15alpha-Hydroxymollic acid

Details

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Internal ID c7c0a969-63b3-4965-b1be-0ecf13950900
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cycloartanols and derivatives
IUPAC Name (1S,3S,4S,6S,7S,8R,11R,12S,13S,15R,16R)-4,6,13-trihydroxy-7,12,16-trimethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid
SMILES (Canonical) CC(CCC=C(C)C)C1CC(C2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C)O
SMILES (Isomeric) C[C@H](CCC=C(C)C)[C@H]1C[C@@H]([C@@]2([C@@]1(CC[C@]34[C@H]2CC[C@@H]5[C@]3(C4)[C@H](C[C@@H]([C@@]5(C)C(=O)O)O)O)C)C)O
InChI InChI=1S/C30H48O5/c1-17(2)8-7-9-18(3)19-14-23(32)28(6)21-11-10-20-27(5,25(34)35)22(31)15-24(33)30(20)16-29(21,30)13-12-26(19,28)4/h8,18-24,31-33H,7,9-16H2,1-6H3,(H,34,35)/t18-,19-,20+,21+,22+,23+,24+,26-,27+,28-,29+,30-/m1/s1
InChI Key YNRJWLCUSNZCQL-CQRFSKKRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H48O5
Molecular Weight 488.70 g/mol
Exact Mass 488.35017463 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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CHEMBL468878

2D Structure

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2D Structure of 15alpha-Hydroxymollic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 - 0.6224 62.24%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6782 67.82%
OATP2B1 inhibitior - 0.5732 57.32%
OATP1B1 inhibitior + 0.8434 84.34%
OATP1B3 inhibitior + 0.7887 78.87%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7223 72.23%
P-glycoprotein inhibitior - 0.5782 57.82%
P-glycoprotein substrate - 0.5361 53.61%
CYP3A4 substrate + 0.6481 64.81%
CYP2C9 substrate - 0.6653 66.53%
CYP2D6 substrate - 0.8408 84.08%
CYP3A4 inhibition - 0.8589 85.89%
CYP2C9 inhibition - 0.6537 65.37%
CYP2C19 inhibition - 0.8333 83.33%
CYP2D6 inhibition - 0.9535 95.35%
CYP1A2 inhibition - 0.8606 86.06%
CYP2C8 inhibition - 0.7458 74.58%
CYP inhibitory promiscuity - 0.8197 81.97%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6704 67.04%
Eye corrosion - 0.9940 99.40%
Eye irritation - 0.9414 94.14%
Skin irritation + 0.5962 59.62%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.6809 68.09%
Human Ether-a-go-go-Related Gene inhibition + 0.7219 72.19%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.6176 61.76%
skin sensitisation - 0.7011 70.11%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.8048 80.48%
Acute Oral Toxicity (c) I 0.7167 71.67%
Estrogen receptor binding + 0.7737 77.37%
Androgen receptor binding + 0.7332 73.32%
Thyroid receptor binding + 0.6132 61.32%
Glucocorticoid receptor binding + 0.7390 73.90%
Aromatase binding + 0.7788 77.88%
PPAR gamma + 0.6060 60.60%
Honey bee toxicity - 0.8616 86.16%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9954 99.54%

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
CHEMBL3837 P07711 Cathepsin L 96.59% 96.61%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.45% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.19% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.20% 96.09%
CHEMBL284 P27487 Dipeptidyl peptidase IV 92.94% 95.69%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 92.56% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 92.40% 90.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 92.32% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 91.45% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.49% 93.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.25% 91.11%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.17% 96.38%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.99% 85.31%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.37% 100.00%
CHEMBL236 P41143 Delta opioid receptor 86.28% 99.35%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.73% 89.34%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.44% 89.50%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.98% 96.47%
CHEMBL2514 O95665 Neurotensin receptor 2 84.93% 100.00%
CHEMBL2581 P07339 Cathepsin D 84.33% 98.95%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 84.18% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.91% 97.09%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.41% 98.75%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 81.59% 96.03%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.79% 95.50%
CHEMBL237 P41145 Kappa opioid receptor 80.14% 98.10%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.11% 90.71%

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.
Acalypha communis

Cross-Links

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PubChem 11005454
LOTUS LTS0028771
wikiData Q105351087