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Search Results for " pten "

36

抑制剂 & 化合物

15

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T7012	VO-Ohpic trihydrate VO-Ohpic	PTEN; Autophagy	Autophagy; PI3K/Akt/mTOR signaling
	VO-Ohpic trihydrate (VO-Ohpic) 是一种有效的磷酸酶和张力蛋白同源物（PTEN）抑制剂，IC50 为 35 nM。
T7953	BpV(HOpic) bpV (HOpic)	PTEN	PI3K/Akt/mTOR signaling
	BpV(HOpic) (bpV (HOpic)) 是 PTEN 选择性抑制剂，IC50=14 nM。BpV(HOpic) 具有神经保护作用。
T6667	SF1670 PTP CD45 Inhibitor,PTPase CD45 Inhibitor	Phosphatase; PTEN; Autophagy	Autophagy; Metabolism; PI3K/Akt/mTOR signaling
	SF1670 (PTPase CD45 Inhibitor) 是一种特异性 PTEN 抑制剂，IC50 为 2 μM。
T6303L	CCT128930 hydrochloride CCT128930 hydrochloride(885499-61-6 Free base)	Apoptosis; Akt; PKA; mTOR; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	CCT128930 hydrochloride (CCT128930 hydrochloride) 是一种选择性 AKT 抑制剂，具有抗肿瘤活性。它通过靶向 AKT 的 Met282 (PKA-AKT 嵌合体的 Met173)，对 PKA 激酶具有 28 倍的选择性，对 p70S6K 具有 20 倍的选择性。
T1952	MK-2206 dihydrochloride MK-2206 2HCl	Apoptosis; Akt; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	MK-2206 dihydrochloride (MK-2206 2HCl) 是一种变构 Akt 抑制剂，抑制 Akt1、Akt2 和 Akt3 (IC50=8/12/65 nM)，具有口服活性的、高效选择性。MK-2206 dihydrochloride 具有抗肿瘤活性。
T14511	BAY1082439 N-[8-[[(2R)-2-羟基-3-(吗啉-4-基)丙基]氧基]-7-甲氧基-2,3-二氢咪唑并[1,2-C]喹唑啉-5-基]-2-甲基吡啶-3-甲酰胺	Apoptosis; PI3K	Apoptosis; PI3K/Akt/mTOR signaling
	BAY1082439 是一种具有口服活性的，选择性 PI3Kα/β/δ抑制剂。它也能抑制 PIK3CA 的突变形式，它对抑制 Pten 丢失的前列腺癌的生长有很强的作用。
T6303	CCT128930	Akt; PKA; S6 Kinase; Autophagy	Autophagy; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	CCT128930 是一种 ATP 竞争性，选择性 AKT 抑制剂。它通过靶向 AKT 的 Met282 (PKA-AKT 嵌合体的 Met173)，对 PKA 激酶具有 28 倍的选择性，对 p70S6K 具有 20 倍的选择性，具有抗肿瘤活性。
T77548	(6Z)-7-Phenyl-7-(3-Pyridinyl)-6-Heptenoic Acid
	(6Z)-7-Phenyl-7-(3-Pyridinyl)-6-Heptenoic Acid 是一种7-phenyl-7-(3-pyridyl)-6-heptenoic acid 衍生物，可用于生物研究。
T81790	Miptenalimab BI-754111
	Miptenalimab (BI-754111)为一种高亲和力抗人LAG-3抗体，其对hLAG-3的结合常数(KD)为88.6 nM。该抗体能有效阻断LAG-3与其主要配体MHC-II之间的相互作用。
T32062	Heptenophos BRN 1978448,BRN1978448,BRN-1978448
	Heptenophos is a biochemical.
T64309	Isometheptene mucate
	Isometheptene mucate 是一种拟交感神经剂，是间接作用的肾上腺素能受体 (adrenergic receptor) 激动剂，能够用于研究偏头痛。
T66069	t-Butyl (3R,5S)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-isopropylidenedioxy-6-heptenoate
	t-Butyl (3R,5S)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-isopropylidenedioxy-6-heptenoate 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T66069，CAS号为 147489-06-3。
T27155	Dexisometheptene TNX 201,TNX-201,(R)-Isometheptene,TNX201
	Dexisometheptene is an antimigraine drug candidate. Dexisometheptene significantly increases the pain threshold of acute pain response, and potently and selectively binds to receptors in the central nervous system known as imidazoline type-1 (I1) receptor
T125501	trans-2-Heptenal
	trans-2-Heptenal 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T125501，CAS号为 18829-55-5。
T33197	m-Anisidine, 4-(3-heptenyloxy)-
	m-Anisidine, 4-(3-heptenyloxy)- is a bioactive chemical.
T130740	7-(4-Hydroxy-3-methoxyphenyl)-1-phenyl-4-hepten-3-
	7-(4-Hydroxy-3-methoxyphenyl)-1-phenyl-4-hepten-3- 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T130740。
