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59

抑制剂 & 化合物

4

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
TP1122L	IGF-I 30-41 acetate(82177-09-1 free base) Insulin-like Growth Factor I (30-41) acetate	Others	Others
	IGF-I 30-41 acetate(82177-09-1 free base) (Insulin-like Growth Factor I (30-41) acetate) 是胰岛素样生长因子 I (IGF-I) 的氨基酸 30 至 41 片段。
T6419	BMS-536924 HY-10262,胰岛素样生长因子-1 受体拮抗剂,BMS 536924,CS-0117	Apoptosis; FAK; MEK; IGF-1R; Src	Angiogenesis; Apoptosis; Cytoskeletal Signaling; MAPK; Tyrosine Kinase/Adaptors
	BMS-536924 (BMS 536924) 是一种具有口服活性，竞争性和选择性的胰岛素样生长因子受体激酶和胰岛素受体抑制剂，IC50分别为 100 nM 和 73 nM。它具有抗癌活性。
T76539	Insulin-like growth factor II
	Insulin-like growth factor II (IGF-2)为人血清中主要生长激素，对神经突生长具有许可性和直接作用，同时增强交感与感觉神经元的生存能力。
TP1122	IGF-I (30-41) Insulin-like Growth Factor I (30-41),IGF-I 30-41
	IGF-I (30-41) is amino acids 30 to 41 fragment of Insulin-like Growth Factor I (IGF-I).
TP1124	IGF-I (24-41) Insulin-like Growth Factor I (24-41),IGF-I 24-41
	IGF-I (24-41) is a 24-41 amino acid fragment of Insulin-like Growth Factor I (IGF-I). IGF-I is partly responsible for systemic GH activities although it possesses a wide number of own properties (anabolic, antioxidant, anti-inflammatory and cytoprotective
T6203	Saxagliptin BMS-477118,沙克列汀,Onglyza,沙格列汀	Proteasome; DPP-4	Proteases/Proteasome; Ubiquitination
	Saxagliptin (BMS-477118) 是一种选择性，可逆性，竞争性和口服活性的二肽基肽酶 4 (DPP-4) (Ki= 0.6-1.3 nM) 抑制剂。Saxagliptin 能够用于 2 型糖尿病的研究。
TP1121	IGF-I (30-41) TFA(82177-09-1,FREE) Insulin-like Growth Factor I (30-41) (TFA)
	IGF-I (30-41) (TFA) is amino acids 30 to 41 fragment of Insulin-like Growth Factor I (IGF-I).
TP1123	IGF-I (24-41) TFA (135861-49-3 free base) Insulin-like Growth Factor I (24-41) (TFA),IGF-I (24-41) TFA
	IGF-I is partly responsible for systemic GH activities although it possesses a wide number of own properties (anabolic, antioxidant, anti-inflammatory and cytoprotective actions).IGF-I (24-41) (TFA) is amino acids 24 to 41 fragment of Insulin-like Growth
T0178	Saxagliptin hydrate 沙格列汀单水化合物,Onglyza hydrate,BMS-477118 hydrate	Proteasome; DPP-4	Proteases/Proteasome; Ubiquitination
	Saxagliptin hydrate (Onglyza hydrate) 是一种选择性，竞争性，可逆性和口服活性的二肽基肽酶 4 (DPP-4) (Ki= 0.6-1.3 nM) 抑制剂。Saxagliptin hydrate 能够用于 2 型糖尿病的研究。
T2349	BMS-754807	Trk receptor; c-Met/HGFR; IGF-1R	Tyrosine Kinase/Adaptors
	BMS754807 是一种可逆的IGF-1R 抑制剂 (IC50:1.8 nM，Ki<2 nM)，也是一种可逆的IR 抑制剂 (IC50:7 nM，Ki<2 nM)。它也抑制 Met (IC50:6 nM)，RON (IC50:44 nM)，TrkA (IC50:7 nM)，TrkB (IC50:4 nM)，AurA (IC50:9 nM) 和 AurB (IC50:25 nM) 的活性。
T8906	NBI-31772 NBI31772,NBI 31772	IGF-1R	Tyrosine Kinase/Adaptors
	NBI-31772 (NBI 31772) 是胰岛素样生长因子-1 结合蛋白 (IGFBP, Ki = 47 nM) 的有效抑制剂。 NBI-31772 可用于 IGF 反应性疾病的研究。
T2189	Sodium orthovanadate Sodium vanadate,钒酸钠,Trisodium vanadate,Sodium pervanadate	ATPase; Phosphatase	Membrane transporter/Ion channel; Metabolism
