Myristoleic acid

Details

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Internal ID 777bb684-81a5-46f2-a15b-eb3ef9c50bbf
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (Z)-tetradec-9-enoic acid
SMILES (Canonical) CCCCC=CCCCCCCCC(=O)O
SMILES (Isomeric) CCCC/C=C\CCCCCCCC(=O)O
InChI InChI=1S/C14H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h5-6H,2-4,7-13H2,1H3,(H,15,16)/b6-5-
InChI Key YWWVWXASSLXJHU-WAYWQWQTSA-N
Popularity 540 references in papers

Physical and Chemical Properties

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Molecular Formula C14H26O2
Molecular Weight 226.35 g/mol
Exact Mass 226.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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544-64-9
(Z)-Tetradec-9-enoic acid
cis-9-tetradecenoic acid
9Z-tetradecenoic acid
9-Tetradecenoic acid, (9Z)-
9-Tetradecenoic acid
(9Z)-tetradec-9-enoic acid
(Z)-9-Tetradecenoicacid
9-Tetradecenoic acid, (Z)-
cis-Delta(9)-tetradecenoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Myristoleic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.8124 81.24%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.6181 61.81%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior - 0.3186 31.86%
OATP1B3 inhibitior - 0.4408 44.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6449 64.49%
P-glycoprotein inhibitior - 0.9662 96.62%
P-glycoprotein substrate - 0.9637 96.37%
CYP3A4 substrate - 0.6935 69.35%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9386 93.86%
CYP2C9 inhibition - 0.8711 87.11%
CYP2C19 inhibition - 0.9373 93.73%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition + 0.8857 88.57%
CYP2C8 inhibition - 0.9454 94.54%
CYP inhibitory promiscuity - 0.9365 93.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6635 66.35%
Carcinogenicity (trinary) Non-required 0.7143 71.43%
Eye corrosion + 0.9709 97.09%
Eye irritation + 0.9637 96.37%
Skin irritation + 0.8485 84.85%
Skin corrosion + 0.7149 71.49%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4542 45.42%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.8470 84.70%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7915 79.15%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6657 66.57%
Acute Oral Toxicity (c) IV 0.7278 72.78%
Estrogen receptor binding - 0.7752 77.52%
Androgen receptor binding - 0.8405 84.05%
Thyroid receptor binding + 0.5192 51.92%
Glucocorticoid receptor binding - 0.6565 65.65%
Aromatase binding - 0.8325 83.25%
PPAR gamma + 0.7496 74.96%
Honey bee toxicity - 0.9958 99.58%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.9575 95.75%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.59% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.90% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.07% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 92.74% 97.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.70% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 88.58% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 85.40% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.37% 96.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.34% 93.56%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.31% 96.00%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 80.82% 92.26%

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.
Cassia fistula
Citrullus colocynthis
Diplotaxis harra
Gladiolus italicus
Gossypium hirsutum
Hoya longifolia
Lactuca saligna
Persicaria minor
Salvia fruticosa
Senna didymobotrya
Trifolium pratense
Ziziphus jujuba

Cross-Links

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PubChem 5281119
NPASS NPC281245
LOTUS LTS0078418
wikiData Q58221