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天然化合物

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カタログ番号	製品名	別名	ターゲット
T38387	Compound C108		GTPase
	Compound C108 is an inhibitor of GTPase-activating protein SH3 domain-binding protein 2 (G3BP2). Compound C108 can be used in studies about breast tumors and esophageal squamous cell carcinoma.		GTPase
T50125	Compound C749
	Compound C749 is a useful organic compound for research related to life sciences. The catalog number is T50125 and the CAS number is 57-03-4.
T6146	Dorsomorphin dihydrochloride	BML-275 2HCl,Compound C dihydrochloride,Dorsomorphin (Compound C) 2HCl,Compound C 2HCl,BML-275 dihydrochloride	AMPK , Autophagy , TGF-beta/Smad
	Dorsomorphin dihydrochloride (BML-275 2HCl) is a potent, selective and ATP-competitive AMPK inhibitor (Ki: 109 nM) and does not exhibit significant activity on structurally related kinases.		AMPK , Autophagy , TGF-beta/Smad
T3964	Glutaminase C-IN-1	Compound 968,Glutaminase Inhibitor Compound 968	Glutaminase
	Glutaminase C-IN-1 (Compound 968) is a Glutaminase C allosteric inhibitor.		Glutaminase
T27635	Isoxepac	Olopatadine USP Related Compound C	Others
	Isoxepac (Olopatadine USP Related Compound C) is a non-steroidal anti-antiphlogistic agent and analgesic.		Others
T126236	Clopidogrel Related Compound C
	Clopidogrel Related Compound C is a useful organic compound for research related to life sciences. The catalog number is T126236 and the CAS number is 120202-71-3.
T1977	Dorsomorphin	Compound C,BML-275	AMPK , Autophagy , TGF-beta/Smad
	Dorsomorphin (BML-275) is an AMPK inhibitor (Ki=109 nM) that is selective and ATP-competitive. Dorsomorphin inhibits the BMP type I receptors ALK2, ALK3, and ALK6. Dorsomorphin induces autophagy, and possesses antitumor ...		AMPK , Autophagy , TGF-beta/Smad
TQ0028	EX229	Compound 991,C991	AMPK
	EX229 (C991) is an allosteric activator of AMPK, with Kds of 0.06 μM, 0.06 μM and 0.51 μM for α1β1γ1, α2β1γ1, and α1β2γ1, respectively.		AMPK
T23734	AMPK activator C2	Compound 2,Compound-2,C2
	AMPK activator C2 is an AMPK allosteric activator.
T20564	Valsartan benzyl ester	Valsartan impurity B,Valsartan related compound C
	Valsartan benzyl ester is a intermediate of Valsartan.
T20942	De(5-carboxamide)oxcarbazepine	Oxcarbazepine related compound E,Oxcarbazepine impurity C
	De(5-carboxamide)oxcarbazepine is used for organic synthesis.
T71507	PF-4522654
	PF-4522654 is a potent and selective 5-HT2C receptor agonist.
T61589	c-Fms-IN-13		c-Fms
	c-Fms-IN-13 (compound 14) is a potent FMS kinase inhibitor (IC50= 17 nM). c-Fms-IN-13 is an anti-inflammatory agent.		c-Fms
T3188	RE-640		CCR , Parasite
	NSC-5844 (RE-640) (RE640) is a bisquinoline compound with C-C chemokine receptor type 1 (CCR1)-agonistic activities.		CCR , Parasite
T8409	SYN1143	RON-IN-1,AMG-1	c-Met/HGFR
	SYN1143 (AMG-1) is a potent inhibitor of human RON and c-Met.In vitro kinase assays showed that compound I is a potent inhibitor of human RON and c-Met with IC50s of 9 and 4 nmol/L, respectively.		c-Met/HGFR
T13623	Compound 48/80 trihydrochloride	C48/80 trihydrochloride	Phospholipase
	Compound 48/80 trihydrochloride (C48/80 trihydrochloride) is a mixture of N-methyl-p-methoxyphenethylamine and formaldehyde in a condensation reaction.Compound 48/80 trihydrochloride is a mast cell degranulator and hista...		Phospholipase
T9628	10074-A4		c-Myc
	10074-A4 is a c-Myc binding compound that associates with c-Myc370–409 and behaves like a “ligand cloud” around a “protein cloud”, with distinct features from that of a non-binding ligand.		c-Myc
T1876	Kobe0065		Apoptosis , Raf , Ras
	Kobe0065 is a novel and effective small-molecule compound inhibiting Ras–Raf interaction by SBDD; shows potent activity to competitively inhibit the binding of H-Ras·GTP to c-Raf-1 RBD with a Ki value of 46 ± 13 μM.		Apoptosis , Raf , Ras
T16436	PBOX 6	PBOX-6	Apoptosis
	PBOX 6 is a pyrrolo-1,5-benzoxazepine (PBOX) compound with anticancer and antitumor activity that inhibits breast cancer cell growth in vitro and selectively induces apoptosis in leukemia cells via c-Jun NH2 terminal kin...		Apoptosis
T68060	Elgodipine
	Elgodipine significantly reduced the incidence and severity of exercise-induced angina pectoris systemically and was able to inhibit vascular smooth muscle proliferation through a mechanism independent of the expression ...
T60485	DIF-3
	DIF-3 is a chemical compound that acts by activating GSK-3β to facilitate the degradation of cyclin D1 and c-Myc, resulting in reduced expression levels of these proteins. In addition, DIF-3 inhibits Wnt/β-catenin signal...
T8839	ICCB280		Apoptosis , Others
	ICCB280 was capable of inducing differentiation and apoptosis of ATRA-resistant patient blasts strongly signify that the activity of this compound can overcome resistance to other current therapies for AML with an unfavo...		Apoptosis , Others
T0825	Ebselen	SPI-1005,PZ-51,CCG-39161	Phosphatase , Virus Protease , Calcium Channel , COX , HIV Protease
	Ebselen (CCG-39161) is a organoselenium compound with anti-inflammatory, anti-oxidant and cytoprotective activity. Ebselen acts as a glutathione peroxidase mimetic and is thereby able to prevent cellular damage induced b...
T4306	CCG-203971	CCG203971	Rho , Ras
	CCG-203971 is an inhibitor of SRE activation in the prostate cancer cell line PC-3 (IC50: 6.4 μM), with 87% inhibition of SRE activation achieved at 100 μM. This compound also inhibits PC-3 cell migration (IC50: 4.2 μM),...		Rho , Ras
T38192	Unifiram		Others
