Naphtho(2,1-a)naphthacene

Details

Top
Internal ID c20510e4-f7ef-41ce-8eb4-60569a1ac066
Taxonomy Benzenoids > Naphthacenes
IUPAC Name hexacyclo[12.12.0.02,11.05,10.016,25.018,23]hexacosa-1(26),2(11),3,5,7,9,12,14,16,18,20,22,24-tridecaene
SMILES (Canonical) C1=CC=C2C(=C1)C=CC3=C2C=CC4=CC5=CC6=CC=CC=C6C=C5C=C43
SMILES (Isomeric) C1=CC=C2C(=C1)C=CC3=C2C=CC4=CC5=CC6=CC=CC=C6C=C5C=C43
InChI InChI=1S/C26H16/c1-2-7-19-14-22-16-26-20(15-21(22)13-18(19)6-1)10-12-24-23-8-4-3-5-17(23)9-11-25(24)26/h1-16H
InChI Key AFVMDRFUJONSCM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H16
Molecular Weight 328.40 g/mol
Exact Mass 328.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.00
Atomic LogP (AlogP) 7.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
Naphtho(2,1-a)naphthacene
220-82-6
naphtho[2,1-a]tetracene
Naphtha(2,1-a)tetracene
DTXSID00176431
AFVMDRFUJONSCM-UHFFFAOYSA-N

2D Structure

Top
2D Structure of Naphtho(2,1-a)naphthacene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.5746 57.46%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.8244 82.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9537 95.37%
OATP1B3 inhibitior + 0.9656 96.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9248 92.48%
P-glycoprotein inhibitior - 0.7359 73.59%
P-glycoprotein substrate - 0.9660 96.60%
CYP3A4 substrate - 0.6610 66.10%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate + 0.3525 35.25%
CYP3A4 inhibition - 0.9288 92.88%
CYP2C9 inhibition - 0.9070 90.70%
CYP2C19 inhibition - 0.8548 85.48%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.6798 67.98%
CYP2C8 inhibition - 0.8123 81.23%
CYP inhibitory promiscuity + 0.5335 53.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4954 49.54%
Eye corrosion + 0.6689 66.89%
Eye irritation + 0.9878 98.78%
Skin irritation + 0.9222 92.22%
Skin corrosion - 0.7730 77.30%
Ames mutagenesis + 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6880 68.80%
Micronuclear - 0.6024 60.24%
Hepatotoxicity + 0.8573 85.73%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.6061 60.61%
Acute Oral Toxicity (c) III 0.7913 79.13%
Estrogen receptor binding + 0.9727 97.27%
Androgen receptor binding + 0.9624 96.24%
Thyroid receptor binding + 0.7741 77.41%
Glucocorticoid receptor binding + 0.8489 84.89%
Aromatase binding + 0.8473 84.73%
PPAR gamma + 0.8739 87.39%
Honey bee toxicity - 0.9014 90.14%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.9800 98.00%
Fish aquatic toxicity + 0.9750 97.50%

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 95.32% 91.11%
CHEMBL240 Q12809 HERG 91.26% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.84% 95.56%
CHEMBL4531 P17931 Galectin-3 83.95% 96.90%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.92% 93.81%
CHEMBL3959 P16083 Quinone reductase 2 80.95% 89.49%

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.
Trifolium hybridum

Cross-Links

Top
PubChem 123039
NPASS NPC184729