1-Chlorotrideca-3,11-dien-5,7,9-triyn-2-ol

Details

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Internal ID 9d08b0c7-7a0d-476b-9698-7de48c9c07b1
Taxonomy Organohalogen compounds > Halohydrins > Chlorohydrins
IUPAC Name 1-chlorotrideca-3,11-dien-5,7,9-triyn-2-ol
SMILES (Canonical) CC=CC#CC#CC#CC=CC(CCl)O
SMILES (Isomeric) CC=CC#CC#CC#CC=CC(CCl)O
InChI InChI=1S/C13H11ClO/c1-2-3-4-5-6-7-8-9-10-11-13(15)12-14/h2-3,10-11,13,15H,12H2,1H3
InChI Key BWFFGWCCMCLGBQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H11ClO
Molecular Weight 218.68 g/mol
Exact Mass 218.0498427 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Chlorotrideca-3,11-dien-5,7,9-triyn-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.8499 84.99%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5978 59.78%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.8309 83.09%
OATP1B3 inhibitior + 0.9529 95.29%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8652 86.52%
P-glycoprotein inhibitior - 0.9449 94.49%
P-glycoprotein substrate - 0.9328 93.28%
CYP3A4 substrate - 0.5757 57.57%
CYP2C9 substrate - 0.7861 78.61%
CYP2D6 substrate - 0.8012 80.12%
CYP3A4 inhibition - 0.8523 85.23%
CYP2C9 inhibition - 0.8417 84.17%
CYP2C19 inhibition - 0.6153 61.53%
CYP2D6 inhibition - 0.9360 93.60%
CYP1A2 inhibition - 0.5307 53.07%
CYP2C8 inhibition - 0.9319 93.19%
CYP inhibitory promiscuity - 0.8369 83.69%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) + 0.6450 64.50%
Carcinogenicity (trinary) Non-required 0.5909 59.09%
Eye corrosion + 0.7164 71.64%
Eye irritation - 0.8298 82.98%
Skin irritation + 0.8146 81.46%
Skin corrosion + 0.9793 97.93%
Ames mutagenesis + 0.6863 68.63%
Human Ether-a-go-go-Related Gene inhibition - 0.6497 64.97%
Micronuclear - 0.9341 93.41%
Hepatotoxicity + 0.5402 54.02%
skin sensitisation - 0.6114 61.14%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.6560 65.60%
Acute Oral Toxicity (c) II 0.7087 70.87%
Estrogen receptor binding - 0.5201 52.01%
Androgen receptor binding - 0.8671 86.71%
Thyroid receptor binding - 0.5417 54.17%
Glucocorticoid receptor binding - 0.6018 60.18%
Aromatase binding - 0.5227 52.27%
PPAR gamma - 0.6618 66.18%
Honey bee toxicity - 0.7505 75.05%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.7877 78.77%

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 89.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.66% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.29% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.23% 91.11%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.36% 90.24%
CHEMBL3401 O75469 Pregnane X receptor 80.21% 94.73%

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.
Carthamus tinctorius

Cross-Links

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PubChem 85927507
LOTUS LTS0259520
wikiData Q104947194