Terpestacin B

Details

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Internal ID 0695ac17-c045-4dac-aa01-86efd48e0db7
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name (1S,2E,5R,9S,11E,15S,16R)-7,15-dihydroxy-6-[(2S)-1-hydroxypropan-2-yl]-2,9,12,16-tetramethyl-19-oxatricyclo[14.2.1.05,9]nonadeca-2,6,11-trien-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H38O5/c1-15-6-9-20(27)25(5)13-11-19(30-25)16(2)7-8-18-21(17(3)14-26)22(28)23(29)24(18,4)12-10-15/h7,10,17-20,26-28H,6,8-9,11-14H2,1-5H3/b15-10+,16-7+/t17-,18-,19+,20+,24+,25-/m1/s1
InChI Key LAJNGEKHZMZDRF-ZPIROSACSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H38O5
Molecular Weight 418.60 g/mol
Exact Mass 418.27192431 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terpestacin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.5701 57.01%
Blood Brain Barrier + 0.6135 61.35%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6953 69.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8855 88.55%
OATP1B3 inhibitior + 0.9751 97.51%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior + 0.5564 55.64%
BSEP inhibitior + 0.8964 89.64%
P-glycoprotein inhibitior - 0.6810 68.10%
P-glycoprotein substrate - 0.6508 65.08%
CYP3A4 substrate + 0.6387 63.87%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8721 87.21%
CYP3A4 inhibition - 0.5090 50.90%
CYP2C9 inhibition - 0.8456 84.56%
CYP2C19 inhibition - 0.8771 87.71%
CYP2D6 inhibition - 0.9331 93.31%
CYP1A2 inhibition - 0.7830 78.30%
CYP2C8 inhibition - 0.6312 63.12%
CYP inhibitory promiscuity - 0.8921 89.21%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5832 58.32%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9403 94.03%
Skin irritation + 0.5441 54.41%
Skin corrosion - 0.9474 94.74%
Ames mutagenesis - 0.7970 79.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4010 40.10%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6538 65.38%
skin sensitisation - 0.8740 87.40%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7762 77.62%
Acute Oral Toxicity (c) III 0.6008 60.08%
Estrogen receptor binding + 0.7373 73.73%
Androgen receptor binding + 0.5371 53.71%
Thyroid receptor binding + 0.5562 55.62%
Glucocorticoid receptor binding + 0.8533 85.33%
Aromatase binding + 0.7054 70.54%
PPAR gamma + 0.5484 54.84%
Honey bee toxicity - 0.8387 83.87%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.8737 87.37%

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 98.07% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.84% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.52% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.83% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.78% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.53% 89.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.31% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.07% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.05% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 83.53% 94.73%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.43% 96.47%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.20% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.22% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.17% 99.23%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.25% 98.75%

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 146683287
LOTUS LTS0011682
wikiData Q105148678