Isobergapten

Modify Date: 2025-08-20 10:36:11

Isobergapten Structure
Isobergapten structure
Common Name Isobergapten
CAS Number 482-48-4 Molecular Weight 216.189
Density 1.368 Boiling Point 412.4±45.0 °C at 760 mmHg
Molecular Formula C12H8O4 Melting Point 224 ºC
MSDS N/A Flash Point 203.2±28.7 °C

 Use of Isobergapten


Isobergapten is an allelopathic inhibitor isolated from seeds of Hevacleum laciniatum[1].

 Names

Name 5-methoxyfuro[2,3-h]chromen-2-one
Synonym More Synonyms

 Isobergapten Biological Activity

Description Isobergapten is an allelopathic inhibitor isolated from seeds of Hevacleum laciniatum[1].
Related Catalog
References

[1]. OLAVI JUNTTILA, et al. Allelopathic Inhibitors in Seeds of Hevacleum laciniatum. Physiologia Plantarum. 1976.

 Chemical & Physical Properties

Density 1.368
Boiling Point 412.4±45.0 °C at 760 mmHg
Melting Point 224 ºC
Molecular Formula C12H8O4
Molecular Weight 216.189
Flash Point 203.2±28.7 °C
Exact Mass 216.042252
PSA 52.58000
LogP 2.34
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.635
InChIKey AJSPSRWWZBBIOR-UHFFFAOYSA-N
SMILES COc1cc2occc2c2oc(=O)ccc12
Storage condition 2-8C

 Safety Information

HS Code 2932999099

 Synthetic Route

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Isobergapten Structure

Isobergapten

CAS#:482-48-4

Literature: Spaeth; Kubiczek Chemische Berichte, 1937 , vol. 70, p. 1253

~%

Isobergapten Structure

Isobergapten

CAS#:482-48-4

Literature: Rodighiero; Antonello Farmaco, Edizione Scientifica, 1955 , vol. 10, p. 889,893

~%

Isobergapten Structure

Isobergapten

CAS#:482-48-4

Literature: Rodighiero; Antonello Farmaco, Edizione Scientifica, 1955 , vol. 10, p. 889,893

~%

Isobergapten Structure

Isobergapten

CAS#:482-48-4

Literature: Spaeth; Kubiczek Chemische Berichte, 1937 , vol. 70, p. 1253

 Customs

HS Code 2932999099
Summary 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 IsobergaptenBioassay

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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
Name: Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
Source: NCGC
Target: N/A
External Id: SERCaMPGLuc-p1-antagonist
Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
Name: ERK5 transcriptional activity HTS
Source: 24565
Target: N/A
External Id: ERK5 transcriptional activity-HTS
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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 Synonyms

5-Methoxy-2H-furo[2,3-h]-1-benzopyran-2-one
isobergaptene
Isobergapten,5-Methoxy-7,8:5',4'-furocumarin
Isobergapten
5-Methoxy-2H-furo(2,3-h)-1-benzopyran-2-one
5-Methoxy-2H-furo[2,3-h]chromen-2-one
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