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Ingredient
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Gene Target
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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
Icariin
2
Clinical Trials
4
Meta-Analyses
42
PubMed References
Top Conditions Studied with Icariin
📋 Sample Trials
NCT01979133
Study of Icariin for Bipolar Disorder and Co-Occurring Substance Use Disorders
Completed · Phase 3
NCT02112123
Icariin to Prevent Corticosteroid-related Memory Changes
Completed · Phase 1
📊 Sample Meta-Analyses
CRD42019148977
The effect of icariin for infertile women with thin endometrium: a systematic review and meta-analysis
Thin endometrium is defined as <7 mm on the day of ovulation, or on the day o
CRD42023412608
Protective effects of Icariin in nephropathy and possible mechanisms of action: a meta-analysis and systematic review of animal studies
CRD42023400169
Preclinical evidence for Icariin against Alzheimer's disease: a meta-analysis and systematic review
📚 Sample References
PMID 31943455
Icariin prevents oestrogen deficiency-induced alveolar bone loss through promoting osteogenesis via STAT3
Cell Prolif · 2020
PMID 31914584
Icariin and its phosphorylated derivatives alleviate intestinal epithelial barrier disruption caused by enterotoxigenic Escherichia coli through modulate p38 MAPK in vivo and in vitro
FASEB J · 2020
PMID 30051466
Icariin protects cardiomyocytes against ischaemia/reperfusion injury by attenuating sirtuin 1-dependent mitochondrial oxidative damage
Br J Pharmacol · 2018
⚗️ All Ingredient data fields for Icariin
⚗️ Identity
Name
Icariin
Aliases / Synonyms
489-32-7; Ieariline; CHEBI:78420; UNII-VNM47R2QSQ; VNM47R2QSQ; 5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; Icariine; Epimedii herba icariin; MFCD00210516
🧪 Chemistry
Molecular Weight
676.6680
LogP
0.0679
Drug-likeness
0.14
Oral Bioavailability
41.5830
H-Bond Acceptors
15
H-Bond Donors
8
Rotatable Bonds
9
🔬 Structures
Canonical SMILES
CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O
Isomeric SMILES
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O
InChIKey
TZJALUIVHRYQQB-XLRXWWTNSA-N
InChI
InChI=1S/C33H40O15/c1-13(2)5-10-17-19(45-33-28(42)26(40)23(37)20(12-34)46-33)11-18(35)21-24(38)31(48-32-27(41)25(39)22(36)14(3)44-32)29(47-30(17)21)15-6-8-16(43-4)9-7-15/h5-9,11,14,20,22-23,25-28,32-37,39-42H,10,12H2,1-4H3/t14-,20+,22-,23+,25+,26-,27+,28+,32-,33+/m0/s1
🔗 External References
HERB DB
PubChem CID
CAS Number
NPASS
NPC5319
HIT
C0135
TCMID
23160
TCMSP
MOL004425
TCM-ID
3598
🔍 Raw view — every non-empty column on this row (33 fields)
name
Icariin
common names
489-32-7; Ieariline; CHEBI:78420; UNII-VNM47R2QSQ; VNM47R2QSQ; 5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; Icariine; Epimedii herba icariin; MFCD00210516
herb ingredient id
HBIN029922
canonical smiles
CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O
isomeric smiles
C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O
inchi
InChI=1S/C33H40O15/c1-13(2)5-10-17-19(45-33-28(42)26(40)23(37)20(12-34)46-33)11-18(35)21-24(38)31(48-32-27(41)25(39)22(36)14(3)44-32)29(47-30(17)21)15-6-8-16(43-4)9-7-15/h5-9,11,14,20,22-23,25-28,32-37,39-42H,10,12H2,1-4H3/t14-,20+,22-,23+,25+,26-,27+,28+,32-,33+/m0/s1
inchikey
TZJALUIVHRYQQB-XLRXWWTNSA-N
mol wt
676.6680
num h acceptors
15
num h donors
8
mol logp
0.0679
num rotatable bonds
9
drug likeness
0.14
ob score
41.5830
cas id
489-32-7
tcmid ingredient id
23160
tcmsp ingredient id
MOL004425
tcm id ingredient id
3598
pubchem cid
5318997
npass id
NPC5319
hit id
C0135
📋 Clinical Trials
2 · subject of clinical studyNCT01979133 Study of Icariin for Bipolar Disorder and Co-Occurring Substance Use Disorders
→ Bipolar Disorder|Substance Use Disorder
NCT02112123 Icariin to Prevent Corticosteroid-related Memory Changes
→ the Pharmacokinetic Profile of Icariin in Humans
📊 Meta-Analyses
4 · systematic reviewCRD42019148977 The effect of icariin for infertile women with thin endometrium: a systematic re
→ Thin endometrium is defined as <7 mm on the day
CRD42023412608 Protective effects of Icariin in nephropathy and possible mechanisms of action:
CRD42023400169 Preclinical evidence for Icariin against Alzheimer's disease: a meta-analysi
CRD42023451564 The shared KEGG pathways between Icariin-targeted genes and Alzheimer's dise
📚 PubMed References
12 · cited researchPMID 31943455 Icariin prevents oestrogen deficiency-induced alveolar bone loss through promoti
Cell Prolif
PMID 31914584 Icariin and its phosphorylated derivatives alleviate intestinal epithelial barri
FASEB J
PMID 30051466 Icariin protects cardiomyocytes against ischaemia/reperfusion injury by attenuat
Br J Pharmacol
PMID 25787271 Icariin promotes angiogenic differentiation and prevents oxidative stress-induce
Stem Cells
PMID 25355404 Icariin attenuates hypoxia-induced oxidative stress and apoptosis in osteoblasts
Cell Prolif
PMID 32011040 Icariin inhibits proliferation, migration, and invasion of medulloblastoma DAOY
Phytother Res
PMID 32082160 Icariin Protects Hippocampal Neurons From Endoplasmic Reticulum Stress and NF-κB
Front Pharmacol
PMID 32124960 Icariin sensitizes human colon cancer cells to TRAIL‑induced apoptosis via ERK‑m
Int J Oncol
PMID 32265695 Icariin Ameliorates Diabetic Cardiomyopathy Through Apelin/Sirt3 Signalling to I
Front Pharmacol
PMID 32348838 Icariin protects rabbit BMSCs against OGD-induced apoptosis by inhibiting ERs-me
Life Sci
PMID 32470450 Icariin protects neurons from endoplasmic reticulum stress-induced apoptosis aft
Life Sci
PMID 32554031 Intranasal delivery of icariin via a nanogel-thermoresponsive hydrogel compound
Int J Pharm
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