Huperzine A

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Huperzine A
Molecular weight
Structure (SMILES)
C/C=C1\[C@H]2C=C(C)C[C@]1(N)c1ccc(=O)[nH]c1C2

  • (-)-huperzine a
  • (-)-selagine
  • (5R,9R,11E)-5-AMINO-11-ETHYLIDENE-5,6,9,10-TETRAHYDRO-7-METHYL-5,9-METHANOCYCLOOCTA(B)PYRIDIN-2(1H)-ONE
  • 5r 9r 11e 5 amino 11 ethylidene 5 6 9 10 tetrahydro 7 methyl 5 9 methanocycloocta b pyridin 2 1h one
  • huperzine a
  • huperzine A
  • Huperzine a
  • Huperzine A
  • HUPERZINE A [MI]
  • HUPERZINE A [VANDF]
  • Huperzine a [WHO-DD]
  • huperzine a 0 4 mg
  • huperzine a 0 8 mg
  • Huperzine A 0.4 mg
  • Huperzine A 0.8 mg
  • huperzine a for injection
  • Huperzine A for Injection
  • huperzine a injection
  • Huperzine A injection
  • Huperzine A Injection
  • huperzine a mi
  • huperzine a oral solution
  • Huperzine A Oral Solution
  • huperzine a vandf
  • huperzine a who dd

And 4 more, listed on the interactive page.

CAS registry numbers
  • 102518-79-6
ChEMBL ID
CHEMBL395280
InChIKey
ZRJBHWIHUMBLCN-YQEJDHNASA-N
PubChem compound IDs
  • 854026
RxNorm IDs (RxCUI)
  • 2267703
FDA ingredient codes (UNII)
  • 0111871I23

Patents
0
Designations
3
First in class
No
Fast track
No
Breakthrough designation
No
Orphan designation
No
Priority review
No
Orphan exclusivity
No
Accelerated approval
No

Pharmacology name
huperzine A
Type
Synthetic organic
Approval recorded by Guide to Pharmacology
Yes

  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    acetylcholinesterase (Yt blood group)
    Gene symbol
    ACHE
    Protein identifier
    P22303
    Median affinity
    7.77
    Affinity units
    pKd
  • Mechanism
    Acetylcholinesterase inhibitor
    Action type
    Inhibitor
    Target
    Acetylcholinesterase
    Protein identifier
    P22303

Open Targets mechanisms

  • Mechanism
    Acetylcholinesterase inhibitor
    Action type
    Inhibitor
    Target
    Acetylcholinesterase

  • Condition
    Substance-Related Disorders
    Highest recorded phase
    1
    Condition identifier
    MONDO:0002491
    Subject identifier
    D019966
  • Condition
    Cocaine-Related Disorders
    Highest recorded phase
    1
    Condition identifier
    MONDO:0004456
    Subject identifier
    D019970
  • Condition
    Alzheimer Disease
    Highest recorded phase
    2
    Condition identifier
    MONDO:0004975
    Subject identifier
    D000544
  • Condition
    Brain Injuries
    Highest recorded phase
    2
    Condition identifier
    MONDO:0043510
    Subject identifier
    D001930

  • Condition identifier
    HP_0100543
  • Condition identifier
    MONDO_0004456
    Highest recorded phase
    1
  • Condition identifier
    MONDO_0004975
  • Condition identifier
    MONDO_0004975
    Highest recorded phase
    4

Hydrogen bond acceptors
2
Hydrogen bond donors
2
Polar surface area
58.88
Calculated partition coefficient (ALogP)
2
Calculated partition coefficient (XLogP)
0
Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Rule-of-five violations
0
Rotatable bonds
0
Heavy atoms
18
Molecular formula
C15H18N2O
Monoisotopic mass
242.141913202
Natural product
Yes

Recorded assays
1,156
Active assays
72

  • Confirmatory
  • Other

Related records

Trials (13)

In development for (4)

Targets (1)