Germanicen

Details

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Internal ID e74f5989-643f-4d58-8dea-c85d0f87e17d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicene
SMILES (Canonical) CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C
SMILES (Isomeric) CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C
InChI InChI=1S/C30H50/c1-25(2)16-17-27(5)18-19-29(7)21(22(27)20-25)10-11-24-28(6)14-9-13-26(3,4)23(28)12-15-30(24,29)8/h20-21,23-24H,9-19H2,1-8H3
InChI Key RKXWJPSYFPRIGF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50
Molecular Weight 410.70 g/mol
Exact Mass 410.391251595 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.90
Atomic LogP (AlogP) 9.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Germanicene
RKXWJPSYFPRIGF-UHFFFAOYSA-N

2D Structure

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2D Structure of Germanicen

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.7006 70.06%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.6465 64.65%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.8691 86.91%
OATP1B3 inhibitior + 0.8746 87.46%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8209 82.09%
P-glycoprotein inhibitior - 0.6454 64.54%
P-glycoprotein substrate - 0.8453 84.53%
CYP3A4 substrate + 0.5955 59.55%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8710 87.10%
CYP2C9 inhibition - 0.7317 73.17%
CYP2C19 inhibition - 0.6019 60.19%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.8422 84.22%
CYP2C8 inhibition - 0.5798 57.98%
CYP inhibitory promiscuity - 0.5141 51.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4857 48.57%
Eye corrosion - 0.9650 96.50%
Eye irritation - 0.8898 88.98%
Skin irritation - 0.6920 69.20%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6815 68.15%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6248 62.48%
skin sensitisation + 0.8341 83.41%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6503 65.03%
Acute Oral Toxicity (c) III 0.6528 65.28%
Estrogen receptor binding + 0.8469 84.69%
Androgen receptor binding + 0.6924 69.24%
Thyroid receptor binding + 0.6781 67.81%
Glucocorticoid receptor binding + 0.8469 84.69%
Aromatase binding + 0.7242 72.42%
PPAR gamma + 0.5973 59.73%
Honey bee toxicity - 0.8222 82.22%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6900 69.00%
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 90.94% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.39% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.78% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.41% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.15% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.23% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.87% 95.56%
CHEMBL2581 P07339 Cathepsin D 83.96% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.66% 85.30%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.20% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.15% 100.00%

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.
Goniophlebium mengtzeense

Cross-Links

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PubChem 609342
LOTUS LTS0114190
wikiData Q105239617