72
36
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T61269 | Anti-osteoporosis agent-1 | ||
Anti-osteoporosis agent-1 (comp 4aa) 作为一种高效的复制蛋白 A(RPA) 抑制剂,表现出其IC50值仅为18 μM。 | |||
T83032 |
Anti-osteoporosis agent-7
|
||
Anti-osteoporosis agent-7 (Compound 133) 作为一种潜在的抗骨质疏松剂,对破骨细胞的形成展示了高度的抑制效果。 | |||
T78816 |
Anti-osteoporosis agent-4
|
NF-κB | NF-κB |
Anti-osteoporosis agent-4 (Compound 11h) 在生物医学领域中表现为有效抑制原代破骨细胞的分化,减弱RANKL诱导的破骨细胞生成,并展示出强抑制作用,具有 IC50 值为358.29 nM。此外,该化合物还能抑制关键的 PI3K/AKT 和 IκBα/NF-κB 信号通路激活,表明其在防治骨质疏松症中的潜在应用价值。 | |||
T10696 |
CB2 modulator 1
|
Cannabinoid Receptor | GPCR/G Protein |
CB2 modulator 1 是一种有效的 CB2 调节剂。 可用于免疫疾病、骨质疏松症、炎症、肾缺血的研究。 | |||
T7469 |
Alendronic Acid
alendronate,阿仑膦酸 |
Others | Others |
Alendronic Acid (alendronate) 是法呢基二磷酸合酶(FDPS)抑制剂,是一种双膦酸盐。它能够抑制破骨细胞介导的骨吸收,对绝经后骨质疏松症,恶性高钙血症和 Paget 病具有疗效。 | |||
T22703 |
CYM-5520
CYM 5520 |
S1P Receptor; LPL Receptor | GPCR/G Protein |
CYM-5520 是一种选择性的变构鞘氨醇 1-磷酸受体 2 (S1PR2) 激动剂,EC50为 480 nM。它可以在 S1PR2 受体中与 S1P 结合,可用于骨质疏松症研究。 | |||
T39508 |
KY-02327
|
Others | Others |
KY-02327 是 KY-02061的一种类似物,具有代谢稳定性。KY-02327是Dishevelled (Dvl)-CXXC5相互作用抑制剂。KY-02327激活Wnt/β-catenin 途径,从而促进成骨细胞分化。 | |||
T9917 |
Denosumab
|
RANKL/RANK | NF-κB |
Denosumab 是能够结合并抑制RANKL 受体激活因子的人单克隆抗体。它具有抗癌活性,可降髋部、低椎骨以及非椎骨骨折的风险。 | |||
T1210 |
Sodium etidronate
依替膦酸钠,Didronel |
Phosphatase | Metabolism |
Sodium etidronate (Didronel) 是一种内源性 pyrophosphate 的合成治疗性 diphosphonate 类似物。作为称为 bisphosphonates 盐类药物家族的一员,etidronate disodium 与内源性 pyrophosphate 的不同之处在于其对酶水解的耐受性。该药剂吸附 hydroxyapatite 细胞并减少破骨细胞的数量,从而抑制异常骨吸收。 Etidronate 还可以直接刺激成骨细胞的骨形成。 | |||
T1850 |
Balicatib
AAE581,巴利卡替 |
Cysteine Protease | Proteases/Proteasome |
Balicatib (AAE581) 是组织蛋白酶K 抑制剂,其对组织蛋白酶K 的抑制作用是组织蛋白酶B、L 和S 的抑制性的10到100倍。 | |||
T0308 |
Etidronic acid
HEDPA,Etidronate,HEDP,羟乙磷酸 |
Apoptosis; Phosphatase; Others; HBV | Apoptosis; Metabolism; Microbiology/Virology; Others |
Etidronic acid (HEDP) 是一种影响钙代谢的二膦酸盐,抑制异位钙化并减缓骨吸收和骨转换,可应用于洗涤,水处理,化妆品和制药业。 | |||
T2334 |
Avanafil
阿伐那非,TA1790 |
PDE | Metabolism |
Avanafil (TA1790) 是一种高活性PDE-5抑制剂,IC50=5.2 nM,对PDE1,PDE6和PDE11活性较低。 | |||
T7839 |
Lasofoxifene Tartrate
CP-336156,酒石酸拉索昔芬 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Lasofoxifene Tartrate (CP-336156) 是一种非甾体类的雌激素受体选择性调节剂 (SERM)。 | |||
T21460 |
Teriparatide acetate
hPTH 1-34 (acetate salt),Parathar acetate,Forteo,醋酸立特帕肽 |
Others | Others |
Teriparatide acetate (Forteo) 是一种 PHT 激动剂,在 HEK293 细胞中的 IC50 为 2 nM。Teriparatide acetate 是一种重组形式的甲状旁腺激素。它是一种有效的合成代谢(即骨骼生长)剂,用于治疗某些形式的骨质疏松症。间歇使用特立帕肽比破骨细胞更能激活成骨细胞,从而导致骨骼整体增加。 | |||
T6374 |
Alfacalcidol
