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150

抑制剂 & 化合物

10

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T21534L	Oxytocin C-terminal tripeptide Acetate Oxytocin C-terminal tripeptide Acetate(2002-44-0 Free base)	Others	Others
	Oxytocin C-terminal tripeptide Acetate 是 Oxytocin 的 C-末端三肽。Oxytocin 是哺乳动物的神经垂体激素，催产素受体的配体。
T21724L	Fas C-Terminal Tripeptide Acetate Fas C-Terminal Tripeptide Acetate (189109-90-8 free base)	Others; Fatty Acid Synthase	Metabolism; Others
	Fas C-Terminal Tripeptide Acetate 显示出对 Fas/FAP-1 结合的抑制活性。
TP2177	Amyloid Precursor C-Terminal Peptide	Others	Others
	Amyloid precursor c-terminal peptide has the amino acid sequence Gly-Tyr-Glu-Asn-Pro-Thr-Tyr-Lys-Phe-Phe-Glu-Gln-Met-Gln-Asn. APP is best known as the precursor molecule whose proteolysis generates beta-amyloid (Aβ), a 37 to 49 amino acid peptide whose am
T9688	CC-90001	JNK	MAPK
	CC-90001 是口服有效的 c-Jun N 末端激酶选择性抑制剂。在基于细胞的模型中，CC-90001显示出对JNK1的选择性是JNK2的 12.9 倍。CC-90001在特发性肺纤维化方面有研究价值。
T11282	FGTI-2734	Transferase	Metabolism
	FGTI-2734 是有效的RAS C-末端法尼基转移酶 (FT) 和香叶烯基转移酶-1 (GGT-1) 抑制剂，IC50s 分别为 250 nM 和 520 nM。它可以阻断 KRAS 的膜定位，从而解决 KRAS 耐药性问题，并抑制突变的 KRAS 胰腺肿瘤。
T6697	TCID UCH-L3 Inhibitor	DUB	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
	TCID (UCH-L3 Inhibitor) 是一种有效的选择性神经元泛素 C 末端水解酶 L3 的 DUB 抑制剂，IC50为 0.6 μM。它对 L1 具有 125 倍的选择性，可减少脑干和脊髓原代神经元中的甘氨酸转运蛋白 GlyT2 泛素化。
T32139	Igercine Ige C-terminal nonapeptide
	Igercine is the C-terminal nonapeptide in immunoglobulin E.
TP2382	Gastrin hexapeptide Tyr-gly-trp-met-asp-phe-NH2,Gastrin C-terminal hexapeptide
	Gastrin hexapeptide is a hexapeptide from porcine antral mucosa.
T21688L	Cytochrome c - pigeon (88-104) Acetate Cytochrome c - pigeon (88-104) Acetate (86579-06-8 Free base)	Others	Others
	Cytochrome c - pigeon (88-104) Acetate (Cytochrome c - pigeon ) 对 COOH 末端序列 88-1041 内的肽具有特异性。
T2343	AS601245	JNK	MAPK
	AS601245 是 c-Jun NH2-末端激酶 (JNK) 的抑制剂，具有神经保护特性。
T21743L	Beta-Lipotropin (1-10), porcine Acetate Beta-Lipotropin (1-10), porcine Acetate(77875-68-4 Free base)	Others	Others
	Beta-Lipotropin (1-10), porcine Acetate (Beta-Lipotropin ) 被发现在其 C 末端序列中包含这些肽的一级结构。
T8931L	ICCB-19 hydrochloride ICCB-19 HCl（750621-52-4 free base）	Apoptosis; Others; Autophagy; RIP kinase	Apoptosis; Autophagy; NF-κB; Others
	ICCB-19 hydrochloride (ICCB-19 HCl) 是RIPK1激酶活性的间接抑制剂。它是一种 TRADD 抑制剂，可与 TRADD 的 N 端结构域结合，破坏其与 TRADD-C 和 TRAF2 的结合，诱导自噬和长寿命蛋白质的降解。
T15729	LDN-91946	DUB	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
	LDN-91946 是一种有效且特异性的泛素 C-末端水解酶-L1 (UCH-L1) 抑制剂（Ki = 2.8 μM）。
T7554	Substance P (7-11) Substance P 7-11(TFA)	Others; Neurokinin receptor	GPCR/G Protein; Neuroscience; Others
	Substance P (7-11) (Substance P 7-11(TFA)) 是神经肽物质P 的C-末端片段，可引起细胞内钙浓度的增加。
TP1315	c-Myc Peptide Trifluoroacetate	Others	Others
	c-Myc Peptide Trifluoroacetate (145646-22-6 free base) 是一种合成肽，对应于人类 c-myc 蛋白的 C 末端氨基酸 (410-419)，参与调控生长相关基因的转录。
T13000	Src Inhibitor 3	Others; Src	Angiogenesis; Others; Tyrosine Kinase/Adaptors
	Src Inhibitor 3 是一种有效的 c-terminal Src 激酶抑制剂（CSK HTRF 中 IC50 <3 nM，Caliper 中 IC50 <4 nM）。 Src Inhibitor 3 增加由 T 细胞受体信号传导诱导的 T 细胞增殖。
T5833	CC-401 Hydrochloride CC401 HCl	JNK	MAPK
	CC-401 Hydrochloride (CC401 HCl) 是 JNK 抑制剂(Ki= 25~50 nM)。
T16436	PBOX 6 PBOX-6	Apoptosis	Apoptosis
