4-Isopropylbenzyl alcohol

Details

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Internal ID 45dc4fb7-c142-416e-9a10-1268b470f83a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (4-propan-2-ylphenyl)methanol
SMILES (Canonical) CC(C)C1=CC=C(C=C1)CO
SMILES (Isomeric) CC(C)C1=CC=C(C=C1)CO
InChI InChI=1S/C10H14O/c1-8(2)10-5-3-9(7-11)4-6-10/h3-6,8,11H,7H2,1-2H3
InChI Key OIGWAXDAPKFNCQ-UHFFFAOYSA-N
Popularity 152 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Cumic alcohol
536-60-7
Cuminol
cuminyl alcohol
(4-Isopropylphenyl)methanol
cuminic alcohol
Cumyl alcohol
p-Cymen-7-ol
CUMIN ALCOHOL
p-Isopropylbenzyl alcohol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Isopropylbenzyl alcohol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.9292 92.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5088 50.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9172 91.72%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9105 91.05%
P-glycoprotein inhibitior - 0.9721 97.21%
P-glycoprotein substrate - 0.9345 93.45%
CYP3A4 substrate - 0.7906 79.06%
CYP2C9 substrate - 0.7802 78.02%
CYP2D6 substrate - 0.7144 71.44%
CYP3A4 inhibition - 0.9152 91.52%
CYP2C9 inhibition - 0.9228 92.28%
CYP2C19 inhibition - 0.8646 86.46%
CYP2D6 inhibition - 0.9444 94.44%
CYP1A2 inhibition - 0.5586 55.86%
CYP2C8 inhibition - 0.9890 98.90%
CYP inhibitory promiscuity - 0.8860 88.60%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5617 56.17%
Carcinogenicity (trinary) Non-required 0.7358 73.58%
Eye corrosion + 0.9010 90.10%
Eye irritation + 0.9629 96.29%
Skin irritation + 0.8134 81.34%
Skin corrosion - 0.7688 76.88%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6928 69.28%
Micronuclear - 0.8741 87.41%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.7897 78.97%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.8208 82.08%
Acute Oral Toxicity (c) III 0.8710 87.10%
Estrogen receptor binding - 0.8962 89.62%
Androgen receptor binding - 0.6232 62.32%
Thyroid receptor binding - 0.8431 84.31%
Glucocorticoid receptor binding - 0.8827 88.27%
Aromatase binding - 0.6310 63.10%
PPAR gamma - 0.8894 88.94%
Honey bee toxicity - 0.9436 94.36%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.5727 57.27%
Fish aquatic toxicity - 0.3675 36.75%

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
CHEMBL2581 P07339 Cathepsin D 95.22% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 92.07% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.19% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.75% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.51% 91.11%
CHEMBL4208 P20618 Proteasome component C5 84.11% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 82.34% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.97% 97.25%

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.
Achillea abrotanoides
Achillea grandifolia
Agastache rugosa
Aizoon africanum
Alangium premnifolium
Angelica acutiloba
Angelica archangelica
Angelica gigas
Angelica sinensis
Angelica taiwaniana
Angelica tarokoensis
Aristolochia kaempferi
Artemisia judaica
Artemisia salsoloides
Asarum canadense
Bellium bellidioides
Bombax ceiba
Caesulia axillaris
Centaurea calcitrapa
Centromadia fitchii
Chrysanthemum indicum
Coespeletia timotensis
Conioselinum anthriscoides
Cuminum cyminum
Cynara humilis
Daucus carota
Delphinium hohenackeri
Diospyros ferrea
Elegia deusta
Elettaria cardamomum
Elwendia persica
Ephedra sinica
Epimedium davidii
Erica glauca
Erysimum odoratum
Eucalyptus camaldulensis
Frullania tamarisci
Garcinia intermedia
Globba variabilis
Gossypium hirsutum
Helianthus annuus
Heterotheca inuloides
Ilex amara
Illicium difengpi
Isodon japonicus
Jacobaea vulgaris
Kielmeyera coriacea
Kitagawia praeruptora
Knightia excelsa
Lasiosiphon lampranthus
Lavandula latifolia
Lavandula stoechas
Leonurus glaucescens
Lepidium draba
Leucas neufliseana
Ligusticum officinale
Ligusticum striatum
Lithospermum officinale
Litsea glutinosa
Magnolia liliiflora
Micromeria pineolens
Myristica fragrans
Nepeta racemosa
Oncosiphon suffruticosus
Origanum hypericifolium
Origanum minutiflorum
Origanum sipyleum
Peumus boldus
Picea abies
Pinellia ternata
Platonia insignis
Plectranthus parishii
Polygala senega
Quercus petraea subsp. petraea
Rhodiola crenulata
Rhodiola rosea
Salacia madagascariensis
Salvia munzii
Sarcococca coriacea
Saussurea lyrata
Sideritis lasiantha
Solanum acaule
Solanum villosum
Sophora koreensis
Swertia delavayi
Synotis cappa
Tabebuia heterophylla
Teucrium polium
Thuja occidentalis
Thymus camphoratus
Thymus longicaulis
Trachelospermum lucidum
Ulmus americana
Vaccinium vitis-idaea
Vepris hiernii
Vismia jefensis
Vitis vinifera
Wikstroemia chamaedaphne
Wollastonia dentata
Wurfbainia neoaurantiaca
Xylopia aromatica
Zanthoxylum armatum
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zea mays

Cross-Links

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PubChem 325
NPASS NPC93843
LOTUS LTS0021403
wikiData Q1143803