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BRCA1

BRCA1 (BReast CAncer gene 1) is a human tumor suppressor gene that plays a critical role in DNA repair, maintaining genomic stability. Mutations in BRCA1 are associated with an increased risk of hereditary breast cancer, ovarian cancer, prostate cancer, and pancreatic cancer. Its protein product participates in homologous recombination, ensuring accurate repair of double-strand DNA breaks. Genetic testing for BRCA1 mutations is crucial for risk assessment and guiding personalized prevention and treatment strategies in affected individuals and families.
Catalog No Product Description CAS No. Purity Structural Formula
BP4730
Yuanhuadine
Yuanhuadine is a natural product found in Daphne genkwa. It has a role as a metabolite.
76402-66-9 98% Yuanhuadine
BP0683
Gomisin D
Gomisin D is a natural product from Schizandra chinensis.
60546-10-3 98% Gomisin D
BP0754
hypocrellin A
Hypocrellin A, an a natural perylene quinine photosensitizers (PSs), can chelate with heavy metal ions, including Au(III) and Pt(IV), to form a 1:2 complex. Hypocrellin A has light-induced antitumor,antifungal and antiviral activities, it also exerts immunomodulatory effects on MHC-restricted presentation of antigen.
77029-83-5 98% hypocrellin A
BP0774
Isobavachin
Isobavachin can stimulate osteoblasts proliferation and differentiation; it also can facilitate mouse embryonic stem cells differentiating into neuronal cells, the mechanism involved protein prenylation and, subsequently, phos-ERK activation and the phos-p38 off pathway. Isobavachin possesses estrogen-like activity in MCF-7/BOS cells, it can significantly stimulate the proliferation of MCF-7/BOS cells in a dose-dependent manner. Isobavachin has cytotoxic effects on H4IIE hepatoma and metabolically poorly active C6 glioma cells.
31524-62-6 98% Isobavachin
BP0098
7-Epitaxol
7-Epitaxol is the major derivative of taxol found in cells and taxol (paclitaxel) is a well-known natural-source cancer drug.
105454-04-4 98% 7-Epitaxol
BP2418 3035699-17-0 98% (2"S)-2",3"-Dihydrodelicaflavone
BP2064
Dulcoside A
Dulcoside A is a sweetener and has antioxidant activity.
64432-06-0 98% Dulcoside A
BP3229
Licarin A
Licarin A and (-)-Licarin A are promising compounds that could be used for the development of schistosomicidal and trypanocidal agents; Licarin A presents effect against Leishmania (Leishmania) major associated with immunomodulation in vitro; (-)-Licarin A has antimycobacterial activity, represents a potentially active anti-tuberculosis agent to treat MDR M. tuberculosis and NTM strains.Licarin A significantly protects primary cultured neuronal cells against glutamate-induced oxidative stress, via antioxidative activities.
51020-86-1 98% Licarin A
BP0414
Cucurbitacin B
Cucurbitacin B is a cucurbitacin in which a lanostane skeleton is multi-substituted with hydroxy, methyl and oxo substituents, with unsaturation at positions 5 and 23; a hydroxy function at C-25 is acetylated. It is a tertiary alpha-hydroxy ketone, a cucurbitacin and a secondary alpha-hydroxy ketone. It derives from a hydride of a lanostane. Cucurbitacin B, an effective HIF-1 inhibitor, has antitumor activity, it inhibits proliferation and induces apoptosis via STAT3 pathway inhibition in A549 lung cancer cells. It inhibited AKT signaling activation through up-regulation of PTEN.
6199-67-3 98% Cucurbitacin B
BP0711
Hederasaponin B
Hederasaponin B has antiviral activity, via inhibiting the viral VP2 protein expression and blocking viral capsid protein synthesis. It also has antitumor activity, and it inhibits the superoxide generation induced by arachidonic acid (AA).
36284-77-2 98% Hederasaponin B
BP4921
Cornoside
Cornoside and Iridoids are chemosystematic markers.
40661-45-8 98% Cornoside
BP0835
Kushenol F
Sophoraflavanone G is a tetrahydroxyflavanone having a structure of naringenin bearing an additional hydroxyl substituent at position 2' as well as a (2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl (lavandulyl) substituent at position 8'. It has a role as an antioxidant, an antimicrobial agent, an antimalarial and a plant metabolite. It is a member of 4'-hydroxyflavanones, a (2S)-flavan-4-one and a tetrahydroxyflavanone. It is functionally related to a (S)-naringenin. Kushenol F is a tyrosinase inhibitor, it shows significant inhibitory effects on monoamine oxidase ( in a dose-dependent manner with IC50 values of 69.9 microM). Kushenol F preferentially inhibits the MAO-B activity than MAO-A activity with the IC50 values of 63.1 and 103.7 microM, respectively.
97938-30-2 98% Kushenol F
BP4638 102421-42-1 98% Yuanamide
SBP02602 911004-72-3 Furowanin A
BP4518
Damulin B
Damulin A and Damulin B as potential activators of AMP-activated protein kinase (AMPK) from Gynostemma pentaphyllum, which may contribute to beneficial effect of G. pentaphyllum on glucose and lipid metabolism.
1202868-75-4 98% Damulin B
BP0530
Embelin
Embelin is a member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxy-1,4-benzoquinone which is substituted by an undecyl group at position 3. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antimicrobial, antineoplastic and inhibitory activity towards hepatitis C protease. It has a role as an antimicrobial agent, an antineoplastic agent, a hepatitis C protease inhibitor and a plant metabolite. Embelin is an inhibitor of X-linked inhibitor of apoptosis (XIAP) with IC50 of 4.1 μM in a cell-free assay.Embelin has antitumor, antioxidant and anti-inflammatory activities. Embelin can enhance TRAIL-induced cell apoptosis through DR4 and DR5 upregulation and decrease IL-6-induced STAT3 phosphorylation, that combination of low-toxicity Embelin and TRAIL may become as a potential antileukemia strategy.
550-24-3 98% Embelin
BP1399
Topotecan Hydrochloride
Topotecan hydrochloride, a topoisomerase I inhibitor, capable of inhibiting tumoral growth in animal models of retinoblastoma. Topotecan hydrochloride liposomes loaded CS/β-GP hydrogel could become a potential formulation for improving the antitumor efficacy of Topotecan hydrochloride. Topotecan hydrochloride is a pyranoindolizinoquinoline. It has a role as an antineoplastic agent and an EC 5.99.1.2 (DNA topoisomerase) inhibitor. It contains a topotecan.
119413-54-6 98% Topotecan Hydrochloride
BP2185 102805-32-3 98% Pseudoginsenoside RC1
BP0456 517-66-8 D-Dicentrine
BP1862
Licarin B
Licarin B can improve insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway in 3T3-L1 adipocytes, it as a promising bioactive for insulin resistance and associated complications through its partial PPARγ activity.
51020-87-2 98% Licarin B