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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H19N2O2.Cl
Molecular Weight 282.766
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
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 ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Hypaphorine Attenuates Lipopolysaccharide-Induced Endothelial Inflammation via Regulation of TLR4 and PPAR-γ Dependent on PI3K/Akt/mTOR Signal Pathway.
2017 Apr 17
Vaccaria hypaphorine alleviates lipopolysaccharide-induced inflammation via inactivation of NFκB and ERK pathways in Raw 264.7 cells.
2017 Feb 20
Hypaphorine, an Indole Alkaloid Isolated from Caragana korshinskii Kom., Inhibites 3T3-L1 Adipocyte Differentiation and Improves Insulin Sensitivity in Vitro.
2017 Jul
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 08:28:44 GMT 2023
Edited
by admin
on Sat Dec 16 08:28:44 GMT 2023
Record UNII
6444YS784R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYPAPHORINE HYDROCHLORIDE
MI  
Common Name English
1H-INDOLE-3-ETHANAMINIUM, .ALPHA.-CARBOXY-N,N,N-TRIMETHYL-, CHLORIDE, (S)-
Systematic Name English
HYPAPHORINE HYDROCHLORIDE [MI]
Common 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 Sat Dec 16 08:28:44 GMT 2023 , Edited by admin on Sat Dec 16 08:28:44 GMT 2023
PRIMARY
CAS
20671-76-5
Created by admin on Sat Dec 16 08:28:44 GMT 2023 , Edited by admin on Sat Dec 16 08:28:44 GMT 2023
PRIMARY
MERCK INDEX
m6170
Created by admin on Sat Dec 16 08:28:44 GMT 2023 , Edited by admin on Sat Dec 16 08:28:44 GMT 2023
PRIMARY Merck Index
FDA UNII
6444YS784R
Created by admin on Sat Dec 16 08:28:44 GMT 2023 , Edited by admin on Sat Dec 16 08:28:44 GMT 2023
PRIMARY