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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYPAPHORINE

SMILES

C[N+](C)(C)[C@@H](CC1=CNC2=C1C=CC=C2)C([O-])=O

InChI

InChIKey=AOHCBEAZXHZMOR-ZDUSSCGKSA-N
InChI=1S/C14H18N2O2/c1-16(2,3)13(14(17)18)8-10-9-15-12-7-5-4-6-11(10)12/h4-7,9,13,15H,8H2,1-3H3/t13-/m0/s1

HIDE SMILES / InChI

Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Hypaphorine is the alkaloid isolated from the seeds of Brazilian medicinal plant Erythrina spp. This compound was investigated for sleep-promoting effects in mice, and the results showed that it significantly increased non-rapid eye movement (NREM) sleep time during the first hour after its administration. Hypaphorine prevented the differentiation of 3T3-L1 preadipocytes into adipocytes by down-regulating hormone-stimulated protein expression of peroxisome proliferator activated receptor γ (PPARγ) and CCAAT/enhancer binding protein (C/EBPα), and their downstream targets, sterol regulatory element binding protein 1 c (SREBP1c) and fatty acid synthase (FAS). Hypaphorine may exert anti-inflammatory actions through the regulation of TLR4 and PPAR-γ dependent on PI3K/Akt/mTOR signal pathways. It is considered as a therapeutic agent that can potentially relieve or ameliorate endothelial inflammation-associated diseases. Hypaphorine was also a key component of Vaccaria segetalis. Vaccaria hypaphorine might be considered as a potential therapeutic agent for treating osteoclast-based bone loss.

Originator

Sources: DOI: 10.1039/CT9119902068

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Interactions of TLR4 and PPARγ, Dependent on AMPK Signalling Pathway Contribute to Anti-Inflammatory Effects of Vaccariae Hypaphorine in Endothelial Cells.
2017
Vaccaria hypaphorine impairs RANKL-induced osteoclastogenesis by inhibition of ERK, p38, JNK and NF-κB pathway and prevents inflammatory bone loss in mice.
2018 Jan
Patents

Sample Use Guides

Mice: 10 and 30 mg/kg (1 d before LPS injection and then every other 7 d.
Route of Administration: Oral
12.5 uM, 25 uM or 50 uM vaccaria hypaphorine markedly disturbed F-actin ring structure, indicating that vaccaria hypaphorine could inhibit bone-resorbing activity of osteoclasts.
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:13:21 GMT 2023
Edited
by admin
on Sat Dec 16 08:13:21 GMT 2023
Record UNII
GJ3358U63L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYPAPHORINE
MI  
Common Name English
L-HYPAPHORINE
Common Name English
TRYPTOPHAN, TRIMETHYLBETAINE
Common Name English
HYPAPHORINE [MI]
Common Name English
HYPAPHORINE, (+)-
Common Name English
TRYPTOPHAN BETAINE
Common Name English
LENTICINE
Common Name English
LENTICIN
Common Name English
GLYYUNNANENINE
Common Name English
1H-INDOLE-3-ETHANAMINIUM, .ALPHA.-CARBOXY-N,N,N-TRIMETHYL-, INNER SALT, (.ALPHA.S)-
Systematic Name English
(.ALPHA.S)-.ALPHA.-CARBOXY-N,N,N-TRIMETHYL-1H-INDOLE-3-ETHANAMINIUM INNER SALT
Systematic Name English
Code System Code Type Description
CAS
487-58-1
Created by admin on Sat Dec 16 08:13:21 GMT 2023 , Edited by admin on Sat Dec 16 08:13:21 GMT 2023
PRIMARY
MERCK INDEX
m6170
Created by admin on Sat Dec 16 08:13:21 GMT 2023 , Edited by admin on Sat Dec 16 08:13:21 GMT 2023
PRIMARY Merck Index
PUBCHEM
442106
Created by admin on Sat Dec 16 08:13:21 GMT 2023 , Edited by admin on Sat Dec 16 08:13:21 GMT 2023
PRIMARY
FDA UNII
GJ3358U63L
Created by admin on Sat Dec 16 08:13:21 GMT 2023 , Edited by admin on Sat Dec 16 08:13:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID70964100
Created by admin on Sat Dec 16 08:13:21 GMT 2023 , Edited by admin on Sat Dec 16 08:13:21 GMT 2023
PRIMARY
CHEBI
5832
Created by admin on Sat Dec 16 08:13:21 GMT 2023 , Edited by admin on Sat Dec 16 08:13:21 GMT 2023
PRIMARY