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⚗️ Ingredient

Parthenolide

1
Clinical Trials
0
Meta-Analyses
17
PubMed References
Top Conditions Studied with Parthenolide
📋 Sample Trials
NCT00133341
Clinical Evaluation of the 3 Allergens: Methyldibromoglutharonitrile, Parthenolide and Goldnatriumthiosulphate
Completed · Phase 2
📊 Sample Meta-Analyses
None linked yet.
📚 Sample References
PMID 31078744
Parthenolide, a feverfew-derived phytochemical, ameliorates obesity and obesity-induced inflammatory responses via the Nrf2/Keap1 pathway
Pharmacol Res · 2019
PMID 28965856
Pharmacological evidence for the bone-autonomous contribution of the NFκB/β-catenin axis to breast cancer related osteolysis
Cancer Lett · 2017
PMID 26821066
The clerodane diterpene casearin J induces apoptosis of T-ALL cells through SERCA inhibition, oxidative stress, and interference with Notch1 signaling
Cell Death Dis · 2016
⚗️ All Ingredient data fields for Parthenolide
⚗️ Identity
Name
Parthenolide
Aliases / Synonyms
20554-84-1; (-)-Parthenolide; MFCD00134592; CHEBI:7939; PARTHENOLIDE [MI]; 2RDB26I5ZB; PARTHENOLIDE [USP-RS]; PARTHENOLIDE [WHO-DD]; CHEMBL465158
🧪 Chemistry
Molecular Weight
248.3220
LogP
2.7620
Drug-likeness
0.286
H-Bond Acceptors
3
🔬 Structures
Canonical SMILES
CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C
Isomeric SMILES
C/C/1=C\CC[C@@]2([C@H](O2)[C@@H]3[C@@H](CC1)C(=C)C(=O)O3)C
InChIKey
KTEXNACQROZXEV-PVLRGYAZSA-N
InChI
InChI=1S/C15H20O3/c1-9-5-4-8-15(3)13(18-15)12-11(7-6-9)10(2)14(16)17-12/h5,11-13H,2,4,6-8H2,1,3H3/b9-5+/t11-,12-,13+,15+/m0/s1
🔗 External References
PubChem CID
SymMap
17112
TCMID
16663
TCM-ID
11954
🔍 Raw view — every non-empty column on this row (29 fields)
name
Parthenolide
common names
20554-84-1; (-)-Parthenolide; MFCD00134592; CHEBI:7939; PARTHENOLIDE [MI]; 2RDB26I5ZB; PARTHENOLIDE [USP-RS]; PARTHENOLIDE [WHO-DD]; CHEMBL465158
herb ingredient id
HBIN038876
canonical smiles
CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C
isomeric smiles
C/C/1=C\CC[C@@]2([C@H](O2)[C@@H]3[C@@H](CC1)C(=C)C(=O)O3)C
inchi
InChI=1S/C15H20O3/c1-9-5-4-8-15(3)13(18-15)12-11(7-6-9)10(2)14(16)17-12/h5,11-13H,2,4,6-8H2,1,3H3/b9-5+/t11-,12-,13+,15+/m0/s1
inchikey
KTEXNACQROZXEV-PVLRGYAZSA-N
mol wt
248.3220
num h acceptors
3
num h donors
0
mol logp
2.7620
num rotatable bonds
0
drug likeness
0.286
symmap mol id
17112
tcmid ingredient id
16663
tcm id ingredient id
11954
pubchem cid
7251185

📋 Clinical Trials

1 · subject of clinical study
NCT00133341 Clinical Evaluation of the 3 Allergens: Methyldibromoglutharonitrile, Parthenoli
→ Allergic Contact Dermatitis

📚 PubMed References

12 · cited research
PMID 31078744 Parthenolide, a feverfew-derived phytochemical, ameliorates obesity and obesity-
Pharmacol Res
PMID 28965856 Pharmacological evidence for the bone-autonomous contribution of the NFκB/β-cate
Cancer Lett
PMID 26821066 The clerodane diterpene casearin J induces apoptosis of T-ALL cells through SERC
Cell Death Dis
PMID 25553117 Parthenolide inhibits cancer stem-like side population of nasopharyngeal carcino
Theranostics
PMID 24387758 Parthenolide induces apoptosis via TNFRSF10B and PMAIP1 pathways in human lung c
J Exp Clin Cancer Res
PMID 23933184 Parthenolide inhibits nociception and neurogenic vasodilatation in the trigemino
Pain
PMID 23674500 KEAP1 is a redox sensitive target that arbitrates the opposing radiosensitive ef
Cancer Res
PMID 23318959 Inhibition of intracellular dipeptidyl peptidases 8 and 9 enhances parthenolide'
Leukemia
PMID 22155272 Bcl-XL, but not Bcl-2, can protect human B-lymphoma cell lines from parthenolide
Cancer Lett
PMID 21719790 The inflammatory cytokines TWEAK and TNFα reduce renal klotho expression through
J Am Soc Nephrol
PMID 21223972 Parthenolide inhibits STAT3 signaling and attenuates angiotensin II-induced left
J Mol Cell Cardiol
PMID 31497910 Parthenolide ameliorates intracerebral hemorrhage-induced brain injury in rats
Phytother Res
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