(3R)-1-chloro-3-phenylhex-5-en-3-ol

Details

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Internal ID 7bae61de-d742-4ad3-bc0f-e05f907fcee1
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name (3R)-1-chloro-3-phenylhex-5-en-3-ol
SMILES (Canonical) C=CCC(CCCl)(C1=CC=CC=C1)O
SMILES (Isomeric) C=CC[C@@](CCCl)(C1=CC=CC=C1)O
InChI InChI=1S/C12H15ClO/c1-2-8-12(14,9-10-13)11-6-4-3-5-7-11/h2-7,14H,1,8-10H2/t12-/m1/s1
InChI Key UCJCMQUVFCYCEH-GFCCVEGCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H15ClO
Molecular Weight 210.70 g/mol
Exact Mass 210.0811428 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R)-1-chloro-3-phenylhex-5-en-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 + 0.9938 99.38%
Caco-2 + 0.9301 93.01%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7356 73.56%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.8899 88.99%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8717 87.17%
P-glycoprotein inhibitior - 0.9724 97.24%
P-glycoprotein substrate - 0.9720 97.20%
CYP3A4 substrate - 0.6535 65.35%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.6699 66.99%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.6494 64.94%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8491 84.91%
CYP1A2 inhibition + 0.5118 51.18%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.7744 77.44%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6540 65.40%
Carcinogenicity (trinary) Non-required 0.6251 62.51%
Eye corrosion - 0.6099 60.99%
Eye irritation + 0.9781 97.81%
Skin irritation + 0.6568 65.68%
Skin corrosion - 0.5599 55.99%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7762 77.62%
Micronuclear - 0.9741 97.41%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.7399 73.99%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.5662 56.62%
Acute Oral Toxicity (c) III 0.7718 77.18%
Estrogen receptor binding - 0.5687 56.87%
Androgen receptor binding - 0.8316 83.16%
Thyroid receptor binding - 0.5792 57.92%
Glucocorticoid receptor binding - 0.6719 67.19%
Aromatase binding - 0.7438 74.38%
PPAR gamma + 0.6780 67.80%
Honey bee toxicity - 0.8785 87.85%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8464 84.64%

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 94.27% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.60% 94.62%
CHEMBL2581 P07339 Cathepsin D 86.37% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.46% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.04% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.76% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.27% 96.09%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.41% 93.81%

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.
Schisandra bicolor

Cross-Links

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PubChem 101354187
LOTUS LTS0180842
wikiData Q105269941