Ophiobolin B Lactone

Details

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Internal ID afbe6afe-57e8-4a1c-a6cf-48893e197ccf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name (1S,3R,6S,7R,9E,13S,15R,16S)-6,15-dihydroxy-3,15-dimethyl-6-[(2S)-6-methylhept-5-en-2-yl]-12-oxatetracyclo[8.5.1.03,7.013,16]hexadec-9-en-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H38O4/c1-15(2)7-6-8-16(3)25(28)12-11-23(4)13-18-21-17(9-10-20(23)25)22(26)29-19(21)14-24(18,5)27/h7,9,16,18-21,27-28H,6,8,10-14H2,1-5H3/b17-9+/t16-,18-,19-,20+,21+,23+,24+,25-/m0/s1
InChI Key QQIDJUCXUQXXFU-MIOWFVLLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H38O4
Molecular Weight 402.60 g/mol
Exact Mass 402.27700969 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.55
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL469915

2D Structure

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2D Structure of Ophiobolin B Lactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.5543 55.43%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6921 69.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8732 87.32%
OATP1B3 inhibitior + 0.9222 92.22%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.6066 60.66%
P-glycoprotein inhibitior - 0.5439 54.39%
P-glycoprotein substrate - 0.6429 64.29%
CYP3A4 substrate + 0.6430 64.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8949 89.49%
CYP3A4 inhibition - 0.6296 62.96%
CYP2C9 inhibition - 0.7598 75.98%
CYP2C19 inhibition - 0.7619 76.19%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.5119 51.19%
CYP2C8 inhibition - 0.7877 78.77%
CYP inhibitory promiscuity - 0.8944 89.44%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5465 54.65%
Eye corrosion - 0.9839 98.39%
Eye irritation - 0.9606 96.06%
Skin irritation + 0.5377 53.77%
Skin corrosion - 0.9357 93.57%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6988 69.88%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5495 54.95%
skin sensitisation - 0.7486 74.86%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8059 80.59%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.6786 67.86%
Acute Oral Toxicity (c) I 0.3722 37.22%
Estrogen receptor binding + 0.9221 92.21%
Androgen receptor binding + 0.5866 58.66%
Thyroid receptor binding + 0.7873 78.73%
Glucocorticoid receptor binding + 0.8241 82.41%
Aromatase binding + 0.6945 69.45%
PPAR gamma + 0.5763 57.63%
Honey bee toxicity - 0.7941 79.41%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9668 96.68%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.78% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.57% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.43% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 93.25% 94.75%
CHEMBL221 P23219 Cyclooxygenase-1 93.23% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.94% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 88.41% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.69% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.58% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.39% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.60% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.58% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.34% 98.95%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.18% 95.71%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.01% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.44% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.18% 95.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.64% 91.07%
CHEMBL284 P27487 Dipeptidyl peptidase IV 80.01% 95.69%

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 10341078
LOTUS LTS0016392
wikiData Q75064784