1-Tridecene-3,5,7,9,11-pentayne

Details

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Internal ID ec92df67-82a3-4040-9941-86f949ec1ed6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name tridec-1-en-3,5,7,9,11-pentayne
SMILES (Canonical) CC#CC#CC#CC#CC#CC=C
SMILES (Isomeric) CC#CC#CC#CC#CC#CC=C
InChI InChI=1S/C13H6/c1-3-5-7-9-11-13-12-10-8-6-4-2/h3H,1H2,2H3
InChI Key KKBHBCOJHHCOCL-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C13H6
Molecular Weight 162.19 g/mol
Exact Mass 162.0469501914 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 1.21
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2060-59-5
UNII-0W1JQG9623
Tridec-1-ene-3,5,7,9,11-pentayne
0W1JQG9623
1-Tridecen-3,5,7,9,11-pentayne
PENTAYNEENE
VINYLPENTAACETYLENE
1-Tridecene-3,5,7,9,11-pentyne
CHEBI:9699
DTXSID40174613
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Tridecene-3,5,7,9,11-pentayne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 + 0.5538 55.38%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.5631 56.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9141 91.41%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8778 87.78%
P-glycoprotein inhibitior - 0.9613 96.13%
P-glycoprotein substrate - 0.9821 98.21%
CYP3A4 substrate - 0.6651 66.51%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8202 82.02%
CYP3A4 inhibition - 0.9539 95.39%
CYP2C9 inhibition - 0.8695 86.95%
CYP2C19 inhibition - 0.9067 90.67%
CYP2D6 inhibition - 0.9671 96.71%
CYP1A2 inhibition - 0.7708 77.08%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.7939 79.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7483 74.83%
Carcinogenicity (trinary) Non-required 0.4259 42.59%
Eye corrosion + 0.9806 98.06%
Eye irritation + 0.6807 68.07%
Skin irritation + 0.8712 87.12%
Skin corrosion + 0.7907 79.07%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7639 76.39%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.7553 75.53%
skin sensitisation + 0.8377 83.77%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.7289 72.89%
Acute Oral Toxicity (c) III 0.4906 49.06%
Estrogen receptor binding - 0.8464 84.64%
Androgen receptor binding - 0.7291 72.91%
Thyroid receptor binding - 0.6436 64.36%
Glucocorticoid receptor binding - 0.7331 73.31%
Aromatase binding + 0.5870 58.70%
PPAR gamma - 0.5793 57.93%
Honey bee toxicity - 0.7388 73.88%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8820 88.20%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 86.65% 96.42%
CHEMBL1951 P21397 Monoamine oxidase A 83.17% 91.49%

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.
Abrus precatorius
Acourtia thurberi
Acritopappus heterolepis
Agrianthus pungens
Arctium lappa
Blumea lacera
Brachylaena discolor var. transvaalensis
Buphthalmum salicifolium
Carthamus tinctorius
Caucasalia pontica
Centaurea benedicta
Centaurea cineraria subsp. cineraria
Centaurea nervosa
Cirsium helenioides
Cirsium japonicum
Cladrastis kentukea
Conocliniopsis prasiifolia
Coreopsis nuecensis
Dimerostemma asperatum
Dimorphotheca tragus
Doronicum hungaricum
Echinacea angustifolia
Flourensia heterolepis
Garcinia multiflora
Geigeria brevifolia
Gnaphalium declinatum
Gymnanthemum myrianthum
Haplocarpha lyrata
Helianthella uniflora
Helichrysum chionosphaerum
Helichrysum fulvum
Ichthyothere connata
Isodon henryi
Iva annua
Lepidaploa chalybaea
Libanothamnus spectabilis
Ligularia thyrsoidea
Lychnophora crispa
Lychnophora salicifolia
Madia sativa
Mattfeldanthus andrade-limae
Morithamnus crassus
Onoseris albicans
Onoseris lopezii
Osteospermum auriculatum
Paralychnophora bicolor
Perymenium featherstonei
Perymenium jelskii
Phlomoides rotata
Piptolepis ericoides
Planaltoa lychnophoroides
Plecostachys serpyllifolia
Pleiotaxis rugosa
Polymnia canadensis
Proteopsis argentea
Pterocaulon rugosum
Ricinus communis
Rudbeckia hirta
Scapania nemorea
Senecio oxyodontus
Smallanthus fruticosus
Smallanthus uvedalia
Symphyopappus reticulatus
Telekia speciosa
Triticum aestivum
Trixis inula
Verbesina luetzelburgii
Vernonia marginata
Wunderlichia mirabilis
Xanthium spinosum subsp. spinosum
Zinnia acerosa
Zinnia peruviana

Cross-Links

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PubChem 441552
NPASS NPC21806
LOTUS LTS0085389
wikiData Q27108474