- Signaling Pathways
- Metabolic Enzyme/Protease
- Cytochrome P450
Cytochrome P450
CYPs
Cytochrome P450 Isoform Specific Products
-
Cytochrome P450
(678)
View all products
-
CYP1
(96)
View all products
-
CYP2
(144)
View all products
-
CYP3
(135)
View all products
-
CYP4
(12)
View all products
-
CYP11
(13)
View all products
-
CYP17
(18)
View all products
-
Aromatase/
CYP19A1 (63)View all products
-
CYP26
(6)
View all products
-
CYP51
(25)
View all products
-
CYP1A2
(11)
View all products
-
CYP2D6
(18)
View all products
-
CYP2C9
(18)
View all products
-
CYP2C19
(9)
View all products
-
CYP3A
(5)
View all products
-
CYP3A4
(31)
View all products
-
CYP17A1
(5)
View all products
All Product Categories
-
Cytochrome P450 Inhibitors
(798)
View all products
-
Cytochrome P450 Agonists
(7)
View all products
-
Cytochrome P450 Antagonists
(4)
View all products
-
Cytochrome P450 Activators
(103)
View all products
-
Cytochrome P450 Modulators
(31)
View all products
-
Cytochrome P450 p53 Activator
(1)
View all products
-
Cytochrome P450 Inducers
(33)
View all products
-
Cytochrome P450 Degraders
(2)
View all products
-
Cytochrome P450 Controls
(7)
View all products
-
Cytochrome P450 Substrates
(55)
View all products
-
Cytochrome P450 Ligands
(3)
View all products
-
Cytochrome P450 Related Products (1219)
Related Products (1219)
-
Antibodies (26)
-
Cytochrome P450 Isoform Comparison
-
17(R)-HETE
0 ImagesCat. No.: HY-116050ACAS No.: 183509-24-217R-HETE is an arachidonic acid metabolite through cytochrome P-450 pathways. 17R-HETE exhibits efficacy in inducing cardic hypertrophy with less efficiency with compared to 17S-HETE. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Methoxsalen-13C,d3
0 ImagesCat. No.: HY-W777749CAS No.: 1246819-63-5Synonyms: 8-Methoxypsoralen-13C,d3; Xanthotoxin-13C,d3; 8-MOP-13C,d3Methoxsalen-13C,d3 (8-Methoxypsoralen-13C,d3) is the deuterium and 13C-labeled Methoxsalen (HY-30151). Methoxsalen (8-Methoxypsoralen) is a furanocoumarin compound used in psoralen, used in studies of psoriasis, eczema, vitiligo and some sun-exposed cutaneous lymphomas, and is a P450 inhibitor. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
CYP1B1-IN-8
0 ImagesCat. No.: HY-161403CAS No.: 3052218-49-9CYP1B1-IN-8 (Compound 14b) is a CYP1B1 inhibitor (IC50: 4.14 × 10–5 nM). CYP1B1-IN-8 reduces the resistance in A549 cells to Paclitaxel (HY-B0015), and inhibits cell migration and invasion. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Rogletimide
0 ImagesCat. No.: HY-106750CAS No.: 92788-10-8Rogletimide is an aromatase inhibitor. Rogletimide can be studied in research on cancer. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Olivetol-d9
0 ImagesCat. No.: HY-W008364S1CAS No.: 137125-92-9 -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Urotensin-II receptor antagonist-1
0 ImagesCat. No.: HY-10672CAS No.: 1034708-07-0Urotensin-II receptor antagonist-1 (compound 1) is a low oral bioavailability (F=0-3%, rat) selective human Urotensin II receptor antagonist, Ki=16 nM (test on HEK293 cells expressing recombinant human UT receptor). Urotensin-II receptor antagonist-1 inhibits cytochrome P450 (IC50=0.75 μM, CYP2D6; 1.4 μM, CYP3A4), inhibits κ-opioid receptor (EC50=3.2 μM), targets cardiac sodium channels (Ki=2.5 μM). -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Vildagliptin carboxylic acid metabolite TFA
0 ImagesCat. No.: HY-G0024ACAS No.: 565453-41-0Synonyms: Vildagliptin carboxy acid metabolite TFAVildagliptin carboxylic acid metabolite (M20.7) TFA is a potent P450 enzyme activity inhibitor. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
BMS-764459
0 ImagesCat. No.: HY-14225CAS No.: 1188407-45-5BMS-764459 is a CRF1 antagonist. BMS-764459 can be used for the research of neurological disorders such as depression and anxiety. BMS-764459 is also an atypical CYP1A1 inducer. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
ASN-001
0 ImagesCat. No.: HY-164457CAS No.: 1429329-63-4ASN-001 is an orally active CYP-17A1 lyase inhibitor that selectively inhibits testosterone synthesis. ASN-001 has anticancer activity and can be used for research in the field of prostate cancer. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Aromatase-IN-5
0 ImagesCat. No.: HY-172783Aromatase-IN-5 (Compound 10) is a potent inhibitor of aromatase with an IC50 value of 0.06 μM. Aromatase-IN-5 effectively blocks estrogen production. Aromatase-IN-5 inhibits the proliferation of breast cancer cell lines like MCF-7, arrests the cell cycle at the G1 phase, and induces apoptosis. Aromatase-IN-5 is promising for research of breast cancer. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
CYP51-IN-26