	Unifiram is a nootropic agent.1It increases acetylcholine (ACh) release in the rat cerebral cortexin vivoand induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the ra...		Others
T32429	KW 2149	KT6149,KW2149,KW-2149
	KW 2149 is a compound derived from mitomycin C.
T79439	c-Myc inhibitor 12		c-Myc
	Compound 67h, also known as c-Myc inhibitor 12, is a potent inhibitor of c-Myc, exhibiting a pEC50 value of 6.4 [1].		c-Myc
T72620	c-Myc inhibitor 9
	c-Myc Inhibitor 9 (Compound 332) is an effective c-Myc inhibitor, exhibiting a logEC50 of ≥6, and demonstrating significant tumor growth inhibition in nude mouse models. This compound is utilized in cancer research.
T10647	c-Fms-IN-8		CSF-1R
	c-Fms-IN-8 is a colony-stimulating factor-1 receptor (CSF-1R, c-FMS) Type II inhibitor (IC50: 9.1 nM). It is compound 4a in the reference.		CSF-1R
T35653	2’-O,4’-C-Methyleneuridine
	2'-O,4'-C-Methyleneuridine (Compound 15a) is a bicyclic nucleoside. [1]. Sharma VK, et al. Chemoenzymatic convergent synthesis of 2'-O,4'-C-methyleneribonucleosides. J Org Chem. 2014 Jul 3;79(13):6336-41.
T41002	HCVP-IN-1
	HCVP-IN-1 (compound 1) is a hepatitis C viral polymerase (HCVP) inhibitor.
T38482	MM 419447
	MM 419447 is a guanylate cyclase-C agonist, and it is a metabolite of linaclotide. This compound, MM 419447, shows promise in the field of irritable bowel syndrome with constipation (IBS-C) research.
T61128	c-ABL-IN-2
	C-ABL-IN-2 is a highly effective inhibitor of the c-Abl protein, which plays a significant role in the development of several diseases, including cancer. This compound exhibits promise for investigating neurodegenerative...
T74554	Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH
	Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH (Compound 21b), an EZH2 degrader, is employed in lymphoma research [1].
T63359	c-Myc inhibitor 4
	c-Myc inhibitor 4 is a potent, orally active c-Myc-reducing compound. c-Myc is an important proto-oncogene, which is closely associated with the development of many tumors.
T61496	NPR-C activator 1
	NPR-C activator 1 (Compound 1) is a potent activator of natriuretic peptide receptor C (NPR-C), a receptor involved in the regulation of vascular homeostasis. It acts as a potent agonist (EC50 ~ 1 μM) of C-type natriuret...
T67796	C-BVDU
	C-BVDU is a very potent and selective anti-herpes-virus compound.
T79438	c-Myc inhibitor 11		c-Myc
	c-Myc inhibitor 11 (Compound 67e), a c-MYC inhibitor (p EC 50 : 6.4), exhibits high clearance, a moderate volume of distribution, and a short half-life in rat pharmacokinetic assays, making it suitable for cancer researc...		c-Myc
T126101	Apigenin 6-C-(2-O-feruloyl)glucoside 8-C-glucoside
	Apigenin 6-C-(2-O-feruloyl)glucoside 8-C-glucoside is a useful organic compound for research related to life sciences and the catalog number is T126101.
T75239	c-Myc inhibitor 10
	C-Myc Inhibitor 10 (compound 17), exhibiting enhanced cellular potency, benefits from increased permeability due to the methylation of the morpholine nitrogen [1].
T79893	Cbl-b-IN-6		E1/E2/E3 Enzyme
	Cbl-b-IN-6 (Compound 246) is an inhibitor of both casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting inhibitory half-maximal inhibitory concentrations (IC50s) of 6.7 nM for Cbl-b and 5.2 nM for c-Cbl, respectivel...		E1/E2/E3 Enzyme
T78602	Chaetoglobosin C
	Chaetoglobosin C (Compound 4), an anthraquinone-chromone derivative of Chaetomium globosum KMITL-N0802, exhibits anti-tuberculosis activity [1].
T18619	Bis-PEG1-C-PEG1-CH2COOH	PROTAC Linker 26	Others
	Bis-PEG1-C-PEG1-CH2COOH (PROTAC Linker 26) is a PEG-based linker suitable for the synthesis of PROTACs, compound complexes that selectively degrade target proteins[1].		Others
T61313	Antitumor agent-70
	Antitumor agent-70 (compound 8b) is a highly potent multi-targeted kinase inhibitor, particularly targeting c-Kit. It demonstrates remarkable anti-tumor activity and the ability to induce cell apoptosis. This compound al...
T32287	Jegosapogenol A	Jegosapogenol,Giganteumgenin M,Proschiwalligenin PB1,Careyagenol A,Saniculagenin D
	Jegosapogenol A is a type of triterpenoid. Triterpenoids are terpene molecules containing six isoprene units. Barringtogenol C is a very weakly acidic compound (based on its pKa) and practically insoluble (in water). Bar...
T71169	XMD-12
	XMD-12, also known as DUN57447, Aurora inhibitor (compound 1) or Aurora-IN-1, is an Auroro inhibitor, which targets Aurora A/B/C. (5.6/18.4/24.6 nM).
T37891	GLP-1(32-36)amide
	GLP-1(32-36)amide is a pentapeptide compound derived from the C terminus of the glucoregulatory hormone GLP-1. This compound has shown potential in inhibiting weight gain and regulating glucose metabolism in diabetic mic...
T79715	c-Met-IN-19		c-Met/HGFR
	c-Met-IN-19 (Compound 21j) is a potent c-Met inhibitor with an IC50 of 1.99 nM and demonstrates cytotoxic effects on various cancer cell lines, including A549, HT-29, SGC-7901, and MDA-MB-231, with IC50 values of 0.25, 0...		c-Met/HGFR
T36615	DPTA NONOate	Dipropylenetriamine NONOate
	DPTA NONOate is a NO donor. It spontaneously dissociates in a pH-dependent, first-order process with a half-life of three hours and five hours at 37°C and 22-25°C, pH 7.4, respectively, to liberate 2 moles of NO per mole...
T79496	Cathepsin C-IN-6
	Cathepsin C-IN-6 (compound 2), an E-64c-hydrazideas-derived inhibitor of cathepsin C, possesses anti-inflammatory properties and impedes neutrophil elastase activation. This compound demonstrates potential efficacy in tr...

