1,3,5-Tributyl-1,3,5-triazinane

Details

Top
Internal ID f4b3aa66-ed51-42f3-a69c-4914dba0ebc4
Taxonomy Organoheterocyclic compounds > Triazinanes > 1,3,5-triazinanes
IUPAC Name 1,3,5-tributyl-1,3,5-triazinane
SMILES (Canonical) CCCCN1CN(CN(C1)CCCC)CCCC
SMILES (Isomeric) CCCCN1CN(CN(C1)CCCC)CCCC
InChI InChI=1S/C15H33N3/c1-4-7-10-16-13-17(11-8-5-2)15-18(14-16)12-9-6-3/h4-15H2,1-3H3
InChI Key OIQDTXAPPNRLAS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H33N3
Molecular Weight 255.44 g/mol
Exact Mass 255.267448065 g/mol
Topological Polar Surface Area (TPSA) 9.70 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

Top
13036-83-4
1,3,5-Triazine, 1,3,5-tributylhexahydro-
1,3,5-Tributylhexahydro-1,3,5-triazine
1,3,5-Triazine,1,3,5-tributylhexahydro-
s-Triazine, 1,3,5-tributylhexahydro-
EINECS 235-905-1
SCHEMBL5487662
DTXSID7065334
OIQDTXAPPNRLAS-UHFFFAOYSA-N
AMY40974
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 1,3,5-Tributyl-1,3,5-triazinane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9527 95.27%
Caco-2 + 0.9254 92.54%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.6251 62.51%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9613 96.13%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.8258 82.58%
P-glycoprotein inhibitior - 0.9508 95.08%
P-glycoprotein substrate - 0.9059 90.59%
CYP3A4 substrate - 0.6831 68.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7560 75.60%
CYP3A4 inhibition - 0.9717 97.17%
CYP2C9 inhibition - 0.8727 87.27%
CYP2C19 inhibition - 0.8709 87.09%
CYP2D6 inhibition - 0.7772 77.72%
CYP1A2 inhibition - 0.6209 62.09%
CYP2C8 inhibition - 0.9942 99.42%
CYP inhibitory promiscuity - 0.9441 94.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6342 63.42%
Eye corrosion + 0.6396 63.96%
Eye irritation + 0.9869 98.69%
Skin irritation + 0.8175 81.75%
Skin corrosion + 0.9366 93.66%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6402 64.02%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5252 52.52%
skin sensitisation - 0.9385 93.85%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7207 72.07%
Acute Oral Toxicity (c) III 0.5730 57.30%
Estrogen receptor binding - 0.8232 82.32%
Androgen receptor binding - 0.9052 90.52%
Thyroid receptor binding - 0.5949 59.49%
Glucocorticoid receptor binding - 0.8223 82.23%
Aromatase binding - 0.8049 80.49%
PPAR gamma - 0.8164 81.64%
Honey bee toxicity - 0.9945 99.45%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6752 67.52%
Fish aquatic toxicity - 0.5484 54.84%

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 94.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.99% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.16% 97.25%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.46% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.50% 92.86%
CHEMBL240 Q12809 HERG 83.05% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.79% 92.08%
CHEMBL2885 P07451 Carbonic anhydrase III 80.65% 87.45%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 80.25% 95.00%

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.
Chimonanthus praecox

Cross-Links

Top
PubChem 83069
NPASS NPC230333