Formosadimer A

Details

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Internal ID 1167b03d-b9a2-453c-818d-4797ce31d98d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,9S,10R,10aS)-10-[[(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl]oxy]-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol
SMILES (Canonical) CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)OC4C(C5=CC(=C(C=C5C6(C4C(CCC6)(C)C)C)OC)C(C)C)O
SMILES (Isomeric) CC(C)C1=C(C=C2C(=C1)C=C[C@@H]3[C@@]2(CCCC3(C)C)C)O[C@H]4[C@H](C5=CC(=C(C=C5[C@@]6([C@@H]4C(CCC6)(C)C)C)OC)C(C)C)O
InChI InChI=1S/C41H58O3/c1-24(2)27-20-26-14-15-34-38(5,6)16-12-18-40(34,9)30(26)22-33(27)44-36-35(42)29-21-28(25(3)4)32(43-11)23-31(29)41(10)19-13-17-39(7,8)37(36)41/h14-15,20-25,34-37,42H,12-13,16-19H2,1-11H3/t34-,35-,36-,37-,40+,41+/m0/s1
InChI Key ZQIWLIFQYJYGHM-OKDLLEDBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C41H58O3
Molecular Weight 598.90 g/mol
Exact Mass 598.43859571 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 12.00
Atomic LogP (AlogP) 10.63
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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(4aS,9S,10R,10aS)-10-[[(4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-yl]oxy]-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol

2D Structure

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2D Structure of Formosadimer A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 - 0.6966 69.66%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7397 73.97%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.8429 84.29%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9943 99.43%
P-glycoprotein inhibitior + 0.8701 87.01%
P-glycoprotein substrate + 0.5167 51.67%
CYP3A4 substrate + 0.6698 66.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3535 35.35%
CYP3A4 inhibition - 0.6905 69.05%
CYP2C9 inhibition - 0.7146 71.46%
CYP2C19 inhibition - 0.5785 57.85%
CYP2D6 inhibition - 0.8949 89.49%
CYP1A2 inhibition + 0.6550 65.50%
CYP2C8 inhibition + 0.6422 64.22%
CYP inhibitory promiscuity - 0.7209 72.09%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8363 83.63%
Carcinogenicity (trinary) Non-required 0.5693 56.93%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9064 90.64%
Skin irritation - 0.7068 70.68%
Skin corrosion - 0.9544 95.44%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7682 76.82%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7245 72.45%
skin sensitisation - 0.7841 78.41%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8043 80.43%
Acute Oral Toxicity (c) III 0.7009 70.09%
Estrogen receptor binding + 0.7747 77.47%
Androgen receptor binding + 0.6764 67.64%
Thyroid receptor binding + 0.6591 65.91%
Glucocorticoid receptor binding + 0.8230 82.30%
Aromatase binding + 0.7183 71.83%
PPAR gamma + 0.7118 71.18%
Honey bee toxicity - 0.6145 61.45%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.9965 99.65%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.72% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.29% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.23% 94.45%
CHEMBL4040 P28482 MAP kinase ERK2 96.73% 83.82%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.83% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.05% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.86% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.73% 98.95%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.18% 91.03%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.99% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.48% 85.14%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 84.47% 97.33%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.09% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.83% 97.14%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.59% 95.56%
CHEMBL4208 P20618 Proteasome component C5 82.86% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.78% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.45% 89.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.34% 96.77%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.01% 90.71%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.21% 89.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.09% 100.00%
CHEMBL2535 P11166 Glucose transporter 80.08% 98.75%

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.
Calocedrus macrolepis
Glaucium oxylobum

Cross-Links

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PubChem 11563385
NPASS NPC269928
LOTUS LTS0014234
wikiData Q105381497