![]() Khellin structure
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Common Name | Khellin | ||
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CAS Number | 82-02-0 | Molecular Weight | 260.242 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 482.1±0.0 °C at 760 mmHg | |
Molecular Formula | C14H12O5 | Melting Point | 150-154ºC | |
MSDS | Chinese USA | Flash Point | 218.8±28.7 °C | |
Symbol |
![]() GHS06 |
Signal Word | Danger |
Use of KhellinKhellin, a naturally occurring furochromone, is an EGFR inhibitor with an IC50 of 0.15 µM. Khelline has anti-proliferative activity in vitro. Khellin has antispasmodic and coronary vasodilator effects[1][2]. |
Name | 4,9-dimethoxy-7-methylfuro[3,2-g]chromen-5-one |
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Synonym | More Synonyms |
Description | Khellin, a naturally occurring furochromone, is an EGFR inhibitor with an IC50 of 0.15 µM. Khelline has anti-proliferative activity in vitro. Khellin has antispasmodic and coronary vasodilator effects[1][2]. |
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Related Catalog | |
Target |
IC50: 0.15 µM (EGFR)[1] |
In Vitro | Khelline exhibits anti-proliferative activity for MCF-7 cells and Hela cells[1]. Khellin causes total relaxation of both NA- and K+-contractions and a change in external calcium concentration[2]. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 482.1±0.0 °C at 760 mmHg |
Melting Point | 150-154ºC |
Molecular Formula | C14H12O5 |
Molecular Weight | 260.242 |
Flash Point | 218.8±28.7 °C |
Exact Mass | 260.068481 |
PSA | 61.81000 |
LogP | 1.77 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.595 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
![]() GHS06 |
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Signal Word | Danger |
Hazard Statements | H301-H315 |
Precautionary Statements | P301 + P310 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T: Toxic; |
Risk Phrases | R25 |
Safety Phrases | 36/37/39-45 |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
RTECS | LV1050000 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 2932999099 |
Precursor 7 | |
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DownStream 10 | |
HS Code | 2932999099 |
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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% |
Validated HPLC and HPTLC methods for simultaneous determination of colchicine and khellin in pharmaceutical formulations.
J. Chromatogr. Sci. 51(3) , 258-65, (2013) The present work describes validated high-performance liquid chromatography (HPLC) and high-performance thin-layer chromatography (HPTLC) methods for the simultaneous determination of colchicine and k... |
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F420H2-dependent degradation of aflatoxin and other furanocoumarins is widespread throughout the actinomycetales.
PLoS ONE 7(2) , e30114, (2012) Two classes of F(420)-dependent reductases (FDR-A and FDR-B) that can reduce aflatoxins and thereby degrade them have previously been isolated from Mycobacterium smegmatis. One class, the FDR-A enzyme... |
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A case study to evaluate the treatment of vitiligo with khellin encapsulated in L-phenylalanin stabilized phosphatidylcholine liposomes in combination with ultraviolet light therapy.
Eur. J. Dermatol. 13(5) , 474-7, (2003) Vitiligo destroys the melanocytes in the epidermis; the inactive melanocytes in the outer root sheaths are not affected. Phosphatidylcholine liposomes are able to target molecules contained in them in... |
Khellin |
4,9-Dimethoxy-7-methyl-5H-furo[3,2-g]-[1]benzopyran-5-one |
Methafrone |
Corafurone |
Ammivisnagen |
coronin |
4,9-Dimethoxy-7-methyl-5-oxofuro[3,2-g][1]benzopyran |
Rykellin |
4,9-Dimethoxy-7-methyl-5H-furo[3,2-g]chromen-5-one |
4,9-Dimethoxy-7-methyl-5-oxo-1,8-dioxabenz[f]indene |
4,9-Dimethoxy-7-methyl-5-oxofuro[3,2-g]-1,2-chromene |
5H-Furo[3,2-g][1]benzopyran-5-one, 4,9-dimethoxy-7-methyl- |
Ammicardine |
5,8-dimethoxy-2-methyl-4',5'-furo-6,7-chromane |
Kelourin |
Ammispasmin |
hellin |
Amicardine |
EINECS 201-392-8 |
MFCD00005007 |
Visammin |
5H-Furo(3,2-g)(1)benzopyran-5-one, 4,9-dimethoxy-7-methyl- |