Bondiol,Etalpha,阿法骨化醇,1-hydroxy Vitamin D3,1.alpha.-Hydroxyvitamin D3,1-hydroxycholecalciferol |
Others | Others |
Alfacalcidol (Etalpha) 是一种维生素 D3 衍生物,是非选择性的维生素 D 受体活化剂,有用于骨质疏松研究的潜力。 | |||
T6739 |
Zoledronic Acid
CGP-4244,CGP42446A,唑来膦酸,Zoledronate,CGP 42446,ZOL 446,Zometa |
Apoptosis; Rho; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint |
Zoledronic Acid (ZOL 446) 是一种含氮二磷酸盐,能抑制破骨细胞的分化和凋亡,具有高效的抗骨质再吸收活性,也有抗癌作用。 | |||
T21299 |
Zoledronic acid monohydrate
唑来膦酸一水合物,zoledronate,ZOL 446,CGP 42446,CGP42446A,Zoledronic acid hydrate |
Apoptosis; Others; Autophagy | Apoptosis; Autophagy; Others |
Zoledronic acid monohydrate (CGP 42446) 是一种含氮二磷酸盐,具有高效的抗骨质再吸收活性。它能抑制破骨细胞的分化和凋亡,有抗癌作用。 | |||
T29164 |
WY-47766
WY47766 |
||
WY-47766, a proton pump inhibitor, is used potentially for the treatment of postmenopausal osteoporosis. | |||
T19501 |
Pamidronate disodium pentahydrate
|
Others | Others |
Pamidronate disodium pentahydrate 能够强化骨骼、预防骨质疏松症。 | |||
T12846 |
SB-423562
|
CaSR | GPCR/G Protein |
SB-423562 是一种钙敏感受体 (CaSR) 拮抗剂,可用于骨质疏松症研究。 | |||
T24182 |
ISX-1
ISX 1 |
Others | Others |
ISX-1 抑制脂肪生成并促进成骨细胞生成。 ISX-1 可用于骨质疏松症和骨质减少症的研究。 | |||
T1599L |
Ibandronate sodium
伊班膦酸钠,Boniva,Ibandronate sodium salt,Bondronat |
HBV; Transferase | Metabolism; Microbiology/Virology |
Ibandronate sodium (Boniva) 是一种高活性的含氮二磷酸盐,可用于骨质疏松的研究。 | |||
TP1215 |
Abaloparatide TFA
BA 058 TFA,Abaloparatide TFA (247062-33-5 free base),BIM 44058 TFA |
Others | Others |
Abaloparatide TFA (BIM 44058 TFA) 是一种甲状旁腺激素相关蛋白 (PTHrP) 类似物药物,与相关药物特立帕肽一样用于治疗骨质疏松症。 | |||
T6539 |
Ibandronate sodium monohydrate
Boniva monohydrate,Bondronat monohydrate,Ibandronate sodium,伊班膦酸钠单水合物,BM-210955,BM-21.0955,伊班膦酸钠一水合物,RPR-102289A |
Apoptosis; Others | Apoptosis; Others |
Ibandronate sodium monohydrate (BM-210955) 是一种高活性的含氮二磷酸盐,可用于骨质疏松。 | |||
TP1040L |
Calcitonin(salmon) Acetate(47931-85-1(free base))
Salmon calcitonin |
CGRP Receptor | GPCR/G Protein; Neuroscience |
Calcitonin(salmon)Acetate (47931-85-1(free base))(Salmon calcitonin) 是一种钙调节激素,用于治疗绝经后至少 5 年的女性骨质疏松症。 | |||
T6373 |
Alendronate sodium hydrate
G-704650,Alendronate,MK 217,Alendronate sodium trihydrate,阿仑膦酸钠,G-704650 Adronat,Fosamax |
Transferase | Metabolism |
Alendronate sodium hydrate (MK 217) 是 farnesyl diphosphate synthase 抑制剂(IC50:460 nM)。 | |||
TP1040 |
Calcitonin (salmon)
鲑降钙素,Calcitonin salmon,Salmon calcitonin |
CGRP Receptor | GPCR/G Protein; Neuroscience |
Calcitonin (salmon) 是一种阿米林和卡西宁受体的双激动剂,是一种钙调节激素,能够刺激骨的生成并能抑制骨吸收。 | |||
T1041 |
Risedronate Sodium
NE 58095 Sodium,Risedronic Acid Sodium,利塞膦酸钠,利赛膦酸钠 |
