Norcapillene

Details

Top
Internal ID 5c7f6430-e5af-4404-ae52-81178e1bd54c
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name penta-1,3-diynylbenzene
SMILES (Canonical) CC#CC#CC1=CC=CC=C1
SMILES (Isomeric) CC#CC#CC1=CC=CC=C1
InChI InChI=1S/C11H8/c1-2-3-5-8-11-9-6-4-7-10-11/h4,6-7,9-10H,1H3
InChI Key ACPMYIIORVILBG-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H8
Molecular Weight 140.18 g/mol
Exact Mass 140.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
Norcapillene
4009-22-7
1-Phenyl-1,3-pentadiyne
penta-1,3-diynyl-benzene
(Penta-1,3-diyn-1-yl)benzene
CHEBI:81344
DTXSID00450687
C17796
Q27155282

2D Structure

Top
2D Structure of Norcapillene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.8384 83.84%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.5459 54.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9619 96.19%
OATP1B3 inhibitior + 0.9690 96.90%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8894 88.94%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9798 97.98%
CYP3A4 substrate - 0.7379 73.79%
CYP2C9 substrate - 0.8245 82.45%
CYP2D6 substrate - 0.7578 75.78%
CYP3A4 inhibition - 0.9460 94.60%
CYP2C9 inhibition - 0.8683 86.83%
CYP2C19 inhibition - 0.9451 94.51%
CYP2D6 inhibition - 0.9703 97.03%
CYP1A2 inhibition - 0.6137 61.37%
CYP2C8 inhibition - 0.9108 91.08%
CYP inhibitory promiscuity - 0.7488 74.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5564 55.64%
Carcinogenicity (trinary) Warning 0.4626 46.26%
Eye corrosion + 0.9935 99.35%
Eye irritation + 0.9295 92.95%
Skin irritation + 0.9582 95.82%
Skin corrosion + 0.5294 52.94%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7802 78.02%
Micronuclear - 0.9250 92.50%
Hepatotoxicity + 0.8343 83.43%
skin sensitisation + 0.9399 93.99%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6711 67.11%
Acute Oral Toxicity (c) III 0.8526 85.26%
Estrogen receptor binding - 0.7818 78.18%
Androgen receptor binding - 0.5957 59.57%
Thyroid receptor binding - 0.8173 81.73%
Glucocorticoid receptor binding - 0.7180 71.80%
Aromatase binding - 0.6284 62.84%
PPAR gamma - 0.8388 83.88%
Honey bee toxicity - 0.9665 96.65%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9035 90.35%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 95.51% 96.42%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.77% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 89.69% 90.17%
CHEMBL2581 P07339 Cathepsin D 87.20% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.01% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.99% 86.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 84.72% 94.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.74% 96.09%

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.
Artemisia capillaris
Artemisia dracunculus
Artemisia monosperma

Cross-Links

Top
PubChem 10983572
NPASS NPC74384
LOTUS LTS0032051
wikiData Q27155282