Linearolide A

Details

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Internal ID f4d1b2c0-8bce-493b-8acf-dcd2b7c890cd
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (9E,11E,15Z)-1,19-dihydroxy-5-[(1E,3E)-6-hydroxy-3,5-dimethylhepta-1,3-dienyl]-6,16,20-trimethoxy-2,10,14-trimethyl-4,21-dioxabicyclo[15.3.1]henicosa-9,11,15-trien-3-one
SMILES (Canonical) CC1CC=CC(=CCCC(C(OC(=O)C(C2(C(C(CC(O2)C(=C1)OC)O)OC)O)C)C=CC(=CC(C)C(C)O)C)OC)C
SMILES (Isomeric) CC\1C/C=C/C(=C/CCC(C(OC(=O)C(C2(C(C(CC(O2)/C(=C1)/OC)O)OC)O)C)/C=C/C(=C/C(C)C(C)O)/C)OC)/C
InChI InChI=1S/C34H54O9/c1-21-12-10-14-22(2)19-30(40-8)31-20-27(36)32(41-9)34(38,43-31)25(5)33(37)42-29(28(39-7)15-11-13-21)17-16-23(3)18-24(4)26(6)35/h10,12-13,16-19,22,24-29,31-32,35-36,38H,11,14-15,20H2,1-9H3/b12-10+,17-16+,21-13+,23-18+,30-19-
InChI Key AJKVFABIUCMHIE-WGZNCOSKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C34H54O9
Molecular Weight 606.80 g/mol
Exact Mass 606.37678330 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Linearolide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5949 59.49%
Caco-2 - 0.7831 78.31%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5738 57.38%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8591 85.91%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9311 93.11%
P-glycoprotein inhibitior + 0.7997 79.97%
P-glycoprotein substrate + 0.7016 70.16%
CYP3A4 substrate + 0.7241 72.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8860 88.60%
CYP3A4 inhibition - 0.8413 84.13%
CYP2C9 inhibition - 0.9257 92.57%
CYP2C19 inhibition - 0.8650 86.50%
CYP2D6 inhibition - 0.9184 91.84%
CYP1A2 inhibition - 0.8771 87.71%
CYP2C8 inhibition + 0.6523 65.23%
CYP inhibitory promiscuity - 0.9508 95.08%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5862 58.62%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.9350 93.50%
Skin irritation - 0.5396 53.96%
Skin corrosion - 0.9151 91.51%
Ames mutagenesis - 0.6208 62.08%
Human Ether-a-go-go-Related Gene inhibition + 0.6658 66.58%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5283 52.83%
skin sensitisation - 0.8196 81.96%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6413 64.13%
Acute Oral Toxicity (c) III 0.5045 50.45%
Estrogen receptor binding + 0.7136 71.36%
Androgen receptor binding + 0.6645 66.45%
Thyroid receptor binding + 0.5609 56.09%
Glucocorticoid receptor binding + 0.7526 75.26%
Aromatase binding + 0.5889 58.89%
PPAR gamma + 0.6308 63.08%
Honey bee toxicity - 0.6798 67.98%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.92% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.62% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.69% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 93.34% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.87% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.71% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 92.31% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.09% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.96% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.80% 97.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.50% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.88% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.39% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.36% 89.00%
CHEMBL2996 Q05655 Protein kinase C delta 87.21% 97.79%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.68% 95.58%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.86% 90.08%
CHEMBL1902 P62942 FK506-binding protein 1A 84.37% 97.05%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.53% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.04% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.80% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 82.65% 91.19%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.41% 93.03%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.87% 99.18%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.69% 96.47%
CHEMBL325 Q13547 Histone deacetylase 1 80.35% 95.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.20% 94.00%

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.
There are no matching plants.

Cross-Links

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PubChem 139585856
LOTUS LTS0104607
wikiData Q77493419