	PBOX 6 是一种 pyrrolo-1,5-benzoxazepine (PBOX) 化合物，具有抗癌抗肿瘤活性，可在体外抑制乳腺癌细胞的生长，在白血病细胞中通过 c-Jun NH2 末端激酶依赖性磷酸化、 Bcl-2 和 Bcl-XL 的失活发生选择性诱导细胞凋亡。
T7677	JNK Inhibitor VIII TCS JNK 6o	JNK	MAPK
	JNK Inhibitor VIII (TCS JNK 6o) 是一种 c-Jun N-末端激酶(JNK-1, -2, -3)抑制剂，对 JNK-1、JNK-2 的IC50值分别是 45 nM 和 160 nM，对JNK-1、JNK-2、JNK-3 的Ki 分别为 2 nM、4 nM、52 nM。
T33519	MTOB α-keto-γ-Methylthiobutyric acid,4-甲硫基-2-氧丁酸钠,KMBA,MTOB salt,4-methylthio 2-oxobutyric acid	Others	Others
	MTOB (α-keto-γ-Methylthiobutyric acid) 是 c 末端结合蛋白 (CtBP) 的底物，可干扰 CtBP 在细胞培养物和小鼠中的致癌活性。它还积极调节 TCF-4 信号传导，导致癌症干细胞 (CSC) 生长和自我更新。
TQ0003L1	740 Y-P acetate PDGFR 740Y-P Acetate,740YPDGFR acetate,740 Y-P acetate(1236188-16-1 Free base)	PI3K	PI3K/Akt/mTOR signaling
	740 Y-P acetate (740YPDGFR acetate) 是一个有效的且具有细胞渗透性的 PI3K 激活剂。740 Y-P acetate 倾向和含有 p85 的 N- 和 C- 末端 SH2 结构域的 GST 融合蛋白结合，但不能单独结合 GST。
T39664	Ethaselen BBSKE
	Ethaselen (BBSKE), a selective thioredoxin reductase (TrxR) inhibitor, is orally active with IC50s of 0.5 and 0.35 μM for wild-type human TrxR1 and rat TrxR1, respectively. Ethaselen specifically binds to the unique selenocysteine-cysteine redox pair located in the C-terminal active site of mammalian TrxR1. As an organoselenium compound, it demonstrates potent antitumor activity against non-small cell lung cancer (NSCLC) by targeting TrxR.
TP1942L1	pep2-AVKI acetate(1315378-69-8 free base)	Others	Others
	pep2-AVKI acetate(1315378-69-8 free base) 选择性破坏 AMPA 受体亚基 GluA2（在 C 末端 PDZ 位点）与与 C 激酶 (PICK1) 相互作用的蛋白质结合的抑制剂肽。不影响 GluA2 与 GRIP 或 ABP 的结合，也不增加 AMPA 电流幅度或影响长期抑制 (LTD)。
T60619	CDK9-IN-15	CDK	Cell Cycle/Checkpoint
	CDK9-IN-15 是一种有效的小分子CDK9抑制剂，可通过降解、抑制 CDK9 来阻断正性转录延长因子 P-TEFb (positive transcription elongation factor b) 对 RNA Poly-II C末端区域的磷酸化，抑制转录，迅速降低细胞内 mRNA 水平，从而引起肿瘤细胞凋亡。
T9996	NCT-58 NCT58	HSP	Cytoskeletal Signaling; Metabolism
	NCT-58是一种有效的C 端HSP90抑制剂。NCT-58不会引起热休克反应（HSR）。NCT-58通过同时下调HER 家族成员以及抑制Akt 磷酸化来激发抗肿瘤活性。NCT-58杀死对曲妥珠单抗耐药的乳腺癌干细胞样细胞。NCT-58诱导HER2阳性乳腺癌细胞凋亡。
TP1897L1	JIP-1 (153-163) acetate(438567-88-5 free base)	JNK	MAPK
	JIP-1 (153-163) acetate(438567-88-5 free base) 是c-Jun N-末端激酶 (JNK) 的肽抑制剂，基于 JNK-interacting protein-1 (JIP-1) 的残基 153-163。以微摩尔范围内的亲和力与 JNK 结合，并抑制 p38 和 ERK。
TP1616L	Hsp70-derived octapeptide acetate Hsp70-derived octapeptide acetate(736171-62-3 free base)	Others	Others
	Hsp70-derived octapeptide acetate (Hsp70-derived octapeptide acetate)(736171-62-3 free base) 是一组含有四肽重复 (TPR) 的蛋白质，已显示与 70 kDa 热休克同源蛋白 (hsc70) 的 C 末端结构域相互作用。在本研究中，含 TPR 的蛋白质，包括 hsc70 相互作用蛋白 (CHIP)、TPR1 和人富含谷氨酰胺的 TPR 含蛋白 (hSGT) 的 C 端，对 DnaJ 和 hsc70 对荧光素酶重折叠的影响进行了调查。
TP1197	Sincalide SQ19844,辛卡利特,CCK-8,Cholecystokinin octapeptide	Others	Others
	Sincalide (CCK-8) 是一种速效的胆囊收缩素的氨基酸多肽激素类似物，可在胆囊造影术中静脉使用。它的肝胆生理作用是增加胆汁的分泌，使胆囊收缩并使 Oddi 的括约肌松弛，从而使胆汁排入十二指肠。它是一种通过注射促进胆囊收缩并帮助诊断胆囊和胰腺疾病的药物。
T22540L	Ac-Endothelin-1 (16-21), human acetate	Others	Others
	Ac-Endothelin-1 (16-21), human acetate 是内皮素家族的主要肽，已被证明在血管和非血管组织中具有多种生物活性。 C-末端片段是 ET 家族肽中高度保守的序列，已显示可区分称为 ETA 和 ETB 的两种 ET 受体亚型，因为它仅激活后者。
T1063	Ticarcillin disodium Ticarpen,Ticarcillin disodium salt,替卡西林二钠	Antibacterial; Antibiotic	Microbiology/Virology
	Ticarcillin disodium (Ticarpen) 主要用于抗革兰氏阴性菌, 特别是绿脓杆菌, 也是少数可研究嗜麦芽感染的抗生素。
T9417L	gamma-preprotachykinin amide (72-92) acetate gamma-preprotachykinin amide (72-92) acetate (114882-65-4 Free base)	Others	Others
