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Dehydrocorybulbine (DHCB) is a natural alkaloid compound derived from the plant Corydalis yanhusuo, traditionally used in Chinese medicine for its analgesic and sedative properties. It acts as a natural painkiller targeting the same pathways as opioids but with fewer side effects, such as respiratory depression and addiction potential. DHCB also has potential antidepressant effects and is considered a promising alternative to traditional opioid medications for pain management.

59870-72-3

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59870-72-3 Usage

Uses

Used in Pain Management:
Dehydrocorybulbine is used as a natural painkiller for its analgesic properties, targeting the same pathways as opioids but with fewer side effects such as respiratory depression and addiction potential.
Used in Traditional Chinese Medicine:
Dehydrocorybulbine is used as a therapeutic agent in traditional Chinese medicine for its analgesic and sedative properties.
Used in Antidepressant Research:
Dehydrocorybulbine is used as a potential antidepressant agent, although further research is needed to fully understand its mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 59870-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,7 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59870-72:
(7*5)+(6*9)+(5*8)+(4*7)+(3*0)+(2*7)+(1*2)=173
173 % 10 = 3
So 59870-72-3 is a valid CAS Registry Number.

59870-72-3Downstream Products

59870-72-3Relevant academic research and scientific papers

A General, Concise Strategy that Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps

Zhou, Shiqiang,Tong, Rongbiao

supporting information, p. 7084 - 7089 (2016/05/19)

A concise, catalytic, and general strategy that allowed efficient total syntheses of 22 natural 13-methylprotoberberines within four steps for each molecule is reported. This synthesis represents the most efficient and shortest route to date, featuring three catalytic processes: CuI-catalyzed redox-A3 reaction, Pd-catalyzed reductive carbocyclization, and PtO2-catalyzed hydrogenation. Importantly, this new strategy to the tetracyclic framework has also been applied to the collective concise syntheses of >30 natural protoberberines (without 13-methyl group) and five aporhoeadane alkaloids.

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