HBV; Transferase | Metabolism; Microbiology/Virology |
Risedronate Sodium (NE 58095 Sodium) 是一种双磷酸盐,对破骨细胞介导的骨吸收具有抑制作用。 | |||
T1641 |
Strontium ranelate
Distrontium renelate,S12911,雷尼酸锶 |
Calcium Channel; CaSR | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism |
Strontium ranelate (S12911) 是抗骨质疏松的药物,能够抑制骨吸收,促进骨形成,进而促使正骨平衡。它还能够激活非骨骼细胞中的钙敏感受体 (CaSR),进而促进肌醇 1,4,5-三磷酸的生成及丝裂原活化的蛋白激酶信号转导。 | |||
T67855 |
ISX-3
|
Others | Others |
ISX-3 是有效的促成骨剂和抗脂肪生成剂。ISX-3 可以增加 PPARγ 的表达。ISX-3 可用于研究骨质减少和骨质疏松症。 | |||
T21535 |
Parathyroid Hormone (1-34), bovine
|
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
Parathyroid Hormone (1-34), bovine 是一种甲状旁腺激素 (PTH) 受体激动剂,是甲状旁腺激素的一部分。 Parathyroid Hormone (1-34), bovine 可用于研究骨质疏松症和甲状旁腺功能衰退。 | |||
T77567 |
BCPA
|
Others | Others |
BCPA 是一种无细胞毒性的 Pin1 调节剂。BCPA 可调节破骨细胞活化,减弱 Pin1 蛋白的减少,从而抑制 RANKL 诱导的破骨细胞发生的受体激活物。BCPA 用于研究骨质疏松。 | |||
T8436 |
Minodronic acid
Phosphonicacid,(1-hydroxy-2-imidazo(1,2-a)pyridin-3-ylethylidene)bis-,ONO-5920,YM-529 |
Apoptosis; P2X Receptor | Apoptosis; Membrane transporter/Ion channel; Neuroscience |
Minodronic acid(YM-529) 是一种 P2X2/3 受体拮抗剂, 具有抗癌活性,可直接或间接的抑制癌细胞增殖,诱导细胞凋亡。Minodronic-acid 对各种类型的癌细胞的转移具有抑制作用。Minodronic-acid 可用于研究骨质疏松。 | |||
T60554 |
Schnurri-3 inhibitor-1
|
Others | Others |
Schnurri-3 inhibitor-1 是有效的 schnurri-3 抑制剂,schnurri-3是成人骨形成的重要调节因子。在成骨细胞系 Shn3FFL 中,Schnurri-3 inhibitor-1 通过 EF1alpha 启动子抑制 Shn3 蛋白表达 (AC50= 2.09 μM)。Schnurri-3 inhibitor-1 可用于骨质疏松症相关的研究。 | |||
T111959 |
IFB-088 acetate
|
||
IFB-088 acetate 是一种苄基胍衍生物,可用于治疗与PPP1R15A 途径相关并与蛋白质错误折叠应激相关的疾病和癌症,如tau 病、突触核蛋白病、多谷氨酰胺和多丙氨酸疾病、白质营养不良、囊性纤维化、多发性硬化症、溶酶体储存障碍、淀粉样变性疾病、炎症、代谢障碍、心血管疾病、骨质疏松症、神经系统创伤等等。 | |||
T31944 |
Glutamine monofluorophosphate
L-Glutamine monofluorophosphate,G-MFP |
||
Glutamine monofluorophosphate is used during the fluorotherapy of osteoporosis. | |||
T28870 |
Strontium Malonate
NBS-101,NBS 101,NBS101 |
||
Strontium Malonate, a calcium-sensing receptor agonist, is used potentially for the treatment of postmenopausal osteoporosis. | |||
T25700L |
Levormeloxifene fumarate
|
||
Levormeloxifene fumarate is an osteoporosis drug and selective estrogen receptor modulator (SERM). | |||
T70305 | Zoledronate trisodium hydrate | ||
Zoledronate trisodium is a Bone Resorption Inhibitor and Osteoporosis Therapy Adjunct | |||
T27825 |
LG190178
LG-190178,LG 190178 |
||
LG190178, a vitamin D receptor (VDR) ligand, is a therapeutic agent used for the treatment of psoriasis, osteoporosis, and secondary hyperparathyroidism. | |||
T26041 | Ranelic acid | ||
