CID 162913601

Details

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Internal ID ad2598c3-1c2c-4020-9f35-f20a648f0d22
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC1C(=O)CC2C(C(CCC2(C13CCC4(O3)COC=C4)C)OC(=O)C)(C)C
SMILES (Isomeric) C[C@H]1C(=O)C[C@@H]2[C@@]([C@]13CC[C@]4(O3)COC=C4)(CC[C@H](C2(C)C)OC(=O)C)C
InChI InChI=1S/C22H32O5/c1-14-16(24)12-17-19(3,4)18(26-15(2)23)6-7-20(17,5)22(14)9-8-21(27-22)10-11-25-13-21/h10-11,14,17-18H,6-9,12-13H2,1-5H3/t14-,17-,18+,20-,21+,22-/m0/s1
InChI Key RWQAIOGLVLEWEL-MUSVXNCESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O5
Molecular Weight 376.50 g/mol
Exact Mass 376.22497412 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.80
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162913601

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 - 0.5164 51.64%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8227 82.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7806 78.06%
OATP1B3 inhibitior + 0.8763 87.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.7982 79.82%
P-glycoprotein inhibitior - 0.4916 49.16%
P-glycoprotein substrate - 0.7176 71.76%
CYP3A4 substrate + 0.6627 66.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8551 85.51%
CYP3A4 inhibition - 0.7956 79.56%
CYP2C9 inhibition - 0.8364 83.64%
CYP2C19 inhibition - 0.8389 83.89%
CYP2D6 inhibition - 0.9478 94.78%
CYP1A2 inhibition - 0.8902 89.02%
CYP2C8 inhibition + 0.5534 55.34%
CYP inhibitory promiscuity - 0.9002 90.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5014 50.14%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9310 93.10%
Skin irritation - 0.6496 64.96%
Skin corrosion - 0.9054 90.54%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7553 75.53%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5185 51.85%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6543 65.43%
Acute Oral Toxicity (c) III 0.5490 54.90%
Estrogen receptor binding + 0.9023 90.23%
Androgen receptor binding + 0.6734 67.34%
Thyroid receptor binding + 0.6925 69.25%
Glucocorticoid receptor binding + 0.7955 79.55%
Aromatase binding + 0.6799 67.99%
PPAR gamma + 0.7172 71.72%
Honey bee toxicity - 0.7875 78.75%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9932 99.32%

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 95.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.13% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.48% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.12% 86.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 90.45% 93.04%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.21% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.73% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.04% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.74% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.34% 99.23%
CHEMBL2581 P07339 Cathepsin D 85.97% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.46% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.62% 94.80%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.32% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 84.09% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.93% 82.69%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.16% 96.77%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.63% 97.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.27% 91.07%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.61% 95.71%

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.
Roylea cinerea

Cross-Links

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PubChem 162913601
LOTUS LTS0015292
wikiData Q105246668