Compounds

Dorsomorphin dihydrochloride

T6146

Synonym: BML-275 2HCl,Compound C dihydrochloride,Dorsomorphin (Compound C) 2HCl,Compound C 2HCl,BML-275 dihydrochloride

Target: AMPK, Autophagy, TGF-beta/Smad

Glutaminase C-IN-1

T3964

Synonym: Compound 968,Glutaminase Inhibitor Compound 968

Target: Glutaminase

Isoxepac

T27635

Synonym: Olopatadine USP Related Compound C

Target: Others

Clopidogrel Related Compound C

Synonym: Compound C,BML-275

Target: AMPK, Autophagy, TGF-beta/Smad

EX229

TQ0028

Synonym: Compound 991,C991

Target: AMPK

AMPK activator C2

T23734

Synonym: Compound 2,Compound-2,C2

Target:

Valsartan benzyl ester

T20564

Synonym: Valsartan impurity B,Valsartan related compound C

Target:

De(5-carboxamide)oxcarbazepine

T20942

Synonym: Oxcarbazepine related compound E,Oxcarbazepine impurity C

Target: CCR, Parasite

SYN1143

T8409

Synonym: RON-IN-1,AMG-1

Target: c-Met/HGFR

Compound 48/80 trihydrochloride

T13623

Synonym: C48/80 trihydrochloride

Target: Phospholipase

Target: Apoptosis, Raf, Ras

Target: Apoptosis, Others

Ebselen

T0825

Synonym: SPI-1005,PZ-51,CCG-39161

Target: Phosphatase, Virus Protease, Calcium Channel, COX, HIV Protease

Synonym: KT6149,KW2149,KW-2149

2’-O,4’-C-Methyleneuridine

Tazemetostat de(methylene morpholine)-O-C3-O-C-COOH

Apigenin 6-C-(2-O-feruloyl)glucoside 8-C-glucoside

Target: E1/E2/E3 Enzyme

Bis-PEG1-C-PEG1-CH2COOH

T18619

Synonym: PROTAC Linker 26

Synonym: Jegosapogenol,Giganteumgenin M,Proschiwalligenin PB1,Careyagenol A,Saniculagenin D