0 ImagesCat. No.: HY-174973CYP51-IN-26 is a CYP51 inhibitor with an IC50 value of approximately 0.40 μM. CYP51-IN-26 eradicates C. auris biofilms. CYP51-IN-26 demonstrates significantly improved intracellular uptake in an accumulation assay. CYP51-IN-26 protects against C. auris infection in both G. mellonella and D. melanogaster models. CYP51-IN-26 can be used for research on fungal infections. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Tolterodine tartrate (Standard)
0 ImagesCat. No.: HY-90010RCAS No.: 124937-52-6Synonyms: Kabi-2234 (Standard); PNU-200583E (Standard)Tolterodine (tartrate) (Standard) is the analytical standard of Tolterodine tartrate. This product is intended for research and analytical applications. Tolterodine ((R)-(+)-Tolterodine) is a mAChR inhibitor and substrate for cytochrome P450 enzymes. Tolterodine competitively binds acetylcholine, reduces sympathetic excitation, and inhibits involuntary bladder muscle contraction. Tolterodine restores the Nrf2/NF-κB signaling pathway, mediates protection against inflammatory response and ferroptosis. Tolterodine ameliorates LPS (HY-D1056)-induced reactive oxygen species production and lipid oxidation. Tolterodine can be used for the research of urinary tract infections and overactive bladder. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
- CYP51-IN-17
-
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
AR-C141990
0 ImagesCat. No.: HY-119996CAS No.: 873327-59-4AR-C141990 (Compound 30) is a potent blocker of the monocarboxylate transporter MCT1 with a Ki of 4.8 nM. AR-C141990 (Compound 30) inhibits CYP3A4 and CYP2C9 with IC50 values of 16 μM. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
(Rac)-Tamsulosin
0 ImagesCat. No.: HY-B0661DCAS No.: 94666-07-6Synonyms: YM12617 free base; (Rac)-LY253351 free base(Rac)-Tamsulosin (YM12617 (free base); (Rac)-LY253351 (free base)) is an isomer of Tamsulosin (HY-B0661). (Rac)-Tamsulosin is a sulfonamide phenethylamine derivative and a competitive antagonist of selective post-synaptic α1-adrenoceptors. (Rac)-Tamsulosin inhibits CYP3A4 activity in a non-competitive, enantiomer-specific manner, with an IC50 and Ki of 6.75 μM. (Rac)-Tamsulosin produces dose-dependent hypotension, preferentially antagonizing α1-adrenoceptor-mediated pressor responses, and inhibits α2-adrenoceptor-mediated pressor responses at high doses. (Rac)-Tamsulosin can be used in research related to various diseases such as metabolism. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
COX-2/Aromatase-IN-1
0 ImagesCat. No.: HY-181235COX-2/Aromatase-IN-1 is a potent dual inhibitor of COX-2 and aromatase. COX-2/Aromatase-IN-1 can simultaneously inhibit COX-2 and aromatase, significantly suppress inflammation and induce proliferation inhibition of breast cancer cells. COX-2/Aromatase-IN-1 exerts anti-breast cancer and anti-inflammatory effects in the MCF-7 breast cancer cell and carrageenan-induced rat paw edema model. COX-2/Aromatase-IN-1 can be used for the study of inflammation and breast cancer. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Anticancer agent 78
0 ImagesCat. No.: HY-151119Anticancer agent 78 is a potent anticancer agent. Anticancer agent 78 shows cytotoxicity. Anticancer agent 78 exhibits anti-aromatase activity with an IC50 value of 0.9 µM. Anticancer agent 78 has the potential for the research of breast cancer. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Galeterone hydrochloride
0 ImagesCat. No.: HY-70006ACAS No.: 1239339-17-3Synonyms: TOK-001 hydrochloride; VN-124-1 hydrochlorideGaleterone (TOK-001) hydrochloride is a potent, orally active molecular glue degrader, which degrades androgen receptor (AR) and its splice variants (AR-Vs) and MAP kinase-interacting serine/threonine protein kinase Mnk1/2. Galeterone hydrochloride also functions as a CYP17 inhibitor (IC50 = 47 nM). Galeterone hydrochloride induces cell apoptosis. Galeterone hydrochloride inhibits tumor growth in human prostate cancer xenograft mouse models. Galeterone hydrochloride can be used for castration resistant prostate cancer (CRPC) and pancreatic ductal adenocarcinoma (PDAC) research[1][2]. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
CYP3A4-IN-1
0 ImagesCat. No.: HY-150574CAS No.: 2771297-34-6CYP3A4-IN-1 (compound 5a) is a potent cytochrome P450 3A4 (CYP3A4) inhibitor with an IC50 value of 0.085 µM. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
-
Phenoxan
0 ImagesCat. No.: HY-N21815CAS No.: 134332-63-1Phenoxan is an inhibitor of cytochrome b and NADH: ubiquinone oxidoreductase. It exerts anti-HIV, antifungal, and cytotoxic effects by inhibiting the electron transport chain, the activity of HIV-1 Reverse Transcriptase, and viral replication. Phenoxan can be used in studies of HIV-1 infection and fungal infections. -
loading...Please select quantityGet Quote
August 31
-
Please select quantity
August 31
Get Quote
loading... -
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
Your Search Returned No Results.
Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.