Abieta-8,11,13,15-tetraen-18-oic acid

Details

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Internal ID 409ef716-8440-4847-98af-7c1f40b12b85
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1R,4aS,10aR)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H26O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12,17H,1,5,7,9-11H2,2-4H3,(H,21,22)/t17-,19-,20-/m1/s1
InChI Key NGBRPGLXCQJIPU-MISYRCLQSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O2
Molecular Weight 298.40 g/mol
Exact Mass 298.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.81
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Abieta-8,11,13,15-tetraen-18-oic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.7824 78.24%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4478 44.78%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.8771 87.71%
OATP1B3 inhibitior - 0.3373 33.73%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.8152 81.52%
P-glycoprotein inhibitior - 0.8511 85.11%
P-glycoprotein substrate - 0.7066 70.66%
CYP3A4 substrate + 0.5902 59.02%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8713 87.13%
CYP3A4 inhibition - 0.7741 77.41%
CYP2C9 inhibition + 0.6292 62.92%
CYP2C19 inhibition + 0.8393 83.93%
CYP2D6 inhibition - 0.8243 82.43%
CYP1A2 inhibition - 0.6479 64.79%
CYP2C8 inhibition + 0.6568 65.68%
CYP inhibitory promiscuity - 0.8180 81.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7911 79.11%
Carcinogenicity (trinary) Non-required 0.6076 60.76%
Eye corrosion - 0.9825 98.25%
Eye irritation - 0.8761 87.61%
Skin irritation - 0.6507 65.07%
Skin corrosion - 0.9763 97.63%
Ames mutagenesis - 0.8044 80.44%
Human Ether-a-go-go-Related Gene inhibition - 0.3814 38.14%
Micronuclear - 0.9441 94.41%
Hepatotoxicity - 0.6948 69.48%
skin sensitisation + 0.5445 54.45%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7798 77.98%
Acute Oral Toxicity (c) III 0.7738 77.38%
Estrogen receptor binding - 0.5143 51.43%
Androgen receptor binding - 0.4846 48.46%
Thyroid receptor binding + 0.6469 64.69%
Glucocorticoid receptor binding - 0.5526 55.26%
Aromatase binding + 0.6952 69.52%
PPAR gamma + 0.8115 81.15%
Honey bee toxicity - 0.9069 90.69%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6400 64.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.26% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 93.83% 83.82%
CHEMBL1951 P21397 Monoamine oxidase A 92.65% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.59% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 90.23% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.55% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.80% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.15% 93.99%
CHEMBL2581 P07339 Cathepsin D 86.65% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.77% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.40% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.28% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.71% 93.04%
CHEMBL4208 P20618 Proteasome component C5 81.47% 90.00%

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.
Callicarpa macrophylla
Larix kaempferi

Cross-Links

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PubChem 15929992
NPASS NPC133809
LOTUS LTS0121512
wikiData Q105178823