Curculigoside B 是从虎杖中分离得到的酚苷类化合物,能促进成骨细胞增殖,减少骨吸收坑面积,减少破骨细胞形成和 TRAP 活性。具有抗骨质疏松和抗氧化活性。
Curculigoside B Chemical Structure
CAS No. : 143601-09-6
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1 mg
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生物活性
Curculigoside B, a phenolic glycoside isolated from Curculigo orchioides, enhances the osteoblast proliferation, decreases the area of bone resorption pit, osteoclastic formation and TRAP activity. Antiosteoporotic and antioxidative activities[1].
分子量
452.41
Formula
C21H24O11
CAS 号
143601-09-6
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Jiao L, et al. Antiosteoporotic activity of phenolic compounds from Curculigo orchioides. Phytomedicine. 2009;16(9):874-881.
Psoralenoside is a benzofuran glycoside from Psoralea corylifolia[1]. Psoralenoside exhibits high binding affinities against histaminergic H1, calmodulin, and voltage-gated L-type calcium channels (E-value≥-6.5 Kcal/mol)[2]. Psoralenoside shows estrogen-like activity, osteoblastic proliferation accelerating activity, antitumor effects and antibacterial activity[3].
IC50 Target[1]
H1 Receptor
;
L-type calcium channel
;
分子量
366.32
Formula
C17H18O9
CAS 号
905954-17-8
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Chun-Feng Qiao, et al.Psoralenoside and isopsoralenoside, two new benzofuran glycosides from Psoralea corylifolia. Chem Pharm Bull (Tokyo). 2006 May;54(5):714-6.
[2]. Muhammad Bilal Riaz, et al. Pharmacological and computational evaluation of fig for therapeutic potential in hyperactive gastrointestinal disorders. BMC Complement Altern Med. 2019 Dec 3;19(1):348.
[3]. Yue-Fei Wang, et al.A UPLC-MS/MS method for in vivo and in vitro pharmacokinetic studies of psoralenoside, isopsoralenoside, psoralen and isopsoralen from Psoralea corylifolia extract. J Ethnopharmacol
Isopsoralenoside is a benzofuran glycoside from Psoralea corylifolia. Isopsoralenoside can be quickly metabolized to Psoralen (HY-N0053) in digestive tract contents. Isopsoralenoside show estrogen-like activity, osteoblastic proliferation accelerating activity, antitumor effects and antibacterial activity[1].
分子量
366.32
Formula
C17H18O9
CAS 号
905954-18-9
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Yue-Fei Wang, et al.A UPLC-MS/MS method for in vivo and in vitro pharmacokinetic studies of psoralenoside, isopsoralenoside, psoralen and isopsoralen from Psoralea corylifolia extract. J Ethnopharmacol
Anemarsaponin E 是从 Anemarrhena asphodeloides 中提取的皂苷,并具有抗炎活性。
Anemarsaponin E Chemical Structure
CAS No. : 136565-73-6
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数量
5 mg
¥3500
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10 mg
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;
50 mg
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;
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生物活性
Anemarsaponin E is extracted from Anemarrhena asphodeloides Bunge and has anti-inflammatory activity.
分子量
935.10
Formula
C46H78O19
CAS 号
136565-73-6
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder
-20deg;C
3 years
4deg;C
2 years
In solvent
-80deg;C
6 months
-20deg;C
1 month
参考文献
[1]. Yang B, et al. Pharmacokinetic comparison of seven major bioactive components in normal and depression model rats after oral administration of Baihe Zhimu decoction by liquid chromatography-tandem mass spectrometry. J Pharm Biomed Anal. 2018 Jan 30;148:119-127.
Nociceptin (1-7) is the N-terminal bioactive fragment of nociceptin (HY-P0183). Nociceptin (1-7) is a potent ORL1 (NOP) receptor agonist with antinociceptive activity. Nociceptin (1-7) combines with nociceptin reduces hyperalgesia in vivo[1].
体内研究 (In Vivo)
Nociceptin (1-7) (intrathecal injection; 150–1200 nmol; single dose) has no significant effect in the nociceptive thermal threshold (hyperalgesia). However, when nociceptin (1–7) is injected simultaneously with nociceptin (3.0 fmol), nociceptin-induced hyperalgesia is significantly reduced[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
Mice[1]
Dosage:
150–1200 nmol
Administration:
Intrathecal injection; single dose
Result:
Co-treatment with nociceptin could reduce hyperalgesia.