T83658	SQLE-IN-1	Antifungal	Microbiology/Virology
	SQLE-IN-1 是一种角鲨烯环氧化酶 (SQLE) 抑制剂，具有抗肿瘤活性，可抑制肝癌细胞系 Huh7 的增殖和迁移能力，抑制细胞胆固醇的生成，增加抑癌基因PTEN的表达，抑制PI3K和AKT的蛋白表达。
T13376	YS-49	RAAS; Akt; PI3K; Adrenergic Receptor	Cytoskeletal Signaling; Endocrinology/Hormones; GPCR/G Protein; Neuroscience; PI3K/Akt/mTOR signaling
	YS-49 是一种PI3K/Akt(RhoA 的下游靶标) 的激活剂，可减少 3-甲基胆碱处理的细胞中 RhoA/PTEN 的激活。它是异喹啉化合物生物碱，因能激活心脏β-adrenoceptors 而具有强烈的正性肌力作用。它能通过诱导血红素加氧酶来抑制血管紧张素 II 刺激 VSMC 细胞的增殖。
T10594	bpV(phen)	PTEN	PI3K/Akt/mTOR signaling
	bpV(phen) is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor (IC50s: 343 nM, 920 nM, and 38 nM for PTP-β, PTP-1B, and PTEN).
T71739	PTPMT1-IN-1
	PTPMT1-IN-1 is a PTEN-like mitochondrial phosphatase PTPMT1 inhibitor.
T26775	Bepafant WEB-2170,WEB2170,STY 2108,STY-2108,WEB 2170
	Bepafant is a platelet activating factor (PAF) antagonist. Bepafant may produce significant anti-inflammatory effects. Bepafant triggered apoptosis in NB4, KG1, and NB4-MR4 cells where PTEN was expressed, but not in THP1 and U937 cells where PTEN was abse
T39929	MS21
	MS21 is a unique AKT degrader that selectively hampers the proliferation of cancers with mutations in the PI3K/PTEN pathway, alongside wild-type KRAS and BRAF.
T71757	SC-10914
	SC10914 is a highly potent PARP inhibitor (PARP1 IC50 = 7.87 nM) with potent anti-proliferative activity against human BRCA deficient tumor cells (MDA-MB-436, BRCA1 deficient, IC50 = 4.03 nM, Capan-1 BRCA2 deficient, IC50 = 11.66 nM) and PTEN deficient tumor cells (HGC-27,PTEN deficient, IC50 = 0.35 μM). SC10914 showed potent anti-tumor activity in BRCA1/2 mutant tumor models and better pharmacokinetics profile has the potential to be selected as the clinical candidate for the treatment of treat...
T71147	PBS-1086
	PBS-1086 is a novel dual inhibitor of the canonical and noncanonical NF-κB pathways, increasing the magnitude and duration of initial EGFR inhibitor response in multiple NSCLC models, decreasing PDHK1 expression, and suppressing phosphorylation of the PDHK1 protein substrate PDHA1 in a panel of PTEN-deficient cell lines.
T60776	Anticancer agent 68
	Anticancer agent 68 is (Compound 12) 是一种抗癌剂。Anticancer agent 68 将细胞阻滞在 G2/M 期并诱导程序性细胞死亡。Anticancer agent 68 通过激活 p53 和 PTEN 诱导上调肿瘤抑制。
T61344	VO-OHPic
	VO-OHPic is a reversible, noncompetitive, and selective inhibitor of PTEN with an IC50 of 46 nM. It effectively attenuates apoptosis, adverse cardiac remodeling, and the presence of pro-inflammatory M1 macrophages in models of doxorubicin-induced cardiomyopathy. Additionally, VO-OHPic inhibits autophagy [1] [2] [3].
T81784	MK-2206 free base	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	MK-2206 free base是一种口服活性、高选择性的变构Akt抑制剂，IC50分别针对Akt1、Akt2、Akt3为8、12和65 nM 。多种乳腺癌细胞系、PIK3CA突变以及PTEN缺失细胞系对此化合物敏感，显示出抗癌活性。
T62609	MK-2206
	MK-2206 是一种具有口服具有活力的、高效选择性的变构 Akt 抑制剂，能够作用于 Akt1 (IC50: 8 nM)、Akt2 (IC50: 12 nM) 和 Akt3 (IC50: 65 nM)。许多乳腺癌细胞系、PIK3CA 突变体和 PTEN 丢失细胞系对 MK-2206 敏感。MK-2206 具有抗癌作用。
T38847	Vevorisertib Vevorisertib,ARQ 751