Synonym: Dipropylenetriamine NONOate

カタログ番号	製品名	別名	ターゲット
T3811	Ginsenoside C-K	Ginsenoside compound K,Ginsenoside K	P450 , cell cycle arrest , COX , NO Synthase
	Ginsenoside C-K (Ginsenoside K) is a bacterial metabolite of G-Rb1 exhibiting anti-inflammatory effects by reducing iNOS and COX-2.		P450 , cell cycle arrest , COX , NO Synthase
T5S1963	Orcinol gentiobioside	Anacardoside	Others
	Orcinol gentiobioside is a natural compound extracted from the rhizomes of C. breviscapa.		Others
TN1949	Moracin C		ROS , NO Synthase
	Moracin C, a natural compound found in Morus mesozygia, Morus alba var. multicaulis, is an anti-inflammatory agent. moracin C inhibits nitric oxide (NO) release and LPS-activated reactive oxygen species (ROS) in cells.		ROS , NO Synthase
T5656	(±)-Norcantharidin	Endothall anhydride,Norcantharidin	EGFR , c-Met/HGFR
	(±)-Norcantharidin (Endothall anhydride) is a synthetic anticancer compound which is a dual inhibitor for c-Met and EGFR in human colon cancers.		EGFR , c-Met/HGFR
T2894	Norcantharidin	Norcantharadine,Endothall anhydride	EGFR , c-Met/HGFR
	Norcantharidin (Norcantharadine) is a synthetic anticancer compound which is a dual inhibitor for c-Met and EGFR in human colon cancers.		EGFR , c-Met/HGFR
TN1195	17-Hydroxy sprengerinin C	17-羟基 SPRENGERININ C	BCL , Others , Caspase
	17-Hydroxy sprengerinin C is a glycoside compound isolated from rhizomes of Polygonatum sibiricum with stronger anticancer activities. 17-Hydroxy sprengerinin C reduces the expression of Blc-2 and pro-caspase3 and increa...		BCL , Others , Caspase
T3671	Vitexin-2"-O-rhamnoside	2''-O-Rhamnosylvitexin,Vitexin-2-O-rhaMnoside,Vitexin-2''-O-rhamnoside,Apigenin-8-C-glucoside	Others
	Vitexin-2"-O-rhamnoside (Apigenin-8-C-glucoside) is a compound contributes to the protection against H O -mediated oxidative stress damage.		Others
T3903	Angoroside C		Prostaglandin Receptor
	Angoroside C is a Potential anti-inflammatory compound. Inhibitor of prostaglandin E2 release in mouse peritoneal macrophages in vitro. Shows potent antioxidative activity in reducing the oxidized OH adducts of dAMP and ...		Prostaglandin Receptor
T3519	Formosanin C	Polyphyllin B	Apoptosis , Caspase
	Formosanin C (Polyphyllin B) is a compound isolated from Rhizoma Paridis, showed pro-apoptosis and immunoregulation with antitumor activity in cultured cells and animal systems.		Apoptosis , Caspase
T2336	Vitamin K2	Menatetrenone	Endogenous Metabolite
	Vitamin K2 (Menatetrenone) is a menaquinone compound and form of vitamin K2 with potential antineoplastic activity. Menatetrenone may act by modulating the signaling of certain tyrosine kinases, thereby affecting several...		Endogenous Metabolite
T3427	Polydatin	Piceid,Polydotin Peceid	Apoptosis , Mitophagy , NF-κB , Autophagy
	Polydatin (Piceid), the glycoside of Resveratrol, is originally isolated from the Chinese herb Polygonum cuspidatum. The compound can inhibit platelet aggregation and elevate the ratios of LDL-C/HDL-C and TC/HDL-C. In th...		Apoptosis , Mitophagy , NF-κB , Autophagy
T5755	Aloesin		Tyrosinase
	Aloesin is a C-glycosylated chromone compound found in aloe (Liliaceae) that inhibits tyrosinase (IC50 = 0.9 mM), an enzyme responsible for catalyzing the first step of the conversion of tyrosine to melanin.		Tyrosinase
TN1861	Licoflavone C	4',5,7-Trihydroxy-8-prenylflavone	Antioxidant , Antifungal
	Licoflavone C (4',5,7-Trihydroxy-8-prenylflavone) is an isoprenoid-based flavonoid compound isolated from the roots of Glycyrrhiza inflata, which possesses antioxidant and antifungal activities, and is known to have a pr...		Antioxidant , Antifungal
T8256	Piperitone		Others
	piperitone is a natural compound from Piper nigrum L		Others
T70955	Vinaxanthone	SM-345431	Phospholipase , Antibacterial
