cis-4-Hydroxy-3-methylundecanoic acid lactone

Details

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Internal ID 575029b4-4869-4b09-a5ac-268a6a0c0fd6
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (4R,5R)-5-heptyl-4-methyloxolan-2-one
SMILES (Canonical) CCCCCCCC1C(CC(=O)O1)C
SMILES (Isomeric) CCCCCCC[C@@H]1[C@@H](CC(=O)O1)C
InChI InChI=1S/C12H22O2/c1-3-4-5-6-7-8-11-10(2)9-12(13)14-11/h10-11H,3-9H2,1-2H3/t10-,11-/m1/s1
InChI Key OGRZZHTVLPTHNR-GHMZBOCLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O2
Molecular Weight 198.30 g/mol
Exact Mass 198.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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cis-4-Hydroxy-3-methylundecanoic acid lactone
5-Heptyl-4-methyldihydro-2(3H)-furanone, cis

2D Structure

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2D Structure of cis-4-Hydroxy-3-methylundecanoic acid lactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8565 85.65%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5004 50.04%
OATP2B1 inhibitior - 0.8466 84.66%
OATP1B1 inhibitior + 0.9325 93.25%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8565 85.65%
P-glycoprotein inhibitior - 0.9227 92.27%
P-glycoprotein substrate - 0.8594 85.94%
CYP3A4 substrate - 0.6051 60.51%
CYP2C9 substrate + 0.6168 61.68%
CYP2D6 substrate - 0.8637 86.37%
CYP3A4 inhibition - 0.8164 81.64%
CYP2C9 inhibition - 0.8952 89.52%
CYP2C19 inhibition - 0.7288 72.88%
CYP2D6 inhibition - 0.9209 92.09%
CYP1A2 inhibition - 0.6792 67.92%
CYP2C8 inhibition - 0.9383 93.83%
CYP inhibitory promiscuity - 0.8907 89.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6911 69.11%
Eye corrosion - 0.6956 69.56%
Eye irritation + 0.9035 90.35%
Skin irritation + 0.6557 65.57%
Skin corrosion - 0.9001 90.01%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5563 55.63%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5826 58.26%
skin sensitisation + 0.4773 47.73%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6268 62.68%
Acute Oral Toxicity (c) III 0.7189 71.89%
Estrogen receptor binding - 0.8893 88.93%
Androgen receptor binding - 0.7462 74.62%
Thyroid receptor binding - 0.8040 80.40%
Glucocorticoid receptor binding - 0.7904 79.04%
Aromatase binding - 0.8324 83.24%
PPAR gamma - 0.8111 81.11%
Honey bee toxicity - 0.9631 96.31%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.8134 81.34%
Fish aquatic toxicity + 0.9249 92.49%

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 95.81% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.24% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.44% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 89.98% 97.79%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.51% 92.08%
CHEMBL299 P17252 Protein kinase C alpha 86.21% 98.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.01% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.00% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.31% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.75% 90.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.40% 91.11%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.23% 94.80%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.68% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.23% 93.56%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 91701100
NPASS NPC192138