Zyggomphic Acid B

Details

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Internal ID ea9f39c3-090c-43ce-8b8e-cb0414e173fa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,3aR,4R,5S,7aS)-3-ethyl-1,4,5,7-tetramethyl-5-[(1E,3E)-2-methyl-4-phenylbuta-1,3-dienyl]-3a,7a-dihydro-1H-indene-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H34O2/c1-7-22-15-19(3)23-20(4)17-26(5,27(6,24(22)23)25(28)29)16-18(2)13-14-21-11-9-8-10-12-21/h8-17,19,23-24H,7H2,1-6H3,(H,28,29)/b14-13+,18-16+/t19-,23-,24+,26+,27+/m1/s1
InChI Key OPQNKFIXMSPDAA-RSTNLCSYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O2
Molecular Weight 390.60 g/mol
Exact Mass 390.255880323 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.92
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL1224899

2D Structure

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2D Structure of Zyggomphic Acid B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5331 53.31%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.3725 37.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8812 88.12%
OATP1B3 inhibitior + 0.9200 92.00%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9381 93.81%
P-glycoprotein inhibitior + 0.6607 66.07%
P-glycoprotein substrate + 0.5241 52.41%
CYP3A4 substrate + 0.6085 60.85%
CYP2C9 substrate - 0.8030 80.30%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.8316 83.16%
CYP2C9 inhibition - 0.6973 69.73%
CYP2C19 inhibition - 0.6032 60.32%
CYP2D6 inhibition - 0.8975 89.75%
CYP1A2 inhibition - 0.7370 73.70%
CYP2C8 inhibition + 0.7110 71.10%
CYP inhibitory promiscuity + 0.6910 69.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6913 69.13%
Carcinogenicity (trinary) Non-required 0.4784 47.84%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.8899 88.99%
Skin irritation + 0.5128 51.28%
Skin corrosion - 0.9364 93.64%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8991 89.91%
Micronuclear - 0.7641 76.41%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation + 0.7691 76.91%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6180 61.80%
Acute Oral Toxicity (c) III 0.7678 76.78%
Estrogen receptor binding + 0.8089 80.89%
Androgen receptor binding + 0.5219 52.19%
Thyroid receptor binding + 0.7483 74.83%
Glucocorticoid receptor binding + 0.6743 67.43%
Aromatase binding + 0.7459 74.59%
PPAR gamma + 0.6592 65.92%
Honey bee toxicity - 0.9125 91.25%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5051 50.51%
Fish aquatic toxicity + 0.9943 99.43%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.46% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.32% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.65% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.38% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.02% 96.00%
CHEMBL2581 P07339 Cathepsin D 88.70% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.76% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.80% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.92% 89.00%
CHEMBL5028 O14672 ADAM10 83.97% 97.50%

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 46938442
LOTUS LTS0164124
wikiData Q105196512