(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol

Details

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Internal ID e6a47586-a0e1-4893-bac9-61524746723c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol
SMILES (Canonical) CC1=CC2C(CCC(C2CC1)(C)O)C(C)C
SMILES (Isomeric) CC1=C[C@H]2[C@@H](CC[C@@](C2CC1)(C)O)C(C)C
InChI InChI=1S/C15H26O/c1-10(2)12-7-8-15(4,16)14-6-5-11(3)9-13(12)14/h9-10,12-14,16H,5-8H2,1-4H3/t12-,13-,14?,15+/m0/s1
InChI Key LHYHMMRYTDARSZ-ZAQQFOKRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.8660 86.60%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4594 45.94%
OATP2B1 inhibitior - 0.8489 84.89%
OATP1B1 inhibitior + 0.9414 94.14%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8915 89.15%
P-glycoprotein inhibitior - 0.9441 94.41%
P-glycoprotein substrate - 0.8538 85.38%
CYP3A4 substrate + 0.5434 54.34%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.8359 83.59%
CYP2C9 inhibition - 0.7000 70.00%
CYP2C19 inhibition - 0.6108 61.08%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition - 0.8334 83.34%
CYP2C8 inhibition - 0.8818 88.18%
CYP inhibitory promiscuity - 0.8326 83.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5844 58.44%
Eye corrosion - 0.9790 97.90%
Eye irritation - 0.6945 69.45%
Skin irritation + 0.6655 66.55%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis - 0.8370 83.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4407 44.07%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5661 56.61%
skin sensitisation + 0.7250 72.50%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7891 78.91%
Acute Oral Toxicity (c) III 0.8519 85.19%
Estrogen receptor binding - 0.8461 84.61%
Androgen receptor binding - 0.5271 52.71%
Thyroid receptor binding - 0.4873 48.73%
Glucocorticoid receptor binding - 0.7209 72.09%
Aromatase binding - 0.8340 83.40%
PPAR gamma - 0.8868 88.68%
Honey bee toxicity - 0.9225 92.25%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9744 97.44%

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 96.96% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.51% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.48% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 88.45% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.27% 100.00%
CHEMBL1871 P10275 Androgen Receptor 85.80% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.65% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 84.94% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.89% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.93% 97.09%
CHEMBL2581 P07339 Cathepsin D 81.45% 98.95%

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.
Achyrospermum africanum
Agastache foeniculum
Agastache rugosa
Ajuga chamaepitys
Angostura trifoliata
Annona cascarilloides
Annona reticulata
Annona squamosa
Aristolochia birostris
Artemisia lagocephala
Austrobaileya scandens
Baccharis dracunculifolia
Bouchardatia neurococca
Brucea javanica
Caesalpinia pulcherrima
Calendula officinalis
Callicarpa americana
Cananga odorata
Chamaecyparis formosensis
Chamaecyparis obtusa
Chromolaena odorata
Chrysopogon zizanioides
Cinnamomum burmanni
Cinnamomum parthenoxylon
Cistus albidus
Cleistopholis patens
Cleome chrysantha
Cleonia lusitanica
Cordia trichotoma
Corymbia citriodora
Cryptomeria japonica
Cymbopogon citratus
Daniellia oliveri
Duguetia confinis
Ekimia bornmuelleri
Entandrophragma cylindricum
Eremanthus arboreus
Erigeron philadelphicus
Ferula flabelliloba
Hedyosmum costaricense
Helichrysum odoratissimum
Humulus lupulus
Hypericum coris
Hyptis suaveolens
Illicium difengpi
Illicium merrillianum
Juniperus comitana
Juniperus communis
Juniperus sabina
Lantana camara
Lavandula stoechas
Lavandula stoechas subsp. luisieri
Leonotis leonurus
Lepechinia chamaedryoides
Lepechinia floribunda
Liatris microcephala
Liquidambar styraciflua
Melissa officinalis
Mentha spicata
Micromeria biflora
Morina persica
Nelumbo lutea
Nepeta trachonitica
Ocimum gratissimum subsp. gratissimum
Origanum vulgare
Pallenis spinosa
Pelargonium endlicherianum
Persea americana
Pimenta dioica
Pimenta racemosa
Pinus pumila
Pinus sylvestris
Piper auritum
Piper cernuum
Piper dactylostigmum
Piper fimbriulatum
Piper gaudichaudianum
Piper guineense
Piper regnellii
Pittosporum viridiflorum
Platostoma africanum
Pongamia pinnata
Prangos uechtritzii
Pseudobrickellia brasiliensis
Pseudotsuga sinensis var. sinensis
Psiadia altissima
Salvia dorisiana
Salvia mirzayanii
Santolina chamaecyparissus
Sassafras albidum
Satureja wiedemanniana
Schinus molle
Senecio adenophyllus
Sideritis lanata
Sideritis lyciae
Solanum tuberosum
Solidago canadensis
Spondias mombin
Stevia rebaudiana
Tagetes lucida
Taiwania cryptomerioides
Tetradenia riparia
Teucrium montanum
Teucrium polium
Teucrium scorodonia
Teucrium stocksianum
Thymus funkii
Thymus riatarum
Thymus willkommii
Thymus zygis
Toona ciliata
Uvaria chamae
Varronia curassavica
Virola surinamensis
Vitex negundo
Xylopia sericea

Cross-Links

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PubChem 5315592
LOTUS LTS0164497
wikiData Q104667224