Wortmannine B4

Details

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Internal ID 4f99e0f0-8a0e-453c-bb18-c00ac75a37b5
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name [(1S,4R,8S,10R,12R,13S,16S,17R)-17-hydroxy-13-(methoxymethyl)-8,12-dimethyl-2,7,15,19-tetraoxo-14-oxa-18-azapentacyclo[10.7.0.01,16.03,11.04,8]nonadec-3(11)-en-10-yl] 2-methylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H31NO9/c1-10(2)20(30)34-12-8-23(3)11(6-7-13(23)27)15-16(12)24(4)14(9-33-5)35-21(31)17-19(29)26-22(32)25(17,24)18(15)28/h10-12,14,17,19,29H,6-9H2,1-5H3,(H,26,32)/t11-,12+,14+,17-,19+,23-,24+,25-/m0/s1
InChI Key QLBVXPPJNPNFMF-AQVWAYKISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H31NO9
Molecular Weight 489.50 g/mol
Exact Mass 489.19988157 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.45
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL4587782

2D Structure

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2D Structure of Wortmannine B4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9681 96.81%
Caco-2 - 0.6422 64.22%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7121 71.21%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8518 85.18%
OATP1B3 inhibitior + 0.9327 93.27%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.4875 48.75%
P-glycoprotein inhibitior + 0.5936 59.36%
P-glycoprotein substrate + 0.5494 54.94%
CYP3A4 substrate + 0.6568 65.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8928 89.28%
CYP3A4 inhibition - 0.8439 84.39%
CYP2C9 inhibition - 0.8834 88.34%
CYP2C19 inhibition - 0.9113 91.13%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.8376 83.76%
CYP2C8 inhibition + 0.5196 51.96%
CYP inhibitory promiscuity - 0.9329 93.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Danger 0.4561 45.61%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.9207 92.07%
Skin irritation - 0.7200 72.00%
Skin corrosion - 0.9202 92.02%
Ames mutagenesis - 0.5237 52.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5585 55.85%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.6110 61.10%
skin sensitisation - 0.8353 83.53%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.4522 45.22%
Acute Oral Toxicity (c) III 0.5897 58.97%
Estrogen receptor binding + 0.6664 66.64%
Androgen receptor binding + 0.7195 71.95%
Thyroid receptor binding - 0.5318 53.18%
Glucocorticoid receptor binding + 0.6976 69.76%
Aromatase binding + 0.6362 63.62%
PPAR gamma + 0.6948 69.48%
Honey bee toxicity - 0.7130 71.30%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9210 92.10%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.90% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.90% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.33% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.24% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.12% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.49% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.95% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.24% 92.62%
CHEMBL2581 P07339 Cathepsin D 90.51% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.10% 100.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.78% 94.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.20% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.51% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 145720817
LOTUS LTS0063871
wikiData Q105223475