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Search Results for " cyp1a1 "

28

Compounds

15

Natural Products

1

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T27109 CYP1A1 inhibitor 8a
CYP1A1 inhibitor 8a is a potent and selective CYP1A1 inhibitor. It antagonizes B[a]P mediated activation of aromatic hydrocarbon receptor (AhR) in yeast cells, thereby protects human cells from CYP1A1-mediated B[a]P toxi...
T5116 Iprodione Others , Reactive Oxygen Species , Antifungal
Iprodione is a fungicide. Iprodione is also used in cannabis testing kits as a component of pesticide mixes.
T10270 BAY 2416964 Aryl Hydrocarbon Receptor
BAY 2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist(example 192, IC50: 341 nM). It has the potential for cancer treatment.
T8729 3-(2-Naphthalenyl)-1-(3-pyridinyl)-2-propen-1-one P450
DMU2105 is a specific CYP1B1 inhibitor(CYP1B1 and CYP1A1 with IC50 of 10 nM and 742 nM, respectively)
T3585 TMS (E)-2,3',4,5'-tetramethoxystilbene,2,3',4,5'-Tetramethoxystilbene P450
TMS (2,3',4,5'-Tetramethoxystilbene) is a very selective and potent competitive inhibitor of P450 1B1 (CYP1A1).
T8728 DMU-2139 P450
DMU2139 is a specific CYP1B1 inhibitor (CYP1B1 and CYP1A1 with IC50 of 9 nM and 795 nM, respectively).
T23151 Phortress NSC 710305 AhR
Phortress (NSC-710305) is a potent AhR ligand with strong binding affinity, which subsequently triggers the transcription of CYP1A1 and induces antitumor activity.
T21507 7-Ethoxyresorufin Resorufin ethyl ether P450 , NO Synthase
7-Ethoxyresorufin (Resorufin ethyl ether) (7-ER) is a fluorometric substrate for and competitive inhibitor of cytochrome P450, especially CYP1A1.
T7696 3-Cyano-7-ethoxycoumarin Others
3-Cyano-7-ethoxycoumarin is cytochrome P450 (CYP) isoforms CYP1A1 and CYP1A2 .
T3158L Harman hydrochloride Harmane hydrochloride(486-84-0 Free base) P450
Harman hydrochloride can directly induce CYP1A1 gene expression in an AhR-dependent manner and may represent a novel mechanism by which harman promotes mutagenicity, co-mutagenicity and carcinogenicity.
T21704 5-fluoro 203 5F-203,NSC-703786 Others
5-fluoro 203 (NSC-703786) is a cytotoxic molecule leading to cell death by forming DNA adducts. 5-fluoro 203 induces aryl hydrocarbon receptor signaling, and elevates expression of CYP1A1. 5-fluoro 203 treatment of cells...
T7088 Diflubenzuron Dimilin,Difubenzuron,Larvakil,Difluron P450
Diflubenzuron (Larvakil) is a benzoyl-urea insecticide, found to be a potent inhibitor of melanosome synthesis in mouse melanoma cells. Diflubenzuron has also been shown to inhibit TCDD-induced CYP1A1 expression in HepG2...
T3637 Pifithrin-β hydrobromide Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide) Ferroptosis , p53
Pifithrin-β hydrobromide (Cyclic PFT-α) is an inhibitor of p53; reversibly blocks p53-dependent transcriptional activation and apoptosis. Protects against neuronal death in models of stroke and neurodegenerative disorder...
T4567 Sulfaphenazole Plisulfan,Raziosulfa,Depocid,Depotsulfonamide P450 , Antibacterial
Sulfaphenazole (Plisulfan) is an inhibitor of CYP2C9 (Ki: 0.3 μM) that demonstrates at least 100-fold selectivity over other CYP450 isoforms (Ki: 63/29 μM for CYP2C8/CYP2C18, respectively, and no activity at CYP1A1, CYP1...
