(3E,4S,5S)-3-dodec-11-ynylidene-4-hydroxy-5-methyloxolan-2-one

Details

Top
Internal ID 22fbd414-0884-434b-aa27-61adda060237
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3E,4S,5S)-3-dodec-11-ynylidene-4-hydroxy-5-methyloxolan-2-one
SMILES (Canonical) CC1C(C(=CCCCCCCCCCC#C)C(=O)O1)O
SMILES (Isomeric) C[C@H]1[C@H](/C(=C\CCCCCCCCCC#C)/C(=O)O1)O
InChI InChI=1S/C17H26O3/c1-3-4-5-6-7-8-9-10-11-12-13-15-16(18)14(2)20-17(15)19/h1,13-14,16,18H,4-12H2,2H3/b15-13+/t14-,16+/m0/s1
InChI Key ZOHSBTYPSYCTIC-WPDDIUJQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C17H26O3
Molecular Weight 278.40 g/mol
Exact Mass 278.18819469 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.36
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3E,4S,5S)-3-dodec-11-ynylidene-4-hydroxy-5-methyloxolan-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9626 96.26%
Caco-2 + 0.6099 60.99%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7564 75.64%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8695 86.95%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.6916 69.16%
P-glycoprotein inhibitior - 0.8758 87.58%
P-glycoprotein substrate - 0.9030 90.30%
CYP3A4 substrate - 0.5057 50.57%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8704 87.04%
CYP3A4 inhibition - 0.8617 86.17%
CYP2C9 inhibition - 0.7860 78.60%
CYP2C19 inhibition - 0.6803 68.03%
CYP2D6 inhibition - 0.9285 92.85%
CYP1A2 inhibition - 0.6130 61.30%
CYP2C8 inhibition - 0.9006 90.06%
CYP inhibitory promiscuity - 0.6399 63.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.4893 48.93%
Eye corrosion - 0.7873 78.73%
Eye irritation - 0.8330 83.30%
Skin irritation - 0.5380 53.80%
Skin corrosion - 0.8664 86.64%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4092 40.92%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5179 51.79%
skin sensitisation - 0.7358 73.58%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5731 57.31%
Acute Oral Toxicity (c) III 0.5804 58.04%
Estrogen receptor binding + 0.5502 55.02%
Androgen receptor binding - 0.7746 77.46%
Thyroid receptor binding + 0.5266 52.66%
Glucocorticoid receptor binding + 0.6063 60.63%
Aromatase binding - 0.5754 57.54%
PPAR gamma - 0.5187 51.87%
Honey bee toxicity - 0.9388 93.88%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5724 57.24%
Fish aquatic toxicity + 0.9040 90.40%

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
CHEMBL2581 P07339 Cathepsin D 93.94% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 91.82% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.98% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 90.90% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.45% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.67% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.61% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.89% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.97% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 84.02% 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.
Cinnamomum kotoense
Lindera communis
Machilus wangchiana

Cross-Links

Top
PubChem 11778320
NPASS NPC150502
LOTUS LTS0121757
wikiData Q105380486