trans-(+)-alpha1-(Hydroxymethyl)-alpha1-methyl-1,4-cyclohexanedimethanol

Details

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Internal ID 3c5eace2-77cc-40a4-a3a7-b5c5f8b537fd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-[4-(hydroxymethyl)cyclohexyl]propane-1,2-diol
SMILES (Canonical) CC(CO)(C1CCC(CC1)CO)O
SMILES (Isomeric) CC(CO)(C1CCC(CC1)CO)O
InChI InChI=1S/C10H20O3/c1-10(13,7-12)9-4-2-8(6-11)3-5-9/h8-9,11-13H,2-7H2,1H3
InChI Key AYKAYXCATARIHK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H20O3
Molecular Weight 188.26 g/mol
Exact Mass 188.14124450 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.53
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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DTXSID401170917
1alpha-(Hydroxymethyl)-4beta-(1,2-dihydroxy-1-methylethyl)cyclohexane
trans-(+)-alpha1-(Hydroxymethyl)-alpha1-methyl-1,4-cyclohexanedimethanol

2D Structure

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2D Structure of trans-(+)-alpha1-(Hydroxymethyl)-alpha1-methyl-1,4-cyclohexanedimethanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9421 94.21%
Caco-2 - 0.5804 58.04%
Blood Brain Barrier - 0.5115 51.15%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6754 67.54%
OATP2B1 inhibitior - 0.8475 84.75%
OATP1B1 inhibitior + 0.9502 95.02%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8041 80.41%
BSEP inhibitior - 0.9288 92.88%
P-glycoprotein inhibitior - 0.9755 97.55%
P-glycoprotein substrate - 0.9015 90.15%
CYP3A4 substrate - 0.6013 60.13%
CYP2C9 substrate - 0.6408 64.08%
CYP2D6 substrate - 0.7850 78.50%
CYP3A4 inhibition - 0.8547 85.47%
CYP2C9 inhibition - 0.8093 80.93%
CYP2C19 inhibition - 0.8614 86.14%
CYP2D6 inhibition - 0.9324 93.24%
CYP1A2 inhibition - 0.8252 82.52%
CYP2C8 inhibition - 0.9292 92.92%
CYP inhibitory promiscuity - 0.9627 96.27%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6727 67.27%
Eye corrosion - 0.9251 92.51%
Eye irritation + 0.6748 67.48%
Skin irritation - 0.7827 78.27%
Skin corrosion - 0.9817 98.17%
Ames mutagenesis - 0.7954 79.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6662 66.62%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6104 61.04%
skin sensitisation - 0.5806 58.06%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4756 47.56%
Acute Oral Toxicity (c) III 0.5110 51.10%
Estrogen receptor binding - 0.8208 82.08%
Androgen receptor binding - 0.8951 89.51%
Thyroid receptor binding - 0.6993 69.93%
Glucocorticoid receptor binding - 0.4691 46.91%
Aromatase binding - 0.8009 80.09%
PPAR gamma - 0.8863 88.63%
Honey bee toxicity - 0.9443 94.43%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.4409 44.09%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.72% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.75% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.00% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 87.50% 95.93%
CHEMBL2581 P07339 Cathepsin D 85.12% 98.95%
CHEMBL237 P41145 Kappa opioid receptor 82.13% 98.10%
CHEMBL2996 Q05655 Protein kinase C delta 81.43% 97.79%

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.
Picea morrisonicola

Cross-Links

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PubChem 91255057
LOTUS LTS0007676
wikiData Q104921164