3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,6,6a,7,8,10,11a-decahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-11-one

Details

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Internal ID e81377c4-ab9b-451a-9378-a6b2e0ca5153
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,6,6a,7,8,10,11a-decahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H39NO3/c1-14-11-21-24(28-13-14)16(3)27(31-21)10-8-19-20-6-5-17-12-18(29)7-9-26(17,4)23(20)25(30)22(19)15(27)2/h5,14-16,18,20-21,23-24,28-29H,6-13H2,1-4H3
InChI Key QRXOCOSLDOPPKH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H39NO3
Molecular Weight 425.60 g/mol
Exact Mass 425.29299411 g/mol
Topological Polar Surface Area (TPSA) 58.60 Ų
XlogP 3.00
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,6,6a,7,8,10,11a-decahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-11-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.5141 51.41%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6033 60.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8713 87.13%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5811 58.11%
BSEP inhibitior + 0.7812 78.12%
P-glycoprotein inhibitior + 0.5777 57.77%
P-glycoprotein substrate + 0.5593 55.93%
CYP3A4 substrate + 0.7104 71.04%
CYP2C9 substrate - 0.7688 76.88%
CYP2D6 substrate - 0.8070 80.70%
CYP3A4 inhibition - 0.9521 95.21%
CYP2C9 inhibition - 0.9101 91.01%
CYP2C19 inhibition - 0.9121 91.21%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition + 0.5306 53.06%
CYP inhibitory promiscuity - 0.9087 90.87%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4961 49.61%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9603 96.03%
Skin irritation - 0.7014 70.14%
Skin corrosion - 0.9133 91.33%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7610 76.10%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7682 76.82%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.5998 59.98%
Acute Oral Toxicity (c) III 0.6302 63.02%
Estrogen receptor binding + 0.7761 77.61%
Androgen receptor binding + 0.7103 71.03%
Thyroid receptor binding + 0.6664 66.64%
Glucocorticoid receptor binding + 0.8536 85.36%
Aromatase binding + 0.7645 76.45%
PPAR gamma + 0.5193 51.93%
Honey bee toxicity - 0.7036 70.36%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.6611 66.11%

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 95.66% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.50% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.77% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.70% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.55% 96.09%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 90.98% 89.05%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.55% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.27% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.56% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.16% 99.23%
CHEMBL255 P29275 Adenosine A2b receptor 88.79% 98.59%
CHEMBL226 P30542 Adenosine A1 receptor 87.47% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.45% 94.45%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 87.44% 88.84%
CHEMBL299 P17252 Protein kinase C alpha 86.03% 98.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.73% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.82% 93.04%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.36% 93.03%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.02% 92.94%
CHEMBL3045 P05771 Protein kinase C beta 82.61% 97.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.52% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.08% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 81.80% 90.17%

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.
Veratrum lobelianum

Cross-Links

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PubChem 163045956
LOTUS LTS0073426
wikiData Q105226726