(1R,8aS)-1,4-dimethyl-7-propan-2-ylidene-2,3,5,6,8,8a-hexahydroazulen-1-ol

Details

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Internal ID 68531733-8803-41f9-8a99-6d336ba5f743
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,8aS)-1,4-dimethyl-7-propan-2-ylidene-2,3,5,6,8,8a-hexahydroazulen-1-ol
SMILES (Canonical) CC1=C2CCC(C2CC(=C(C)C)CC1)(C)O
SMILES (Isomeric) CC1=C2CC[C@@]([C@H]2CC(=C(C)C)CC1)(C)O
InChI InChI=1S/C15H24O/c1-10(2)12-6-5-11(3)13-7-8-15(4,16)14(13)9-12/h14,16H,5-9H2,1-4H3/t14-,15+/m0/s1
InChI Key ZVIMQWMKXPGGTC-LSDHHAIUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,8aS)-1,4-dimethyl-7-propan-2-ylidene-2,3,5,6,8,8a-hexahydroazulen-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 + 0.9958 99.58%
Caco-2 + 0.8730 87.30%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5558 55.58%
OATP2B1 inhibitior - 0.8417 84.17%
OATP1B1 inhibitior + 0.9127 91.27%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8077 80.77%
P-glycoprotein inhibitior - 0.8905 89.05%
P-glycoprotein substrate - 0.8780 87.80%
CYP3A4 substrate + 0.5370 53.70%
CYP2C9 substrate - 0.7433 74.33%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9330 93.30%
CYP2C9 inhibition - 0.6586 65.86%
CYP2C19 inhibition - 0.6796 67.96%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition - 0.6614 66.14%
CYP2C8 inhibition - 0.9488 94.88%
CYP inhibitory promiscuity - 0.8694 86.94%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5615 56.15%
Eye corrosion - 0.9677 96.77%
Eye irritation + 0.9549 95.49%
Skin irritation + 0.7019 70.19%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.8137 81.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3715 37.15%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6217 62.17%
skin sensitisation + 0.5784 57.84%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6027 60.27%
Acute Oral Toxicity (c) III 0.7692 76.92%
Estrogen receptor binding - 0.8335 83.35%
Androgen receptor binding - 0.5794 57.94%
Thyroid receptor binding - 0.6566 65.66%
Glucocorticoid receptor binding - 0.7723 77.23%
Aromatase binding - 0.7859 78.59%
PPAR gamma - 0.7424 74.24%
Honey bee toxicity - 0.8984 89.84%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9354 93.54%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.39% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.29% 91.11%
CHEMBL2581 P07339 Cathepsin D 83.42% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.19% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.52% 100.00%

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.
Asarum caulescens

Cross-Links

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PubChem 163012438
LOTUS LTS0001141
wikiData Q105384321