Tertacyclo(6,3,2,o(2,5),o(1,8)tridecan-9-ol

Details

Top
Internal ID 4be92cb8-a0f1-4493-abf1-570cb0c0b069
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name tetracyclo[6.3.2.01,8.02,5]tridecan-9-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O/c14-11-4-6-12-7-8-13(11,12)5-3-9-1-2-10(9)12/h9-11,14H,1-8H2
InChI Key VXFNNTKJEWQORX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H20O
Molecular Weight 192.30 g/mol
Exact Mass 192.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Tertacyclo(6,3,2,o(2,5),o(1,8)tridecan-9-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.5692 56.92%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9546 95.46%
OATP1B3 inhibitior + 0.9575 95.75%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8756 87.56%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.9395 93.95%
CYP3A4 substrate - 0.5348 53.48%
CYP2C9 substrate - 0.7698 76.98%
CYP2D6 substrate + 0.3659 36.59%
CYP3A4 inhibition - 0.9414 94.14%
CYP2C9 inhibition - 0.8126 81.26%
CYP2C19 inhibition - 0.7830 78.30%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.7306 73.06%
CYP2C8 inhibition - 0.9398 93.98%
CYP inhibitory promiscuity - 0.9621 96.21%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.4893 48.93%
Eye corrosion - 0.8351 83.51%
Eye irritation + 0.9129 91.29%
Skin irritation + 0.6663 66.63%
Skin corrosion - 0.7590 75.90%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7097 70.97%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5726 57.26%
skin sensitisation - 0.5501 55.01%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6499 64.99%
Acute Oral Toxicity (c) III 0.8308 83.08%
Estrogen receptor binding - 0.7262 72.62%
Androgen receptor binding + 0.6340 63.40%
Thyroid receptor binding - 0.7470 74.70%
Glucocorticoid receptor binding - 0.5870 58.70%
Aromatase binding - 0.7081 70.81%
PPAR gamma - 0.8562 85.62%
Honey bee toxicity - 0.8618 86.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.6845 68.45%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.58% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.14% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.03% 97.09%
CHEMBL240 Q12809 HERG 86.15% 89.76%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.97% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.67% 96.61%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.04% 93.04%
CHEMBL226 P30542 Adenosine A1 receptor 84.08% 95.93%
CHEMBL204 P00734 Thrombin 82.82% 96.01%
CHEMBL237 P41145 Kappa opioid receptor 82.30% 98.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.08% 91.11%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.16% 99.18%
CHEMBL238 Q01959 Dopamine transporter 81.01% 95.88%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.97% 92.94%
CHEMBL1871 P10275 Androgen Receptor 80.15% 96.43%

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.
Cyperus rotundus

Cross-Links

Top
PubChem 163194666
LOTUS LTS0121286
wikiData Q105298464