T2196 Fipronil Fluocyanobenpyrazole,Termidor P450 , GluCls , GABA Receptor
Fipronil (Fluocyanobenpyrazole) is a broad-use insecticide that belongs to the phenylpyrazole chemical family. Fipronil is a broad-spectrum insecticide that disrupts the insect central nervous system by blocking GABA-gat...
T73040 CYP1B1-IN-4 P450
CYP1B1-IN-4, a 2,4-diarylthiazole compound, exhibits selective inhibition of CYP1B1 (IC50=0.2 nM), demonstrating minimal cytotoxicity and high stability in human and rat liver microsomes [1].
T73039 CYP1B1-IN-3
CYP1B1-IN-3 is a potent, selective inhibitor of CYP1B1, exhibiting IC50 values of 6.6 nM for CYP1B1, 347.3 nM for CYP1A1, and >10000 nM for CYP1A2. It also impedes cell migration and invasion, and inhibits the P-gp, AKT/...
T9704 1-Ethynylpyrene P450
1-Ethynylpyrene is an aryl acetylenic inhibitor of CYTP450 1A1(IC50=0.18 μM), 1A2(IC50 = 0.32 μM), and 2B1(IC50 = 0.04 μM).
T73042 CYP1B1-IN-5 P450
CYP1B1-IN-5 is a selective and potent cytochrome P450 1B1 (CYP1B1) inhibitor with an IC50 of 4.7 nM.CYP1B1-IN-5 can be used for the study of metabolism-related diseases.
T32136 ICT2700 de OH CPI MI,deOHCPIMI,de-OH-CPI-MI,ICT 2700,ICT-2700
ICT2700 is a potent cytotoxin selectively by CYP1A1 as a tumor-selective treatment for human bladder cancers.
T72552 Antitumor agent-88
Antitumor agent-88, a competitive inhibitor of CYP1A1 (K i: 1.4 μM), demonstrates significant antimitotic activity by arresting cells in the G2/M phase and disrupting the microtubule network and cytoskeleton in CYP1A1-ex...
T12449 Phortress free base Others
Phortress free base is a P450 CYP1A1-activated antitumor prodrug with antitumor activity.
T36793 Dolutegravir M1
Dolutegravir M1 is a metabolite of the HIV integrase inhibitor dolutegravir .1It is formed primarily by the cytochrome P450 (CYP) isoforms CYP1A1 and CYP1B1. 1.Zhu, J., Wang, P., Li, F., et al.CYP1A1 and 1B1-mediated met...
T70257 Avitriptan HCl
Avitriptan, also known as BMS-180048, is a selective 5-HT1-like receptor agonist. Avitriptan is an effective compound for the treatment of migraine headaches with a prolonged duration of response. Avitriptan Is a Ligan...
T72551 Antitumor agent-87
Antitumor agent-87 is a potent compound with antitumoral activity, demonstrating a high affinity for CYP1A1, evidenced by a K i value of 0.23 µM. It exhibits antiproliferative effects and induces cell cycle arrest at the...
T35855 AAA
AAA is an antagonist of G protein-coupled receptor 75 (GPR75).1It increases basal GPR75 protein levels and inhibits 20-HETE-induced reductions in GPR75 protein levels in PC3 cells. AAA (5 and 10 μM) also reduces 20-HETE-...
T36039 16α-Hydroxyestrone
The naturally-occurring estrogens are estrone , estradiol , and estriol . 16α-hydroxy Estrone (16α-OHE1) is a hydroxylated metabolite of E1 as well as an interconversion product with E2. E1 is 16α-hydroxylated by cytochr...
T36215 17R(18S)-EpETE
17R(18S)-EpETE is an oxylipin and a cytochrome P450 metabolite of eicosapentaenoic acid .1,217R(18S)-EpETE is an activator of large-conductance calcium-activated potassium (BKCa) channels, increasing the potassium curren...

