(+)-Cepharanthine
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(+)-Cepharanthine
structure -
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CAS No:
481-49-2
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Formula:
C37H38N2O6
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Chemical Name:
(+)-Cepharanthine
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Synonyms:
1H-4,6:16,19-Dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2′,3′:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline,2,3,13,14,14a,15,26,26a-octahydro-22,30-dimethoxy-1,14-dimethyl-,(14aS,26aR)-;Cepharanthine;Oxyacanthan,6′,12′-dimethoxy-2,2′-dimethyl-6,7-[methylenebis(oxy)]-;(14aS,26aR)-2,3,13,14,14a,15,26,26a-Octahydro-22,30-dimethoxy-1,14-dimethyl-1H-4,6:16,19-dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2′,3′:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline;O-Methylcepharanoline;Cepharanthin;1H-4,6:16,19-Dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2′,3′:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline,2,3,13,14,14a,15,26,26a-octahydro-22,30-dimethoxy-1,14-dimethyl-,[14aS-(14aR*,26aS*)]-;Cepharantin;(+)-Cepharanthine;NSC 623442;SML 1269;1413-58-7;30255-28-8
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CAS No:
Description
Cepharanthine, an alkaloid derived from Stephania cepharantha Hayata, with possesses anti-inflammatory and antioxidative activities[1][2][3]. Cepharanthine attenuates muscle and kidney injuries induced by limb ischemia/reperfusion (I/R)[3]. Cepharanthine induces autophagy, apoptosis and cell cycle arrest in breast cancer cells[4]. Cepharanthine inhibits the HIV-1 entry process by reducing plasma membrane fluidity[5].
Cepharanthine is a bisbenzylisoquinoline alkaloid from tubers of Stephania; stimulates recovery of immunologic function in lymphatic system after administration of antineoplastic agents or x-irradiation. It is a member of isoquinolines and a bisbenzylisoquinoline alkaloid.
Characteristics
61.9
6.5
Yellow powder.
1.2±0.1 g/cm3
140-145 °C
1.608
Store cool and dry in sealed containers.
Oral-rat LD50: 2000 mg/kg; Oral-Mouse LD50: 1900 mg/kg
Thermal decomposition to emit toxic nitrogen oxide fumes
D20 +277° (c = 2 in chloroform)
Safety Information
NONH for all modes of transport
FK0527000
The warehouse is low-temperature, ventilated and dry
P301 + P312 + P330
H302
Drug Information
Agents obtained from higher plants that have demonstrable cytostatic or antineoplastic activity. (See all compounds classified as Antineoplastic Agents, Phytogenic.)|Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Drugs used to protect against ionizing radiation. They are usually of interest for use in radiation therapy but have been considered for other purposes, e.g. military. (See all compounds classified as Radiation-Protective Agents.)
cepharanthin
Computed Properties
Molecular Weight:606.7
XLogP3:6.5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:2
Exact Mass:606.27298694
Monoisotopic Mass:606.27298694
Topological Polar Surface Area:61.9
Heavy Atom Count:45
Complexity:994
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Not yet clear
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