收缩剂，血管舒张剂，也是一种中枢作用的神经递质。
T2S1464	Thiocolchicoside 硫秋水仙苷;噻可撒可,Thiocolchicine 2-glucoside analog,硫秋水仙苷,Coltramyl	Others; GABA Receptor	Membrane transporter/Ion channel; Neuroscience; Others
	Thiocolchicoside (Thiocolchicine 2-glucoside analog) 是秋水仙碱的半合成硫衍生物，是竞争性 GABAA 受体拮抗剂和甘氨酸受体拮抗剂。它是肌肉松弛剂，具有抗炎作用，可用于缓解疼痛的研究。
TC0019	Pregnenolone acetate 孕烯醇酮醋酸酯,3β-Hydroxy-5-pregnen-20-one acetate	Cannabinoid Receptor; Endogenous Metabolite	GPCR/G Protein; Metabolism
	Pregnenolone acetate 是一种强大的神经类固醇，是各种类固醇激素（包括类固醇酮）的主要前体。它作为大麻素 CB1 受体的信号特异性抑制剂，抑制由 CB1 受体介导的四氢大麻酚 (THC) 的作用。它可以保护大脑免受大麻中毒。
T10933	D-Cysteine	Endogenous Metabolite; Antibacterial	Metabolism; Microbiology/Virology
	D-Cysteine 是一种大肠杆菌生长的有力抑制剂，是半胱氨酸的 D 型异构体。它由 D-氨基酸氧化酶介导产生 H2S，是一种对抗小脑共济失调的神经保护剂。 D-半胱氨酸可以抑制由变形链球菌和链球菌血红蛋白形成的两种生物膜的生长和致龋性。
T6S0221	Eriocitrin eriodictyol 7-rutinoside,圣草次甙,Eriodictyol-7-O-Rutinoside,Eriodictioside,圣草次甙；圣草次苷,Eriodictyol glycoside	Apoptosis; Carbonic Anhydrase	Apoptosis; Metabolism
	Eriocitrin (Eriodictyol-7-O-Rutinoside) 是从柠檬中分离出来的一种黄酮类天然产物，是强效的抗氧化剂。它通过激活线粒体涉及的内在信号传导途径来触发细胞凋亡。它通过上调 p53、cyclin A、cyclin D3 和 CDK6 使 S 期细胞周期停滞，从而抑制肝癌细胞的增殖。
T40803	Isoanthricin (Rac)-Deoxypodophyllotoxin
	Isoanthricin, also known as (Rac)-Deoxypodophyllotoxin, is the racemate form of Deoxypodophyllotoxin, a powerful compound with noteworthy antitumor and anti-inflammatory properties.
T7980	Hesperidin methylchalcone	NF-κB	NF-κB
	Hesperidin methylchalcone 抑制氧化应激，细胞因子产生和NF-κB 活化。它能够抑制炎症和疼痛，具有血管保护作用。
TN2726	Jatrophane 5	P-gp	Membrane transporter/Ion channel; Neuroscience
	Jatrophane 5 demonstrates the most powerful inhibition of P-gp, higher than R(+)-verapamil and tariquidar in colorectal multi-drug resistant (MDR) cells (DLD1-TxR).
T38838	QS-21 Stimulon,QS-21
	QS-21, an immunostimulatory saponin, is a powerful vaccine adjuvant that stimulates both Th2 humoral and Th1 cell-mediated immune responses by interacting with antigen presenting cells (APCs) and T cells. Additionally, QS-21 activates the NLRP3 inflammasome, leading to the release of cytokines IL-1β and IL-18, which are dependent on caspase-1.
T72731	Acremoxanthone C
	Acremoxantone C 是一种有效的钙调素(CaM)抑制剂，存在于 Purpureocillium lilacinum 中。Acremoxantone C 与人钙调素 (hCaM) 生物传感器 hCaM M124C mBBr 结合，Kd 为 18.25 nM。
T37687	Cyclic ADP-ribose ammonium
	Cyclic ADP-ribose ammonium (cADPR ammonium) is a powerful calcium mobilization second messenger synthesized from NAD+ by an ADP-ribosyl cyclase. It primarily raises cytosolic calcium levels through Ryanodine receptor-mediated release from the endoplasmic reticulum, while also facilitating extracellular influx through the opening of TRPM2 channels [1][2][3].
T79931	Mutanocyclin
	Mutanocyclin 作为一种效能显著的抗真菌剂，能够抑制白色念珠菌 (C. albicans) 的丝状形成，并下调 HWP1、ECE1、FLO8、TEC1 基因的 mRNA 表达水平。此外，Mutanocyclin 在体外小鼠模型中亦能有效抑制酵母形态的发展。
T35895	Ingenol 3,20-dibenzoate
	Ingenol 3,20-dibenzoate is a powerful activator of protein kinase C (PKC) isoforms. It effectively induces the translocation of nPKC-delta, -epsilon, and -theta as well as PKC-mu from the cytosolic fraction to the particulate fraction. Through de novo synthesis of macromolecules, it triggers apoptosis with characteristic morphology. Moreover, Ingenol 3,20-dibenzoate enhances IFN-γ production and degranulation in NK cells, particularly when stimulated by NSCLC cells[1][2].
T71750	Quinolactacin A1
	Quinolactacin A1 是一种有效的乙酰胆碱酯酶 (AChE) 抑制剂，可从Penicillium citrinum 中得到。Quinolactacin A1 可用于阿尔茨海默病的研究。
T16574	Pregnenolone monosulfate sodium salt 3β-Hydroxy-5-pregnen-20-one monosulfate sodium salt	Others	Others
	Pregnenolone monosulfate sodium salt is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone monosulfate sodium salt can protect the brain from cannabis intoxication. Pregnenolone monosulfate sodi
TN2727	Jatrophane 2	P-gp; Antifection	Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience
	2,5,7,8,9,14-Hexaacetoxy-3-benzoyloxy-15-hydroxyjatropha-6(17),11E-diene (Jatrophane 2 ) exhibits significant antifeedant activity against a generalist plant-feeding insect, the cotton bollworm (Helicoverpa armigera). Jatrophane 2 also demonstrates the mo

