Chondrillast-7-enol

Details

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Internal ID a789a41e-e7da-434f-a6b4-cd2bd9119f85
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (3S,5S,9R,10S,13R,14R,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES (Canonical) CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C
SMILES (Isomeric) CC[C@@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C)C(C)C
InChI InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h11,19-23,25-27,30H,7-10,12-18H2,1-6H3/t20-,21+,22+,23+,25-,26+,27+,28+,29-/m1/s1
InChI Key YSKVBPGQYRAUQO-XCFYOIDPSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C29H50O
Molecular Weight 414.70 g/mol
Exact Mass 414.386166214 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 9.10
Atomic LogP (AlogP) 8.02
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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Poriferast-7-en-3beta-ol
Dihydrochondrillasterol
18525-35-4
(3S,5S,9R,10S,13R,14R,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Stigmast-7-en-3-ol
22-Dihydrochondrillasterol
5.alpha.-Stigmast-7-en-3.beta.-ol, (24S)-
Stigmast-7-en-3-ol, (3.beta.,5.alpha.,24S)-
Stigmast-7-en-3-ol,(3.beta
poriferst-7-enol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Chondrillast-7-enol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6429 64.29%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4872 48.72%
OATP2B1 inhibitior - 0.5862 58.62%
OATP1B1 inhibitior + 0.8252 82.52%
OATP1B3 inhibitior + 0.9834 98.34%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6966 69.66%
P-glycoprotein inhibitior - 0.5468 54.68%
P-glycoprotein substrate + 0.6050 60.50%
CYP3A4 substrate + 0.6435 64.35%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8031 80.31%
CYP2C9 inhibition - 0.8613 86.13%
CYP2C19 inhibition - 0.7651 76.51%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.9019 90.19%
CYP2C8 inhibition - 0.8095 80.95%
CYP inhibitory promiscuity + 0.5816 58.16%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5992 59.92%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9340 93.40%
Skin irritation + 0.5848 58.48%
Skin corrosion - 0.9453 94.53%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4757 47.57%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5688 56.88%
skin sensitisation + 0.5663 56.63%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.7956 79.56%
Acute Oral Toxicity (c) III 0.7147 71.47%
Estrogen receptor binding + 0.7654 76.54%
Androgen receptor binding + 0.5253 52.53%
Thyroid receptor binding + 0.6577 65.77%
Glucocorticoid receptor binding + 0.8014 80.14%
Aromatase binding - 0.6241 62.41%
PPAR gamma + 0.5223 52.23%
Honey bee toxicity - 0.8554 85.54%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9929 99.29%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.36% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 96.40% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.76% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.73% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.33% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.76% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.52% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.15% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.02% 93.56%
CHEMBL240 Q12809 HERG 86.08% 89.76%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.98% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.35% 90.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.29% 95.89%
CHEMBL2581 P07339 Cathepsin D 85.11% 98.95%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 83.22% 92.88%
CHEMBL1977 P11473 Vitamin D receptor 82.74% 99.43%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.68% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.54% 89.62%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.04% 92.62%
CHEMBL268 P43235 Cathepsin K 80.19% 96.85%

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.
Artemisia vestita
Melia azedarach
Monochaetum vulcanicum
Phellodendron chinense

Cross-Links

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PubChem 5283639
NPASS NPC257347
LOTUS LTS0132904
wikiData Q76294340