CID 15127236

Details

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Internal ID a37a4f82-e82f-44f1-aa27-c9af063b9b4f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES (Canonical) CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OS(=O)(=O)O)C)C)C2C1)C)C(=O)O)C
SMILES (Isomeric) C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O)C)C)(C)C)OS(=O)(=O)O
InChI InChI=1S/C30H48O6S/c1-25(2)14-16-30(24(31)32)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(36-37(33,34)35)26(3,4)21(27)10-13-29(22,28)7/h8,20-23H,9-18H2,1-7H3,(H,31,32)(H,33,34,35)/t20-,21-,22+,23-,27-,28+,29+,30-/m0/s1
InChI Key HPTCFCREEHCWMI-GTOFXWBISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H48O6S
Molecular Weight 536.80 g/mol
Exact Mass 536.31716042 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 7.10
Atomic LogP (AlogP) 7.06
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

2D Structure

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2D Structure of CID 15127236

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9685 96.85%
Caco-2 - 0.6792 67.92%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6122 61.22%
OATP2B1 inhibitior - 0.5669 56.69%
OATP1B1 inhibitior - 0.3629 36.29%
OATP1B3 inhibitior + 0.8792 87.92%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9086 90.86%
P-glycoprotein inhibitior - 0.5056 50.56%
P-glycoprotein substrate - 0.8150 81.50%
CYP3A4 substrate + 0.6626 66.26%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.9150 91.50%
CYP2C9 inhibition - 0.7952 79.52%
CYP2C19 inhibition - 0.7537 75.37%
CYP2D6 inhibition - 0.8731 87.31%
CYP1A2 inhibition - 0.7816 78.16%
CYP2C8 inhibition + 0.4797 47.97%
CYP inhibitory promiscuity - 0.8357 83.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6283 62.83%
Eye corrosion - 0.9824 98.24%
Eye irritation - 0.9236 92.36%
Skin irritation - 0.7380 73.80%
Skin corrosion - 0.8633 86.33%
Ames mutagenesis - 0.9264 92.64%
Human Ether-a-go-go-Related Gene inhibition - 0.4933 49.33%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.7726 77.26%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7786 77.86%
Acute Oral Toxicity (c) III 0.6300 63.00%
Estrogen receptor binding + 0.6778 67.78%
Androgen receptor binding + 0.6950 69.50%
Thyroid receptor binding + 0.5987 59.87%
Glucocorticoid receptor binding + 0.7984 79.84%
Aromatase binding + 0.7508 75.08%
PPAR gamma + 0.5678 56.78%
Honey bee toxicity - 0.8129 81.29%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5095 50.95%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.53% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.74% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.29% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 86.53% 91.19%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.52% 85.31%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.62% 93.03%
CHEMBL2581 P07339 Cathepsin D 84.37% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.30% 96.77%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.55% 82.69%
CHEMBL5255 O00206 Toll-like receptor 4 83.55% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.24% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.47% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.96% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.49% 95.89%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.36% 95.17%

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.
Gypsophila pacifica
Hedera caucasigena
Hedera helix

Cross-Links

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PubChem 15127236
LOTUS LTS0113012
wikiData Q105031883