Subamolide B

Details

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Internal ID 0fae4b77-0c19-4de6-a198-e1abfa91fe5e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name (3E,4R,5R)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one
SMILES (Canonical) CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O
SMILES (Isomeric) CCCCCCCCCCCCC/C=C/1\[C@H]([C@](OC1=O)(C)OC)O
InChI InChI=1S/C20H36O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(21)20(2,23-3)24-19(17)22/h16,18,21H,4-15H2,1-3H3/b17-16+/t18-,20-/m1/s1
InChI Key YLCXJNOKPGBEPM-DPBVHHOFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H36O4
Molecular Weight 340.50 g/mol
Exact Mass 340.26135963 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 6.50
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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CHEMBL220075
(3E,4R,5R)-4-hydroxy-5-methoxy-5-methyl-3-tetradecylideneoxolan-2-one

2D Structure

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2D Structure of Subamolide B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9364 93.64%
Caco-2 + 0.7735 77.35%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6363 63.63%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.8525 85.25%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.7090 70.90%
P-glycoprotein inhibitior - 0.6247 62.47%
P-glycoprotein substrate - 0.8518 85.18%
CYP3A4 substrate + 0.5863 58.63%
CYP2C9 substrate - 0.6100 61.00%
CYP2D6 substrate - 0.8701 87.01%
CYP3A4 inhibition - 0.5435 54.35%
CYP2C9 inhibition - 0.7131 71.31%
CYP2C19 inhibition + 0.5625 56.25%
CYP2D6 inhibition - 0.8795 87.95%
CYP1A2 inhibition - 0.5295 52.95%
CYP2C8 inhibition - 0.5659 56.59%
CYP inhibitory promiscuity - 0.6674 66.74%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6275 62.75%
Eye corrosion - 0.9757 97.57%
Eye irritation - 0.5474 54.74%
Skin irritation - 0.5235 52.35%
Skin corrosion - 0.9592 95.92%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4056 40.56%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5831 58.31%
skin sensitisation - 0.7971 79.71%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.6551 65.51%
Acute Oral Toxicity (c) III 0.4397 43.97%
Estrogen receptor binding + 0.5551 55.51%
Androgen receptor binding - 0.6226 62.26%
Thyroid receptor binding + 0.6007 60.07%
Glucocorticoid receptor binding + 0.6260 62.60%
Aromatase binding - 0.6282 62.82%
PPAR gamma + 0.6249 62.49%
Honey bee toxicity - 0.9353 93.53%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.8513 85.13%
Fish aquatic toxicity + 0.9797 97.97%

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 97.09% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.35% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 92.93% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.52% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.01% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.78% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.28% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.71% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.09% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 85.47% 90.17%
CHEMBL299 P17252 Protein kinase C alpha 82.72% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.19% 97.25%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.26% 92.62%

Cross-Links

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PubChem 16104907
NPASS NPC286770
LOTUS LTS0229167
wikiData Q105350065