(3R,6R)-6-ethenyl-2,2,6-trimethyloxan-3-ol

Details

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Internal ID 3ad2302a-d5a0-4cb4-accb-7c1bce55ab40
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name (3R,6R)-6-ethenyl-2,2,6-trimethyloxan-3-ol
SMILES (Canonical) CC1(C(CCC(O1)(C)C=C)O)C
SMILES (Isomeric) C[C@@]1(CC[C@H](C(O1)(C)C)O)C=C
InChI InChI=1S/C10H18O2/c1-5-10(4)7-6-8(11)9(2,3)12-10/h5,8,11H,1,6-7H2,2-4H3/t8-,10+/m1/s1
InChI Key BCTBAGTXFYWYMW-SCZZXKLOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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UNII-N1ME467AVA
N1ME467AVA
cis-linalol pyranoxide
cis-Linalool 3,7-oxide
24048-52-0
Linalool oxide pyranoid, cis-(+-)-
FEMA No. 4593, cis-(+-)-
(+)-cis-Linalool 3,7-oxide
(3R,6R)-6-ethenyl-2,2,6-trimethyloxan-3-ol
2H-Pyran-3-ol, 6-ethenyltetrahydro-2,2,6-trimethyl-, (3R,6R)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (3R,6R)-6-ethenyl-2,2,6-trimethyloxan-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 + 0.7583 75.83%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5703 57.03%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9477 94.77%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9517 95.17%
P-glycoprotein inhibitior - 0.9774 97.74%
P-glycoprotein substrate - 0.9614 96.14%
CYP3A4 substrate + 0.5192 51.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7078 70.78%
CYP3A4 inhibition - 0.7449 74.49%
CYP2C9 inhibition - 0.9073 90.73%
CYP2C19 inhibition - 0.8361 83.61%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.7977 79.77%
CYP2C8 inhibition - 0.8974 89.74%
CYP inhibitory promiscuity - 0.9659 96.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8628 86.28%
Carcinogenicity (trinary) Non-required 0.6494 64.94%
Eye corrosion - 0.9249 92.49%
Eye irritation + 0.7140 71.40%
Skin irritation + 0.5898 58.98%
Skin corrosion - 0.7755 77.55%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6575 65.75%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5124 51.24%
skin sensitisation + 0.7232 72.32%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5594 55.94%
Acute Oral Toxicity (c) III 0.8445 84.45%
Estrogen receptor binding - 0.8068 80.68%
Androgen receptor binding - 0.8942 89.42%
Thyroid receptor binding - 0.7556 75.56%
Glucocorticoid receptor binding - 0.5872 58.72%
Aromatase binding - 0.8615 86.15%
PPAR gamma - 0.7999 79.99%
Honey bee toxicity - 0.8237 82.37%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.4934 49.34%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.28% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.02% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.32% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.21% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.54% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.60% 95.89%

Cross-Links

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PubChem 6428574
NPASS NPC198031
LOTUS LTS0266946
wikiData Q27284396