	Vinaxanthone (SM-345431) is a small molecule compound derived from Penicillium chrysogenum that is a selective and potent semaphorin3A, phospholipase C (PLC), and FabI inhibitor, inhibiting semaphorin3A and FabI.Vinaxant...		Phospholipase , Antibacterial
T37341	N-Acetyltyramine		Antibacterial
	N-acetyltyramine is a metabolite of the biogenic amine tyramine . It enhances cytotoxicity of doxorubicin in resistant P388 murine leukemia cells with an IC50 value of 0.13 μg/ml compared with an IC50 value of 0.48 μg/ml...		Antibacterial
T2163	Dihydrocapsaicin	CCRIS1589,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide	Others , TRP/TRPV Channel
	Dihydrocapsaicin (CCRIS1589) is isolated from Capsicum fruit. Capsaicin is the primary active component of the heat and pain-eliciting lipid soluble fraction of the Capsicum pepper. Like capsaicin, dihydrocapsaicin is an...		Others , TRP/TRPV Channel
T81903	Lupulone C
	Lupulone C (Compound 9) serves as an inhibitor of nitric oxide (NO) production [1].
T81930	Linderanine C	(-)-Linderanine C
	Linderanine C ((-)-Linderanine C) (compound 6), a sesquiterpenoid, can be extracted from the roots of Wuyao [1].
T39098	Pulsatilloside C
	Pulsatilloside C, an isolated compound from Pulsatilla koreana, exhibits notable inhibition of adipocyte differentiation.
T82506	Edgeworoside C
	Edgeworoside C (compound 5), a coumarin derivative, has been isolated from the flower buds of Edgeworthia chrysantha [1].
T82688	Condurango glycoside C
	Condurango glycoside C, isolated from Marsdenia cundurango's bark [1], is a chemical compound.
T82001	Justin C
	Justin C (compound 14), a natural product extracted from Justicia procumbens, has potential applications in cancer research [1].
T82783	Cannflavin C
	Cannflavin C, also referred to as compound 5, is extractable from Cannabis sativa and exhibits antioxidant activity [1].
T83150	Ajugasterone C 2-acetate
	Ajugasterone C 2-acetate, an ecdysteroid extractable from Cyanotis arachnoidea [1], is a chemical compound.
T81809	Methylkushenol C
	Methylkushenol C, a phenolic compound, can be isolated from Sophora flavescens [1].
T81189	Schizolaenone C
	Schizolaenone C, a natural compound isolated from Schizolaena hystrix, demonstrates anti-proliferative and anti-oxidative properties [1] [2].
T83276	6,8-Di-C-β-D-xylopyranoside
	6,8-Di-C-β-D-xylopyranoside (compound 3bb) is a xylopyranoside that has been isolated from the orchid Dendrobium huoshanensis [1].
T80938	Triptotriterpenic acid C
	Triptotriterpenic acid C, an ursolic-type compound, can be isolated from the total glycosides extracted from the root of Tripterygium wilfordii Hook.f [1].
T81687	Neohelmanthicin C
	Neohelminthicin C is a compound belonging to the phenylpropionic acid class [1].
T81601	Ophiopogonone C
	Ophiopogonone C (compound 3), an isoflavone, has been isolated from the ethanol extract of the tubers of Ophiopogon japonicus [1].
T83272	6′-O-β-D-Glucopyranosylphlorigidoside C
	Compound 1, known as 6′-O-β-D-Glucopyranosylphlorigidoside C, is an iridoid glycoside extractable from the plant Lamiophlomis rotata [1].
T74203	Licoagrochalcone C
	Licoagrochalcone C, a flavonoid compound, demonstrates potent inhibitory effects on NF-κB transcription and significantly reduces LPS-induced NO production, showcasing its bioactive properties [1] [2].
T81980	Kissoone C
	Kissoone C (compound 3), a sesquiterpene with a three-membered ring structure, has been isolated from valerian root. This compound has been found to promote nerve growth factor (NGF)-mediated neurite outgrowth in PC12D c...
T82982	Aplyronine C
	Aplyronine C, an active compound, exhibits potent antitumor activity and demonstrates cytotoxicity against HeLa-S3 cells, with an IC50 value of 22 nM, suggesting potential use in cancer research [1].
TN6284	Taiwanin C		Antioxidant , Immunology/Inflammation related
