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Gene Target
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Disease
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trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
⚗️ Ingredient
Oroxin a
16
Clinical Trials
0
Meta-Analyses
0
PubMed References
Top Conditions Studied with Oroxin a
📋 Sample Trials
NCT00234949
A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderate Uncomplicated Skin Infections
Completed · Phase 4
NCT00352612
Comparison of Cephalexin Versus Clindamycin for Suspected CA-MRSA Skin Infections
Completed · Phase 4
NCT02100826
A Study of Cephalexin in Healthy Participants
Completed · Phase 1
📊 Sample Meta-Analyses
None linked yet.
📚 Sample References
None linked yet.
⚗️ All Ingredient data fields for Oroxin a
⚗️ Identity
Name
Oroxin a
Aliases / Synonyms
57396-78-8; baicalein-7-o-glucoside; 5,6-dihydroxy-2-phenyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; baicalein 7-O-glucoside; OroxinA; Baicalein-7-O-glucoside; Baikalin; Baicalein 7-O-glucopyranoside; CHEMBL516858; SCHEMBL6238244
🧪 Chemistry
Molecular Weight
432.3810
LogP
0.0499
Drug-likeness
0.31
Oral Bioavailability
9.5820
H-Bond Acceptors
10
H-Bond Donors
6
Rotatable Bonds
4
🔬 Structures
Canonical SMILES
C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O
Isomeric SMILES
C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
InChIKey
IPQKDIRUZHOIOM-IAAKTDFRSA-N
InChI
InChI=1S/C21H20O10/c22-8-14-17(25)19(27)20(28)21(31-14)30-13-7-12-15(18(26)16(13)24)10(23)6-11(29-12)9-4-2-1-3-5-9/h1-7,14,17,19-22,24-28H,8H2/t14-,17-,19+,20-,21-/m1/s1
🔗 External References
HERB DB
PubChem CID
CAS Number
SymMap
10840
TCMID
31760
TCMSP
MOL009754
TCM-ID
1894
🔍 Raw view — every non-empty column on this row (32 fields)
name
Oroxin a
common names
57396-78-8; baicalein-7-o-glucoside; 5,6-dihydroxy-2-phenyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; baicalein 7-O-glucoside; OroxinA; Baicalein-7-O-glucoside; Baikalin; Baicalein 7-O-glucopyranoside; CHEMBL516858; SCHEMBL6238244
herb ingredient id
HBIN038299
canonical smiles
C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O
isomeric smiles
C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
inchi
InChI=1S/C21H20O10/c22-8-14-17(25)19(27)20(28)21(31-14)30-13-7-12-15(18(26)16(13)24)10(23)6-11(29-12)9-4-2-1-3-5-9/h1-7,14,17,19-22,24-28H,8H2/t14-,17-,19+,20-,21-/m1/s1
inchikey
IPQKDIRUZHOIOM-IAAKTDFRSA-N
mol wt
432.3810
num h acceptors
10
num h donors
6
mol logp
0.0499
num rotatable bonds
4
drug likeness
0.31
ob score
9.5820
cas id
57396-78-8
symmap mol id
10840
tcmid ingredient id
31760
tcmsp ingredient id
MOL009754
tcm id ingredient id
1894
pubchem cid
5320313
🏥 Linked Health Topics
2 · diseases via target pathways📋 Clinical Trials
12 · subject of clinical studyNCT00234949 A Study to Compare Cefdinir and Cephalexin for the Treatment of Mild to Moderate
→ Mild to Moderate Uncomplicated Skin and Skin Struc
NCT00352612 Comparison of Cephalexin Versus Clindamycin for Suspected CA-MRSA Skin Infection
→ Staphylococcal Infection|Abscess|Staphylococcal Sk
NCT02100826 A Study of Cephalexin in Healthy Participants
→ Healthy Volunteers
NCT02490670 A Study of Cephalexin Liquid in Healthy Participants
→ Healthy
NCT01029782 Comparison of Intravenous Cefazolin Plus Oral Probenecid With Oral Cephalexin fo
→ Cellulitis
NCT01073540 Cross-over Study to Prove Bioequivalence Between Two Brands of Cefalexin Suspens
→ Anti-Infective Agents
NCT01105208 Cross Over Study to Prove Bioequivalence Between Two Brands of Cefalexin Suspens
→ Anti-Infective Agents
NCT01767532 Bioequivalence Study of Cephalexin Suspension 125
→ Infections, Respiratory Tract
NCT01767571 Bioequivalence Study of Cephalexin Suspension 250
→ Infections, Respiratory Tract
NCT02123446 A Study of Cephalexin Capsules in Healthy Participants
→ Healthy Volunteers
NCT02123459 A Study of Cephalexin Suspension in Healthy Participants
→ Healthy Volunteers
NCT02123472 A Study of Cephalexin Liquid for Pediatrics in Healthy Adults Participants
→ Healthy Volunteers
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