1-Hydroxycyclocolorenone

Details

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Internal ID 6564e398-0b17-4870-b074-20767d3b7531
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Aromadendrane sesquiterpenoids > 5,10-cycloaromadendrane sesquiterpenoids
IUPAC Name (1aS,4S,4aR,7bR)-4a-hydroxy-1,1,4,7-tetramethyl-1a,2,3,4,5,7b-hexahydrocyclopropa[e]azulen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-8-5-6-10-13(14(10,3)4)12-9(2)11(16)7-15(8,12)17/h8,10,13,17H,5-7H2,1-4H3/t8-,10-,13-,15+/m0/s1
InChI Key ZBZKCPGSZOLGGP-LGRMDKJXSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Hydroxycyclocolorenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.7743 77.43%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6141 61.41%
OATP2B1 inhibitior - 0.8470 84.70%
OATP1B1 inhibitior + 0.9301 93.01%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8947 89.47%
P-glycoprotein inhibitior - 0.8866 88.66%
P-glycoprotein substrate - 0.8897 88.97%
CYP3A4 substrate + 0.6000 60.00%
CYP2C9 substrate - 0.8284 82.84%
CYP2D6 substrate - 0.8927 89.27%
CYP3A4 inhibition - 0.9159 91.59%
CYP2C9 inhibition - 0.6613 66.13%
CYP2C19 inhibition - 0.6126 61.26%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.5584 55.84%
CYP2C8 inhibition - 0.9055 90.55%
CYP inhibitory promiscuity - 0.8955 89.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4963 49.63%
Eye corrosion - 0.9832 98.32%
Eye irritation - 0.6272 62.72%
Skin irritation + 0.6300 63.00%
Skin corrosion - 0.9437 94.37%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6552 65.52%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5550 55.50%
skin sensitisation - 0.5850 58.50%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.4658 46.58%
Acute Oral Toxicity (c) III 0.5307 53.07%
Estrogen receptor binding - 0.5485 54.85%
Androgen receptor binding - 0.5207 52.07%
Thyroid receptor binding - 0.5753 57.53%
Glucocorticoid receptor binding - 0.7140 71.40%
Aromatase binding - 0.7655 76.55%
PPAR gamma - 0.8033 80.33%
Honey bee toxicity - 0.8660 86.60%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9626 96.26%

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
CHEMBL2039 P27338 Monoamine oxidase B 90.88% 92.51%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.04% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.83% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.98% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.70% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.62% 93.99%
CHEMBL2581 P07339 Cathepsin D 82.41% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.38% 93.04%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.18% 93.03%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.10% 93.00%

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.
Porella vernicosa
Vatica harmandiana

Cross-Links

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PubChem 44566212
NPASS NPC182848
LOTUS LTS0221575
wikiData Q105370907