Fercomin

Details

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Internal ID ca8e0f63-15e3-4075-92e8-21456383470e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(1R,3aR,4R,8aS)-8a-hydroxy-3a,6-dimethyl-3-oxo-1-propan-2-yl-2,4,7,8-tetrahydro-1H-azulen-4-yl] 4-methoxybenzoate
SMILES (Canonical) CC1=CC(C2(C(=O)CC(C2(CC1)O)C(C)C)C)OC(=O)C3=CC=C(C=C3)OC
SMILES (Isomeric) CC1=C[C@H]([C@]2(C(=O)C[C@@H]([C@]2(CC1)O)C(C)C)C)OC(=O)C3=CC=C(C=C3)OC
InChI InChI=1S/C23H30O5/c1-14(2)18-13-19(24)22(4)20(12-15(3)10-11-23(18,22)26)28-21(25)16-6-8-17(27-5)9-7-16/h6-9,12,14,18,20,26H,10-11,13H2,1-5H3/t18-,20-,22-,23+/m1/s1
InChI Key UJYSKNUHBUUKAD-URHOCTSQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H30O5
Molecular Weight 386.50 g/mol
Exact Mass 386.20932405 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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[(1R,3aR,4R,8aS)-8a-hydroxy-3a,6-dimethyl-3-oxo-1-propan-2-yl-2,4,7,8-tetrahydro-1H-azulen-4-yl] 4-methoxybenzoate
4-Methoxybenzoic acid (1R)-1,2,3,3a,4,7,8,8a-octahydro-8abeta-hydroxy-3abeta,6-dimethyl-1beta-(1-methylethyl)

2D Structure

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2D Structure of Fercomin

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 + 0.6838 68.38%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8080 80.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8988 89.88%
OATP1B3 inhibitior - 0.2627 26.27%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7071 70.71%
BSEP inhibitior - 0.4632 46.32%
P-glycoprotein inhibitior + 0.6978 69.78%
P-glycoprotein substrate - 0.6070 60.70%
CYP3A4 substrate + 0.6598 65.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8563 85.63%
CYP3A4 inhibition - 0.7011 70.11%
CYP2C9 inhibition + 0.7088 70.88%
CYP2C19 inhibition + 0.6588 65.88%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition + 0.7112 71.12%
CYP2C8 inhibition - 0.5873 58.73%
CYP inhibitory promiscuity - 0.9232 92.32%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6191 61.91%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9377 93.77%
Skin irritation - 0.5583 55.83%
Skin corrosion - 0.9486 94.86%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6817 68.17%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5591 55.91%
skin sensitisation - 0.7813 78.13%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6675 66.75%
Acute Oral Toxicity (c) II 0.5411 54.11%
Estrogen receptor binding + 0.7581 75.81%
Androgen receptor binding + 0.7551 75.51%
Thyroid receptor binding + 0.6788 67.88%
Glucocorticoid receptor binding + 0.6358 63.58%
Aromatase binding + 0.8129 81.29%
PPAR gamma + 0.5247 52.47%
Honey bee toxicity - 0.8057 80.57%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.12% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.94% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.50% 96.09%
CHEMBL4208 P20618 Proteasome component C5 94.26% 90.00%
CHEMBL2581 P07339 Cathepsin D 93.37% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.91% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.71% 86.33%
CHEMBL2535 P11166 Glucose transporter 88.49% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.47% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.13% 91.11%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.56% 91.07%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.16% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.49% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 84.14% 91.19%
CHEMBL2996 Q05655 Protein kinase C delta 83.52% 97.79%
CHEMBL221 P23219 Cyclooxygenase-1 82.15% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 81.77% 93.31%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.79% 85.31%

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.
Daucus carota subsp. carota
Ferula communis
Ferula jaeschkeana
Ferula sinaica
Ferula tingitana
Ferula vesceritensis

Cross-Links

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PubChem 14486243
LOTUS LTS0045781
wikiData Q105274302