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Details

Stereochemistry ACHIRAL
Molecular Formula C8H15NO
Molecular Weight 141.2108
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PSEUDOTROPINE

SMILES

CN1[C@H]2CC[C@@H]1C[C@@H](O)C2

InChI

InChIKey=CYHOMWAPJJPNMW-RNLVFQAGSA-N
InChI=1S/C8H15NO/c1-9-6-2-3-7(9)5-8(10)4-6/h6-8,10H,2-5H2,1H3/t6-,7+,8-

HIDE SMILES / InChI

Molecular Formula C8H15NO
Molecular Weight 141.2108
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Pseudotropine (ψ-tropine, or psi-tropine) is an isomer of tropine. Pseudotropine is formed during NADPH-dependent reduction of the 3-carbonyl group of tropinone to a beta-hydroxyl group. Tropinone reductase-II is an enzyme responsible for this transformation. It is known, that tropinone reductase-II is also a key enzyme in the biosynthetic pathway of tropane alkaloids, which include medicinally important compounds such as hyoscyamine (atropine) and cocaine.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Virtual combinatorial syntheses and computational screening of new potential anti-herpes compounds.
1999 Aug 26
The new neuromuscular blocking agents: do they offer any advantages?
2001 Dec
Neuromuscular pharmacology of TAAC3, a new nondepolarizing muscle relaxant with rapid onset and ultrashort duration of action.
2002 Apr
Structure-activity relationships among derivatives of dicarboxylic acid esters of tropine.
2002 Oct
Calystegines in wild and cultivated Erythroxylum species.
2005 Jun
Quaternary derivatives of granatanol diesters: potent, ultrashort acting non-depolarizing neuromuscular relaxants.
2006 Jul 4
The functional divergence of short-chain dehydrogenases involved in tropinone reduction.
2008 May
Treatment of Cushing disease: overview and recent findings.
2010 Oct 21
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 09:58:30 GMT 2023
Edited
by admin
on Sat Dec 16 09:58:30 GMT 2023
Record UNII
L9Q7Z9D09L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PSEUDOTROPINE
MI  
Common Name English
PSEUDOTROPINE [MI]
Common Name English
PSEUDOTROPANOL
Common Name English
.PSI.-TROPINE
Common Name English
8-AZABICYCLO(3.2.1)OCTAN-3-OL, 8-METHYL-, (3-EXO)-
Common Name English
3-PSEUDOTROPANOL
Common Name English
NSC-43871
Code English
3.BETA.-TROPANOL
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
205-226-5
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
DRUG BANK
DB04026
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
WIKIPEDIA
Pseudotropine
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
CHEBI
15742
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
CAS
135-97-7
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID501026533
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
MERCK INDEX
m9300
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY Merck Index
NSC
43871
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
CHEBI
57493
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY
FDA UNII
L9Q7Z9D09L
Created by admin on Sat Dec 16 09:58:30 GMT 2023 , Edited by admin on Sat Dec 16 09:58:30 GMT 2023
PRIMARY