CID 73836482

Details

Top
Internal ID 7a1281b1-f2bd-4370-aafc-c48d57be5ae5
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids
IUPAC Name
SMILES (Canonical) CC1C2CC=C3C2(COC14C(CC(O4)(C)C)O)C(=O)CC5(C3CCC6C5(CC7=NC8=C(CC9(C(C8)CCC1C9CC(C2(C1=CC1C2(C(C2(O1)C(CC(O2)(C)C)O)C)O)C)O)C)N=C7C6)C)O
SMILES (Isomeric) CC1C2CC=C3C2(COC14C(CC(O4)(C)C)O)C(=O)CC5(C3CCC6C5(CC7=NC8=C(CC9(C(C8)CCC1C9CC(C2(C1=CC1C2(C(C2(O1)C(CC(O2)(C)C)O)C)O)C)O)C)N=C7C6)C)O
InChI InChI=1S/C54H74N2O10/c1-26-31-14-15-32-33-13-11-29-17-37-39(21-48(29,8)51(33,61)24-41(58)50(31,32)25-63-53(26)42(59)22-45(3,4)65-53)56-36-16-28-10-12-30-34(47(28,7)20-38(36)55-37)18-40(57)49(9)35(30)19-44-52(49,62)27(2)54(64-44)43(60)23-46(5,6)66-54/h15,19,26-31,33-34,40,42-44,57,59-62H,10-14,16-18,20-25H2,1-9H3
InChI Key FQBRNFTWXHGHOY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C54H74N2O10
Molecular Weight 911.20 g/mol
Exact Mass 910.53434656 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 5.65
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 73836482

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 - 0.8565 85.65%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5218 52.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8392 83.92%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9499 94.99%
P-glycoprotein inhibitior + 0.7530 75.30%
P-glycoprotein substrate + 0.7056 70.56%
CYP3A4 substrate + 0.7412 74.12%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8265 82.65%
CYP3A4 inhibition - 0.8767 87.67%
CYP2C9 inhibition - 0.8640 86.40%
CYP2C19 inhibition - 0.8764 87.64%
CYP2D6 inhibition - 0.8948 89.48%
CYP1A2 inhibition - 0.5243 52.43%
CYP2C8 inhibition + 0.7540 75.40%
CYP inhibitory promiscuity - 0.7819 78.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5221 52.21%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9024 90.24%
Skin irritation - 0.6847 68.47%
Skin corrosion - 0.9294 92.94%
Ames mutagenesis - 0.6178 61.78%
Human Ether-a-go-go-Related Gene inhibition + 0.6646 66.46%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5533 55.33%
skin sensitisation - 0.8282 82.82%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.9021 90.21%
Acute Oral Toxicity (c) III 0.6563 65.63%
Estrogen receptor binding + 0.7694 76.94%
Androgen receptor binding + 0.7781 77.81%
Thyroid receptor binding + 0.6114 61.14%
Glucocorticoid receptor binding + 0.7641 76.41%
Aromatase binding + 0.6393 63.93%
PPAR gamma + 0.7993 79.93%
Honey bee toxicity - 0.6825 68.25%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9576 95.76%

Targets

Top

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 96.86% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.10% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.28% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.28% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.00% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.42% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.05% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.99% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.89% 82.69%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 88.95% 96.39%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 87.63% 98.46%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.75% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.80% 94.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 83.18% 97.33%
CHEMBL1937 Q92769 Histone deacetylase 2 83.03% 94.75%
CHEMBL1871 P10275 Androgen Receptor 82.94% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.41% 95.89%
CHEMBL2581 P07339 Cathepsin D 82.37% 98.95%
CHEMBL259 P32245 Melanocortin receptor 4 80.81% 95.38%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.77% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.34% 89.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 73836482
LOTUS LTS0088336
wikiData Q104999519