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⚗️ Ingredient

Delphinidin

0
Clinical Trials
0
Meta-Analyses
5
PubMed References
📋 Sample Trials
None linked yet.
📊 Sample Meta-Analyses
None linked yet.
📚 Sample References
PMID 27393705
Dual Inhibition of PI3K/Akt and mTOR by the Dietary Antioxidant, Delphinidin, Ameliorates Psoriatic Features In Vitro and in an Imiquimod-Induced Psoriasis-Like Disease in Mice
Antioxid Redox Signal · 2017
PMID 25749779
Inhibitory Effect of Delphinidin on Extracellular Matrix Production via the MAPK/NF-κB Pathway in Nasal Polyp-Derived Fibroblasts
Allergy Asthma Immunol Res · 2015
PMID 25533330
Topical application of delphinidin reduces psoriasiform lesions in the flaky skin mouse model by inducing epidermal differentiation and inhibiting inflammation
Br J Dermatol · 2015
⚗️ All Ingredient data fields for Delphinidin
⚗️ Identity
Name
Delphinidin
Aliases / Synonyms
Delphinidin chloride; 528-53-0; Delphinidine; 8012-95-1; Delphinidol; Ephdine; PARAFFIN; Delfinidol chloride; CCRIS 2518
🧪 Chemistry
Molecular Weight
338.6990
LogP
-0.3815
Drug-likeness
0.263
Oral Bioavailability
40.6350
H-Bond Acceptors
6
H-Bond Donors
6
Rotatable Bonds
1
🔬 Structures
Canonical SMILES
C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O.[Cl-]
Isomeric SMILES
C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O.[Cl-]
InChIKey
FFNDMZIBVDSQFI-UHFFFAOYSA-N
InChI
InChI=1S/C15H10O7.ClH/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6;/h1-5H,(H5-,16,17,18,19,20,21);1H
🔗 External References
PubChem CID
CAS Number
SymMap
215
TCMID
5010
TCMSP
MOL004798
TCM-ID
5075
🔍 Raw view — every non-empty column on this row (34 fields)
name
Delphinidin
common names
Delphinidin chloride; 528-53-0; Delphinidine; 8012-95-1; Delphinidol; Ephdine; PARAFFIN; Delfinidol chloride; CCRIS 2518
herb ingredient id
HBIN023132
canonical smiles
C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O.[Cl-]
isomeric smiles
C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O.[Cl-]
inchi
InChI=1S/C15H10O7.ClH/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6;/h1-5H,(H5-,16,17,18,19,20,21);1H
inchikey
FFNDMZIBVDSQFI-UHFFFAOYSA-N
mol wt
338.6990
num h acceptors
6
num h donors
6
mol logp
-0.3815
num rotatable bonds
1
drug likeness
0.263
ob score
40.6350
cas id
528-53-0
symmap mol id
215
tcmid ingredient id
5010
tcmsp ingredient id
MOL004798
tcm id ingredient id
5075
pubchem cid
68245
tcmsp mol id
MOL004798
tcmsp molecule id
4798

🌿 Related Herbs

1 · contains this compound

🧬 Gene / Protein Targets

8 · directly binds these targets
AR
Gene AR
NCOA2
Gene NCOA2
Prostaglandin G/H synthase 1
Prostaglandin G/H synthase 2
Heat shock protein HSP 90
Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit, gamma isoform
Nitric oxide synthase, inducible
Carbonic anhydrase II

📚 PubMed References

5 · cited research
PMID 27393705 Dual Inhibition of PI3K/Akt and mTOR by the Dietary Antioxidant, Delphinidin, Am
Antioxid Redox Signal
PMID 25749779 Inhibitory Effect of Delphinidin on Extracellular Matrix Production via the MAPK
Allergy Asthma Immunol Res
PMID 25533330 Topical application of delphinidin reduces psoriasiform lesions in the flaky ski
Br J Dermatol
PMID 31963866 Cytoprotective Effects of Delphinidin for Human Chondrocytes against Oxidative S
Antioxidants (Basel)
PMID 33274001 Inhibitory Effect of Delphinidin on Oxidative Stress Induced by H2O2 in HepG2 Ce
Oxid Med Cell Longev
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_pinyin matching herbs.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