Ranelic acid is an organic acid capable of chelating metal cations. Strontium ranelate, the strontium salt of Ranelic acid, is utilized to treat osteoporosis and increase bone mineral density. | |||
T11914 |
LY88074 Trimethyl ether
|
Others | Others |
LY88074 Trimethyl ether is useful for inhibiting various conditions associated with estrogen deprivation syndrome, such as osteoporosis and hyperlipidemia. | |||
T31624 |
Encaleret
JIT305,JIT 305 |
||
Encaleret( JIT-305) is an antagonist of oral calcium-sensing receptor (CaSR), it is used for the treatment of osteoporosis. | |||
T69778 |
iso-Dehydrozingerone
|
||
iso-Dehydrozingerone is a novel osteoclastogenesis inhibitor, preventing ovariectomy-induced osteoporosis in ddY mice. | |||
T15749 |
LGD-2226
|
Androgen Receptor | Endocrinology/Hormones |
LGD-2226 is a selective and orally active androgen receptor modulator (EC50: 0.2 nM, Ki: 1.5 nM for the human androgen receptor). LGD-2226 can be used for muscle wasting, osteoporosis, and sexual dysfunction. | |||
T19305 |
Eldecalcitol-d6
|
Others | Others |
Eldecalcitol is an orally active analogue of active vitamin D used in the treatment of osteoporosis. Eldecalcitol-d6 is the deuterium labeled Eldecalcitol. | |||
T11913 |
LY88074 Methyl ether
|
Others | Others |
LY88074 Methyl ether is effective in inhibiting conditions associated with estrogen deprivation syndrome, such as osteoporosis and hyperlipidemia, which occur due to various estrogen-deficient states. | |||
T15206 |
Eldecalcitol
艾地骨化醇,ED-71,2-(3-hydroxypropoxy)-1,25-dihydroxyvitamin D3 |
Others | Others |
Eldecalcitol possesses a potent inhibitory effect on bone resorption and induces a significant increase in bone mineral density. Eldecalcitol is an orally active analogue of active vitamin D. It also is used in the treatment of osteoporosis . | |||
T16394 |
ONO-5334
|
Cysteine Protease | Proteases/Proteasome |
ONO-5334 is an effective and selective cathepsin K inhibitor (Ki: 0.10 nM, 0.049 nM, and 0.85 nM for human, rabbit, and rat cathepsin K, respectively). ONO-5334 has the potential for the study of osteoporosis. | |||
TP1027 |
Calcitonin, eel TFA (57014-02-5 free base)
Thyrocalcitonin eel (TFA),Calcitonin, eel TFA |
||
Calcitonin,eel TFA is a thyroid hormone polypeptide that can regulate calcium homeostasis and is widely used in the study of postmenopausal osteoporosis. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T83033 | Anti-osteoporosis agent-2 | ||
Anti-osteoporosis agent-2 (Compound 10)为抗骨质疏松剂,能抑制RANKL诱导的破骨细胞分化。 | |||
TN1124 |
Neoeriocitrin
|
AChE | Neuroscience |
Neoeriocitrin 是一种有效的乙酰胆碱酯酶抑制剂,分离于自百日草,在 MC3T3-E1 中显示出对增殖和成骨分化的活性。 | |||
