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trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
⚗️ Ingredient
Cannabigerol
3
Clinical Trials
0
Meta-Analyses
4
PubMed References
Top Conditions Studied with Cannabigerol
📋 Sample Trials
NCT05088018
Swallowable Cannabigerol Tablets for Sleep Quality In Veterans (Veterans Exploring Cannabigerol for Sleep)
Completed
NCT05257044
Acute Effects of Cannabigerol
Completed · Phase 1
NCT05743985
Efficacy and Safety of Hemp-derived, Full Spectrum Cannabigerol (CBG) in Adults
Completed
📊 Sample Meta-Analyses
None linked yet.
📚 Sample References
PMID 25252936
Neuroprotective properties of cannabigerol in Huntington's disease: studies in R6/2 mice and 3-nitropropionate-lesioned mice
Neurotherapeutics · 2015
PMID 31941059
Neuroprotective and Neuromodulatory Effects Induced by Cannabidiol and Cannabigerol in Rat Hypo-E22 cells and Isolated Hypothalamus
Antioxidants (Basel) · 2020
PMID 35297036
Inhibition of sodium conductance by cannabigerol contributes to a reduction of dorsal root ganglion neuron excitability
Br J Pharmacol · 2022
⚗️ All Ingredient data fields for Cannabigerol
⚗️ Identity
Name
Cannabigerol
Aliases / Synonyms
25654-31-3; 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-pentylbenzene-1,3-diol; Cannabigerol (CBG); 2808-33-5; UNII-J1K406072N; CHEBI:69477; CBG; J1K406072N; CHEMBL497318
🧪 Chemistry
Molecular Weight
316.4850
LogP
6.0657
Drug-likeness
0.429
H-Bond Acceptors
2
H-Bond Donors
2
Rotatable Bonds
9
🔬 Structures
Canonical SMILES
CCCCCC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)C)O
Isomeric SMILES
CCCCCC1=CC(=C(C(=C1)O)C/C=C(\C)/CCC=C(C)C)O
InChIKey
QXACEHWTBCFNSA-SFQUDFHCSA-N
InChI
InChI=1S/C21H32O2/c1-5-6-7-11-18-14-20(22)19(21(23)15-18)13-12-17(4)10-8-9-16(2)3/h9,12,14-15,22-23H,5-8,10-11,13H2,1-4H3/b17-12+
🔗 External References
HERB DB
PubChem CID
CAS Number
NPASS
NPC201662
HIT
C1212
TCMID
3081
TCM-ID
5966
🔍 Raw view — every non-empty column on this row (31 fields)
name
Cannabigerol
common names
25654-31-3; 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-pentylbenzene-1,3-diol; Cannabigerol (CBG); 2808-33-5; UNII-J1K406072N; CHEBI:69477; CBG; J1K406072N; CHEMBL497318
herb ingredient id
HBIN019565
canonical smiles
CCCCCC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)C)O
isomeric smiles
CCCCCC1=CC(=C(C(=C1)O)C/C=C(\C)/CCC=C(C)C)O
inchi
InChI=1S/C21H32O2/c1-5-6-7-11-18-14-20(22)19(21(23)15-18)13-12-17(4)10-8-9-16(2)3/h9,12,14-15,22-23H,5-8,10-11,13H2,1-4H3/b17-12+
inchikey
QXACEHWTBCFNSA-SFQUDFHCSA-N
mol wt
316.4850
num h acceptors
2
num h donors
2
mol logp
6.0657
num rotatable bonds
9
drug likeness
0.429
cas id
25654-31-3
tcmid ingredient id
3081
tcm id ingredient id
5966
pubchem cid
5315659
npass id
NPC201662
hit id
C1212
📋 Clinical Trials
3 · subject of clinical studyNCT05088018 Swallowable Cannabigerol Tablets for Sleep Quality In Veterans (Veterans Explori
→ Sleep
NCT05257044 Acute Effects of Cannabigerol
→ Focus: To Examine Acute Effects of CBG on Anxiety,
NCT05743985 Efficacy and Safety of Hemp-derived, Full Spectrum Cannabigerol (CBG) in Adults
→ Health, Subjective|Inflammatory Response|Adverse E
📚 PubMed References
4 · cited researchPMID 25252936 Neuroprotective properties of cannabigerol in Huntington's disease: studies in R
Neurotherapeutics
PMID 31941059 Neuroprotective and Neuromodulatory Effects Induced by Cannabidiol and Cannabige
Antioxidants (Basel)
PMID 35297036 Inhibition of sodium conductance by cannabigerol contributes to a reduction of d
Br J Pharmacol
PMID 35740979 Cannabidiol and Cannabigerol Inhibit Cholangiocarcinoma Growth In Vitro via Dive
Biomolecules
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