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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H28O2
Molecular Weight 240.3816
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROXIMADIOL

SMILES

CC(C)(O)[C@@H]1CC[C@@]2(C)CCC[C@@](C)(O)[C@@H]2C1

InChI

InChIKey=LKKDASYGWYYFIK-QHSBEEBCSA-N
InChI=1S/C15H28O2/c1-13(2,16)11-6-9-14(3)7-5-8-15(4,17)12(14)10-11/h11-12,16-17H,5-10H2,1-4H3/t11-,12-,14-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H28O2
Molecular Weight 240.3816
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Proximadiol was isolated from the rhizomes of Zingiber mekongense and leaves of Blumea balsamifera. Compound lacks ativiral and antibacterial activity. Proximadiol was found to inhibit platelet-activating factor receptor binding on platelets at micromolar concentrations.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Inhibitory effect of compounds from Goniothalamus tapis Miq. and Goniothalamus uvaroides King on platelet-activating factor receptor binding.
2012-05
A new diarylheptanoid from the rhizomes of Zingiber mekongense.
2011-06
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
The reaction mixture consisted of 200 mL of washed rabbit platelet suspension, 25 mL of 3H-PAF (2.0 nM) with or without unlabelled PAF (2.0 mM) and 15 mL of sample or control solution. The final concentrations of sample in the reaction mixtures were 18.2, 9.1, 4.5, 1.8 and 0.9 mg/mL. The reaction mixture was incubated at room temperature for 1 h. The free and bound ligands were separated by filtration technique using Whatman GF/C glass fibre filters. The final concentration of DMSO (control) in the reaction mixture was fixed at 0.1% to avoid interference with the receptor binding studies. The reaction mixture with 0.1% DMSO in saline was used as a control and cedrol was used as a positive control. The radioactivity was measured by scintillation counting. The difference between total radioactivities of bound 3H-PAF in the absence and presence of excess unlabelled PAF is defined as specific binding of the radiolabelled ligand.
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:34:57 GMT 2025
Edited
by admin
on Mon Mar 31 22:34:57 GMT 2025
Record UNII
Y2KBV9FZ9M
Record Status Validated (UNII)
Record Version
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Name Type Language
PROXIMADIOL
Common Name English
J13.424D
Preferred Name English
(1R,4AR,7R,8AR)-7-(2-HYDROXY-2-PROPANYL)-1,4A-DIMETHYLDECAHYDRO-1-NAPHTHALENOL
Systematic Name English
CRYPTOMERIDIOL
Common Name English
2-NAPHTHALENEMETHANOL, DECAHYDRO-8-HYDROXY-.ALPHA.,.ALPHA.,4A,8-TETRAMETHYL-, (2R-(2.ALPHA.,4A.ALPHA.,8.BETA.,8A.BETA.))-
Systematic Name English
5.BETA.,7.BETA.H,10.ALPHA.-EUDESMANE-4,11-DIOL
Common Name English
2-NAPHTHALENEMETHANOL, 1,2.BETA.,3,4,4A,5,6,7,8,8A.BETA.-DECAHYDRO-8.BETA.-HYDROXY-.ALPHA.,.ALPHA.,4A.ALPHA.,8-TETRAMETHYL-
Systematic Name English
2-NAPHTHALENEMETHANOL, DECAHYDRO-8-HYDROXY-.ALPHA.,.ALPHA.,4A,8-TETRAMETHYL-, (2R,4AR,8R,8AR)-
Systematic Name English
(2R,8R,8A.BETA.)-DECAHYDRO-8-HYDROXY-.ALPHA.,.ALPHA.,4A.ALPHA.,8-TETRAMETHYL-2-NAPHTHALENEMETHANOL
Systematic Name English
SELINA-4,7-DIOL
Common Name English
SELINANE-4.ALPHA.,11-DIOL
Common Name English
Code System Code Type Description
PUBCHEM
165258
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
EPA CompTox
DTXSID001317282
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
CAS
4666-84-6
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
FDA UNII
Y2KBV9FZ9M
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
RXCUI
2562551
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
EVMPD
SUB69958
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
DAILYMED
Y2KBV9FZ9M
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
SMS_ID
100000135241
Created by admin on Mon Mar 31 22:34:57 GMT 2025 , Edited by admin on Mon Mar 31 22:34:57 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
Isolated from the from Heartwood.
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ACTIVE MOIETY