	Vevorisertib (ARQ 751) is a highly effective oral compound that selectively inhibits pan-AKT serine/threonine kinases such as AKT1 (with an IC50 value of 0.55 nM), AKT2 (with an IC50 value of 0.81 nM), and AKT3 (with an IC50 value of 1.31 nM). This compound, either as a standalone treatment option or in combination with other anti-cancer agents, is ideally suited for conducting research on solid tumors characterized by PIK3CA/AKT/PTEN mutations[4].
T35491	3,5-dimethyl PIT-1
	PtdIns-(3,4,5)-P3 (PIP3) serves as an anchor for the binding of signal transduction proteins bearing pleckstrin homology (PH) domains such as phosphatidylinositol 3-kinase (PI3K) or PTEN. Protein binding to PIP3 is important for cytoskeletal rearrangement and membrane trafficking and initiates an intricate signaling cascade that has been implicated in cancer. 3,5-dimethyl PIT-1 is a dimethyl analog of PIT-1, the selective inhibitor of PIP3/Akt PH domain binding, that is designed for more favorab...
T63879	microRNA-21-IN-1
	microRNA-21-IN-1（compound 7A）是一种高效microRNA抑制剂，对Hela和HCT-116细胞显示出抗增殖活性，IC50值分别为5.5 μM和2.8 μM，并能促进Hela细胞凋亡(apoptosis)。该化合物通过上调microRNA-21下游功能靶点（PTEN、EGR1、SLIT2）的表达，有助于抗癌研究。
T27621	Ipatasertib HCl GDC0068,RG 7440,GDC 0068,RG-7440,GDC-0068,RG7440
	Ipatasertib is an orally active, potent and selective Akt inhibitor with antitumor activity. Inhibition of Akt activity by Ipatasertib resulted in blockade of cell-cycle progression and reduced viability of cancer cell lines. Markers of Akt activation, in
T37029	PtdIns-(3,4,5)-P3-biotin (sodium salt) PtdIns-(3,4,5)-P3-biotin (sodium salt)
	The PtdIn phosphates play an important role in the generation and transduction of intracellular signals. PtdIns-(3,4,5)-P3-biotin is an affinity probe which allows the PIP3 to be detected through an interaction with the biotin ligand. This design allows PtdIns-(3,4,5)-P3-biotin to serve as a general probe for any protein with a high affinity binding interaction with inositol-(3,4,5)-triphosphate phospholipids, such as phosphatidylinositol 3-kinase, PTEN, or PH-domain-containing proteins.
T70552	Ipatasertib tosylate
	Ipatasertib, also known as GDC0068, is an orally active, potent and selective Akt inhibitor. GDC-0068 blocked Akt signaling both in cultured human cancer cell lines and in tumor xenograft models. Inhibition of Akt activity by GDC-0068 resulted in blockade of cell-cycle progression and reduced viability of cancer cell lines. Markers of Akt activation, including high-basal phospho-Akt levels, PTEN loss, and PIK3CA kinase domain mutations, correlate with sensitivity to GDC-0068. In multiple tumor...
T75238	YS-49 monohydrate
	YS-49 (单水合物) 作为PI3K/Akt（RhoA的下游靶点）的激活剂，有效降低3-甲基胆碱处理的细胞中RhoA/PTEN的活性。此外，YS-49通过促进血红素加氧酶（HO-1）的表达，抑制血管紧张素II（Ang II）诱导的血管平滑肌细胞（VSMC）增殖。作为一种异喹啉化合物生物碱，YS-49因激活心脏β-adrenoceptors而显示出显著的正性肌力效应。
T65598	Cefminox sodium
	Cefminox (Sodium) is a new cephamycin antibiotic possessing a D-amino acid moiety derived from D-cysteine at the C-7B side chain. Cefminox is active against a wide range of bacteria, especially Gram-negative and anaerobic bacteria. Cefminox shows excellent in vivo efficacy (ED50) which is higher than would be expected from its in vitro activity (MIC). Moreover, cefminox possesses more potent activity in suppression of bacterial regrowth than other cephems[1]. Cefminox (Sodium) was the most activ...

