U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C20H23NO4
Molecular Weight 341.4009
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CORYDINE

SMILES

[H][C@]12CC3=C(C(OC)=C(OC)C=C3)C4=C1C(CCN2C)=CC(OC)=C4O

InChI

InChIKey=IDQUPXZJURZAGF-ZDUSSCGKSA-N
InChI=1S/C20H23NO4/c1-21-8-7-12-10-15(24-3)19(22)18-16(12)13(21)9-11-5-6-14(23-2)20(25-4)17(11)18/h5-6,10,13,22H,7-9H2,1-4H3/t13-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H23NO4
Molecular Weight 341.4009
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Corydine is a naturally occurring compound which can be extracted from plants such as Chelidonium majus, Corydalis marschalliana, C. bulbosa, C slivenensis, Glaucium grandiflorum. Corydine has shown some efficacy as an anti-cancer compound in several cell models and was examined along with related compounds from Stephania dinklagei for antiprotozoal activities. (+)- and (-)- Corydine were tested as neuromuscular blocking agents were it was found that there was a modest preference for (+)-corydine.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P24941
Gene ID: 1017.0
Gene Symbol: CDK2
Target Organism: Homo sapiens (Human)
Target ID: P08684
Gene ID: 1576.0
Gene Symbol: CYP3A4
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Selective ther cleavage in the aporphine series. Conversion of (S)-bulbocapnine into (S)-corytuberine and (S)-corydine methyl ether.
1976 Nov 3
Alkaloids from Corydalis marschalliana.
1981 Mar
Alkaloids from Corydalis bulbosa.
1981 Sep
Alkaloids of Corydalis slivenensis.
1982 Mar
Alkaloids of Turkish Glaucium species.
1982 Nov
Corydine and norcorydine from the roots of Chelidonium majus.
1998 Jun
Cytotoxic and DNA damaging activity of some aporphine alkaloids from Stephania dinklagei.
2003 Sep
Identification of candidate genes involved in isoquinoline alkaloids biosynthesis in Dactylicapnos scandens by transcriptome analysis.
2017 Aug 22
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:06:32 GMT 2023
Edited
by admin
on Sat Dec 16 08:06:32 GMT 2023
Record UNII
1O1D15OP5R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CORYDINE
MI  
Common Name English
D-CORYDINE
Common Name English
(6AS)-5,6,6A,7-TETRAHYDRO-2,10,11-TRIMETHOXY-6-METHYL-4H-DIBENZO(DE,G)QUINOLIN-1-OL
Systematic Name English
(S)-(+)-CORYDINE
Common Name English
GLAUCENTRINE
Common Name English
(+)-CORYDINE
Common Name English
CORYDINE [MI]
Common Name English
CORYTUBERINE METHYL ETHER [MI]
Common Name English
GLAUCENTRIN
Common Name English
O11-METHYLCORYTUBERINE
Common Name English
4H-DIBENZO(DE,G)QUINOLIN-1-OL, 5,6,6A,7-TETRAHYDRO-2,10,11-TRIMETHOXY-6-METHYL-, (6AS)-
Systematic Name English
Code System Code Type Description
DAILYMED
1O1D15OP5R
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY
RXCUI
2593178
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID00963883
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY
FDA UNII
1O1D15OP5R
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY
CAS
476-69-7
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY
MERCK INDEX
m3803
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY Merck Index
MERCK INDEX
m3807
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY Merck Index
PUBCHEM
10153
Created by admin on Sat Dec 16 08:06:32 GMT 2023 , Edited by admin on Sat Dec 16 08:06:32 GMT 2023
PRIMARY