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Ingredient
44,598
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Gene Target
15,695
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Disease
30,467
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Evidence
23,295
trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
⚗️ Ingredient
Diosmetin
0
Clinical Trials
0
Meta-Analyses
11
PubMed References
📋 Sample Trials
None linked yet.
📊 Sample Meta-Analyses
None linked yet.
📚 Sample References
PMID 30825187
Diosmetin induces apoptosis and enhances the chemotherapeutic efficacy of paclitaxel in non-small cell lung cancer cells via Nrf2 inhibition
Br J Pharmacol · 2019
PMID 31833613
Diosmetin exhibits anti-proliferative and anti-inflammatory effects on TNF-α-stimulated human rheumatoid arthritis fibroblast-like synoviocytes through regulating the Akt and NF-κB signaling pathways
Phytother Res · 2020
PMID 33449987
Diosmetin attenuates metabolic syndrome and left ventricular alterations via the suppression of angiotensin II/AT 1 receptor/gp91 phox/p-NF-κB protein expression in high-fat diet fed rats
Food Funct · 2021
⚗️ All Ingredient data fields for Diosmetin
⚗️ Identity
Name
Diosmetin
Aliases / Synonyms
520-34-3; 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one; Luteolin 4'-methyl ether; 4'-Methylluteolin; Salinigricoflavonol; Diosmetine; Pillon; 3',5,7-trihydroxy-4'-methoxyflavone; 5,7,3'-Trihydroxy-4'-methoxyflavone
🧪 Chemistry
Molecular Weight
300.2660
LogP
2.5854
Drug-likeness
0.672
Oral Bioavailability
31.1380
H-Bond Acceptors
6
H-Bond Donors
3
Rotatable Bonds
2
🔬 Structures
Canonical SMILES
COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
Isomeric SMILES
COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
InChIKey
MBNGWHIJMBWFHU-UHFFFAOYSA-N
InChI
InChI=1S/C16H12O6/c1-21-13-3-2-8(4-10(13)18)14-7-12(20)16-11(19)5-9(17)6-15(16)22-14/h2-7,17-19H,1H3
🔗 External References
HERB DB
PubChem CID
CAS Number
NPASS
NPC52005
HIT
C0026
SymMap
5049
TCMID
6451; 21760
TCMSP
MOL002881
TCM-ID
12601
🔍 Raw view — every non-empty column on this row (36 fields)
name
Diosmetin
common names
520-34-3; 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one; Luteolin 4'-methyl ether; 4'-Methylluteolin; Salinigricoflavonol; Diosmetine; Pillon; 3',5,7-trihydroxy-4'-methoxyflavone; 5,7,3'-Trihydroxy-4'-methoxyflavone
herb ingredient id
HBIN024184
canonical smiles
COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
isomeric smiles
COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O
inchi
InChI=1S/C16H12O6/c1-21-13-3-2-8(4-10(13)18)14-7-12(20)16-11(19)5-9(17)6-15(16)22-14/h2-7,17-19H,1H3
inchikey
MBNGWHIJMBWFHU-UHFFFAOYSA-N
mol wt
300.2660
num h acceptors
6
num h donors
3
mol logp
2.5854
num rotatable bonds
2
drug likeness
0.672
ob score
31.1380
cas id
520-34-3
symmap mol id
5049
tcmid ingredient id
6451; 21760
tcmsp ingredient id
MOL002881
tcm id ingredient id
12601
pubchem cid
5281612
npass id
NPC52005
hit id
C0026
tcmsp mol id
MOL002881
tcmsp molecule id
2881
🌿 Related Herbs
1 · contains this compound🧬 Gene / Protein Targets
10 · directly binds these targetsNCOA1
Gene NCOA1
NCOA2
Gene NCOA2
Prostaglandin G/H synthase 1
Prostaglandin G/H synthase 2
Heat shock protein HSP 90
Dipeptidyl peptidase IV
Trypsin-1
Nitric oxide synthase, inducible
mRNA of PKA Catalytic Subunit C-alpha
Calmodulin
🏥 Linked Health Topics
30 · diseases via target pathwaysCardiovascular disease, unspecified
disease
Chronic inflammatory diseases
disease
Alzheimer'S Disease
syndrome
Arthritis
syndrome
Renal Cell Carcinoma
disease
Carpal Tunnel Syndrome
syndrome
Endometriosis
syndrome
Inflammation
phenotype
Meningioma
disease
Myocardial Infarction
syndrome
Peutz-Jeghers Syndrome
syndrome
Malignant Mesothelioma
disease
Colorectal cancer
disease
Cancer, unspecific
disease
Lung Cancer
disease
Osteoarthritis
disease
Breast cancer
disease
Prostate cancer
disease
Rheumatoid arthritis, unspecified
disease
Analgesics
disease
Stroke
disease
Inflammatory diseases
disease
Bladder cancer
disease
Abdominal aortic aneurysm
disease
Adenomatous polyposis
disease
Carcinoma in situ, unspecified
disease
Dysmenorrhea, unspecified
disease
Genitourinary tumors
disease
Gestational hypertension
disease
Oropharyngeal squamous cell carcinoma
disease
📚 PubMed References
11 · cited researchPMID 30825187 Diosmetin induces apoptosis and enhances the chemotherapeutic efficacy of paclit
Br J Pharmacol
PMID 31833613 Diosmetin exhibits anti-proliferative and anti-inflammatory effects on TNF-α-sti
Phytother Res
PMID 33449987 Diosmetin attenuates metabolic syndrome and left ventricular alterations via the
Food Funct
PMID 34091150 Diosmetin ameliorate type 2 diabetic mellitus by up-regulating Corynebacterium g
Phytomedicine
PMID 34262136 Diosmetin has therapeutic efficacy in colitis regulating gut microbiota, inflamm
Acta Pharmacol Sin
PMID 34573119 Diosmetin Ameliorates Vascular Dysfunction and Remodeling by Modulation of Nrf2/
Antioxidants (Basel)
PMID 34922636 Diosmetin inhibits cell proliferation and promotes apoptosis through STAT3/c-Myc
Biol Res
PMID 35242278 Diosmetin Protects against Cardiac Hypertrophy via p62/Keap1/Nrf2 Signaling Path
Oxid Med Cell Longev
PMID 35481411 Diosmetin attenuates oxidative stress-induced damage to lens epithelial cells vi
Bioengineered
PMID 35684047 Diosmetin Targeted at Peroxisome Proliferator-Activated Receptor Gamma Alleviate
Nutrients
PMID 35955819 Lobelia chinensis Extract and Its Active Compound, Diosmetin, Improve Atopic Der
Int J Mol Sci
How relationships are computed
- Clinical Trials / Meta-Analyses / References: direct foreign-key link via
subject_entity_id(Phase 2d wireup) - Formula ↔ Herbs: text bridge via
formulas.herbs_in_pinyinmatchingherbs.pinyin_name - Herb ↔ Ingredient:
ACTIVE — direct link via
herb_ingredients - Ingredient ↔ Target:
ACTIVE — direct link via
ingredient_targets - Target ↔ Disease:
ACTIVE — direct link via
target_health_topics - Herb → Target → Disease (full chemical spine): ACTIVE — joins all three link tables