Neoruscogenin

Details

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Internal ID 6fef6718-2557-41be-8931-0ec27140efb8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14,16-diol
SMILES (Canonical) CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6
SMILES (Isomeric) C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4([C@@H](C[C@@H](C5)O)O)C)C)O[C@]16CCC(=C)CO6
InChI InChI=1S/C27H40O4/c1-15-7-10-27(30-14-15)16(2)24-22(31-27)13-21-19-6-5-17-11-18(28)12-23(29)26(17,4)20(19)8-9-25(21,24)3/h5,16,18-24,28-29H,1,6-14H2,2-4H3/t16-,18+,19+,20-,21-,22-,23+,24-,25-,26-,27+/m0/s1
InChI Key ALTRINCJVPIQNK-NHIXJPGBSA-N
Popularity 66 references in papers

Physical and Chemical Properties

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Molecular Formula C27H40O4
Molecular Weight 428.60 g/mol
Exact Mass 428.29265975 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.60
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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17676-33-4
25(27)-Dehydroruscogenin
delta5-Convallamarogenin
D4E4KC2TUK
Spirosta-5,25(27)-diene-1beta,3beta-diol
EINECS 241-660-1
Spirosta-5,25(27)-diene-1,3-diol, (1b,3b)-
Spirosta-5,25(27)-diene-1,3-diol, (1beta,3beta)-
Spirosta-5,25(27)-dien-1beta,3beta-diol
(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14,16-diol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Neoruscogenin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9388 93.88%
Caco-2 - 0.6039 60.39%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5749 57.49%
OATP2B1 inhibitior - 0.7121 71.21%
OATP1B1 inhibitior + 0.8881 88.81%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8666 86.66%
P-glycoprotein inhibitior - 0.5953 59.53%
P-glycoprotein substrate + 0.5846 58.46%
CYP3A4 substrate + 0.7312 73.12%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.7501 75.01%
CYP3A4 inhibition - 0.8196 81.96%
CYP2C9 inhibition - 0.9233 92.33%
CYP2C19 inhibition - 0.9378 93.78%
CYP2D6 inhibition - 0.9318 93.18%
CYP1A2 inhibition - 0.7966 79.66%
CYP2C8 inhibition + 0.6585 65.85%
CYP inhibitory promiscuity - 0.9045 90.45%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4395 43.95%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9575 95.75%
Skin irritation + 0.5754 57.54%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6985 69.85%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8547 85.47%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8232 82.32%
Acute Oral Toxicity (c) III 0.5205 52.05%
Estrogen receptor binding + 0.7558 75.58%
Androgen receptor binding + 0.7174 71.74%
Thyroid receptor binding + 0.6757 67.57%
Glucocorticoid receptor binding + 0.8236 82.36%
Aromatase binding + 0.7718 77.18%
PPAR gamma + 0.5551 55.51%
Honey bee toxicity - 0.6912 69.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9770 97.70%

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 98.14% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 95.60% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.67% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 93.24% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.58% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.68% 95.89%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 86.59% 89.05%
CHEMBL1871 P10275 Androgen Receptor 86.57% 96.43%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.61% 86.00%
CHEMBL2996 Q05655 Protein kinase C delta 84.79% 97.79%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.50% 94.45%
CHEMBL242 Q92731 Estrogen receptor beta 83.76% 98.35%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.70% 86.33%
CHEMBL5028 O14672 ADAM10 82.80% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.69% 89.00%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 81.79% 87.16%
CHEMBL221 P23219 Cyclooxygenase-1 81.48% 90.17%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.32% 93.04%
CHEMBL1977 P11473 Vitamin D receptor 80.25% 99.43%

Cross-Links

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PubChem 9910474
NPASS NPC281471