分子量
655.70
Formula
C31H41N7O9
CAS 号
178249-42-8
Sequence Shortening
FGGFTGA
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. T Sakurada, et al. Nociceptin (1 – 7) antagonizes nociceptin-induced hyperalgesia in mice.Br J Pharmacol. 1999 Nov;128(5):941-4.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
α-Terpineol(Synonyms: α-松油醇) 纯度: ≥98.0%
α-Terpineol 从蓝桉 (Eucalyptus globulus Labill) 中分离出来,对牙周病和致龋菌具有很强的抗菌活性。 α-Terpineol 具有抗真菌活性 T. mentagrophytes,这种活性可能导致不可逆转的细胞分裂。
α-Terpineol Chemical Structure
CAS No. : 98-55-5
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价格
是否有货
数量
Free Sample (0.1-0.5 mg)
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10 mM * 1 mL in DMSO
¥550
In-stock
100 mg
¥500
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200 mg
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500 mg
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α-Terpineol 相关产品
•相关化合物库:
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生物活性
α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].
分子量
154.25
Formula
C10H18O
CAS 号
98-55-5
中文名称
α-松油醇
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Park SN, et al. Antimicrobial effect of linalool and α-terpineol against periodontopathic and cariogenic bacteria. Anaerobe. 2012 Jun;18(3):369-72.
[2]. Park MJ, et al. Effect of citral, eugenol, nerolidol and alpha-terpineol on the ultrastructural changes of Trichophyton mentagrophytes. Fitoterapia. 2009 Jul;80(5):290-6.
Phillyrin is isolated from Forsythia suspensa Vahl (Oleaceae), has antibacterial and anti-inflammatory activities. Phillyrin has potential inductive effects on rat CYP1A2 and CYP2D1 activities, without affecting CYP2C11 and CYP3A1/2 activities[1]. Phillyrin has anti-influenza A virus activities[2].
IC50 & Target
CYP1A2; CYP2D1[1]
体外研究 (In Vitro)
Phillyrin (1–5 μM; pretreatment 1 hour; 24 hours) inhibits high glucose-induced FAS protein significantly in HepG2 cells[1]. Phillyrin (1–5 μM; pretreatment 1 hour; 24 hours) inhibits high glucose-induced FAS mRNA expression by suppressing SREBP-1c activation in human HepG2 hepatocytes[1].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
RT-PCR[1]
Cell Line:
Human HepG2 hepatocyte cells
Concentration:
1 μM; 2.5 μM; 5 μM
Incubation Time:
24 hours
Result:
Reduced FAS and SREBP-1c mRNA expression.
分子量
534.55
Formula
C27H34O11
CAS 号
487-41-2
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Cheng Y, et al. Effects of phillyrin and forsythoside A on rat cytochrome P450 activities in vivo and in vitro. Xenobiotica. 2017 Apr;47(4):297-303.
[2]. Qu XY, et al. Protective effects of phillyrin against influenza A virus in vivo. Arch Pharm Res. 2016 Jul;39(7):998-1005.
[3]. Do MT, et al. Phillyrin attenuates high glucose-induced lipid accumulation in human HepG2 hepatocytes through the activation of LKB1/AMP-activated protein kinase-dependent signalling. Food Chem. 2013 Jan 15;136(2):415-25.
Sideroxylin is a C-methylated flavone isolated from Callistemon lanceolatus and exerts antimicrobial activity against Staphylococcus aureus. Sideroxylin inhibits ovarian cancer cell proliferation and induces apoptosis, causing DNA fragmentation, depolarization of the mitochondrial membrane, the generation of reactive oxygen species (ROS)[1].
分子量
312.32
Formula
C18H16O5
CAS 号
3122-87-0
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Sunwoo Park, et al. Sideroxylin (Callistemon Lanceolatus) Suppressed Cell Proliferation and Increased Apoptosis in Ovarian Cancer Cells Accompanied by Mitochondrial Dysfunction, the Generation of Reactive Oxygen Species, and an Increase of Lipid Peroxidation. J Cell Physiol. 2018 Nov;233(11):8597-8604.