Compounds

CYP1A1 inhibitor 8a
T27109
Synonym:
Target:
Iprodione
T5116
Synonym:
Target: Others, Reactive Oxygen Species, Antifungal
BAY 2416964
T10270
Synonym:
Target: Aryl Hydrocarbon Receptor
3-(2-Naphthalenyl)-1-(3-pyridinyl)-2-propen-1-one
T8729
Synonym:
Target: P450
TMS
T3585
Synonym: (E)-2,3',4,5'-tetramethoxystilbene,2,3',4,5'-Tetramethoxystilbene
Target: P450
DMU-2139
T8728
Synonym:
Target: P450
Phortress
T23151
Synonym: NSC 710305
Target: AhR
7-Ethoxyresorufin
T21507
Synonym: Resorufin ethyl ether
Target: P450, NO Synthase
3-Cyano-7-ethoxycoumarin
T7696
Synonym:
Target: Others
Harman hydrochloride
T3158L
Synonym: Harmane hydrochloride(486-84-0 Free base)
Target: P450
5-fluoro 203
T21704
Synonym: 5F-203,NSC-703786
Target: Others
Diflubenzuron
T7088
Synonym: Dimilin,Difubenzuron,Larvakil,Difluron
Target: P450
Pifithrin-β hydrobromide
T3637
Synonym: Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide)
Target: Ferroptosis, p53
Sulfaphenazole
T4567
Synonym: Plisulfan,Raziosulfa,Depocid,Depotsulfonamide
Target: P450, Antibacterial
Fipronil
T2196
Synonym: Fluocyanobenpyrazole,Termidor
Target: P450, GluCls, GABA Receptor
CYP1B1-IN-4
T73040
Synonym:
Target: P450
CYP1B1-IN-3
T73039
Synonym:
Target:
1-Ethynylpyrene
T9704
Synonym:
Target: P450
CYP1B1-IN-5
T73042
Synonym:
Target: P450
ICT2700
T32136
Synonym: de OH CPI MI,deOHCPIMI,de-OH-CPI-MI,ICT 2700,ICT-2700
Target:
Antitumor agent-88
T72552
Synonym:
Target:
Phortress free base
T12449
Synonym:
Target: Others
Dolutegravir M1
T36793
Synonym:
Target:
Avitriptan HCl
T70257
Synonym:
Target:
Antitumor agent-87
T72551
Synonym:
Target:
AAA
T35855
Synonym:
Target:
16α-Hydroxyestrone
T36039
Synonym:
Target:
17R(18S)-EpETE
T36215
Synonym:
Target:
Cat No. Product Name Synonyms Targets
T8198 Visnagin Others
Visnagin has acute hypotensive, anti-inflammatory, and neuroprotective effects, it protects against doxorubicin-induced cardiomyopathy through modulation of mitochondrial malate dehydrogenase.
T5786 TETRAHYDROPIPERINE Cosmoperine P450 , TRP/TRPV Channel
Tetrahydropiperine (Cosmoperine) is a natural product derived from piperine, can be used to treat convulsion, epilepsy, relieve pain, and control insects.
T9328 Ellagic Acid Dihydrate P450
Ellagic Acid Dihydrate inhibit the CYP1A1-dependent activation of benzo[a]pyrene.
T2949 Alizarin Mordant Red 11,Anthraquinonic P450
Alizarin (Mordant Red 11), a red dye derived from the roots of plants of the madder genus, inhibits P450 isoform CYP1A1( IC50 = 6.2 μM), CYP1A2 (IC50 =10.0 μM )and CYP1B1(IC50 = 2.7 μM).
T7472 7-Hydroxyflavone P450
7-Hydroxyflavone is a potent inhibitor of CYP1A1 with a Ki value of 0.015 μM and exhibits 6-fold greater selectivity for CYP1A1 over CYP1A2.with anti-inflammatory activity
T5S0669 Bergamottin 5-Geranoxypsoralen,Bergamotine,Bergaptin P450
1. Bergamottin (5-Geranoxypsoralen) can significantly reduce blood glucose and increase glucose tolerance and insulin sensitivity in KK-A<sup>y</sup>diabetic mice.
T3668 Galangin Norizalpinin,3,5,7-Trihydroxyflavone ERK , P450 , NF-κB , Autophagy
Galangin (Norizalpinin) is an agonist/antagonist of the arylhydrocarbon receptor, and also shows inhibition of CYP1A1 activity.
T11218 ε-​Viniferin epsilon-Viniferin P450
ε-Viniferin (epsilon-Viniferin) a dimer of resveratrol, shows the inhibitory effects of epsilon-viniferin on human CYP1A1, CYP1A2, CYP1B1, CYP2A6, CYP2B6, CYP2E1, CYP3A4 and CYP4A activities.
TN1724 Harmalol hydrochloride Harmidol hydrochloride P450 , Antioxidant
Harmalol hydrochloride (Harmidol hydrochloride) is a β-carboline alkaloid that can be extracted from the seeds of Peganum harmala L. Harmalol hydrochloride is the major metabolite of Harmaline and significantly inhibits ...
T5582 β-​Apo-​8'-​carotenal trans-β-apo-8'-carotenal,Apocarotenal Others , P450
β-Apo-8'-carotenal (Apocarotenal) is a carotenoid found in spinach and citrus fruits. Apocarotenal is used in fat-based food (margarine, sauces, salad dressing), beverages, dairy products, and sweets.
TN1222 26-Deoxyactein 27-Deoxyactein,23-epi-26-Deoxyactein NOS , CDK , NO Synthase
23-epi-26-Deoxyactein (27-Deoxyactein) has anti-inflammatory activity, it inhibits nitric oxide production by reducing iNOS expression without affecting activity of the enzyme. It also has anti-cancer activity, it can in...
T3736 Olivetol 5-Pentylresorcinol,5-n-Amylresorcinol Cannabinoid Receptor , P450 , IκB/IKK
Olivetol (5-n-Amylresorcinol) (5-pentylresorcinol, 5-pentyl-1,3-benzenediol) is an organic compound found in certain species of lichen; it is also a precursor in various syntheses of tetrahydrocannabinol. Olivetol has an...
TQ0276 Methysticin DL-Methysticin,(±)-Methystici P450
Methysticin, a major kavalactone extracted from kava, can induce CYP1A1.
T3776 Rhapontigenin Protigenin P450 , Antibacterial , Antifungal
Rhapontigenin (Protigenin) is a mechanism-based, selective inactivator of cytochrome P450 1A1 (IC50: 400 nM), an aryl hydrocarbon hydroxylase which activates polycyclic aromatic hydrocarbons that act as procarcinogens. R...
T13670L (Z)-Ligustilide cis-Ligustilide,Ligustilide A Antibacterial
(Z)-Ligustilide (Ligustilide A) , an active ingredient isolated from the medicinal plants Angelica acutiloba and Cnidium officinale, inhibits benzo(a)pyrene-induced CYP1A1 upregulation in cultured human keratinocytes via...

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPH-01182 CYP1A1 Protein, Human, Recombinant (His) Human E. coli
CYP1A1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 63.7 kDa and the accession number is P04798.
TargetMol