2-Nonen-4-yne, (Z)-

Details

Top
Internal ID bb09aa19-917b-4f95-9847-173f5d8ab99c
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (Z)-non-2-en-4-yne
SMILES (Canonical) CCCCC#CC=CC
SMILES (Isomeric) CCCCC#C/C=C\C
InChI InChI=1S/C9H14/c1-3-5-7-9-8-6-4-2/h3,5H,4,6,8H2,1-2H3/b5-3-
InChI Key VSLJPTWFNWRVBG-HYXAFXHYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C9H14
Molecular Weight 122.21 g/mol
Exact Mass 122.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
(Z)-non-2-en-4-yne
(Z)-2-Nonen-4-yne
(2Z)-2-Nonen-4-yne
(2Z)-2-Nonen-4-yne #
VSLJPTWFNWRVBG-HYXAFXHYSA-N
56392-46-2

2D Structure

Top
2D Structure of 2-Nonen-4-yne, (Z)-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.9459 94.59%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4381 43.81%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.8491 84.91%
OATP1B3 inhibitior + 0.9378 93.78%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9131 91.31%
P-glycoprotein inhibitior - 0.9859 98.59%
P-glycoprotein substrate - 0.8990 89.90%
CYP3A4 substrate - 0.6470 64.70%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9672 96.72%
CYP2C9 inhibition - 0.8984 89.84%
CYP2C19 inhibition - 0.9007 90.07%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.5637 56.37%
CYP2C8 inhibition - 0.8977 89.77%
CYP inhibitory promiscuity - 0.6239 62.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5337 53.37%
Eye corrosion + 0.9372 93.72%
Eye irritation + 0.9419 94.19%
Skin irritation + 0.8374 83.74%
Skin corrosion - 0.9057 90.57%
Ames mutagenesis - 0.8237 82.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5950 59.50%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6338 63.38%
skin sensitisation + 0.9488 94.88%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6952 69.52%
Acute Oral Toxicity (c) III 0.6182 61.82%
Estrogen receptor binding - 0.7983 79.83%
Androgen receptor binding - 0.8277 82.77%
Thyroid receptor binding - 0.7094 70.94%
Glucocorticoid receptor binding - 0.7742 77.42%
Aromatase binding - 0.8413 84.13%
PPAR gamma - 0.7751 77.51%
Honey bee toxicity - 0.9336 93.36%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9444 94.44%

Targets

Top

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
CHEMBL221 P23219 Cyclooxygenase-1 90.00% 90.17%
CHEMBL2581 P07339 Cathepsin D 89.54% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.26% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.08% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.40% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.51% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 84.44% 96.42%
CHEMBL2996 Q05655 Protein kinase C delta 83.35% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 83.11% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.02% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 82.43% 89.63%

Plants that contains it

Top
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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

Top
PubChem 5367386
NPASS NPC158993
LOTUS LTS0036596
wikiData Q105292295