T5S1172 |
Tiliroside
银椴甙,Tribuloside,银椴苷;椴树苷 |
Antioxidant | oxidation-reduction |
Tiliroside (Tribuloside) 是糖苷类黄酮,是 α-淀粉酶的非竞争性抑制剂(Ki:84.2 μM)。它抑制胃肠道中碳水化合物的消化和葡萄糖的吸收,具有抗糖尿病作用。 | |||
T3408 |
Syringin
Lilacin,Syringoside,eleutheroside-b,Methoxyconiferine,紫丁香苷 |
NOS; Autophagy | Autophagy; Immunology/Inflammation |
Syringin (eleutheroside-b) 是欧丁香中的一种苯丙素类天然产物,通过抑制自噬来防止压力超载引起的心肌肥厚,具有抗肿瘤、抗增殖、抗骨质疏松、免疫调节和血小板聚集抑制作用。 | |||
TN7036 |
N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide
(9Z,12Z,15Z)-N-[(3-Methoxyphenyl)methyl]-9,12,15-octadecatrienamide,间-甲氧基苄基-亚麻酰胺,Macamide Impurity 14 |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
N-(3-Methoxybenzyl)-(9Z,12Z,15Z)-octadecatrienamide (Macamide Impurity 14) 是一种从玛卡中分离得到的玛卡酰胺。它能够激活典型的Wnt/β‐catenin 信号通路,诱导间充质干细胞成骨分化和随后的骨形成,可用于研究骨质疏松症。 | |||
T3906 |
Epimedin A
|
Others | Others |
Epimedin A 是一种提取自草本淫羊藿中的天然化合物。 | |||
TQ0172 |
2''-O-Rhamnosylicariside II
|
Others | Others |
2''-O-Rhamnosylicariside II 是天然来源的黄酮类糖苷化合物,可能对改善绝经后骨质疏松有益处。 | |||
TN1076 |
Oleonuezhenide
|
Others | Others |
Oleonuezhenide 分离自 Fructus Ligustri Lucidi 中,具有神经保护活性。 | |||
T6S2146 |
Epimedin B
朝藿定B,Epmedin B |
Others | Others |
Epimedin B (Epmedin B) 是一种天然活性成分,来自淫羊藿,据报道其就有抗骨质疏松症的潜能。 | |||
T2O2798 |
D-(+)-Trehalose
Ergot Sugar,D-Trehalose,Mycose,D-(+)-Trehalose Anhydrous,D-海藻糖,Trehalose |
Others; Endogenous Metabolite | Metabolism; Others |
D-(+)-Trehalose (Mycose) 来源于自Saccharomyces cerevisiae,常用作食品成分和药物赋形剂。 | |||
T3130 |
Testosterone phenylpropionate
Testosterone hydrocinnamate,苯丙酸睾酮,Retandrol,Testosterone 17-phenylpropionate |
Others | Others |
Testosterone phenylpropionate (Testosterone 17-phenylpropionate) 是一种长效雄激素。d3-Testosterone phenylpropionate 可用作内标物。 | |||
T7106 |
Menaquinone-4
四烯甲萘醌,Vitamin K2,Menaquinone K4 |
Others; Endogenous Metabolite | Metabolism; Others |
Menaquinone-4 (Vitamin K2) 是维生素 K 的一种,用作止血剂,有潜力用于骨质疏松的研究。 | |||
T3396 |
Baohuoside I
Icariside-II,宝藿苷I,Icariin-II,宝藿苷 I |
Apoptosis; CXCR | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation |
Baohuoside I (Icariside-II) 是从朝鲜淫羊藿中得到的一种黄酮类天然产物,是CXCR4抑制剂,抑制 CXCR4 的表达,诱导凋亡,具有抗肿瘤活性。 | |||
T5751 |
Tigogenin
|
Others | Others |
Tigogenin 是甾体皂甙元,普遍用于甾体类药物的合成。它能够阻碍小鼠骨髓基质细胞脂肪细胞分化,促使成骨细胞的分化。 | |||
T3397 |
Epmedin C
淫羊霍定C,Baohuoside-VI,Epimedin C |
Others | Others |
Epmedin C (Baohuoside-VI) 是天然化合物,在切除卵巢的小鼠体内与雌性激素作用相似。 | |||
T6S2252 |
Sweroside
|
Others | Others |
Sweroside 是分离自Lonicera japonica 中,具有细胞保护、抗骨质疏松和保护肝脏活性。 | |||
T8709 |
Nandrolone phenylpropionate
Nandrolone phenpropionate,苯丙酸诺龙 |
Androgen Receptor | Endocrinology/Hormones |