	Taiwanin C is a compound extracted from the Taiwan plant Cryptocarya chinensis, which belongs to the lignan class of compounds and has many biological activities such as anti-inflammatory, antioxidant and anticancer. The...		Antioxidant , Immunology/Inflammation related
T75570	Justicidin C
	Justicidin C, a lignan compound, exhibits potent antiviral properties, particularly against vesicular stomatitis virus, with minimal cytotoxicity observed in rabbit lung cells (RL-33) [1].
T75577	3′-Omethyl-5′-hydroxydiplacone
	3′-Omethyl-5′-hydroxydiplacone (compound 2), a C-6-geranylflavonoid isolated from the ethanol extract of Paulownia tomentosa fruits, exhibits antibacterial activity against Gram-positive bacteria [1].
T81425	Polyporusterone C
	Polyporusterone C (Compound 3), a natural product extracted from Polyporus umbellatus, exhibits cytotoxic activities, displaying IC50 values of 37, 26, and 42 μg/mL against L-1210 cells after 3, 5, and 7 days of treatmen...
T83026	Antioxidant agent-18
	Antioxidant Agent-18 (Compound 5), a flavonol glycoside derived from Ginkgo biloba, exhibits antioxidant properties through its ability to scavenge DPPH radicals (IC50: 15.8 μM) and reduce cytochrome c (IC50: 14.7 μM).
TN2360	Falcarinol	Falcarinol,Panaxynol	HSP
	Falcarinol, also known as Panaxynol, is a naturally occurring compound that acts as an orally active inhibitor of Hsp90. It effectively targets both the N-terminal and C-terminal regions of Hsp90, displaying high selecti...		HSP
T82565	Diayangambin	Syringaresinol dimethyl ether,Lirioresinol C dimethyl ether
	Diayangambin (Syringaresinol dimethyl ether; Lirioresinol C dimethyl ether) is a compound that inhibits cell proliferation, exhibiting an IC50 value of 1.5 μM in human monocytes. Additionally, it demonstrates immunosuppr...
T75527	Chrexanthomycin C
	Chrexanthomycin C, an orally active marine-derived natural product, exhibits significant bioactivities and shows a binding affinity for DNA [(G4C2)4 G4] with a dissociation constant (Kd) of 2.8 mM. This compound holds po...
T80950	Tricetin 7-O-glucoside
	Chemical Compound 77298-67-0 exhibits high thermal stability and outstanding resistance to both corrosion and oxidation, suitable for extreme environmental conditions. Its melting point lies above 3500°C. The compound de...
T81333	Qianhucoumarin C
	Qianhucoumarin C, a coumarin derivative isolated from the roots of Peucedanum praeruptorum, exhibits potential medicinal properties such as anti-inflammatory, antioxidant, and anticancer effects. This compound plays a si...
T73673	Thiomarinol A
	Thiomarinol A (4-Hydroxythiomarinol C), a potent antibiotic, is a hybrid compound comprising dithiolopyrrolone and marinolic acid, exhibiting antimicrobial activity. It effectively inhibits MRSA IleRS in a dose-dependent...
T81484	Phorbol 12-tiglate
	Phorbol 12-tiglate, a derivative of Phorbol, which in turn is a hydrolyzed product of Croton oil, plays a role in tumor promotion through activation of protein kinase C. This compound and its related derivatives are empl...
T81168	Shishijimicin C
	Shishijimicin C, a novel antitumor agent isolated from the ascidian Didemnum proliferum, exhibits highly potent cytotoxicities and anti-tumor activities. This compound also serves as a click chemistry reagent, featuring ...
T75621	Secalonic acid D
	Secalonic acid D, a toxic compound effective against tumor cells, is derived from the metabolites of Aspergillus aculeatus. It operates by activating GSK3-β and degrading β-catenin, consequently down-regulating c-Myc exp...
T72235	Antibacterial synergist 2
	Antibacterial synergist 2, functioning as a biofilm inhibitor, demonstrates inhibitory effects against pathogens such as S. enterica, S. aureus, P. aeruginosa, and C. albicans. This compound is applicable in research con...
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天然物製品

