Isolinderanolide B

Details

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Internal ID f5d21db0-c0e6-4383-9d72-c5b23e6e6f6e
Taxonomy Organoheterocyclic compounds > Oxolanes
IUPAC Name (3Z,4R)-4-hydroxy-5-methylidene-3-tetradecylideneoxolan-2-one
SMILES (Canonical) CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O
SMILES (Isomeric) CCCCCCCCCCCCC/C=C\1/[C@H](C(=C)OC1=O)O
InChI InChI=1S/C19H32O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-17-18(20)16(2)22-19(17)21/h15,18,20H,2-14H2,1H3/b17-15-/t18-/m0/s1
InChI Key FCLYKYQBTSMTJB-SOBQPUOHSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O3
Molecular Weight 308.50 g/mol
Exact Mass 308.23514488 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.05
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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Linderanolide B
Isolinderanolide B
SCHEMBL12272483
BDBM50559077

2D Structure

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2D Structure of Isolinderanolide B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9824 98.24%
Caco-2 - 0.5275 52.75%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5420 54.20%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8347 83.47%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.5379 53.79%
P-glycoprotein inhibitior - 0.7166 71.66%
P-glycoprotein substrate - 0.9080 90.80%
CYP3A4 substrate - 0.5210 52.10%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8681 86.81%
CYP3A4 inhibition - 0.7633 76.33%
CYP2C9 inhibition - 0.8037 80.37%
CYP2C19 inhibition - 0.5473 54.73%
CYP2D6 inhibition - 0.8830 88.30%
CYP1A2 inhibition + 0.5359 53.59%
CYP2C8 inhibition - 0.8590 85.90%
CYP inhibitory promiscuity - 0.6861 68.61%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5876 58.76%
Eye corrosion - 0.9247 92.47%
Eye irritation + 0.6833 68.33%
Skin irritation + 0.6452 64.52%
Skin corrosion - 0.8742 87.42%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7107 71.07%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6561 65.61%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5316 53.16%
Acute Oral Toxicity (c) III 0.6026 60.26%
Estrogen receptor binding + 0.6020 60.20%
Androgen receptor binding - 0.6875 68.75%
Thyroid receptor binding + 0.6961 69.61%
Glucocorticoid receptor binding + 0.6242 62.42%
Aromatase binding - 0.6935 69.35%
PPAR gamma + 0.7406 74.06%
Honey bee toxicity - 0.9742 97.42%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.7506 75.06%
Fish aquatic toxicity + 0.9927 99.27%

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
CHEMBL2581 P07339 Cathepsin D 97.89% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 92.74% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.32% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.75% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.22% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.35% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 86.10% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 85.85% 89.63%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 83.26% 96.37%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.25% 93.56%
CHEMBL299 P17252 Protein kinase C alpha 82.98% 98.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.12% 99.23%

Cross-Links

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PubChem 53308122
NPASS NPC223476
LOTUS LTS0266554
wikiData Q104399412