Nandrolone phenylpropionate (Nandrolone phenpropionate) 是一种合成代谢类固醇,是一种 19-nortestosterone 的衍生物。它能够促进蛋白质合成,用于缓解组织分解代谢,可以用于骨质疏松症和特纳综合征的研究。 | |||
TN7242 |
5-Hydroxyvanillin
3,4-Dihydroxy-5-methoxybenzaldehyde |
Antifungal | Microbiology/Virology |
5-Hydroxyvanillin (3,4-Dihydroxy-5-methoxybenzaldehyde) 可从籼稻中就分离得到对金黄色葡萄球菌具有抑制作用,可用于治疗和预防骨质疏松症。 | |||
TN6900 |
Reptoside
|
Others | Others |
Reptoside 可从杜仲和 Ajuga chamaepitys (L.) Schreb 根部和地上部分中提取,是杜仲治疗骨质疏松症的活性环烯醚萜苷之一。 | |||
TJS0856 |
Dalbergin
黄檀素,6-Hydroxy-7-Methoxy-4-Phenylcoumarin |
Others | Others |
Dalbergin (6-Hydroxy-7-Methoxy-4-Phenylcoumarin) 是一种 Dalbergia Sissoo Linn. knot wood 提取物的成分。它具有强大的抗氧化活性。 | |||
T1549 |
Raloxifene hydrochloride
LY156758 hydrochloride,盐酸雷洛昔芬,Raloxifene HCl,LY139481 hydrochloride,Keoxifene hydrochloride,LY156758 (Keoxifene) HCl |
Estrogen Receptor/ERR; Others; MAO; Estrogen/progestogen Receptor; Autophagy | Autophagy; Endocrinology/Hormones; Metabolism; Neuroscience; Others |
Raloxifene hydrochloride (LY156758 hydrochloride) 是一种选择性且可口服的雌激素受体调节剂,用于预防绝经后妇女的骨质疏松症。它对骨骼和胆固醇代谢具有雌激素激动作用,但对乳腺和子宫组织具有完全的雌激素拮抗作用。 | |||
T3S0364 |
L-Arginine
L-精氨酸,L-Arg,(S)-(+)-Arginine |
IL Receptor; Endogenous Metabolite; NO Synthase | Immunology/Inflammation; Metabolism |
L-Arginine (L-Arg) 是内皮型一氧化氮合酶(eNOS) 的底物。L-Arginine 通过阳离子氨基酸转运体家族转运到血管平滑肌细胞,并被代谢成一氧化氮、多胺或 L-脯氨酸。 | |||
T2768 |
Saikosaponin A
柴胡皂苷A,柴胡皂苷 A |
NF-κB; Antibacterial; Liver X Receptor | Metabolism; Microbiology/Virology; NF-κB |
Saikosaponin A 是银柴胡中的主要活性成分,有抗炎活性,可上调 LXRα的表达。 | |||
T7190 |
Actein
|
Apoptosis; Akt; JNK; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Actein 是从升麻的根茎中分离的一种三萜糖苷,通过促进ROS/JNK 活化和钝化人膀胱癌中的AKT 途径来抑制细胞增殖,诱导自噬和凋亡。 | |||
TN5888 |
Toddaculin
|
Others | Others |
Toddaculin 是一种天然香豆素,抑制过度的破骨细胞活性并增强成骨细胞分化和矿化。它可诱导白血病细胞分化和凋亡,具有抗炎活性。 | |||
T6S2099 |
Geraniin
|
Antioxidant; TNF | Apoptosis; oxidation-reduction |
Geraniin 是一种肿瘤坏死因子α释放抑制剂,其IC50值为 43 μM,具有抗肿瘤、抗炎和抗高血糖活性。 | |||
T3673 |
Mollugin
大叶茜草素,Rubimaillin |
HER; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Mollugin (Rubimaillin) 是Rubia cordifolia L.中主要的生物活性成分。它能通过 p38-Smad 信号通路增强 BMP-2 的成骨作用。它通过抑制 TNF-α 诱导的 NF-κB 激活起抗癌疗效。 | |||
T6S1559 |
Aurantio-obtusin
|
Others | Others |
Aurantio-obtusin 是从决明子中分离出的蒽醌类化合物,具有抗炎、抗凝血、抗氧化、抗高血压的活性。它能抑制 IgE 介导的肥大细胞和过敏模型中的过敏反应,具有研究过敏相关疾病的潜力。在大鼠中,它通过内皮细胞 PI3K/AKT/ eNOS 依赖信号通路放松全身动脉,是潜在的新型血管扩张剂。 | |||
TMA0132 | Dihydrophaseic acid | Others | Others |
Dihydrophaseic acid 3'-O-b-D-glucopyranoside (D3G) can increase the proliferation and differentiation of osteoblast cells and enhance bone formation, suggests that D3G may be a good candidate for the treatment of osteoporosis. | |||