	gamma-preprotachykinin amide (72-92) acetate 是一种 21 个氨基酸的肽，属于速激肽 (TK) 家族，在其 C 末端序列中包括神经激肽 A (NKA)。它对中枢 NK-2 受体的亲和力高于 NKA；它对 NK-1 受体的亲和力较低，但是，它有效地刺激唾液分泌，这是由 NK-1 受体激活介导的。
T3627	IQ-1S free acid IQ-1,IQ-1S,IQ-1S (free acid)	NF-κB; JNK	MAPK; NF-κB
	IQ-1S free acid (IQ-1S) 是 NF-κB/激活蛋白1 (AP-1) 抑制剂(IC50:2.3±0.41 μM)。它对 JNK1(Kd:240 nM)、JNK2(Kd:360 nM) 和 JNK3(Kd:100 nM)的都具有高的结合亲和力。
TP1604L	Thioredoxin reductase peptide acetate Thioredoxin reductase peptide acetate(950890-23-0 free base)	Others	Others
	Thioredoxin reductase peptide acetate(950890-23-0 free base) 对应于硫氧还蛋白还原酶 (TrxR) 中的 53–67 位残基，用于硫氧还蛋白还原酶研究。哺乳动物硫氧还蛋白还原酶 (TR) 催化硫氧还蛋白 (Trx) 的氧化还原活性二硫键的还原，并且在结构和谷胱甘肽还原酶的作用机制，除了 C 末端的 16 个氨基酸延伸部分含有一个罕见的连位硒硫键。
T3157	COH29 RNR Inhibitor COH29	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	COH29 (RNR Inhibitor COH29) 是一种口服可用的芳香族取代噻唑，是人类核糖核苷酸还原酶 (RNR) 的抑制剂，具有潜在的抗肿瘤活性。它抑制核糖核苷酸还原酶的IC50为 16 μM。
T24830	SR-4326
	SR-4326 is a c-Jun N-terminal Kinase 3 inhibitor.
T13779	MPT0B392	Others	Others
	MPT0B392 is an orally active quinoline derivative, induces c-Jun N-terminal kinase (JNK) activation.
T33654	Neurokinin A-OH Nka OH,NkaOH,Nka-OH
	Neurokinin A-OH is the C-terminal free acid derivative of neurokinin A.
T69527	Erioflorin
	Erioflorin is an ATP-competitive selective c-Jun N-terminal kinase (JNK) inhibitor.
T29702	AG 85-12 AG-85-12,AG85-12
	AG 85-12 is a mimic of the C-terminal portion of angiotensin I.
T29590	Acetoxycycloheximide
	Acetoxycycloheximide induces cell surface TNF receptor 1. It also rapidly induces apoptosis mediated by the release of cytochrome c via activation of c-Jun N-terminal kinase.
T24203	Jmv 170 Jmv-170,Jmv170
	Jmv 170 is the C-terminal heptapeptide of cholecystokinin. It has partial agonist CCK activity on pancreatic amylase release.
T27529	HC-3 HC 3
	HC-3 inhibits ChoK by binding at the conserved hydrophobic groove on the C-terminal lobe.
T33960	Phaseolotoxin Phaseolotoxin A
	Phaseolotoxin is an exotoxin from Pseudomonas sp.; cleavage of C terminal alanine and homoarginine from phaseolotoxin leaves octicidine.
T20492	Tetragastrin Cholecystokinin tetrapeptide,Gastrin tetrapeptide
	Tetragastrin is the C-terminal tetrapeptide of gastrin. It has the same physiological and pharmacological activity as gastrin.
T25553	Jmv 332 Jmv-332,Jmv332
	Jmv 332 is a cyclic analog of the C-terminal hexapeptide of CCK. It is a CCK/gastrin receptor agonist.
T15265	EZ-482	Others	Others
	EZ-482 is a novel ligand of apolipoprotein (apoE). EZ-482 binds to apoE4 by a unique N-terminal allosteric effect and it also binds to sites on apoE in the C-terminal domain (Kds: 5-10 μM for apoE3 and apoE4).
T25896	Octicidine ASOHO
	Octicidine is derived from phaseolotoxin by the removal of C-terminal dipeptide. It is a transition state analog that irreversibly suppresses ornithine carbamoyltransferase.
T71038	MDL-28050
	MDL-28050 is a synthetic analog of hirudin 55-65 C-terminal fragment and a peptide inhibitor.
T37128	Chemerin-9, Mouse
	Chemokine-like receptor 1 (CMKLR1) agonist (EC50 = 42 nM). Corresponds to C-terminal of full length mouse Chemerin, amino acids 148 - 156.
T11330L	FTI-2148	Others	Others
	FTI-2148 is an inhibitor of RAS C-terminal mimetic dual farnesyl transferase (FT-1) and geranylgeranyl transferase-1 (GGT-1) (IC50s: 1.4 nM and 1.7 μM, respectively).

