Candicine

Details

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Internal ID f2f4bcd6-824a-49d5-a1eb-df6e10b9b0ec
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenethylamines
IUPAC Name 2-(4-hydroxyphenyl)ethyl-trimethylazanium
SMILES (Canonical) C[N+](C)(C)CCC1=CC=C(C=C1)O
SMILES (Isomeric) C[N+](C)(C)CCC1=CC=C(C=C1)O
InChI InChI=1S/C11H17NO/c1-12(2,3)9-8-10-4-6-11(13)7-5-10/h4-7H,8-9H2,1-3H3/p+1
InChI Key PTOJXIKSKSASRB-UHFFFAOYSA-O
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18NO+
Molecular Weight 180.27 g/mol
Exact Mass 180.138839198 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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6656-13-9
Candicin
2-(4-hydroxyphenyl)ethyl-trimethylazanium
4-Hydroxy-N,N,N-trimethylbenzeneethanaminium
AMMONIUM, (p-HYDROXYPHENETHYL)TRIMETHYL-
BRN 4133224
Benzeneethanaminium, 4-hydroxy-N,N,N-trimethyl-
5V2TJ5H9Z8
CHEBI:3350
MLS001048976
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Candicine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8722 87.22%
Caco-2 + 0.9651 96.51%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6461 64.61%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.8896 88.96%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9553 95.53%
P-glycoprotein inhibitior - 0.9715 97.15%
P-glycoprotein substrate - 0.8312 83.12%
CYP3A4 substrate - 0.6843 68.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4098 40.98%
CYP3A4 inhibition - 0.9760 97.60%
CYP2C9 inhibition - 0.9442 94.42%
CYP2C19 inhibition - 0.9570 95.70%
CYP2D6 inhibition - 0.6086 60.86%
CYP1A2 inhibition - 0.7449 74.49%
CYP2C8 inhibition + 0.5225 52.25%
CYP inhibitory promiscuity - 0.9842 98.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7837 78.37%
Eye corrosion - 0.8713 87.13%
Eye irritation + 0.9922 99.22%
Skin irritation + 0.5288 52.88%
Skin corrosion + 0.7084 70.84%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6924 69.24%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.7752 77.52%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.6867 68.67%
Acute Oral Toxicity (c) III 0.6826 68.26%
Estrogen receptor binding - 0.6534 65.34%
Androgen receptor binding + 0.5956 59.56%
Thyroid receptor binding - 0.6996 69.96%
Glucocorticoid receptor binding - 0.7644 76.44%
Aromatase binding - 0.5357 53.57%
PPAR gamma - 0.6452 64.52%
Honey bee toxicity - 0.9726 97.26%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.5463 54.63%

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
CHEMBL2581 P07339 Cathepsin D 93.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.59% 96.09%
CHEMBL242 Q92731 Estrogen receptor beta 84.91% 98.35%
CHEMBL3401 O75469 Pregnane X receptor 81.20% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.12% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.01% 99.17%

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.
Alphonsea lutea
Fagaropsis glabra
Oplopanax elatus
Phellodendron amurense
Phellodendron chinense
Senegalia berlandieri
Zanthoxylum martinicense
Zanthoxylum rhoifolium

Cross-Links

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PubChem 23135
NPASS NPC78096
LOTUS LTS0149083
wikiData Q5031710