	Sodium orthovanadate 是一种蛋白酪氨酸磷酸酶，碱性磷酸酶和一些ATP 酶的抑制剂，有可能充当磷酸盐类似物。它具有胰岛素样作用、对心室肌的正性肌力作用和其他代谢作用。
T78097L	Mazdutide acetate（2259884-03-0 free base） Mazdutide acetate（2259884-03-0 free base）,OXM-3 acetate,LY-3305677 acetate,IBI-362 acetate	Glucagon Receptor	GPCR/G Protein
	Mazdutide acetate 是一种高效的胰高血糖素样肽 (GLP-1R) 与胰高血糖素受体 (GCGR) 的共激动剂，是一种胃泌酸调节素类似物。Mazdutide acetate可刺激小鼠胰岛的胰岛素分泌，可用于研究肥胖和 2 型糖尿病 (T2D) 。
T68405	KW-2450 free base	IGF-1R	Tyrosine Kinase/Adaptors
	KW-2450 free base 是一种 IGF-1R/IR和酪氨酸激酶多重抑制剂具有抗肿瘤活性。KW-2450 free base 在小鼠 HT-29/GFP 结肠癌异种移植模型中显示出适度的生长抑制活性并抑制 IGF-1 诱导的信号转导。
T76810	Ganitumab AMG 479	IGF-1R	Tyrosine Kinase/Adaptors
	Ganitumab (AMG 479) 是一种高效的1型胰岛素样生长因子受体 (IGF1R) 单克隆抗体。Ganitumab 在低浓度下识别与 IGF1R 结合，KD 值为0.22 nM，Ganitumab 对小鼠 IGF1R 与 IGF1 和 IGF2 的相互作用有抑制作用。Ganitumab 可用于研究癌症。
T6017	Linsitinib OSI-906,林西替尼	IGF-1R	Tyrosine Kinase/Adaptors
	Linsitinib (OSI-906) 是选择性的、有效的、具有口服活性的IGF-1和胰岛素受体(IR)的双重抑制剂，IC50分别为 35 和 75 nM。
T2160	Suramin Sodium Salt 苏拉明钠,BAY-205,Suramin hexasodium salt,苏拉明钠盐,NF-060	Apoptosis; Phosphatase; SARS-CoV; Sirtuin; Reverse Transcriptase; Topoisomerase; Parasite	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology
	Suramin Sodium Salt (BAY-205) 是可逆的竞争性蛋白酪氨酸磷酸酶抑制剂。它抑制 IP5K，是抗寄生虫，抗肿瘤和抗血管生成剂。它是sirtuins 的有效抑制剂，也是 SARS-CoV-2 RNA 依赖性 RNA 聚合酶抑制剂。
T25123	AZ12253801 AZ 12253801,AZ-12253801
	AZ12253801 is a type 1 insulin-like growth factor receptor (IGF-1R) inhibitor.
T70568	H-1356
	H-1356 is an insulin-like growth factor 1(IGF-I) analog that inhibits autophosphorylation of IGF-I receptor.
T24106	GSK2163632A GSK-2163632-A,GSK 2163632 A
	GSK2163632A is an insulin-like growth factor 1 receptor inhibitor that acts by binding to a novel region of the GRK active site cleft.
TP2209	Xenin-8	Others	Others
	neurotensin-like peptide that modulate pancreatic insulin and glucagon secretion/effects
TP1361	S961 TFA (1083433-49-1 free base) S961 TFA
	S961 TFA is A high affinity insulin receptor (IR) antagonist with IC50 for hir-a, hir-b and human insulin-like growth factor I receptor (higf-ir) at 0.048, 0.027 and 630 nM, respectively.
T25110	AS1069562 AS-1069562,AS 1069562
	AS1069562 is an inhibitor of serotonin (5-HT) and norepinephrine (NE) reuptake which acts by notably restoring reduced insulin-like growth factor 1 and fibroblast growth factor 2 mRNA levels in dorsal root ganglion and spinal cord, respectively.
T16101	ML-290	RXFP receptor	GPCR/G Protein
	ML-290 是一个松弛素/胰岛素样肽受体 (RXFP1) 偏向变构激动剂，为抗纤维化基因激活剂，EC50为 94 nM。
T80871	Veligrotug	IGF-1R	Tyrosine Kinase/Adaptors
	Veligrotug为IgG1-kappa型抗IGF1R（胰岛素样生长因子1受体，CD221）嵌合单克隆抗体。
T76043L	S961 acetate
	S961 acetate 是一种高亲和力的胰岛素受体 (insulin receptor, IR) 拮抗剂，对 HIR-A，HIR-B 和人胰岛素样生长因子 I 受体 (HIGF-IR) 的 IC50分别为 0.048，0.027 和 630 nM。
T24620	PF-06372222 PF-0637222,PF0637222,PF 0637222
