Trichobotrysin B

Details

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Internal ID 4ea2b5d4-d779-41f0-a8c3-649bf084d36f
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-alkylpyrrolidines
IUPAC Name (3Z,5R)-3-[[(1S,2R,4aR,8S,8aR)-2-[(2S,3S)-2,3-dimethyloxiran-2-yl]-3,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-hydroxymethylidene]-1-methyl-5-propan-2-ylpyrrolidine-2,4-dione
SMILES (Canonical) CC1CCCC2C1C(C(C(=C2)C)C3(C(O3)C)C)C(=C4C(=O)C(N(C4=O)C)C(C)C)O
SMILES (Isomeric) C[C@H]1CCC[C@@H]2[C@@H]1[C@@H]([C@H](C(=C2)C)[C@]3([C@@H](O3)C)C)/C(=C/4\C(=O)[C@H](N(C4=O)C)C(C)C)/O
InChI InChI=1S/C25H37NO4/c1-12(2)21-23(28)19(24(29)26(21)7)22(27)18-17-13(3)9-8-10-16(17)11-14(4)20(18)25(6)15(5)30-25/h11-13,15-18,20-21,27H,8-10H2,1-7H3/b22-19-/t13-,15-,16-,17+,18-,20-,21+,25+/m0/s1
InChI Key PEBQSWUQULBCGF-SFOAYJPGSA-N
Popularity 0 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 4.80
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 B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9732 97.32%
Caco-2 + 0.6381 63.81%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5408 54.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8738 87.38%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7822 78.22%
BSEP inhibitior - 0.6420 64.20%
P-glycoprotein inhibitior + 0.6072 60.72%
P-glycoprotein substrate - 0.6064 60.64%
CYP3A4 substrate + 0.6550 65.50%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.7898 78.98%
CYP2C9 inhibition - 0.7439 74.39%
CYP2C19 inhibition - 0.7581 75.81%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.7011 70.11%
CYP2C8 inhibition - 0.8055 80.55%
CYP inhibitory promiscuity - 0.8682 86.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4693 46.93%
Eye corrosion - 0.9841 98.41%
Eye irritation - 0.9378 93.78%
Skin irritation - 0.7469 74.69%
Skin corrosion - 0.8883 88.83%
Ames mutagenesis + 0.5130 51.30%
Human Ether-a-go-go-Related Gene inhibition - 0.5089 50.89%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.8276 82.76%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.6124 61.24%
Acute Oral Toxicity (c) III 0.5821 58.21%
Estrogen receptor binding + 0.6562 65.62%
Androgen receptor binding + 0.6967 69.67%
Thyroid receptor binding + 0.5910 59.10%
Glucocorticoid receptor binding + 0.6142 61.42%
Aromatase binding + 0.5636 56.36%
PPAR gamma + 0.7322 73.22%
Honey bee toxicity - 0.8694 86.94%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9329 93.29%

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 99.73% 83.82%
CHEMBL2581 P07339 Cathepsin D 98.10% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.42% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.10% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.54% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.47% 99.23%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.40% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.80% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.31% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 81.99% 92.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.79% 90.08%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.72% 85.11%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.26% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.21% 97.25%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.91% 93.99%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.89% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.85% 89.00%

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 132594640
LOTUS LTS0222113
wikiData Q77570651