poricoic acid H

Details

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Internal ID 959faee2-cb34-4bf1-8b27-998edb5d35d1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2R)-2-[(2R,3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-2-hydroxy-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,5,7,8,9-octahydrocyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid
SMILES (Canonical) CC(C)C(=C)CCC(C1C(CC2(C1(CCC3=C2CCC(C3(C)CCC(=O)O)C(=C)C)C)C)O)C(=O)O
SMILES (Isomeric) CC(C)C(=C)CC[C@H]([C@H]1[C@@H](C[C@@]2([C@@]1(CCC3=C2CC[C@H]([C@]3(C)CCC(=O)O)C(=C)C)C)C)O)C(=O)O
InChI InChI=1S/C31H48O5/c1-18(2)20(5)9-10-21(28(35)36)27-25(32)17-31(8)24-12-11-22(19(3)4)29(6,15-14-26(33)34)23(24)13-16-30(27,31)7/h18,21-22,25,27,32H,3,5,9-17H2,1-2,4,6-8H3,(H,33,34)(H,35,36)/t21-,22+,25-,27+,29+,30-,31+/m1/s1
InChI Key GKXXWKRLARTIQL-SMFZDKLCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C31H48O5
Molecular Weight 500.70 g/mol
Exact Mass 500.35017463 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 6.70
Atomic LogP (AlogP) 7.02
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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CHEBI:68356
CHEMBL251767
SCHEMBL6281047
GKXXWKRLARTIQL-SMFZDKLCSA-
HY-N11656
CS-0675968
Q27136853
(2R)-2-[(2R,3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-2-hydroxy-3a,6,9b-trimethyl-7-(prop-1-en-2-yl)-2,3,3a,4,5,6,7,8,9,9b-decahydro-1H-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid
(2R)-2-[(2R,3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-2-hydroxy-3a,6,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,4,5,7,8,9-octahydrocyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid
InChI=1/C31H48O5/c1-18(2)20(5)9-10-21(28(35)36)27-25(32)17-31(8)24-12-11-22(19(3)4)29(6,15-14-26(33)34)23(24)13-16-30(27,31)7/h18,21-22,25,27,32H,3,5,9-17H2,1-2,4,6-8H3,(H,33,34)(H,35,36)/t21-,22+,25-,27+,29+,30-,31+/m1/s1

2D Structure

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2D Structure of poricoic acid H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.4912 49.12%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8561 85.61%
OATP2B1 inhibitior - 0.7074 70.74%
OATP1B1 inhibitior + 0.8394 83.94%
OATP1B3 inhibitior - 0.5674 56.74%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6282 62.82%
BSEP inhibitior + 0.7920 79.20%
P-glycoprotein inhibitior - 0.4622 46.22%
P-glycoprotein substrate - 0.5340 53.40%
CYP3A4 substrate + 0.6786 67.86%
CYP2C9 substrate - 0.8404 84.04%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition - 0.7946 79.46%
CYP2C9 inhibition - 0.9225 92.25%
CYP2C19 inhibition - 0.9462 94.62%
CYP2D6 inhibition - 0.9583 95.83%
CYP1A2 inhibition - 0.9483 94.83%
CYP2C8 inhibition - 0.5655 56.55%
CYP inhibitory promiscuity - 0.8942 89.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7204 72.04%
Eye corrosion - 0.9945 99.45%
Eye irritation - 0.9093 90.93%
Skin irritation + 0.6903 69.03%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis - 0.7278 72.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6851 68.51%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6561 65.61%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.8286 82.86%
Acute Oral Toxicity (c) III 0.6127 61.27%
Estrogen receptor binding + 0.6572 65.72%
Androgen receptor binding + 0.7425 74.25%
Thyroid receptor binding + 0.5904 59.04%
Glucocorticoid receptor binding + 0.7484 74.84%
Aromatase binding + 0.6745 67.45%
PPAR gamma + 0.5546 55.46%
Honey bee toxicity - 0.8177 81.77%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7100 71.00%
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 98.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.56% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.48% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.87% 90.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.19% 95.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.20% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 88.72% 91.19%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 87.46% 95.50%
CHEMBL4040 P28482 MAP kinase ERK2 86.76% 83.82%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.53% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.99% 85.14%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.52% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.15% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.94% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.98% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.87% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.92% 95.50%

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 10918099
LOTUS LTS0134201
wikiData Q27136853