化合物

Oxytocin C-terminal tripeptide Acetate

Cat.No: T21534L

Synonym: Oxytocin C-terminal tripeptide Acetate(2002-44-0 Free base)

Target: Others

Fas C-Terminal Tripeptide Acetate

Cat.No: T21724L

Synonym: Fas C-Terminal Tripeptide Acetate (189109-90-8 free base)

Target: Others, Fatty Acid Synthase

Amyloid Precursor C-Terminal Peptide

Cat.No: TP2177

Target: Others

Cat.No: T9688

Target: JNK

Cat.No: T11282

Target: Transferase

Cat.No: T6697

Synonym: UCH-L3 Inhibitor

Target: DUB

Cat.No: T32139

Synonym: Ige C-terminal nonapeptide

Gastrin hexapeptide

Cat.No: TP2382

Synonym: Tyr-gly-trp-met-asp-phe-NH2,Gastrin C-terminal hexapeptide

Cytochrome c - pigeon (88-104) Acetate

Cat.No: T21688L

Synonym: Cytochrome c - pigeon (88-104) Acetate (86579-06-8 Free base)

Target: Others

Cat.No: T2343

Target: JNK

Beta-Lipotropin (1-10), porcine Acetate

Cat.No: T21743L

Synonym: Beta-Lipotropin (1-10), porcine Acetate(77875-68-4 Free base)

