Proximadiol

Details

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Internal ID c032bc0f-ef93-4767-b397-0dbce7b3ec29
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol
SMILES (Canonical) CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O
SMILES (Isomeric) C[C@]12CCC[C@@]([C@@H]1C[C@@H](CC2)C(C)(C)O)(C)O
InChI 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
InChI Key LKKDASYGWYYFIK-QHSBEEBCSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O2
Molecular Weight 240.38 g/mol
Exact Mass 240.208930132 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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Cryptomeridiol
4666-84-6
Selina-4,7-diol
UNII-Y2KBV9FZ9M
Y2KBV9FZ9M
Selinane-4.alpha.,11-diol
(1R,4aR,7R,8aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol
CHEBI:67796
J13.424D
5.beta.,7.beta.H,10.alpha.-Eudesmane-4,11-diol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Proximadiol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.7948 79.48%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5736 57.36%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9319 93.19%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8693 86.93%
P-glycoprotein inhibitior - 0.9389 93.89%
P-glycoprotein substrate - 0.9267 92.67%
CYP3A4 substrate + 0.5584 55.84%
CYP2C9 substrate - 0.5427 54.27%
CYP2D6 substrate - 0.7259 72.59%
CYP3A4 inhibition - 0.9233 92.33%
CYP2C9 inhibition - 0.8269 82.69%
CYP2C19 inhibition - 0.8244 82.44%
CYP2D6 inhibition - 0.9632 96.32%
CYP1A2 inhibition - 0.5339 53.39%
CYP2C8 inhibition - 0.6772 67.72%
CYP inhibitory promiscuity - 0.9366 93.66%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6706 67.06%
Eye corrosion - 0.9553 95.53%
Eye irritation + 0.7411 74.11%
Skin irritation - 0.5614 56.14%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7050 70.50%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5269 52.69%
skin sensitisation + 0.6178 61.78%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6692 66.92%
Acute Oral Toxicity (c) III 0.9222 92.22%
Estrogen receptor binding - 0.5210 52.10%
Androgen receptor binding - 0.7933 79.33%
Thyroid receptor binding - 0.5361 53.61%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.7209 72.09%
PPAR gamma - 0.7829 78.29%
Honey bee toxicity - 0.8692 86.92%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9015 90.15%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.19% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 94.53% 97.79%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 92.25% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.57% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.18% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.05% 97.09%
CHEMBL284 P27487 Dipeptidyl peptidase IV 87.57% 95.69%
CHEMBL1937 Q92769 Histone deacetylase 2 86.19% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.16% 91.11%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.55% 93.04%
CHEMBL1871 P10275 Androgen Receptor 84.72% 96.43%
CHEMBL3920 Q04759 Protein kinase C theta 84.30% 97.69%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 83.43% 95.58%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.79% 100.00%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 82.34% 98.99%
CHEMBL259 P32245 Melanocortin receptor 4 81.46% 95.38%
CHEMBL238 Q01959 Dopamine transporter 81.31% 95.88%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Acacia linarioides
Achillea clypeolata
Acorus calamus
Alpinia flabellata
Anadenanthera colubrina
Angelica japonica
Anodendron affine
Aquilegia viridiflora
Artemisia campestris
Artemisia pygmaea
Astragalus kabadianus
Baccharis truncata
Benincasa hispida
Blumea balsamifera
Breonia chinensis
Brombya platynema
Calycanthus chinensis
Campylotropis hirtella
Carissa spinarum
Cedrela salvadorensis
Centaurea benedicta
Cerbera odollam
Ceropegia dichotoma
Chamaecyparis formosensis
Chenopodium vulvaria
Chloranthus fortunei
Chrysanthemum indicum
Chuquiraga erinacea
Cichorium endivia
Cipadessa baccifera
Clinopodium gracile
Coelogyne prolifera
Commiphora myrrha
Crinum moorei
Crotalaria candicans
Cryptomeria japonica
Cuphea hyssopifolia
Cylindrolobus mucronatus
Daphne arisanensis
Dendrobium loddigesii
Denhamia disperma
Distephanus angulifolius
Eucalyptus apodophylla
Euphorbia palustris
Euphorbia pithyusa
Farfugium japonicum
Fouquieria diguetii
Fritillaria monantha
Galium latoramosum
Garcinia gummi-gutta
Glycosmis macrophylla
Goniothalamus tapis
Guadua angustifolia
Gypsophila perfoliata
Hedychium coronarium
Hertia cheirifolia
Holarrhena floribunda
Hypericum polyanthemum
Jaborosa leucotricha
Juglans mandshurica
Juniperus drupacea
Kiggelaria africana
Lathyrus latifolius
Licaria chrysophylla
Lippia abyssinica
Lophostemon confertus
Lupinus luteus
Magnolia obovata
Mentha × gentilis
Morinda morindoides
Mortonia palmeri
Ononis spinosa
Ononis viscosa
Orbivestus karaguensis
Ormosia hosiei
Ornithoglossum viride
Paragynoxys meridana
Pedicularis rex
Pentaclethra macrophylla
Periploca sepium
Perymenium jelskii
Petasites radiatus
Phenax angustifolius
Pinalia japonica
Pinus edulis
Plectranthus hereroensis
Posidonia oceanica
Potentilla candicans
Prunus mahaleb
Pterocarpus erinaceus
Pterocaulon virgatum
Pyrus bourgaeana
Ratibida mexicana
Rhamnus cathartica
Rhamnus formosana
Rhodiola semenovii
Salvia broussonetii
Salvia sessei
Sandoricum koetjape
Santolina canescens
Schizanthus tricolor
Sedum sarmentosum
Senecio ruwenzoriensis
Senna didymobotrya
Sonneratia caseolaris
Sorbus torminalis
Sphaeranthus confertifolius
Sphaeranthus indicus
Spiraea formosana
Stephania zippeliana
Strychnos elaeocarpa
Strychnos wallichiana
Suaeda maritima
Taraxacum platycarpum
Tinadendron noumeanum
Trichilia havanensis
Tripterospermum lanceolatum
Triunia erythrocarpa
Vachellia leucophloea
Veronica liwanensis
Veronica polita
Viburnum betulifolium
Zingiber mekongense
Zingiber ottensii

Cross-Links

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PubChem 165258
NPASS NPC36002
LOTUS LTS0133156
wikiData Q27136273