(4(S)-(+)-Ipomeanol)

Details

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Internal ID 7aaa4a15-ff5a-4fc4-ab2b-0e3cc35d1a3a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name (4S)-1-(furan-3-yl)-4-hydroxypentan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O3/c1-7(10)2-3-9(11)8-4-5-12-6-8/h4-7,10H,2-3H2,1H3/t7-/m0/s1
InChI Key RJYQLMILDVERHH-ZETCQYMHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O3
Molecular Weight 168.19 g/mol
Exact Mass 168.078644241 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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(4(S)-(+)-Ipomeanol)
CHEMBL1965801
NSC-644432
1-(3-Furyl)-4(S)-hydroxy-1-pentanone
NCI60_015056

2D Structure

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2D Structure of (4(S)-(+)-Ipomeanol)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7814 78.14%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6585 65.85%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8220 82.20%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9240 92.40%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9161 91.61%
CYP3A4 substrate - 0.6525 65.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7615 76.15%
CYP3A4 inhibition - 0.9468 94.68%
CYP2C9 inhibition - 0.9043 90.43%
CYP2C19 inhibition - 0.7643 76.43%
CYP2D6 inhibition - 0.9369 93.69%
CYP1A2 inhibition - 0.6167 61.67%
CYP2C8 inhibition - 0.9639 96.39%
CYP inhibitory promiscuity - 0.9242 92.42%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5370 53.70%
Eye corrosion - 0.5893 58.93%
Eye irritation + 0.7376 73.76%
Skin irritation + 0.7518 75.18%
Skin corrosion + 0.5471 54.71%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7716 77.16%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5716 57.16%
skin sensitisation - 0.7048 70.48%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5481 54.81%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6918 69.18%
Acute Oral Toxicity (c) III 0.6421 64.21%
Estrogen receptor binding - 0.9550 95.50%
Androgen receptor binding - 0.8980 89.80%
Thyroid receptor binding - 0.8788 87.88%
Glucocorticoid receptor binding - 0.8406 84.06%
Aromatase binding - 0.8811 88.11%
PPAR gamma - 0.8066 80.66%
Honey bee toxicity - 0.9779 97.79%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.6102 61.02%

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
CHEMBL221 P23219 Cyclooxygenase-1 94.45% 90.17%
CHEMBL2581 P07339 Cathepsin D 91.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.18% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.23% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.59% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 84.67% 83.82%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.37% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.16% 96.00%

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.
Artemisia gilvescens
Datura stramonium
Oenanthe fistulosa

Cross-Links

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PubChem 6711829
NPASS NPC79557