2,3-Dehydro-4alpha-hydroxylongilactone

Details

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Internal ID f9af504e-7e83-49cb-833a-baf8747b7977
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Eudesmanolides, secoeudesmanolides, and derivatives
IUPAC Name (1R,2R,3R,6R,7S,8R,9S,12S,13R,14R,15R,16R)-3,6,8,14,15-pentahydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-4-en-11-one
SMILES (Canonical) CC1C(C(C2C3(C(C=CC(C3C(C4C2(C1C(=O)O4)C)O)(C)O)O)C)O)O
SMILES (Isomeric) C[C@H]1[C@H]([C@@H]([C@@H]2[C@]3([C@@H](C=C[C@@]([C@@H]3[C@H]([C@@H]4[C@]2([C@H]1C(=O)O4)C)O)(C)O)O)C)O)O
InChI InChI=1S/C19H28O7/c1-7-9-16(24)26-15-12(23)13-17(2,25)6-5-8(20)18(13,3)14(19(9,15)4)11(22)10(7)21/h5-15,20-23,25H,1-4H3/t7-,8-,9-,10-,11+,12-,13+,14-,15-,17-,18+,19+/m1/s1
InChI Key XLXUQTXHTMEKFB-ZSODICBDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O7
Molecular Weight 368.40 g/mol
Exact Mass 368.18350323 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.80
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3-Dehydro-4alpha-hydroxylongilactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9243 92.43%
Caco-2 - 0.7372 73.72%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5095 50.95%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8838 88.38%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8837 88.37%
P-glycoprotein inhibitior - 0.8190 81.90%
P-glycoprotein substrate - 0.7082 70.82%
CYP3A4 substrate + 0.5749 57.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8723 87.23%
CYP3A4 inhibition - 0.7256 72.56%
CYP2C9 inhibition - 0.9476 94.76%
CYP2C19 inhibition - 0.9449 94.49%
CYP2D6 inhibition - 0.9544 95.44%
CYP1A2 inhibition - 0.8087 80.87%
CYP2C8 inhibition - 0.8856 88.56%
CYP inhibitory promiscuity - 0.7455 74.55%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.3803 38.03%
Eye corrosion - 0.9797 97.97%
Eye irritation - 0.9701 97.01%
Skin irritation - 0.5741 57.41%
Skin corrosion - 0.8977 89.77%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6278 62.78%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7578 75.78%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.6554 65.54%
Nephrotoxicity + 0.8018 80.18%
Acute Oral Toxicity (c) III 0.4569 45.69%
Estrogen receptor binding + 0.6279 62.79%
Androgen receptor binding + 0.5494 54.94%
Thyroid receptor binding + 0.6433 64.33%
Glucocorticoid receptor binding + 0.6730 67.30%
Aromatase binding - 0.5388 53.88%
PPAR gamma - 0.5392 53.92%
Honey bee toxicity - 0.8609 86.09%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9103 91.03%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.41% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.10% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.06% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.62% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.44% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.00% 97.25%
CHEMBL2581 P07339 Cathepsin D 81.40% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.50% 94.73%

Cross-Links

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PubChem 101499157
NPASS NPC91160
LOTUS LTS0127516
wikiData Q105330526