Terreusterpene B

Details

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Internal ID 63d3bef7-962b-473a-8c17-69607b376740
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name dimethyl (1S,4R,6R,8S,9S,10R,12S,13R,15S)-15-acetyloxy-4,6,8,10,14,14-hexamethyl-7,18-dioxo-5,19-dioxapentacyclo[10.5.2.01,13.02,10.04,8]nonadec-2-ene-6,9-dicarboxylate
SMILES (Canonical) CC(=O)OC1CCC23C(C1(C)C)C(CC4(C2=CC5(C(C4C(=O)OC)(C(=O)C(O5)(C)C(=O)OC)C)C)C)OC3=O
SMILES (Isomeric) CC(=O)O[C@H]1CC[C@]23[C@@H](C1(C)C)[C@H](C[C@]4(C2=C[C@@]5([C@]([C@H]4C(=O)OC)(C(=O)[C@](O5)(C)C(=O)OC)C)C)C)OC3=O
InChI InChI=1S/C29H38O10/c1-14(30)37-17-10-11-29-16-13-26(5)27(6,21(32)28(7,39-26)22(33)36-9)19(20(31)35-8)25(16,4)12-15(38-23(29)34)18(29)24(17,2)3/h13,15,17-19H,10-12H2,1-9H3/t15-,17-,18+,19-,25-,26+,27+,28+,29+/m0/s1
InChI Key PTFJEMZXUZKAKS-OSUWAKPISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H38O10
Molecular Weight 546.60 g/mol
Exact Mass 546.24649740 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terreusterpene B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 - 0.7071 70.71%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7527 75.27%
OATP2B1 inhibitior - 0.7192 71.92%
OATP1B1 inhibitior + 0.8716 87.16%
OATP1B3 inhibitior + 0.9281 92.81%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9384 93.84%
P-glycoprotein inhibitior + 0.8061 80.61%
P-glycoprotein substrate - 0.5807 58.07%
CYP3A4 substrate + 0.7102 71.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.7338 73.38%
CYP2C9 inhibition - 0.7982 79.82%
CYP2C19 inhibition - 0.8311 83.11%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition - 0.6980 69.80%
CYP2C8 inhibition + 0.4850 48.50%
CYP inhibitory promiscuity - 0.8668 86.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.4247 42.47%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8649 86.49%
Skin irritation - 0.6109 61.09%
Skin corrosion - 0.8790 87.90%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6460 64.60%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.7754 77.54%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.9246 92.46%
Acute Oral Toxicity (c) III 0.4724 47.24%
Estrogen receptor binding + 0.7633 76.33%
Androgen receptor binding + 0.7584 75.84%
Thyroid receptor binding + 0.6710 67.10%
Glucocorticoid receptor binding + 0.7743 77.43%
Aromatase binding + 0.7308 73.08%
PPAR gamma + 0.6974 69.74%
Honey bee toxicity - 0.7136 71.36%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9835 98.35%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.12% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.87% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.23% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.37% 91.11%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.84% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.59% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 87.30% 91.19%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.78% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.46% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.71% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.16% 97.09%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.95% 97.28%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.57% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.66% 94.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.84% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.41% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.32% 95.71%

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 139193858
LOTUS LTS0208833
wikiData Q105214611