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Every herb, ingredient, formula, gene target, and disease — connected through real research. Search, pick a subject, and navigate the graph in any direction.
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Herb
6,826
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Ingredient
44,598
→
🧬
Gene Target
15,695
→
🏥
Disease
30,467
→
🧪
Evidence
23,295
trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
⚗️ Ingredient
Allicin
1
Clinical Trials
1
Meta-Analyses
7
PubMed References
Top Conditions Studied with Allicin
📋 Sample Trials
NCT04545879
Investigating the Gut Microbiota Modulation Effects of Allicin for Cardiovascular Disease Protection and Establishing Microbiota Directed Personalized Nutrition Guidance With Novel Humanized Gnotobiotic Mice Model, Microbial Culturomics and Metabolomic Technique
Completed
📊 Sample Meta-Analyses
CRD42019118199
Allicin for helicobacter pylori eradication: a meta-analysis of randomized controlled trials
Helicobacter pylori (H. pylori) is classified as class I carcinogens by the worl
📚 Sample References
PMID 32808945
Allicin inhibits osteoblast apoptosis and steroid-induced necrosis of femoral head progression by activating the PI3K/AKT pathway
Food Funct · 2020
PMID 33203103
Effects of Allicin on Pathophysiological Mechanisms during the Progression of Nephropathy Associated to Diabetes
Antioxidants (Basel) · 2020
PMID 34777295
The Effect of Allicin on the Proteome of SARS-CoV-2 Infected Calu-3 Cells
Front Microbiol · 2021
⚗️ All Ingredient data fields for Allicin
⚗️ Identity
Name
Allicin
Aliases / Synonyms
539-86-6; Diallyl thiosulfinate; S-allyl prop-2-ene-1-sulfinothioate; Diallyldisulfid-S-oxid; Thio-2-propene-1-sulfinic acid S-allyl ester; Allylthiosulphinic acid allyl ester; 2-Propene-1-sulfinothioic acid, S-2-propenyl ester; DADSO; S-Allyl acrylo-1-sulphinothioate
🧪 Chemistry
Molecular Weight
162.2790
LogP
1.7553
Drug-likeness
0.452
Oral Bioavailability
78.4130
H-Bond Acceptors
2
Rotatable Bonds
5
🔬 Structures
Canonical SMILES
C=CCSS(=O)CC=C
Isomeric SMILES
C=CCSS(=O)CC=C
InChIKey
JDLKFOPOAOFWQN-UHFFFAOYSA-N
InChI
InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2
🔗 External References
HERB DB
PubChem CID
CAS Number
NPASS
NPC2088
HIT
C0872
SymMap
280
TCMID
920; 34844
TCMSP
MOL008354
TCM-ID
7011
🔍 Raw view — every non-empty column on this row (34 fields)
name
Allicin
common names
539-86-6; Diallyl thiosulfinate; S-allyl prop-2-ene-1-sulfinothioate; Diallyldisulfid-S-oxid; Thio-2-propene-1-sulfinic acid S-allyl ester; Allylthiosulphinic acid allyl ester; 2-Propene-1-sulfinothioic acid, S-2-propenyl ester; DADSO; S-Allyl acrylo-1-sulphinothioate
herb ingredient id
HBIN015200
canonical smiles
C=CCSS(=O)CC=C
isomeric smiles
C=CCSS(=O)CC=C
inchi
InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-4H,1-2,5-6H2
inchikey
JDLKFOPOAOFWQN-UHFFFAOYSA-N
mol wt
162.2790
num h acceptors
2
num h donors
0
mol logp
1.7553
num rotatable bonds
5
drug likeness
0.452
ob score
78.4130
cas id
539-86-6
symmap mol id
280
tcmid ingredient id
920; 34844
tcmsp ingredient id
MOL008354
tcm id ingredient id
7011
pubchem cid
65036
npass id
NPC2088
hit id
C0872
🏥 Linked Health Topics
1 · diseases via target pathways📋 Clinical Trials
1 · subject of clinical studyNCT04545879 Investigating the Gut Microbiota Modulation Effects of Allicin for Cardiovascula
→ Atherosclerosis
📊 Meta-Analyses
1 · systematic reviewCRD42019118199 Allicin for helicobacter pylori eradication: a meta-analysis of randomized contr
→ Helicobacter pylori (H. pylori) is classified as c
📚 PubMed References
7 · cited researchPMID 32808945 Allicin inhibits osteoblast apoptosis and steroid-induced necrosis of femoral he
Food Funct
PMID 33203103 Effects of Allicin on Pathophysiological Mechanisms during the Progression of Ne
Antioxidants (Basel)
PMID 34777295 The Effect of Allicin on the Proteome of SARS-CoV-2 Infected Calu-3 Cells
Front Microbiol
PMID 35046802 Protective Effects of Allicin on Acute Myocardial Infarction in Rats via Hydroge
Front Pharmacol
PMID 35784719 Allicin Facilitates Airway Surface Liquid Hydration by Activation of CFTR
Front Pharmacol
PMID 36355777 Allicin ameliorates imiquimod-induced psoriasis-like skin inflammation via distu
Br J Pharmacol
PMID 36430776 Allicin and Capsaicin Ameliorated Hypercholesterolemia by Upregulating LDLR and
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