Ginsenoside C-K

T3811

Synonym: Ginsenoside compound K,Ginsenoside K

Target: P450, cell cycle arrest, COX, NO Synthase

Orcinol gentiobioside

T5S1963

Synonym: Anacardoside

Target: ROS, NO Synthase

(±)-Norcantharidin

T5656

Synonym: Endothall anhydride,Norcantharidin

Target: EGFR, c-Met/HGFR

Norcantharidin

T2894

Synonym: Norcantharadine,Endothall anhydride

Target: EGFR, c-Met/HGFR

17-Hydroxy sprengerinin C

TN1195

Synonym: 17-羟基 SPRENGERININ C

Target: BCL, Others, Caspase

Vitexin-2"-O-rhamnoside

T3671

Synonym: 2''-O-Rhamnosylvitexin,Vitexin-2-O-rhaMnoside,Vitexin-2''-O-rhamnoside,Apigenin-8-C-glucoside

Target: Prostaglandin Receptor

Formosanin C

T3519

Synonym: Polyphyllin B

Target: Apoptosis, Caspase

Vitamin K2

T2336

Synonym: Menatetrenone

Target: Endogenous Metabolite

Polydatin

T3427

Synonym: Piceid,Polydotin Peceid

Target: Apoptosis, Mitophagy, NF-κB, Autophagy

Synonym: 4',5,7-Trihydroxy-8-prenylflavone

Target: Antioxidant, Antifungal

Target: Phospholipase, Antibacterial

N-Acetyltyramine

T37341

Synonym:

Target: Antibacterial

Dihydrocapsaicin

T2163

Synonym: CCRIS1589,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide

Target: Others, TRP/TRPV Channel

Synonym: (-)-Linderanine C

Condurango glycoside C

Ajugasterone C 2-acetate

6,8-Di-C-β-D-xylopyranoside

T83276

Synonym:

