Trichobotrysin C

Details

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Internal ID 536d45a8-e15e-4a12-a863-fb29542741d8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3Z,5R)-3-[[(1aS,2S,3S,3aR,4S,7aR,7bR)-2-[(E)-but-2-en-2-yl]-1a,4-dimethyl-3,3a,4,5,6,7,7a,7b-octahydro-2H-naphtho[1,2-b]oxiren-3-yl]-hydroxymethylidene]-1-methyl-5-propan-2-ylpyrrolidine-2,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H37NO4/c1-8-13(4)19-17(16-14(5)10-9-11-15(16)23-25(19,6)30-23)21(27)18-22(28)20(12(2)3)26(7)24(18)29/h8,12,14-17,19-20,23,27H,9-11H2,1-7H3/b13-8+,21-18-/t14-,15+,16+,17-,19+,20+,23+,25-/m0/s1
InChI Key QVIXMXLKXIWYKD-VNBVSDCXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H37NO4
Molecular Weight 415.60 g/mol
Exact Mass 415.27225866 g/mol
Topological Polar Surface Area (TPSA) 70.10 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trichobotrysin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9567 95.67%
Caco-2 + 0.6262 62.62%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5026 50.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8731 87.31%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7072 70.72%
BSEP inhibitior + 0.5566 55.66%
P-glycoprotein inhibitior + 0.6255 62.55%
P-glycoprotein substrate - 0.5171 51.71%
CYP3A4 substrate + 0.6322 63.22%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.8673 86.73%
CYP2C9 inhibition - 0.7770 77.70%
CYP2C19 inhibition - 0.7680 76.80%
CYP2D6 inhibition - 0.9170 91.70%
CYP1A2 inhibition - 0.7072 70.72%
CYP2C8 inhibition - 0.8069 80.69%
CYP inhibitory promiscuity - 0.8877 88.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.4960 49.60%
Eye corrosion - 0.9835 98.35%
Eye irritation - 0.9286 92.86%
Skin irritation - 0.7449 74.49%
Skin corrosion - 0.8925 89.25%
Ames mutagenesis - 0.6040 60.40%
Human Ether-a-go-go-Related Gene inhibition - 0.5623 56.23%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8241 82.41%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.7292 72.92%
Acute Oral Toxicity (c) III 0.5755 57.55%
Estrogen receptor binding + 0.6804 68.04%
Androgen receptor binding + 0.7140 71.40%
Thyroid receptor binding + 0.6056 60.56%
Glucocorticoid receptor binding + 0.6523 65.23%
Aromatase binding + 0.5802 58.02%
PPAR gamma + 0.7517 75.17%
Honey bee toxicity - 0.7314 73.14%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9268 92.68%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.81% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.16% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.86% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.59% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.34% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.34% 96.77%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.79% 93.04%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.67% 93.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.97% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.36% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.87% 99.23%
CHEMBL3384 Q16512 Protein kinase N1 82.78% 80.71%
CHEMBL340 P08684 Cytochrome P450 3A4 82.25% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.03% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.65% 97.09%

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 139584168
LOTUS LTS0019315
wikiData Q77280457