天然产物

Cat.No: TP1180

Synonym: 尾海兔素10,NSC 376128,DLS 10

Target: Microtubule Associated

3-Indolepropionic acid

Cat.No: T5297

Synonym: Indolepropionic acid,IPA,indole-3-propionic acid,吲哚-3-丙酸

Target: Antioxidant, Reactive Oxygen Species, Endogenous Metabolite

Cat.No: T3749

Synonym: 连苯三酚,Piral,焦榈酚,1,2,3-trihydroxybenzene

Target: Apoptosis, Others, Endogenous Metabolite, Antifungal

Cat.No: T0965

Synonym: Ergamine,组胺

Target: 5-HT Receptor, Endogenous Metabolite, Histamine Receptor

Cat.No: S00015

Target: Apoptosis, Others, Autophagy

Histamine dihydrochloride

Cat.No: T6534

Synonym: 组胺二盐酸盐,peremin,Ceplene,Histamine 2HCl

Target: Endogenous Metabolite, Histamine Receptor

Thiocolchicoside

Cat.No: T2S1464

Synonym: 硫秋水仙苷;噻可撒可,Thiocolchicine 2-glucoside analog,硫秋水仙苷,Coltramyl

Target: Others, GABA Receptor

Pregnenolone acetate

Cat.No: TC0019

Synonym: 孕烯醇酮醋酸酯,3β-Hydroxy-5-pregnen-20-one acetate

Target: Cannabinoid Receptor, Endogenous Metabolite

Cat.No: T10933

Target: Endogenous Metabolite, Antibacterial

Cat.No: T6S0221

Synonym: eriodictyol 7-rutinoside,圣草次甙,Eriodictyol-7-O-Rutinoside,Eriodictioside,圣草次甙；圣草次苷,Eriodictyol glycoside

Target: Apoptosis, Carbonic Anhydrase

Cat.No: T40803

Synonym: (Rac)-Deoxypodophyllotoxin

Hesperidin methylchalcone

Cat.No: T7980

Target: NF-κB

Cat.No: TN2726

Target: P-gp

Cat.No: T38838

Synonym: Stimulon,QS-21

Acremoxanthone C

Cat.No: T72731

Cyclic ADP-ribose ammonium

Cat.No: T37687

Cat.No: T79931

Ingenol 3,20-dibenzoate

Cat.No: T35895

Quinolactacin A1

Cat.No: T71750

Pregnenolone monosulfate sodium salt

Cat.No: T16574

Synonym: 3β-Hydroxy-5-pregnen-20-one monosulfate sodium salt

Target: Others

Cat.No: TN2727

Target: P-gp, Antifection

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