Formic acid, 3,7,11-trimethyl-1,6,10-dodecatrien-3-yl ester

Details

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Internal ID f7e99fd7-2455-4324-a45d-427a475e23fc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(6E)-3,7,11-trimethyldodeca-1,6,10-trien-3-yl] formate
SMILES (Canonical) CC(=CCCC(=CCCC(C)(C=C)OC=O)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CCC(C)(C=C)OC=O)/C)C
InChI InChI=1S/C16H26O2/c1-6-16(5,18-13-17)12-8-11-15(4)10-7-9-14(2)3/h6,9,11,13H,1,7-8,10,12H2,2-5H3/b15-11+
InChI Key GJPVEZJRYIBIOD-RVDMUPIBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H26O2
Molecular Weight 250.38 g/mol
Exact Mass 250.193280068 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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NSC72039
7149-36-2
DTXSID00418606
GJPVEZJRYIBIOD-RVDMUPIBSA-N
NSC-72039
(4E)-1,5,9-Trimethyl-1-vinyl-4,8-decadienyl formate #
Formic acid, 3,7,11-trimethyl-1,6,10-dodecatrien-3-yl ester

2D Structure

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2D Structure of Formic acid, 3,7,11-trimethyl-1,6,10-dodecatrien-3-yl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.7238 72.38%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5893 58.93%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9174 91.74%
OATP1B3 inhibitior + 0.8189 81.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6198 61.98%
P-glycoprotein inhibitior - 0.9468 94.68%
P-glycoprotein substrate - 0.9155 91.55%
CYP3A4 substrate + 0.5380 53.80%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8255 82.55%
CYP3A4 inhibition - 0.8538 85.38%
CYP2C9 inhibition - 0.8119 81.19%
CYP2C19 inhibition - 0.6866 68.66%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition - 0.6402 64.02%
CYP2C8 inhibition - 0.8766 87.66%
CYP inhibitory promiscuity - 0.8037 80.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5133 51.33%
Eye corrosion + 0.4692 46.92%
Eye irritation + 0.9318 93.18%
Skin irritation + 0.7601 76.01%
Skin corrosion - 0.9959 99.59%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7599 75.99%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5898 58.98%
skin sensitisation + 0.8331 83.31%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7883 78.83%
Acute Oral Toxicity (c) III 0.8527 85.27%
Estrogen receptor binding - 0.7630 76.30%
Androgen receptor binding - 0.8291 82.91%
Thyroid receptor binding - 0.6542 65.42%
Glucocorticoid receptor binding - 0.5832 58.32%
Aromatase binding - 0.6375 63.75%
PPAR gamma - 0.4853 48.53%
Honey bee toxicity - 0.5657 56.57%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9848 98.48%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.11% 92.08%
CHEMBL2581 P07339 Cathepsin D 90.25% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.69% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.84% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.63% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.66% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.51% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.44% 91.11%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.34% 80.78%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 5363406
NPASS NPC292322