2,4,7-Trimethyl-2,3,4,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-ol

Details

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Internal ID 5e3dfd23-e539-48f8-a4f0-12ff6f6b7f65
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 2,4,7-trimethyl-1,3,4,6,7,7a-hexahydrocyclopenta[c]pyridin-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H19NO/c1-7-5-12(3)6-10-8(2)11(13)4-9(7)10/h4,7-8,10-11,13H,5-6H2,1-3H3
InChI Key PMOIEWXMDSFOBY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H19NO
Molecular Weight 181.27 g/mol
Exact Mass 181.146664230 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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DTXSID40840164
2,4,7-Trimethyl-2,3,4,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-ol

2D Structure

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2D Structure of 2,4,7-Trimethyl-2,3,4,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9222 92.22%
Caco-2 + 0.7983 79.83%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5006 50.06%
OATP2B1 inhibitior - 0.8458 84.58%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9805 98.05%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9781 97.81%
P-glycoprotein inhibitior - 0.9593 95.93%
P-glycoprotein substrate - 0.8425 84.25%
CYP3A4 substrate - 0.5781 57.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4937 49.37%
CYP3A4 inhibition - 0.9223 92.23%
CYP2C9 inhibition - 0.8335 83.35%
CYP2C19 inhibition - 0.8632 86.32%
CYP2D6 inhibition - 0.6406 64.06%
CYP1A2 inhibition - 0.5493 54.93%
CYP2C8 inhibition - 0.9896 98.96%
CYP inhibitory promiscuity - 0.8899 88.99%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5721 57.21%
Eye corrosion - 0.9568 95.68%
Eye irritation - 0.7716 77.16%
Skin irritation - 0.6281 62.81%
Skin corrosion - 0.7400 74.00%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4009 40.09%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7967 79.67%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.7052 70.52%
Acute Oral Toxicity (c) III 0.6057 60.57%
Estrogen receptor binding - 0.9086 90.86%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7125 71.25%
Glucocorticoid receptor binding - 0.8031 80.31%
Aromatase binding - 0.8683 86.83%
PPAR gamma - 0.8650 86.50%
Honey bee toxicity - 0.9559 95.59%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity - 0.4824 48.24%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.77% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.23% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.04% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.01% 85.14%

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.
Tecoma stans

Cross-Links

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PubChem 71420990
LOTUS LTS0140596
wikiData Q82829000