	PF-06372222 is a small-molecule negative allosteric modulator of the glucagon receptor (GCGR). PF-06372222 is also an antagonist for glucagon-like peptide-1 receptor GLP-1R, which inhibits glucagon secretion and glucose-dependent insulin secretion.
T30538	BMS-695735 CHEMBL459729,DNC008930,BMS 695735,BMS695735,BDBM27888
	BMS-695735, a benzimidazole inhibitor of insulin-like growth factor-1 receptor, has broad-spectrum antitumor activity in vivo. It was found that BMS-695735 had strong inhibition of CYP3A4, induction of CYP3A4 mediated by PXR transactivation, poor water so
TP1795	S961
	S961是一种高亲和力和选择性胰岛素受体(IR)拮抗剂，接近闪烁计数法试验中对HIR-A、HIR-B 和人胰岛素样生长因子I 受体(HIGF-IR)的ic50分别为0.048、0.027和630 nM。
T76043	S961 TFA
	S961 TFA为一种与胰岛素受体（insulin receptor, IR）高亲和力相结合的拮抗剂，其IC50值对HIR-A、HIR-B及人胰岛素样生长因子I受体（HIGF-IR）分别为0.048、0.027及630 nM。
T38584	ALK-IN-12
	ALK-IN-12 is a highly potent and orally active inhibitor of anaplastic lymphoma kinase (ALK), demonstrating an exceptional IC50 value of 0.18 nM. Additionally, ALK-IN-12 displays inhibitory activity against insulin-like growth factor 1 receptor (IGF1R) and insulin receptor (InsR), with IC50 values of 20.3 nM and 90.6 nM, respectively. Notably, its antitumor effects have been observed, making it a promising compound for targeted cancer therapy.
T80605	Dusigitumab MEDI 573	IGF-1R	Tyrosine Kinase/Adaptors
	Dusigitumab (MEDI 573)为一种人源化IgG2λ单克隆抗体，具有特异性针对IGF2和IGF1。
T38502	IGF-1R inhibitor-2
	IGF-1R inhibitor-2 (example 121) is a compound that inhibits the insulin-like growth factor-1 receptor (IGF-1R). By downregulating the IGF-1R, it has the potential to reverse the transformed phenotype of tumor cells and make them more susceptible to apoptosis.
T61506	NBI-31772 hydrate
	NBI-31772 hydrate is a powerful inhibitor of the interaction between insulin-like growth factor (IGF) and IGF-binding proteins (IGFBPs). It acts as a nonpeptide ligand, effectively releasing bioactive IGF-I from the IGF-I/IGFBP-3 complex (Ki values for all six human subtypes range from 1-24 nM). This compound demonstrates significant anxiolytic and antidepressant-like effects [1] [2] [3].
TP1241	Adrenocorticotropic Hormone (ACTH) (18-39), human ACTH (18-39), human
	Adrenocorticotropic Hormone (ACTH) (18-39) is known as the Corticotropin-like Intermediate Lobe Peptide. It stimulates insulin secretion as well as amylase and protein secretion in a dose-dependent manner similar to those of secretin and carbamylcholine.
T76330	Human glucagon-like peptide-1-(7-36)-Lys(Biotin) amide
	Human glucagon-like peptide-1-(7-36)-Lys(Biotin) amide 是一种带有生物素标签的Glucagon-like peptide-1-(7-36)，后者为一种具备提升胰岛素释放功能，从而表现出抗糖尿病活性的胃肠道肽。
T70876	KW-2450 Tosylate
