Tecostanine

Details

Top
Internal ID af0dac02-1ee4-4715-96d1-c2988d5c7e62
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (2,7-dimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-4-yl)methanol
SMILES (Canonical) CC1CCC2C1CN(CC2CO)C
SMILES (Isomeric) CC1CCC2C1CN(CC2CO)C
InChI InChI=1S/C11H21NO/c1-8-3-4-10-9(7-13)5-12(2)6-11(8)10/h8-11,13H,3-7H2,1-2H3
InChI Key CRVXJVHSLVEDRI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H21NO
Molecular Weight 183.29 g/mol
Exact Mass 183.162314293 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
BRN 1422487
Octahydro-2,7-dimethyl-1H-2-pyrindine-4-methanol
708-18-9
AC1L3RGJ
1H-2-Pyrindine-4-methanol, octahydro-2,7-dimethyl-
LS-148644
5-21-01-00349 (Beilstein Handbook Reference)
CHEBI:9425
SCHEMBL22926628
DTXSID10991071
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Tecostanine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9066 90.66%
Caco-2 + 0.7621 76.21%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.7747 77.47%
OATP2B1 inhibitior - 0.8441 84.41%
OATP1B1 inhibitior + 0.9605 96.05%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.9715 97.15%
P-glycoprotein inhibitior - 0.9685 96.85%
P-glycoprotein substrate - 0.7914 79.14%
CYP3A4 substrate - 0.5602 56.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.6139 61.39%
CYP3A4 inhibition - 0.9747 97.47%
CYP2C9 inhibition - 0.9074 90.74%
CYP2C19 inhibition - 0.9401 94.01%
CYP2D6 inhibition - 0.8373 83.73%
CYP1A2 inhibition - 0.8003 80.03%
CYP2C8 inhibition - 0.9683 96.83%
CYP inhibitory promiscuity - 0.9866 98.66%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6816 68.16%
Eye corrosion - 0.7863 78.63%
Eye irritation + 0.7782 77.82%
Skin irritation - 0.6448 64.48%
Skin corrosion + 0.5663 56.63%
Ames mutagenesis - 0.8078 80.78%
Human Ether-a-go-go-Related Gene inhibition - 0.3918 39.18%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation - 0.7688 76.88%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7657 76.57%
Acute Oral Toxicity (c) III 0.8182 81.82%
Estrogen receptor binding - 0.8753 87.53%
Androgen receptor binding - 0.5433 54.33%
Thyroid receptor binding - 0.7203 72.03%
Glucocorticoid receptor binding - 0.7806 78.06%
Aromatase binding - 0.7845 78.45%
PPAR gamma - 0.8882 88.82%
Honey bee toxicity - 0.9529 95.29%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.7595 75.95%

Targets

Top

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 96.27% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.57% 97.25%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 88.71% 98.46%
CHEMBL2581 P07339 Cathepsin D 82.52% 98.95%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 80.61% 93.90%

Plants that contains it

Top
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

Top
PubChem 120773
LOTUS LTS0004299
wikiData Q27108388