Climacostol

Details

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Internal ID 501ad2b9-fcb2-4411-8407-3d7cba92eb6f
Taxonomy Benzenoids > Phenols > Benzenediols > Resorcinols
IUPAC Name 5-[(Z)-non-2-enyl]benzene-1,3-diol
SMILES (Canonical) CCCCCCC=CCC1=CC(=CC(=C1)O)O
SMILES (Isomeric) CCCCCC/C=C\CC1=CC(=CC(=C1)O)O
InChI InChI=1S/C15H22O2/c1-2-3-4-5-6-7-8-9-13-10-14(16)12-15(17)11-13/h7-8,10-12,16-17H,2-6,9H2,1H3/b8-7-
InChI Key VKWFGJNPZKSIEL-FPLPWBNLSA-N
Popularity 12 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) 40.50 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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253158-28-0
5-[(Z)-non-2-enyl]benzene-1,3-diol
DTXSID90443780
5-((Z)-non-2-enyl)benzene-1,3-diol
RefChem:918821
DTXCID30394601
5-((Z)-non-2-en-1-yl)resorcinol
(Z)-5-(non-2-en-1-yl)benzene-1,3-diol
5-(2Z)-2-Nonen-1-yl-1,3-benzenediol
5-(2Z)-2-Nonenyl-1,3-benzenediol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Climacostol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.8795 87.95%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.5227 52.27%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.7293 72.93%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.6493 64.93%
P-glycoprotein inhibitior - 0.9494 94.94%
P-glycoprotein substrate - 0.8392 83.92%
CYP3A4 substrate - 0.6324 63.24%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate + 0.3567 35.67%
CYP3A4 inhibition + 0.8505 85.05%
CYP2C9 inhibition - 0.5926 59.26%
CYP2C19 inhibition + 0.5358 53.58%
CYP2D6 inhibition - 0.7401 74.01%
CYP1A2 inhibition + 0.7543 75.43%
CYP2C8 inhibition + 0.5280 52.80%
CYP inhibitory promiscuity + 0.8169 81.69%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7411 74.11%
Carcinogenicity (trinary) Non-required 0.6401 64.01%
Eye corrosion + 0.4493 44.93%
Eye irritation + 0.8455 84.55%
Skin irritation + 0.7645 76.45%
Skin corrosion + 0.6007 60.07%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6480 64.80%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5839 58.39%
skin sensitisation + 0.8229 82.29%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5491 54.91%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6906 69.06%
Acute Oral Toxicity (c) III 0.7916 79.16%
Estrogen receptor binding + 0.7015 70.15%
Androgen receptor binding - 0.5451 54.51%
Thyroid receptor binding + 0.5788 57.88%
Glucocorticoid receptor binding - 0.5585 55.85%
Aromatase binding + 0.6070 60.70%
PPAR gamma + 0.9186 91.86%
Honey bee toxicity - 0.9905 99.05%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.8650 86.50%
Fish aquatic toxicity + 0.9895 98.95%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.27% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.87% 92.08%
CHEMBL2581 P07339 Cathepsin D 96.24% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.16% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.70% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.88% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.24% 86.33%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.50% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.47% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 82.87% 97.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.13% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10704873
NPASS NPC168528
LOTUS LTS0031631
wikiData Q76415918