Lipocarbazole A4

Details

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Internal ID f33bcc8c-66e7-40f7-ac6f-ca8f24f51cd7
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 1-heptadecyl-2-methyl-9H-carbazol-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H45NO/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-25-24(2)29(32)23-27-26-21-18-19-22-28(26)31-30(25)27/h18-19,21-23,31-32H,3-17,20H2,1-2H3
InChI Key INOUAYJXXCWXDA-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H45NO
Molecular Weight 435.70 g/mol
Exact Mass 435.350115059 g/mol
Topological Polar Surface Area (TPSA) 36.00 Ų
XlogP 12.30
Atomic LogP (AlogP) 9.75
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 16

Synonyms

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1-heptadecyl-2-methyl-9H-carbazol-3-ol
RefChem:153608
CHEBI:199784

2D Structure

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2D Structure of Lipocarbazole A4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5251 52.51%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5932 59.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7711 77.11%
OATP1B3 inhibitior + 0.9338 93.38%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9547 95.47%
P-glycoprotein inhibitior + 0.6452 64.52%
P-glycoprotein substrate - 0.6177 61.77%
CYP3A4 substrate + 0.5533 55.33%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.4117 41.17%
CYP3A4 inhibition + 0.7672 76.72%
CYP2C9 inhibition + 0.5694 56.94%
CYP2C19 inhibition + 0.7668 76.68%
CYP2D6 inhibition - 0.5099 50.99%
CYP1A2 inhibition + 0.9632 96.32%
CYP2C8 inhibition + 0.7996 79.96%
CYP inhibitory promiscuity + 0.9306 93.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5737 57.37%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.8107 81.07%
Skin irritation - 0.8029 80.29%
Skin corrosion - 0.7937 79.37%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7826 78.26%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5077 50.77%
skin sensitisation - 0.7701 77.01%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.9179 91.79%
Acute Oral Toxicity (c) III 0.6094 60.94%
Estrogen receptor binding + 0.7764 77.64%
Androgen receptor binding + 0.8097 80.97%
Thyroid receptor binding + 0.5870 58.70%
Glucocorticoid receptor binding + 0.5779 57.79%
Aromatase binding + 0.6799 67.99%
PPAR gamma + 0.6468 64.68%
Honey bee toxicity - 0.9804 98.04%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.8028 80.28%
Fish aquatic toxicity + 0.9921 99.21%

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
CHEMBL240 Q12809 HERG 99.90% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.96% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.24% 91.49%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 97.22% 92.08%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 94.86% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.15% 93.99%
CHEMBL1781 P11387 DNA topoisomerase I 91.70% 97.00%
CHEMBL255 P29275 Adenosine A2b receptor 91.35% 98.59%
CHEMBL2885 P07451 Carbonic anhydrase III 90.98% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.64% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.64% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.31% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.72% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 86.31% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.85% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 85.40% 89.63%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.17% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.07% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.88% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.79% 94.45%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 81.78% 85.40%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.84% 94.80%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.65% 91.81%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.54% 91.79%
CHEMBL1937 Q92769 Histone deacetylase 2 80.20% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 44512451
LOTUS LTS0199913
wikiData Q75067808