1-Methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol

Details

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Internal ID 4950d23a-8877-49cc-9a76-b43b83f26980
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 1-methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-1-ol
SMILES (Canonical) CC1(CCC2C1CCCCC2=C)O
SMILES (Isomeric) CC1(CCC2C1CCCCC2=C)O
InChI InChI=1S/C12H20O/c1-9-5-3-4-6-11-10(9)7-8-12(11,2)13/h10-11,13H,1,3-8H2,2H3
InChI Key ZBACDSGBJUIJGT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O
Molecular Weight 180.29 g/mol
Exact Mass 180.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.89
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 1-Methyl-4-methylidene-2,3,3a,5,6,7,8,8a-octahydroazulen-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 + 0.9952 99.52%
Caco-2 + 0.7577 75.77%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.7352 73.52%
OATP2B1 inhibitior - 0.8369 83.69%
OATP1B1 inhibitior + 0.8758 87.58%
OATP1B3 inhibitior + 0.9164 91.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9245 92.45%
P-glycoprotein inhibitior - 0.9676 96.76%
P-glycoprotein substrate - 0.9342 93.42%
CYP3A4 substrate + 0.5320 53.20%
CYP2C9 substrate - 0.7433 74.33%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9120 91.20%
CYP2C9 inhibition - 0.7146 71.46%
CYP2C19 inhibition - 0.6086 60.86%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.5515 55.15%
CYP2C8 inhibition - 0.7201 72.01%
CYP inhibitory promiscuity - 0.9091 90.91%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5125 51.25%
Eye corrosion - 0.9537 95.37%
Eye irritation + 0.9521 95.21%
Skin irritation + 0.6415 64.15%
Skin corrosion - 0.9208 92.08%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5406 54.06%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5935 59.35%
skin sensitisation + 0.5869 58.69%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6344 63.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6354 63.54%
Acute Oral Toxicity (c) III 0.7278 72.78%
Estrogen receptor binding - 0.8637 86.37%
Androgen receptor binding - 0.6077 60.77%
Thyroid receptor binding - 0.8620 86.20%
Glucocorticoid receptor binding - 0.6446 64.46%
Aromatase binding - 0.7703 77.03%
PPAR gamma - 0.8445 84.45%
Honey bee toxicity - 0.9500 95.00%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9450 94.50%

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 97.58% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.10% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.29% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.14% 96.09%
CHEMBL206 P03372 Estrogen receptor alpha 86.09% 97.64%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.08% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.70% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.80% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 84.59% 95.38%
CHEMBL226 P30542 Adenosine A1 receptor 83.45% 95.93%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.52% 95.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.87% 93.04%
CHEMBL237 P41145 Kappa opioid receptor 80.40% 98.10%

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.
Dictamnus dasycarpus

Cross-Links

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PubChem 163023922
LOTUS LTS0213559
wikiData Q105370418