TN6568 |
Glycinol
|
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Glycinol enhances osteogenic differentiation and attenuates the effects of age on mesenchymal stem cells, it could as a potential preventive or treatment for osteoporosis. Glycinol also has antidiuretic activity. | |||
T81761 |
Morusignin L
|
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Morusignin L为一种表现出抗骨质疏松症效应的化学物质。 | |||
T39445 |
Korepimedoside C
Epimedin I,朝藿苷丙 |
||
Korepimedoside C, also known as Epimedin I, is a flavonol glycoside derived from the aerial parts of Epimedium koreanum Nakai. Epimedium koreanum Nakai is a renowned Chinese herbal medicine that has been extensively studied for its potential in addressing impotence, osteoporosis, immune suppression, and cardiovascular diseases. | |||
TN3753 |
Dalbergioidin
|
Tyrosinase; ROS; Akt; PI3K; TGF-beta/Smad | Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Proteases/Proteasome; Stem Cells |
Dalbergioidin exhibits tyrosinase inhibitory activity with an IC50 of 20 mM. It shows a melanin biosynthesis inhibition zone in the culture plate of Streptomyces bikiniensis that has commonly been used as an indicator organism. Dalbergioidin protects MC3T3-E1 osteoblastic cells against H2O2-induced cell damage through activation of the PI3K/AKT/SMAD1 pathway, suggests that it may be useful in bone metabolism diseases, particularly osteoporosis. Dalbergioidin also ameliorates doxorubicin-induced ... | |||
TN1431 |
Baohuoside VII
宝藿苷,宝藿苷VII |
Others | Others |
Baohuoside aglycone possesses cardioprotective effect in prevention of ischemia/ reperfusion injury and reduce the myocardial infraction, the mechnism is due to the reduction of the injury of free radicals. Baohuoside VII in vivo exhibits significant anti | |||
TN3144 |
6,4'-Dihydroxy-7-methoxyflavanone
檀木 |
ERK; IL Receptor; Antioxidant; TNF; NF-κB; MAPK; Prostaglandin Receptor; JNK; Autophagy | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; MAPK; NF-κB; oxidation-reduction |
6,4'-Dihydroxy-7-methoxyflavanone 是一种从 Dalbergia odorifera T. Chen (Leguminosae) 的心材中分离出来的生物活性化合物,具有抗氧化、抗炎和神经保护作用。 6,4'-二羟基-7-甲氧基黄烷酮可用于治疗破骨性骨病如骨质疏松症、类风湿性关节炎和牙周病的研究。 | |||
TN4334 | Isotaxiresinol | TNF | Apoptosis |
Isotaxiresinol prevents d-GalN/LPS-induced hepatic injury by inhibiting hepatocyte apoptosis through the blocking of TNF-alpha and IFN-gamma production by activated macrophages and direct inhibition of the apoptosis induced by TNF-alpha. Isotaxiresinol ma |