5-Chloro-5,6-dihydro-2-(2,4,6-octatriynylidene)-2H-pyran

Details

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Internal ID 8f588fed-8f88-4271-8d0a-debac6b9755d
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name (6E)-3-chloro-6-octa-2,4,6-triynylidene-2,3-dihydropyran
SMILES (Canonical) CC#CC#CC#CC=C1C=CC(CO1)Cl
SMILES (Isomeric) CC#CC#CC#C/C=C/1\C=CC(CO1)Cl
InChI InChI=1S/C13H9ClO/c1-2-3-4-5-6-7-8-13-10-9-12(14)11-15-13/h8-10,12H,11H2,1H3/b13-8+
InChI Key KSDSGWWDSHLQBZ-MDWZMJQESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H9ClO
Molecular Weight 216.66 g/mol
Exact Mass 216.0341926 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Chloro-5,6-dihydro-2-(2,4,6-octatriynylidene)-2H-pyran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.5237 52.37%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5967 59.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9049 90.49%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8354 83.54%
P-glycoprotein inhibitior - 0.9574 95.74%
P-glycoprotein substrate - 0.8443 84.43%
CYP3A4 substrate - 0.5130 51.30%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8238 82.38%
CYP3A4 inhibition - 0.8851 88.51%
CYP2C9 inhibition - 0.6570 65.70%
CYP2C19 inhibition + 0.7035 70.35%
CYP2D6 inhibition - 0.9169 91.69%
CYP1A2 inhibition + 0.6594 65.94%
CYP2C8 inhibition - 0.9073 90.73%
CYP inhibitory promiscuity + 0.5644 56.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6570 65.70%
Carcinogenicity (trinary) Non-required 0.5593 55.93%
Eye corrosion + 0.5598 55.98%
Eye irritation - 0.8869 88.69%
Skin irritation + 0.6468 64.68%
Skin corrosion - 0.5065 50.65%
Ames mutagenesis + 0.5746 57.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6233 62.33%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5428 54.28%
skin sensitisation - 0.5475 54.75%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6654 66.54%
Acute Oral Toxicity (c) III 0.4554 45.54%
Estrogen receptor binding - 0.6847 68.47%
Androgen receptor binding - 0.5831 58.31%
Thyroid receptor binding - 0.5818 58.18%
Glucocorticoid receptor binding - 0.5369 53.69%
Aromatase binding - 0.4829 48.29%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.6089 60.89%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.6496 64.96%

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 88.89% 91.11%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 87.37% 96.42%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.65% 94.80%
CHEMBL3401 O75469 Pregnane X receptor 82.97% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.84% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.05% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.71% 96.09%

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.
Anaphalis margaritacea
Chlorophytum malayense

Cross-Links

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PubChem 5315840
NPASS NPC71915