Target: Others

ICCB-19 hydrochloride

Cat.No: T8931L

Synonym: ICCB-19 HCl（750621-52-4 free base）

Target: Apoptosis, Others, Autophagy, RIP kinase

Cat.No: T15729

Target: DUB

Substance P (7-11)

Cat.No: T7554

Synonym: Substance P 7-11(TFA)

Target: Others, Neurokinin receptor

c-Myc Peptide Trifluoroacetate

Cat.No: TP1315

Target: Others

Src Inhibitor 3

Cat.No: T13000

Target: Others, Src

CC-401 Hydrochloride

Cat.No: T5833

Synonym: CC401 HCl

Target: JNK

Cat.No: T16436

Synonym: PBOX-6

Target: Apoptosis

JNK Inhibitor VIII

Cat.No: T7677

Synonym: TCS JNK 6o

Target: JNK

Cat.No: T33519

Synonym: α-keto-γ-Methylthiobutyric acid,4-甲硫基-2-氧丁酸钠,KMBA,MTOB salt,4-methylthio 2-oxobutyric acid

Target: Others

740 Y-P acetate

Cat.No: TQ0003L1

Synonym: PDGFR 740Y-P Acetate,740YPDGFR acetate,740 Y-P acetate(1236188-16-1 Free base)

Target: PI3K

Cat.No: T39664

Synonym: BBSKE

pep2-AVKI acetate(1315378-69-8 free base)

Cat.No: TP1942L1

Target: Others

Cat.No: T60619

Target: CDK

Cat.No: T9996

Synonym: NCT58

Target: HSP

JIP-1 (153-163) acetate(438567-88-5 free base)

Cat.No: TP1897L1

Target: JNK

Hsp70-derived octapeptide acetate

Cat.No: TP1616L

Synonym: Hsp70-derived octapeptide acetate(736171-62-3 free base)

Target: Others

Cat.No: TP1197

Synonym: SQ19844,辛卡利特,CCK-8,Cholecystokinin octapeptide

Target: Others

Ac-Endothelin-1 (16-21), human acetate

Cat.No: T22540L

Target: Others

Ticarcillin disodium

Cat.No: T1063

Synonym: Ticarpen,Ticarcillin disodium salt,替卡西林二钠

Target: Antibacterial, Antibiotic

gamma-preprotachykinin amide (72-92) acetate

Cat.No: T9417L

Synonym: gamma-preprotachykinin amide (72-92) acetate (114882-65-4 Free base)

Target: Others

IQ-1S free acid

Cat.No: T3627

Synonym: IQ-1,IQ-1S,IQ-1S (free acid)

Target: NF-κB, JNK

Thioredoxin reductase peptide acetate

Cat.No: TP1604L

Synonym: Thioredoxin reductase peptide acetate(950890-23-0 free base)

