1-(3,3-Dimethyl allyl)-2-hydroxy-3-formyl-8-meth-oxycarbazole

Details

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Internal ID c27542b7-1d68-4186-97e7-19c4bc85a5d4
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 2-hydroxy-8-methoxy-1-(3-methylbut-2-enyl)-9H-carbazole-3-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H19NO3/c1-11(2)7-8-14-17-15(9-12(10-21)19(14)22)13-5-4-6-16(23-3)18(13)20-17/h4-7,9-10,20,22H,8H2,1-3H3
InChI Key QHPQTMWHKFLVSR-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H19NO3
Molecular Weight 309.40 g/mol
Exact Mass 309.13649347 g/mol
Topological Polar Surface Area (TPSA) 62.30 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3,3-Dimethyl allyl)-2-hydroxy-3-formyl-8-meth-oxycarbazole

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 + 0.7402 74.02%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6734 67.34%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.7834 78.34%
OATP1B3 inhibitior + 0.9324 93.24%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8169 81.69%
P-glycoprotein inhibitior - 0.5580 55.80%
P-glycoprotein substrate - 0.6390 63.90%
CYP3A4 substrate + 0.6027 60.27%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.7955 79.55%
CYP3A4 inhibition + 0.6286 62.86%
CYP2C9 inhibition + 0.6705 67.05%
CYP2C19 inhibition + 0.8353 83.53%
CYP2D6 inhibition - 0.6789 67.89%
CYP1A2 inhibition + 0.9007 90.07%
CYP2C8 inhibition + 0.6527 65.27%
CYP inhibitory promiscuity + 0.9632 96.32%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5659 56.59%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.5291 52.91%
Skin irritation - 0.8436 84.36%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5340 53.40%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8356 83.56%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8100 81.00%
Acute Oral Toxicity (c) III 0.6069 60.69%
Estrogen receptor binding + 0.9479 94.79%
Androgen receptor binding + 0.7639 76.39%
Thyroid receptor binding + 0.7620 76.20%
Glucocorticoid receptor binding + 0.9555 95.55%
Aromatase binding + 0.7673 76.73%
PPAR gamma + 0.8756 87.56%
Honey bee toxicity - 0.8658 86.58%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6234 62.34%
Fish aquatic toxicity + 0.9527 95.27%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 98.47% 98.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.04% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.00% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.77% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.88% 86.33%
CHEMBL2535 P11166 Glucose transporter 93.00% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.31% 85.14%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.96% 91.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.40% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 86.73% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.84% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 85.25% 90.20%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.50% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.33% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.93% 95.50%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.50% 100.00%

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.
Bergera koenigii
Clausena harmandiana

Cross-Links

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PubChem 129710379
LOTUS LTS0043620
wikiData Q105221074