化合物

VO-Ohpic trihydrate

Cat.No: T7012

Synonym: VO-Ohpic

Target: PTEN, Autophagy

Cat.No: T7953

Synonym: bpV (HOpic)

Target: PTEN

Cat.No: T6667

Synonym: PTP CD45 Inhibitor,PTPase CD45 Inhibitor

Target: Phosphatase, PTEN, Autophagy

CCT128930 hydrochloride

Cat.No: T6303L

Synonym: CCT128930 hydrochloride(885499-61-6 Free base)

Target: Apoptosis, Akt, PKA, mTOR, Autophagy

MK-2206 dihydrochloride

Cat.No: T1952

Synonym: MK-2206 2HCl

Target: Apoptosis, Akt, Autophagy

Cat.No: T14511

Synonym: N-[8-[[(2R)-2-羟基-3-(吗啉-4-基)丙基]氧基]-7-甲氧基-2,3-二氢咪唑并[1,2-C]喹唑啉-5-基]-2-甲基吡啶-3-甲酰胺

Target: Apoptosis, PI3K

Cat.No: T6303

Target: Akt, PKA, S6 Kinase, Autophagy

(6Z)-7-Phenyl-7-(3-Pyridinyl)-6-Heptenoic Acid

Cat.No: T77548

Cat.No: T81790

Synonym: BI-754111

Cat.No: T32062

Synonym: BRN 1978448,BRN1978448,BRN-1978448

Isometheptene mucate

Cat.No: T64309

t-Butyl (3R,5S)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-isopropylidenedioxy-6-heptenoate

Cat.No: T66069

Dexisometheptene

Cat.No: T27155

Synonym: TNX 201,TNX-201,(R)-Isometheptene,TNX201

trans-2-Heptenal

Cat.No: T125501

m-Anisidine, 4-(3-heptenyloxy)-

Cat.No: T33197

7-(4-Hydroxy-3-methoxyphenyl)-1-phenyl-4-hepten-3-

Cat.No: T130740

Cat.No: T83658

Target: Antifungal

Cat.No: T13376

Target: RAAS, Akt, PI3K, Adrenergic Receptor

Cat.No: T10594

Target: PTEN

Cat.No: T71739

Cat.No: T26775

Synonym: WEB-2170,WEB2170,STY 2108,STY-2108,WEB 2170

Cat.No: T39929

Cat.No: T71757

Cat.No: T71147

Anticancer agent 68

Cat.No: T60776

Cat.No: T61344

MK-2206 free base

Cat.No: T81784

Target: Akt

Cat.No: T62609

Cat.No: T38847

Synonym: Vevorisertib,ARQ 751

3,5-dimethyl PIT-1

Cat.No: T35491

microRNA-21-IN-1

Cat.No: T63879

Ipatasertib HCl

Cat.No: T27621

Synonym: GDC0068,RG 7440,GDC 0068,RG-7440,GDC-0068,RG7440

PtdIns-(3,4,5)-P3-biotin (sodium salt)

Cat.No: T37029

Synonym: PtdIns-(3,4,5)-P3-biotin (sodium salt)

