Drug Information
Drug (ID: DG00010) and It's Reported Resistant Information
Name |
Baicalein
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Synonyms |
Baicalein; 491-67-8; 5,6,7-Trihydroxyflavone; 5,6,7-trihydroxy-2-phenyl-4H-chromen-4-one; Noroxylin; Biacalein; BaiKalein; Baicelein; UNII-49QAH60606; NSC661431; NSC 661431; CHEMBL8260; 5,6,7-trihydroxy-2-phenylchromen-4-one; CHEBI:2979; FXNFHKRTJBSTCS-UHFFFAOYSA-N; MFCD00017459; 4H-1-Benzopyran-4-one, 5,6,7-trihydroxy-2-phenyl-; 49QAH60606; 5,7-Trihydroxyflavone; 5,6,7-trihydroxy-2-phenyl-chromen-4-one; Sho-saiko-to; SMR000112462; SR-01000597499; Baicalein, 8; Baicalein,(S); 3WL; Baicalein, 14; Baicalein, 98%; AC1NQYPP; Tocris-1761
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Indication |
In total 1 Indication(s)
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Structure | |||||
Target | Arachidonate 5-lipoxygenase (5-LOX) | LOX5_HUMAN | [1] | ||
L-selectin (SELL) | LYAM1_HUMAN | [1] | |||
Lactoylglutathione lyase (GLO1) | LGUL_HUMAN | [1] | |||
P-selectin (SELP) | LYAM3_HUMAN | [1] | |||
Prolyl endopeptidase (PREP) | PPCE_HUMAN | [1] | |||
Tumor necrosis factor (TNF) | TNFA_HUMAN | [1] | |||
Xanthine dehydrogenase/oxidase (XDH) | XDH_HUMAN | [1] | |||
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Formula |
C15H10O5
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IsoSMILES |
C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O
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InChI |
1S/C15H10O5/c16-9-6-11(8-4-2-1-3-5-8)20-12-7-10(17)14(18)15(19)13(9)12/h1-7,17-19H
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InChIKey |
FXNFHKRTJBSTCS-UHFFFAOYSA-N
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PubChem CID | |||||
ChEBI ID | |||||
TTD Drug ID | |||||
DrugBank ID |
Type(s) of Resistant Mechanism of This Drug
EADR: Epigenetic Alteration of DNA, RNA or Protein
UAPP: Unusual Activation of Pro-survival Pathway
Drug Resistance Data Categorized by Their Corresponding Diseases
ICD-02: Benign/in-situ/malignant neoplasm
Liver cancer [ICD-11: 2C12]
Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
Epigenetic Alteration of DNA, RNA or Protein (EADR) | ||||
Key Molecule: NF-kappaB interacting LncRNA (NKILA) | [2] | |||
Molecule Alteration | Expression | Up-regulation |
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Sensitive Disease | Hepatocellular carcinoma [ICD-11: 2C12.2] | |||
Experimental Note | Revealed Based on the Cell Line Data | |||
Cell Pathway Regulation | Cell apoptosis | Activation | hsa04210 | |
Cell invasion | Inhibition | hsa05200 | ||
Cell viability | Inhibition | hsa05200 | ||
NF-kappaB signaling pathway | Inhibition | hsa04064 | ||
In Vitro Model | HepG2 cells | Liver | Homo sapiens (Human) | CVCL_0027 |
HCCLM3 cells | Liver | Homo sapiens (Human) | CVCL_6832 | |
Hep3B cells | Liver | Homo sapiens (Human) | CVCL_0326 | |
SMMC7721 cells | Uterus | Homo sapiens (Human) | CVCL_0534 | |
QSG-7701 cells | Liver | Homo sapiens (Human) | CVCL_6944 | |
In Vivo Model | Nude mouse xenograft model | Mus musculus | ||
Experiment for Molecule Alteration |
qRT-PCR | |||
Experiment for Drug Resistance |
Luminescent cell viability assay; TUNEL assay; Transwell assay | |||
Mechanism Description | NkILA inhibited IkBalpha phosphorylation and enhanced the inhibitory roles of baicalein on NF-kB signaling in HCC cells. | |||
Unusual Activation of Pro-survival Pathway (UAPP) | ||||
Key Molecule: NF-kappa-B inhibitor alpha (NFKBIA) | [2] | |||
Molecule Alteration | Phosphorylation | Down-regulation |
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Sensitive Disease | Hepatocellular carcinoma [ICD-11: 2C12.2] | |||
Experimental Note | Revealed Based on the Cell Line Data | |||
Cell Pathway Regulation | Cell apoptosis | Activation | hsa04210 | |
Cell invasion | Inhibition | hsa05200 | ||
Cell viability | Inhibition | hsa05200 | ||
NF-kappaB signaling pathway | Inhibition | hsa04064 | ||
In Vitro Model | HepG2 cells | Liver | Homo sapiens (Human) | CVCL_0027 |
HCCLM3 cells | Liver | Homo sapiens (Human) | CVCL_6832 | |
Hep3B cells | Liver | Homo sapiens (Human) | CVCL_0326 | |
SMMC7721 cells | Uterus | Homo sapiens (Human) | CVCL_0534 | |
QSG-7701 cells | Liver | Homo sapiens (Human) | CVCL_6944 | |
In Vivo Model | Nude mouse xenograft model | Mus musculus | ||
Experiment for Molecule Alteration |
Western blot analysis | |||
Experiment for Drug Resistance |
Luminescent cell viability assay; TUNEL assay; Transwell assay | |||
Mechanism Description | NkILA inhibited IkBalpha phosphorylation and enhanced the inhibitory roles of baicalein on NF-kB signaling in HCC cells. |
Cervical cancer [ICD-11: 2C77]
Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
Epigenetic Alteration of DNA, RNA or Protein (EADR) | ||||
Key Molecule: Long non-protein coding RNA (BDLNR) | [1] | |||
Molecule Alteration | Expression | Up-regulation |
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Sensitive Disease | Cervical cancer [ICD-11: 2C77.0] | |||
Experimental Note | Revealed Based on the Cell Line Data | |||
Cell Pathway Regulation | PI3K/AKT signaling pathway | Inhibition | hsa04151 | |
In Vitro Model | Hela cells | Cervix uteri | Homo sapiens (Human) | CVCL_0030 |
Siha cells | Cervix uteri | Homo sapiens (Human) | CVCL_0032 | |
Caski cells | Uterus | Homo sapiens (Human) | CVCL_1100 | |
ME-180 cells | Uterus | Homo sapiens (Human) | CVCL_1401 | |
Experiment for Molecule Alteration |
qRT-PCR | |||
Experiment for Drug Resistance |
Glo cell viability assays | |||
Mechanism Description | Baicalein inhibits cervical cancer progression via downregulating long noncoding RNA BDLNR and its downstream PI3 k/Akt pathway. BDLNR physically bound to YBX1, recruited YBX1 to PIk3CA promoter, activated PIk3CA expression and PI3 k/Akt pathway. |
References
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