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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H19N2O2.Cl
Molecular Weight 282.766
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYPAPHORINE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=NZXZRRFENSICAK-ZOWNYOTGSA-N
InChI=1S/C14H18N2O2.ClH/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;1H/t13-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 1 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Vaccaria hypaphorine impairs RANKL-induced osteoclastogenesis by inhibition of ERK, p38, JNK and NF-κB pathway and prevents inflammatory bone loss in mice.
2018-01
Hypaphorine, an Indole Alkaloid Isolated from Caragana korshinskii Kom., Inhibites 3T3-L1 Adipocyte Differentiation and Improves Insulin Sensitivity in Vitro.
2017-07
Hypaphorine Attenuates Lipopolysaccharide-Induced Endothelial Inflammation via Regulation of TLR4 and PPAR-γ Dependent on PI3K/Akt/mTOR Signal Pathway.
2017-04-17
Vaccaria hypaphorine alleviates lipopolysaccharide-induced inflammation via inactivation of NFκB and ERK pathways in Raw 264.7 cells.
2017-02-20
Interactions of TLR4 and PPARγ, Dependent on AMPK Signalling Pathway Contribute to Anti-Inflammatory Effects of Vaccariae Hypaphorine in Endothelial Cells.
2017
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 Mon Mar 31 22:06:19 GMT 2025
Edited
by admin
on Mon Mar 31 22:06:19 GMT 2025
Record UNII
6444YS784R
Record Status Validated (UNII)
Record Version
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Name Type Language
HYPAPHORINE HYDROCHLORIDE
MI  
Common Name English
HYPAPHORINE HYDROCHLORIDE [MI]
Preferred Name English
1H-INDOLE-3-ETHANAMINIUM, .ALPHA.-CARBOXY-N,N,N-TRIMETHYL-, CHLORIDE, (S)-
Systematic Name English
(.ALPHA.S)-.ALPHA.-CARBOXY-N,N,N-TRIMETHYL-1H-INDOLE-3-ETHANAMINIUM CHLORIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
91617793
Created by admin on Mon Mar 31 22:06:19 GMT 2025 , Edited by admin on Mon Mar 31 22:06:19 GMT 2025
PRIMARY
CAS
20671-76-5
Created by admin on Mon Mar 31 22:06:19 GMT 2025 , Edited by admin on Mon Mar 31 22:06:19 GMT 2025
PRIMARY
MERCK INDEX
m6170
Created by admin on Mon Mar 31 22:06:19 GMT 2025 , Edited by admin on Mon Mar 31 22:06:19 GMT 2025
PRIMARY Merck Index
FDA UNII
6444YS784R
Created by admin on Mon Mar 31 22:06:19 GMT 2025 , Edited by admin on Mon Mar 31 22:06:19 GMT 2025
PRIMARY