Ipatasertib tosylate

Cat.No: T70552

YS-49 monohydrate

Cat.No: T75238

Cefminox sodium

Cat.No: T65598

Cat. No.	Product Name	Target	Signaling Pathways
T3780	Oroxin B Hypocretin-2,木蝴蝶苷B	Apoptosis; PTEN; Antioxidant; PI3K; Autophagy	Apoptosis; Autophagy; oxidation-reduction; PI3K/Akt/mTOR signaling
	Oroxin B (Hypocretin-2) 是从传统中草药木蝴蝶中分离出来的黄酮类天然产物，在恶性淋巴瘤细胞中诱导肿瘤抑制性 ER 应激。它通过上调 PTEN，下调 COX-2，VEGF，PI3K 和 p-AKT，对肝癌细胞具有明显的抑制作用，诱导细胞早期凋亡。
TN1362	Afzelin 阿福豆苷,Kaempferol-3-O-rhamnoside	PTEN; p38 MAPK; TNF; Mitochondrial Metabolism; Antibacterial; Prostaglandin Receptor; Autophagy	Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling
	Afzelin (Kaempferol-3-O-rhamnoside) 具有多种细胞活性，例如 DNA 保护、抗菌、抗氧化和抗炎以及 UV 吸收活性，并且可以通过 UV 吸收和细胞活性的组合保护人体皮肤免受 UVB 引起的损伤。 Afzelin 减轻线粒体损伤，增强线粒体生物合成并降低线粒体自噬相关蛋白、parkin 和 putative kinase 1 的水平。
T6S2116	Ginkgolic acid C17:1 银杏酸 C17:1,银杏酸C17:1	Phosphatase; PTEN	Metabolism; PI3K/Akt/mTOR signaling
	Ginkgolic acid C17:1 是分离自银杏叶中，通过诱导PTEN 和SHP-1酪氨酸磷酸酶抑制组成型和诱导型 STAT3 活化。它具有抗癌活性。
T2852	Citropten Limettin,Citroptene,Limetin,5, 7-Dimethoxycoumarin,柠美内脂,5,7-二甲氧基香豆素,5,7-Dimethoxycoumarin	Others	Others
	Citropten (Limetin) 是一种香豆素，分离自佛手柑油中，对 A2058 人黑色素瘤细胞株具有抗增殖作用。
T2143	Bergapten 5-Methoxypsoralen,佛手柑内酯,香柑内酯	P450; Autophagy	Autophagy; Metabolism
	Bergapten (5-Methoxypsoralen) 是白芷中的一种香豆素，也是一种补骨脂素，可抑制细胞复制。
T2S1702	(5R,6E)-5-Hydroxy-1,7-diphenyl-6-hepten-3-one 1,7-双苯-5-羟基-6-庚烯-3-酮,(5R)-trans-1,7-diphenyl-5-hydroxy-6-hept,5-Hydroxy-1,7-diphenyl-6-hepten-3-one	Antioxidant	oxidation-reduction
	(5R,6E)-5-Hydroxy-1,7-diphenyl-6-hepten-3-one ((5R)-trans-1,7-diphenyl-5-hydroxy-6-hept) 是一种胡桃的二氯甲烷提取物，具有抗氧化作用。
T4115	Auraptene 橙皮油内酯,7-geranyloxycoumarin,橙皮油素	MMP; BACE	Neuroscience; Proteases/Proteasome
	Auraptene 是一种丰富的天然香叶氧基香豆素。它能够抑制基质金属蛋白酶 2 以及关键炎症因子，包括 IL-6，IL-8 和趋化因子 (C-C 基序) 配体-5 (CCL5）的分泌。
T5747	ISOBERGAPTEN	Others	Others
	Isobergapten 是一种化感抑制剂，分离自Hevacleum laciniatum 种子。
TN1345	8-Hydroxybergapten 8-羟基佛手柑内酯,8-羟基佛手苷内酯	Others	Others
	8-hydroxybergapten 具有优异的抗皱效果。在离散的 O-甲基转移酶介导的反应中，它被 Ruta 细胞的无细胞提取物 O-甲基化为异青霉素。
TN2523	1,7-Diphenyl-5-hydroxy-4,6-hepten-3-one	Others	Others
	1,7-Diphenyl-5-hydroxy-4,6-hepten-3-one是一种天然产物，属于姜科山姜属，其产品编号为 TN2523，CAS号为 87095-77-0。1,7-Diphenyl-5-hydroxy-4,6-hepten-3-one可用作对照参考。
TN5075	Subelliptenone G	Others	Others
	Subelliptenone G is a natural product from Garcinia hanburyi Hook.f.
TN3218	7-(4-Hydroxyphenyl)-1-phenyl-4-hepten-3-one	Beta Amyloid; PI3K; mTOR	Neuroscience; PI3K/Akt/mTOR signaling
	7-(4-Hydroxyphenyl)-1-phenyl-4-hepten-3-one as a beneficial compound to ameliorate the deleterious effects of Aβ on dendrite integrity and cell survival, and may provide new insights on drug discovery of Alzheimer's disease (AD).
TN2522	1,7-Diphenyl-4-hepten-3-one	Others	Others
	1,7-Diphenyl-4-hepten-3-one has feeding deterrent activities against Tribolium castaneum.
TN1415	Auraptenol 酸橙素烯醇	5-HT Receptor	GPCR/G Protein; Neuroscience
	Auraptenol possesses robust antidepressant-like efficacy in mice.
T3404	Cucurbitacin B Cuc B,葫芦素B,DATISCACIN,葫芦素 B,Amarine	Apoptosis; PTEN; Integrin; Endogenous Metabolite; HIF; STAT; Autophagy	Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
	Cucurbitacin B (Cuc B) 是一具有抗癌活性的天然产物。

