Ponganpin

Modify Date: 2025-09-21 18:18:23

Ponganpin Structure
Ponganpin structure
Common Name Ponganpin
CAS Number 481-99-2 Molecular Weight 336.29500
Density 1.5g/cm3 Boiling Point 514.1ºC at 760 mmHg
Molecular Formula C19H12O6 Melting Point N/A
MSDS N/A Flash Point 264.7ºC

 Names

Name 2-(1,3-benzodioxol-5-yl)-3-methoxyfuro[2,3-h]chromen-4-one
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.5g/cm3
Boiling Point 514.1ºC at 760 mmHg
Molecular Formula C19H12O6
Molecular Weight 336.29500
Flash Point 264.7ºC
Exact Mass 336.06300
PSA 71.04000
LogP 3.94350
Vapour Pressure 1.11E-10mmHg at 25°C
Index of Refraction 1.707
InChIKey IGFBIJDAWSAJIF-UHFFFAOYSA-N
SMILES COc1c(-c2ccc3c(c2)OCO3)oc2c(ccc3occc32)c1=O

 Synthetic Route

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Ponganpin Structure

Ponganpin

CAS#:481-99-2

Literature: Row Austral. J. scient. Res., 1952 , vol. 5, p. 754,758

~%

Ponganpin Structure

Ponganpin

CAS#:481-99-2

Literature: Aneja et al. Tetrahedron, 1958 , vol. 2, p. 203,209

~%

Ponganpin Structure

Ponganpin

CAS#:481-99-2

Literature: Aneja et al. Tetrahedron, 1958 , vol. 2, p. 203,209

~%

Ponganpin Structure

Ponganpin

CAS#:481-99-2

Literature: Row Austral. J. scient. Res., 1952 , vol. 5, p. 754,758

~%

Ponganpin Structure

Ponganpin

CAS#:481-99-2

Literature: Aneja et al. Tetrahedron, 1958 , vol. 2, p. 203,209

 PonganpinBioassay

View more

Name: Anti-neuroinflammatory activity against mouse BV2 cells assessed as inhibition of LPS...
Source: ChEMBL
Target: BV-2
External Id: CHEMBL3583454
Name: Inhibition of human CYP1A1 expressed in human HEK293 cells using 7-ethoxyresorufin as...
Source: ChEMBL
Target: Cytochrome P450 1A1
External Id: CHEMBL4675252
Name: Cytotoxicity against mouse BV2 cells assessed as reduction of cell viability at IC50 ...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3583455
Name: Inhibition of human CYP1B1 expressed in human HEK293 cells using 7-ethoxyresorufin as...
Source: ChEMBL
Target: Cytochrome P450 1B1
External Id: CHEMBL4675251
Name: Inhibition of human CYP1A1 expressed in sacchrosomes using 7-ethoxyresorufin as subst...
Source: ChEMBL
Target: Cytochrome P450 1A1
External Id: CHEMBL4675254
Name: Inhibition of human CYP1B1 expressed in sacchrosomes using 7-ethoxyresorufin as subst...
Source: ChEMBL
Target: Cytochrome P450 1B1
External Id: CHEMBL4675253
Name: Inhibition of rat alpha-glucosidase assessed as p-nitrophenol release at 50 ug/ml
Source: ChEMBL
Target: N/A
External Id: CHEMBL1038573
Name: Induction of cell cycle arrest in human MCF7 over expressing CYP1A cells assessed as ...
Source: ChEMBL
Target: MCF7
External Id: CHEMBL4675236
Name: Induction of cell cycle arrest in human MCF7 over expressing CYP1A cells assessed as ...
Source: ChEMBL
Target: MCF7
External Id: CHEMBL4675235
Name: Cell cycle arrest in human MCF-7 cells over expressing CYP1A1 assessed as down regula...
Source: ChEMBL
Target: MCF7
External Id: CHEMBL4675238
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 Synonyms

Pongapin
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