	KW-2450 Tosylate is an orally bioavailable inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and insulin receptor (IR) tyrosine kinases with potential antineoplastic activity. IGF-1R/IR inhibitor KW-2450 Tosylate selectively binds to and inhibits the activities of IGF-1R and IR, which may result in the inhibition of tumor cell proliferation and the induction of tumor cell apoptosis. IGF-R1 and IR tyrosine kinases, overexpressed in a variety of human cancers, play significant roles in t...
T76759	Robatumumab
	Robatumumab (Sch 717454) 为针对人胰岛素样生长因子 1 受体(anti-humanIGF-1R)的抗体，展现出抗肿瘤及阻止癌细胞增殖的作用，适用于骨肉瘤与尤文肉瘤的研究。
T63019	GKA50 quarterhydrate
	GKA50 quarterhydrate 是一种有效的葡萄糖激酶激活剂，其 EC50 值为 33 nM。GKA50 quarterhydrate 是一种啮齿动物和人类胰岛中 β 细胞代谢的葡萄糖样激活剂，也是一种 Ca2+依赖性胰岛素分泌调节剂。GKA50 quarterhydrate 能够刺激小鼠胰岛分泌胰岛素，可以显著降低高脂喂养的雌性大鼠血糖。
T76746	Figitumumab
	Figitumumab (CP-751871) 为一种高效对抗胰岛素样生长因子 1 受体 (IGF1R) 的全人单克隆抗体。通过阻断 IGF1 与 IGF1R 的结合，其 IC50 值达到 1.8 nM。
T75157L	Cimdelirsen sodium
	Cimdelirsen (sodium) 为针对肝脏的反义寡核苷酸，通过减少生长激素受体(GHr)合成，抑制生长激素(GH)的过度分泌效应，进而降低肢端肥大症患者体内循环胰岛素样生长因子-1 (IGF-1)水平。
T64252	Efpeglenatide
	Efpeglenatide 是一种胰高血糖素样肽 (GLP-1) 受体的长效激动剂。Efpeglenatide 能够改善糖尿病和肥胖小鼠模型的胰岛素敏感性，并减缓其体重减轻的作用。Efpeglenatide 已经被用于 II 型糖尿病的研究。
T73702	Mecasermin
	Mecasermin（Human IGF-I; FK 780），一种重组人胰岛素样生长因子I（IGF-I），主要用于研究因生长激素（GH）受体缺陷或GH抑制抗体导致的GH不敏感性而引起的生长障碍。
T64553	GLP-1(7-37) TFA salt
	The truncated glucagon-like peptides GLP-1(7-37) is naturally occurring peptide product of the preproglucagon gene that are synthesized primarily in the intestine and acts as incretin that are released from the intestine into the bloodstream in response to food and stimulate insulin secretion. GLP-1(7-37) produced a dose-related enhancement of the glucose-stimulated increase in plasma insulin concentration and an increased rate of glucose infusion in Sprague-Dawley Rats at a dosing rang of 0.5, ...
T76291	Des His1, Glu8 Exendin-4
	Des His1, Glu8 Exendin-4 是一种高效的GLP-1-R（胰高血糖素样肽-1 受体）拮抗剂，主要通过调控胰岛素分泌和抑制葡萄糖生成来维持葡萄糖稳态。该化合物广泛应用于2型糖尿病及胃肠道相关研究领域。
TP1148	Glucagon-like peptide 1 (1-37), human HuGLP-1
	Glucagon-like peptide 1 (1-37), human is a highly potent agonist of the GLP-1 receptor.Pancreatic hormone synthesized by post-translational processing of proglucagon. Unlike truncated forms of GLP-1, it has no effect on food intake in rats and does not en
T21691	NVP DPP 728 dihydrochloride
	NVP-DPP728 是一种有效、可逆、腈依赖性二肽基肽酶 IV (DPP-IV)抑制剂，Ki 值为 11 nM。NVP-DPP728 可抑制胰高血糖素样肽-1 (GLP-1)的降解，从而增强响应于葡萄糖摄入的胰岛素释放。NVP-DPP728 可用于糖尿病研究。
T75157	Cimdelirsen
	Cimdelirsen为针对肝脏的反义寡核苷酸，通过降低生长激素受体(GHr)的合成量，来减少生长激素(GH)过量分泌所导致的不良影响，进而在肢端肥大症患者中降低循环胰岛素样生长因子-1(IGF-1)的水平。
T76012	IGF-I (30-41) (TFA)
	IGF-I (30-41) (TFA) 是类胰岛素生长因子I 30 至 41 的氨基酸片段。IGF-I 对生长激素的活性有着重要的作用，但是IGF-I 本身也具有一些自身的特性，如合成代谢、抗氧化、抗炎和细胞保护作用。
T76333	(Ser8)-GLP-1 (7-36) amide, human
	(Ser8)-GLP-1 (7-36) amide, human 为源自胰高血糖素原的胰高血糖素样肽-1酰胺，属于 GLP-1(1-36) 酰胺肽裂解产物。作为肠促胰岛素激素，该化合物促进胰腺 β 细胞在葡萄糖依赖性条件下分泌胰岛素，并对消化道的运动与分泌功能产生影响。