天然产物

Cat.No: T3780

Synonym: Hypocretin-2,木蝴蝶苷B

Target: Apoptosis, PTEN, Antioxidant, PI3K, Autophagy

Cat.No: TN1362

Synonym: 阿福豆苷,Kaempferol-3-O-rhamnoside

Target: PTEN, p38 MAPK, TNF, Mitochondrial Metabolism, Antibacterial, Prostaglandin Receptor, Autophagy

Ginkgolic acid C17:1

Cat.No: T6S2116

Synonym: 银杏酸 C17:1,银杏酸C17:1

Target: Phosphatase, PTEN

Cat.No: T2852

Synonym: Limettin,Citroptene,Limetin,5, 7-Dimethoxycoumarin,柠美内脂,5,7-二甲氧基香豆素,5,7-Dimethoxycoumarin

Target: Others

Cat.No: T2143

Synonym: 5-Methoxypsoralen,佛手柑内酯,香柑内酯

Target: P450, Autophagy

(5R,6E)-5-Hydroxy-1,7-diphenyl-6-hepten-3-one

Cat.No: T2S1702

Synonym: 1,7-双苯-5-羟基-6-庚烯-3-酮,(5R)-trans-1,7-diphenyl-5-hydroxy-6-hept,5-Hydroxy-1,7-diphenyl-6-hepten-3-one

Target: Antioxidant

Cat.No: T4115

Synonym: 橙皮油内酯,7-geranyloxycoumarin,橙皮油素

Target: MMP, BACE

Cat.No: T5747

Target: Others

8-Hydroxybergapten

Cat.No: TN1345

Synonym: 8-羟基佛手柑内酯,8-羟基佛手苷内酯

Target: Others

1,7-Diphenyl-5-hydroxy-4,6-hepten-3-one

Cat.No: TN2523

Target: Others

Subelliptenone G

Cat.No: TN5075

Target: Others

7-(4-Hydroxyphenyl)-1-phenyl-4-hepten-3-one

Cat.No: TN3218

Target: Beta Amyloid, PI3K, mTOR

1,7-Diphenyl-4-hepten-3-one

Cat.No: TN2522

Target: Others

Cat.No: TN1415

Synonym: 酸橙素烯醇

Target: 5-HT Receptor

Cat.No: T3404

Synonym: Cuc B,葫芦素B,DATISCACIN,葫芦素 B,Amarine

Target: Apoptosis, PTEN, Integrin, Endogenous Metabolite, HIF, STAT, Autophagy

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