Target:

Triptotriterpenic acid C

6′-O-β-D-Glucopyranosylphlorigidoside C

Target: Antioxidant, Immunology/Inflammation related

3′-Omethyl-5′-hydroxydiplacone

Synonym: Falcarinol,Panaxynol

Target: HSP

Diayangambin

T82565

Synonym: Syringaresinol dimethyl ether,Lirioresinol C dimethyl ether

Tricetin 7-O-glucoside

Antibacterial synergist 2

T72235

Synonym:

Target:

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Recombinant Proteins

Species：

Expression System：

Tag：

カタログ番号	製品名	Species	Expression System
TMPY-02787	Aconitase 2 Protein, Mouse, Recombinant (His & GST)	Mouse	Baculovirus-Insect Cells
	A homozygous missense mutation was identified in the ACO2 gene (c.1240T>G p.Phe414Val) that segregated with HSP complicated by intellectual disability and microcephaly. Lymphoblastoid cell lines of homozygous carrier pat...
TMPY-02545	Aconitase 2 Protein, Human, Recombinant (His & GST)	Human	Baculovirus-Insect Cells
	A homozygous missense mutation was identified in the ACO2 gene (c.1240T>G p.Phe414Val) that segregated with HSP complicated by intellectual disability and microcephaly. Lymphoblastoid cell lines of homozygous carrier pat...
TMPK-01456	HLA-C*03:04&B2M&KRAS G12D (GADGVGKSAL) Tetramer Protein, Human, MHC (His & Avi)	Human	HEK293
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-pr...
TMPK-01450	HLA-C*03:04&B2M&KRAS G12D (GADGVGKSAL) Monomer Protein, Human, MHC (His & Avi), Biotinylated	Human	HEK293
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-pr...
TMPK-01451	HLA-C 03:04&B2M&KRAS G12D (GADGVGKSAL) Monomer Protein, Human, MHC (His & Avi)	Human	HEK293
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-pr...

Aconitase 2 Protein, Mouse, Recombinant (His & GST)

TMPY-02787

Species: Mouse

Expression System: Baculovirus-Insect Cells

Aconitase 2 Protein, Human, Recombinant (His & GST)

TMPY-02545

Species: Human

Expression System: Baculovirus-Insect Cells

HLA-C*03:04&B2M&KRAS G12D (GADGVGKSAL) Tetramer Protein, Human, MHC (His & Avi)

TMPK-01456

Species: Human

Expression System: HEK293

HLA-C*03:04&B2M&KRAS G12D (GADGVGKSAL) Monomer Protein, Human, MHC (His & Avi), Biotinylated

TMPK-01450

Species: Human

Expression System: HEK293

HLA-C 03:04&B2M&KRAS G12D (GADGVGKSAL) Monomer Protein, Human, MHC (His & Avi)

TMPK-01451

Species: Human

Expression System: HEK293

カタログ番号	製品名
L4010	Bioactive Compounds Library Max	22555 compounds
	A collection of 22555 bioactive compounds for high-throughput screening, high-content screening, cell induction and target identification.
L3800	NF-κB Signaling Compound Library	729 compounds
	A unique collection of 729 compounds targeting NF-κB signaling for high throughput screening and high content screening;
L1720	Nucleotide Compound Library	334 compounds
	A unique collection of 334 nucleoside and nucleotide analogues, can be used for research and development of anti-viral, anti-tumor, anti-fungal, and anti-depressive drugs;
L2193	Anti-Liver Cancer Compound Library	1787 compounds
	1787 species of compounds related to liver cancer that can be used in anti-liver cancer drug development and pharmacological studies.
L2550	Glutamine Metabolism Compound Library	565 compounds
	A unique collection of 565 glutamine metabolism related compounds can be used for high throughput screening (HTS) and high content screening (HCS), and also is an effective tool for research in glutamine metabolism and ...

ライブラリー

Bioactive Compounds Library Max

L4010

Compounds: 22555

NF-κB Signaling Compound Library

L3800

Compounds: 729

Nucleotide Compound Library

L1720

Compounds: 334

Anti-Liver Cancer Compound Library

L2193

Compounds: 1787

Glutamine Metabolism Compound Library

L2550

Compounds: 565