化合物

IGF-I 30-41 acetate(82177-09-1 free base)

Cat.No: TP1122L

Synonym: Insulin-like Growth Factor I (30-41) acetate

Target: Others

Cat.No: T6419

Synonym: HY-10262,胰岛素样生长因子-1 受体拮抗剂,BMS 536924,CS-0117

Target: Apoptosis, FAK, MEK, IGF-1R, Src

Insulin-like growth factor II

Cat.No: T76539

Cat.No: TP1122

Synonym: Insulin-like Growth Factor I (30-41),IGF-I 30-41

Cat.No: TP1124

Synonym: Insulin-like Growth Factor I (24-41),IGF-I 24-41

Cat.No: T6203

Synonym: BMS-477118,沙克列汀,Onglyza,沙格列汀

Target: Proteasome, DPP-4

IGF-I (30-41) TFA(82177-09-1,FREE)

Cat.No: TP1121

Synonym: Insulin-like Growth Factor I (30-41) (TFA)

IGF-I (24-41) TFA (135861-49-3 free base)

Cat.No: TP1123

Synonym: Insulin-like Growth Factor I (24-41) (TFA),IGF-I (24-41) TFA

Saxagliptin hydrate

Cat.No: T0178

Synonym: 沙格列汀单水化合物,Onglyza hydrate,BMS-477118 hydrate

Target: Proteasome, DPP-4

Cat.No: T2349

Target: Trk receptor, c-Met/HGFR, IGF-1R

Cat.No: T8906

Synonym: NBI31772,NBI 31772

Target: IGF-1R

Sodium orthovanadate

Cat.No: T2189

Synonym: Sodium vanadate,钒酸钠,Trisodium vanadate,Sodium pervanadate

Target: ATPase, Phosphatase

Mazdutide acetate（2259884-03-0 free base）

Cat.No: T78097L

Synonym: Mazdutide acetate（2259884-03-0 free base）,OXM-3 acetate,LY-3305677 acetate,IBI-362 acetate

Target: Glucagon Receptor

KW-2450 free base

Cat.No: T68405

Target: IGF-1R

Cat.No: T76810

Synonym: AMG 479

Target: IGF-1R

Cat.No: T6017

Synonym: OSI-906,林西替尼

Target: IGF-1R

Suramin Sodium Salt

Cat.No: T2160

Synonym: 苏拉明钠,BAY-205,Suramin hexasodium salt,苏拉明钠盐,NF-060

Target: Apoptosis, Phosphatase, SARS-CoV, Sirtuin, Reverse Transcriptase, Topoisomerase, Parasite

Cat.No: T25123

Synonym: AZ 12253801,AZ-12253801

Cat.No: T70568

Cat.No: T24106

Synonym: GSK-2163632-A,GSK 2163632 A

Cat.No: TP2209

Target: Others

S961 TFA (1083433-49-1 free base)

