Thiersindole B

Details

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Internal ID 1c10c782-efdd-4801-9f29-d7d160c794f4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3aS,4S,6aS,7R,8S,10aR)-7-(1H-indol-3-ylmethyl)-3a,7,8-trimethyl-1-propan-2-ylidene-3,4,5,6,6a,8,9,10-octahydro-2H-cyclopenta[j]naphthalen-4-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H39NO/c1-18(2)22-13-14-27(5)25(30)11-10-24-26(4,19(3)12-15-28(22,24)27)16-20-17-29-23-9-7-6-8-21(20)23/h6-9,17,19,24-25,29-30H,10-16H2,1-5H3/t19-,24-,25-,26+,27+,28-/m0/s1
InChI Key YPVANRVLBISMCS-HCCSKZQKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H39NO
Molecular Weight 405.60 g/mol
Exact Mass 405.303164868 g/mol
Topological Polar Surface Area (TPSA) 36.00 Ų
XlogP 7.20
Atomic LogP (AlogP) 7.04
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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(3aS,4S,6aS,7R,8S,10aR)-7-(1H-indol-3-ylmethyl)-3a,7,8-trimethyl-1-propan-2-ylidene-3,4,5,6,6a,8,9,10-octahydro-2H-cyclopenta[j]naphthalen-4-ol
(3aS,4S,6aS,7R,8S,10aR)-7-(1H-indol-3-ylmethyl)-3a,7,8-trimethyl-1-propan-2-ylidene-3,4,5,6,6a,8,9,10-octahydro-2H-cyclopenta(j)naphthalen-4-ol
RefChem:189388
610317-21-0
CHEBI:199973

2D Structure

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2D Structure of Thiersindole B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6579 65.79%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.3728 37.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8986 89.86%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9472 94.72%
P-glycoprotein inhibitior + 0.5852 58.52%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6942 69.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3578 35.78%
CYP3A4 inhibition + 0.8033 80.33%
CYP2C9 inhibition - 0.6977 69.77%
CYP2C19 inhibition + 0.5951 59.51%
CYP2D6 inhibition - 0.8232 82.32%
CYP1A2 inhibition + 0.6648 66.48%
CYP2C8 inhibition + 0.5823 58.23%
CYP inhibitory promiscuity + 0.8860 88.60%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5693 56.93%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9563 95.63%
Skin irritation - 0.7017 70.17%
Skin corrosion - 0.9126 91.26%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition + 0.9379 93.79%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.7013 70.13%
skin sensitisation - 0.7240 72.40%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.9076 90.76%
Acute Oral Toxicity (c) III 0.6586 65.86%
Estrogen receptor binding + 0.7469 74.69%
Androgen receptor binding + 0.6912 69.12%
Thyroid receptor binding + 0.8112 81.12%
Glucocorticoid receptor binding + 0.7081 70.81%
Aromatase binding + 0.7141 71.41%
PPAR gamma - 0.5099 50.99%
Honey bee toxicity - 0.8219 82.19%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9836 98.36%

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 99.59% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 98.99% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.73% 93.99%
CHEMBL2581 P07339 Cathepsin D 97.40% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.35% 96.09%
CHEMBL325 Q13547 Histone deacetylase 1 97.06% 95.92%
CHEMBL1914 P06276 Butyrylcholinesterase 94.68% 95.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.15% 90.08%
CHEMBL3310 Q96DB2 Histone deacetylase 11 93.95% 88.56%
CHEMBL2996 Q05655 Protein kinase C delta 93.22% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.74% 95.56%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 90.22% 85.49%
CHEMBL1951 P21397 Monoamine oxidase A 90.15% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.20% 92.62%
CHEMBL5805 Q9NR97 Toll-like receptor 8 89.14% 96.25%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.06% 94.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.12% 97.09%
CHEMBL1944 P08473 Neprilysin 87.91% 92.63%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.22% 92.94%
CHEMBL3524 P56524 Histone deacetylase 4 85.01% 92.97%
CHEMBL5028 O14672 ADAM10 83.88% 97.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.53% 100.00%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.48% 97.64%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 82.71% 95.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.11% 95.89%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.59% 90.71%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 81.45% 91.43%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.00% 91.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.90% 89.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 80.85% 89.44%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.75% 85.30%
CHEMBL1829 O15379 Histone deacetylase 3 80.51% 95.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 80.12% 80.96%

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.
Machilus obovatifolia

Cross-Links

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PubChem 11047787
NPASS NPC186827
LOTUS LTS0264275
wikiData Q75068700