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Herb Integrative Database
Traditional Medicine Data Platform
Ingredients

Sulfuretin

C15H10O5

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Entity Type
Ingredients
Relation Groups
2
Relation Preview
15

Basic Information

Grouped by core information, identifiers, and descriptions.

Core Information

Name
Sulfuretin
Molecular Formula
C15H10O5
Molecular Weight
No data
Canonical SMILES
C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)O)O
Isomeric SMILES
C1=CC(=C(C=C1/C=C\2/C(=O)C3=C(O2)C=C(C=C3)O)O)O
InChI
InChI=1S/C15H10O5/c16-9-2-3-10-13(7-9)20-14(15(10)19)6-8-1-4-11(17)12(18)5-8/h1-7,16-18H/b14-6-
Oral Bioavailability
No data
Drug Likeness
0.547
DL Score
No data
Caco-2 Permeability
No data
ALogP
No data
Bioavailability Score
No data

Identifiers

InChI Key
No data
PubChem CID
No data

Description and Extensions

Toxicity Information
No data
Related

Related Entities

Direct relations and traceable candidates grouped by relation type.

Source HerbsActive Targets

Active Targets

ingredient target8 Targets
GraphMore Targets
02
ALPG
alkaline phosphatase, germ cell
alkaline phosphatase, germ cell
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03
ALPI
alkaline phosphatase, intestinal
alkaline phosphatase, intestinal
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04
ALPL
alkaline phosphatase, biomineralization associated
alkaline phosphatase, biomineralization associated
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05
APEX1
apurinic/apyrimidinic endodeoxyribonuclease 1
apurinic/apyrimidinic endodeoxyribonuclease 1
DetailsGraph
06
APOBEC3F
apolipoprotein B mRNA editing enzyme catalytic subunit 3F
apolipoprotein B mRNA editing enzyme catalytic subunit 3F
DetailsGraph
07
APOBEC3G
apolipoprotein B mRNA editing enzyme catalytic subunit 3G
apolipoprotein B mRNA editing enzyme catalytic subunit 3G
DetailsGraph