(2S)-5-hydroxy-2,7-dimethyl-2-(4-methylpent-3-enyl)chromene-6-carbaldehyde

Details

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Internal ID b8c269a0-cebc-4d3b-b2d1-591608d4ddf7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans
IUPAC Name (2S)-5-hydroxy-2,7-dimethyl-2-(4-methylpent-3-enyl)chromene-6-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H22O3/c1-12(2)6-5-8-18(4)9-7-14-16(21-18)10-13(3)15(11-19)17(14)20/h6-7,9-11,20H,5,8H2,1-4H3/t18-/m0/s1
InChI Key HTJFTUURCKWZOG-SFHVURJKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O3
Molecular Weight 286.40 g/mol
Exact Mass 286.15689456 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.42
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-5-hydroxy-2,7-dimethyl-2-(4-methylpent-3-enyl)chromene-6-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.6895 68.95%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7309 73.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7181 71.81%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7053 70.53%
P-glycoprotein inhibitior - 0.9032 90.32%
P-glycoprotein substrate - 0.7364 73.64%
CYP3A4 substrate + 0.5737 57.37%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.7823 78.23%
CYP3A4 inhibition - 0.7550 75.50%
CYP2C9 inhibition - 0.5064 50.64%
CYP2C19 inhibition + 0.6233 62.33%
CYP2D6 inhibition - 0.7898 78.98%
CYP1A2 inhibition + 0.7840 78.40%
CYP2C8 inhibition - 0.6568 65.68%
CYP inhibitory promiscuity + 0.5272 52.72%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9618 96.18%
Carcinogenicity (trinary) Non-required 0.6511 65.11%
Eye corrosion - 0.9925 99.25%
Eye irritation + 0.6290 62.90%
Skin irritation - 0.6204 62.04%
Skin corrosion - 0.9278 92.78%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4484 44.84%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.5303 53.03%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6334 63.34%
Acute Oral Toxicity (c) III 0.6793 67.93%
Estrogen receptor binding + 0.9178 91.78%
Androgen receptor binding - 0.5361 53.61%
Thyroid receptor binding + 0.7617 76.17%
Glucocorticoid receptor binding + 0.7661 76.61%
Aromatase binding + 0.6031 60.31%
PPAR gamma + 0.8643 86.43%
Honey bee toxicity - 0.8939 89.39%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9702 97.02%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.78% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 97.01% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.64% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.36% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.20% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 92.36% 98.11%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 90.12% 83.57%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.60% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.90% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.61% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.01% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.44% 96.09%

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.
Peperomia blanda
Silybum marianum

Cross-Links

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PubChem 101396972
NPASS NPC238063
LOTUS LTS0081771
wikiData Q105033453