Target: Others

Cat.No: T3157

Synonym: RNR Inhibitor COH29

Target: DNA/RNA Synthesis

Cat.No: T24830

Cat.No: T13779

Target: Others

Neurokinin A-OH

Cat.No: T33654

Synonym: Nka OH,NkaOH,Nka-OH

Cat.No: T69527

Cat.No: T29702

Synonym: AG-85-12,AG85-12

Acetoxycycloheximide

Cat.No: T29590

Cat.No: T24203

Synonym: Jmv-170,Jmv170

Cat.No: T27529

Synonym: HC 3

Cat.No: T33960

Synonym: Phaseolotoxin A

Cat.No: T20492

Synonym: Cholecystokinin tetrapeptide,Gastrin tetrapeptide

Cat.No: T25553

Synonym: Jmv-332,Jmv332

Cat.No: T15265

Target: Others

Cat.No: T25896

Synonym: ASOHO

Cat.No: T71038

Chemerin-9, Mouse

Cat.No: T37128

Cat.No: T11330L

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
T0518	Methacycline hydrochloride Rondomycin,盐酸甲烯土霉素,盐酸美他环素,Methacycline HCl	ribosome; Antibacterial; Antibiotic	Microbiology/Virology
	Methacycline hydrochloride (Rondomycin) 是四环素抗生素，可抑制细菌蛋白质的合成。它是上皮-间质转化 (EMT) 抑制剂。它在体外可阻断 EMT，体内抑制纤维发生，不会直接影响 TGF-β1 Smad 信号传导。它是抗菌剂，有潜力研究肺纤维化。
T3892	Isoacteoside 异麦角甾苷,Isoverbascoside	NF-κB	NF-κB
	Isoacteoside 具有抗炎作用，通过作用于 caspase-1、丝裂原活化蛋白激酶（c-Jun N-末端激酶、p38、细胞外信号调节蛋白激酶）和核因子-kappa B 途径介导。
T3908	10-Gingerol 10-姜酚	Apoptosis	Apoptosis
	10-Gingerol 是一种姜根脂的主要刺激性成分，具有抗炎、抗氧化和抗增殖作用，能够抑制 MDA-MB-231 肿瘤细胞的增殖(IC50:12.1 μM)。
T4757	L-Homoserine (S)-2-氨基-4-羟基丁酸,(S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID	Others; Endogenous Metabolite	Metabolism; Others
	L-Homoserine ((S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID) 是天然存在的非蛋白丝氨酸，是合成苏氨酸、蛋氨酸和赖氨酸的共有中间体。它是氨基酸丝氨酸的更具反应性的变体。
TWS1977	Kamebakaurin 尾叶香茶菜丙素,Kamebakaurine	NF-κB	NF-κB
	Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物，是一种NF-κB 的抑制剂，能够抑制 p50 的 DNA 结合活性。
T6S1597	Mulberroside A 桑皮苷 A,桑皮苷A	TNF; Tyrosinase; Interleukin	Apoptosis; Immunology/Inflammation; Proteases/Proteasome
	Mulberroside A 是桑中的一种主要活性成分，可降低TNF-α、IL-1β和IL-6的表达，抑制 NALP3、caspase-1 和 NF-κB 的激活以及 ERK、JNK 和 p38 的磷酸化。它抑制蘑菇酪氨酸酶，具有抗炎和抗细胞凋亡作用。
TN1448	(-)-Bornyl acetate L-(-)-Bornyl acetate,左旋乙酸冰片酯,Bornyl acetate,(-)-乙酸龙脑酯	p38 MAPK; NF-κB; JNK; Antifungal	MAPK; Microbiology/Virology; NF-κB
	(-)-Bornyl acetate (L-(-)-Bornyl acetate) 是存在于牛膝草油中的一种具有抗真菌活性的 (+)-Bornyl acetate 低活性异构体。
T4889	2,6-Diaminoheptanedioic acid	Others; Endogenous Metabolite	Metabolism; Others
	2,6-Diaminoheptanedioic acid 是内源性代谢产物的一种。
T6S1572	Sauchinone	ERK; p38 MAPK; NF-κB	MAPK; NF-κB
	Sauchinone 是一种从Saururus chinensis 中获得的非对映异构的木脂素。它通过抑制I-κBα磷酸化和p65核易位来抑制 LPS 诱导的 iNOS，TNF-α 和 COX-2 表达。它具有抗炎和抗氧化活性。
TN2360	Falcarinol Falcarinol,Panaxynol,人参炔醇	HSP	Cytoskeletal Signaling; Metabolism
	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 selectivity with minimal toxicities. Furthermore, Falcarinol (Panaxynol) demonstrates the ability to induce apoptosis.

天然产物

Methacycline hydrochloride

Cat.No: T0518

Synonym: Rondomycin,盐酸甲烯土霉素,盐酸美他环素,Methacycline HCl

Target: ribosome, Antibacterial, Antibiotic

Cat.No: T3892

Synonym: 异麦角甾苷,Isoverbascoside

Target: NF-κB

Cat.No: T3908

Synonym: 10-姜酚

Target: Apoptosis

Cat.No: T4757

Synonym: (S)-2-氨基-4-羟基丁酸,(S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID

Target: Others, Endogenous Metabolite

Cat.No: TWS1977

Synonym: 尾叶香茶菜丙素,Kamebakaurine

Target: NF-κB

Cat.No: T6S1597

Synonym: 桑皮苷 A,桑皮苷A

Target: TNF, Tyrosinase, Interleukin

(-)-Bornyl acetate

Cat.No: TN1448

Synonym: L-(-)-Bornyl acetate,左旋乙酸冰片酯,Bornyl acetate,(-)-乙酸龙脑酯

Target: p38 MAPK, NF-κB, JNK, Antifungal

2,6-Diaminoheptanedioic acid

Cat.No: T4889

Target: Others, Endogenous Metabolite

Cat.No: T6S1572

Target: ERK, p38 MAPK, NF-κB

Cat.No: TN2360

Synonym: Falcarinol,Panaxynol,人参炔醇

Target: HSP

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