Cat.No: TP1361

Synonym: S961 TFA

Cat.No: T25110

Synonym: AS-1069562,AS 1069562

Cat.No: T16101

Target: RXFP receptor

Cat.No: T80871

Target: IGF-1R

Cat.No: T76043L

Cat.No: T24620

Synonym: PF-0637222,PF0637222,PF 0637222

Cat.No: T30538

Synonym: CHEMBL459729,DNC008930,BMS 695735,BMS695735,BDBM27888

Cat.No: TP1795

Cat.No: T76043

Cat.No: T38584

Cat.No: T80605

Synonym: MEDI 573

Target: IGF-1R

IGF-1R inhibitor-2

Cat.No: T38502

NBI-31772 hydrate

Cat.No: T61506

Adrenocorticotropic Hormone (ACTH) (18-39), human

Cat.No: TP1241

Synonym: ACTH (18-39), human

Human glucagon-like peptide-1-(7-36)-Lys(Biotin) amide

Cat.No: T76330

KW-2450 Tosylate

Cat.No: T70876

Cat.No: T76759

GKA50 quarterhydrate

Cat.No: T63019

Cat.No: T76746

Cimdelirsen sodium

Cat.No: T75157L

Cat.No: T64252

Cat.No: T73702

GLP-1(7-37) TFA salt

Cat.No: T64553

Des His1, Glu8 Exendin-4

Cat.No: T76291

Glucagon-like peptide 1 (1-37), human

Cat.No: TP1148

Synonym: HuGLP-1

NVP DPP 728 dihydrochloride

Cat.No: T21691

Cat.No: T75157

IGF-I (30-41) (TFA)

Cat.No: T76012

(Ser8)-GLP-1 (7-36) amide, human

Cat.No: T76333

Cat. No.	Product Name	Target	Signaling Pathways
T3823	D-Pinitol Pinitol,Inzitol,D-(+)-Pinitol,D-松醇,Methylinositol,3-O-Methyl-D-chiro-inositol	Others; Influenza Virus	Microbiology/Virology; Others
	D-Pinitol (Methylinositol) 是一种存在于几种植物中，如松科和豆科植物的天然产物，具有抗病毒、杀幼虫、降血糖活性和心血管系统保护作用。
T5915	D-chiro-Inositol D-手性肌醇,D-(+)-CHIRO-INOSITOL	Endogenous Metabolite	Metabolism
	D-chiro-Inositol (D-(+)-CHIRO-INOSITOL) 是肌醇差向异构体，存在于某些哺乳动物糖基磷脂酰肌醇蛋白锚和具有胰岛素样生物特性的肌醇磷脂聚糖中。它能够抑制高血糖，改善胰岛素抵抗。它用于多囊卵巢综合征和糖尿病的相关研究。
TN2080	Pinoresinol 松脂酚，松脂素,(+)-Pinoresinol	Apoptosis; NF-κB; CDK; p53	Apoptosis; Cell Cycle/Checkpoint; NF-κB
	Pinoresinol ((+)-Pinoresinol) 是一种植物来源的木质素，具有抗炎、保肝和杀真菌活性。它导致 CDK 抑制剂 p21(WAF1/Cip1) 在 mRNA 和蛋白质水平上调，抑制 NF-kappaB 和激活蛋白 1 。
T3S0027	Picropodophyllotoxin AXL 1717,Picropodophyllin,苦鬼臼毒素	IGF-1R	Tyrosine Kinase/Adaptors
	Picropodophyllotoxin (AXL 1717) 是一种环木脂素生物碱，存在于五月树(Podophyllum peltatum) 中，是一种具有潜在抗肿瘤活性的胰岛素样生长因子 1 受体 (IGF1R) 的小分子抑制剂。它特异性抑制 IGF1R 的活性并下调细胞表达，而不干扰其他生长因子受体的活性，例如胰岛素受体、表皮生长因子、血小板衍生生长因子、成纤维细胞生长因子和肥大/干细胞生长因子 (KIT) ）。该药剂在抑制肿瘤细胞增殖和诱导肿瘤细胞凋亡方面显示出有效的活性。 IGF1R 是一种在多种人类癌症中过度表达的受体酪氨酸激酶，在多种癌细胞的生长和存活中起关键作用。

天然产物

Cat.No: T3823

Synonym: Pinitol,Inzitol,D-(+)-Pinitol,D-松醇,Methylinositol,3-O-Methyl-D-chiro-inositol

Target: Others, Influenza Virus

D-chiro-Inositol

Cat.No: T5915

Synonym: D-手性肌醇,D-(+)-CHIRO-INOSITOL

Target: Endogenous Metabolite

Cat.No: TN2080

Synonym: 松脂酚，松脂素,(+)-Pinoresinol

Target: Apoptosis, NF-κB, CDK, p53

Picropodophyllotoxin

Cat.No: T3S0027

Synonym: AXL 1717,Picropodophyllin,苦鬼臼毒素

Target: IGF-1R

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