Rostratamine

Details

Top
Internal ID f72d540e-5f2c-4daf-9234-092911b5c122
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Pregnane steroids > Gluco/mineralocorticoids, progestogins and derivatives
IUPAC Name [(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-3,8,14,17-tetrahydroxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] pyridine-3-carboxylate
SMILES (Canonical) CC(=O)C1(CCC2(C1(C(CC3C2(CC=C4C3(CCC(C4)O)C)O)OC(=O)C5=CN=CC=C5)C)O)O
SMILES (Isomeric) CC(=O)[C@@]1(CC[C@]2([C@@]1([C@@H](C[C@H]3[C@]2(CC=C4[C@@]3(CC[C@@H](C4)O)C)O)OC(=O)C5=CN=CC=C5)C)O)O
InChI InChI=1S/C27H35NO7/c1-16(29)25(32)10-11-27(34)24(25,3)21(35-22(31)17-5-4-12-28-15-17)14-20-23(2)8-7-19(30)13-18(23)6-9-26(20,27)33/h4-6,12,15,19-21,30,32-34H,7-11,13-14H2,1-3H3/t19-,20+,21+,23-,24+,25+,26-,27+/m0/s1
InChI Key GQDQWQRPCUUAFD-LLFZLOFHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C27H35NO7
Molecular Weight 485.60 g/mol
Exact Mass 485.24135246 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

Top
12-O-nicotinyldeacetylmetaplexigenin

2D Structure

Top
2D Structure of Rostratamine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9419 94.19%
Caco-2 - 0.7632 76.32%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7176 71.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8929 89.29%
OATP1B3 inhibitior + 0.8909 89.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8092 80.92%
BSEP inhibitior + 0.9639 96.39%
P-glycoprotein inhibitior - 0.5124 51.24%
P-glycoprotein substrate + 0.6036 60.36%
CYP3A4 substrate + 0.7002 70.02%
CYP2C9 substrate - 0.8041 80.41%
CYP2D6 substrate - 0.8732 87.32%
CYP3A4 inhibition - 0.8138 81.38%
CYP2C9 inhibition - 0.8537 85.37%
CYP2C19 inhibition - 0.8218 82.18%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition - 0.5462 54.62%
CYP2C8 inhibition + 0.8708 87.08%
CYP inhibitory promiscuity - 0.8667 86.67%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5997 59.97%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9458 94.58%
Skin irritation - 0.5892 58.92%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis - 0.6570 65.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4024 40.24%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5949 59.49%
skin sensitisation - 0.8517 85.17%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7874 78.74%
Acute Oral Toxicity (c) III 0.3276 32.76%
Estrogen receptor binding + 0.7254 72.54%
Androgen receptor binding + 0.7184 71.84%
Thyroid receptor binding + 0.5755 57.55%
Glucocorticoid receptor binding + 0.7494 74.94%
Aromatase binding + 0.7470 74.70%
PPAR gamma - 0.5738 57.38%
Honey bee toxicity - 0.7005 70.05%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9679 96.79%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.26% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 93.85% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.68% 86.33%
CHEMBL2581 P07339 Cathepsin D 92.31% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.80% 90.17%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.85% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.15% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.85% 99.23%
CHEMBL2535 P11166 Glucose transporter 86.06% 98.75%
CHEMBL226 P30542 Adenosine A1 receptor 85.13% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.00% 95.89%
CHEMBL255 P29275 Adenosine A2b receptor 84.61% 98.59%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.09% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.65% 89.00%
CHEMBL2243 O00519 Anandamide amidohydrolase 81.45% 97.53%
CHEMBL5028 O14672 ADAM10 80.49% 97.50%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 80.40% 95.71%

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.
Araujia sericifera
Marsdenia rostrata

Cross-Links

Top
PubChem 44575623
LOTUS LTS0088572
wikiData Q105015323