82 Results for "

quinazoline

" in MedChemExpress (MCE) Product Catalog:
Products (82)

82 Results for "quinazoline" in MCE Product Catalog:

8
8 Publications Verification
Cat. No.: HY-B0371F
CAS No.: 63074-08-8
Terazosin hydrochloride is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin hydrochloride works by relaxing blood vessels and the opening of the bladder. Terazosin hydrochloride has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment .
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8
8 Publications Verification
Cat. No.: HY-N6607
CAS No.: 13220-57-0
Tryptanthrin is an indole quinazoline that could be an alkaloid from indigo-bearing plants. Tryptanthrin is a potent and orally active cellular Leukotriene (LT) biosynthesis inhibitor. Tryptanthrin has anticancer activity. Tryptanthrin suppresses the expression levels of NOS1, COX-2, and NF-κB and regulates the expression levels of IL-2, IL-10, and TNF-α .
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8
8 Publications Verification
Cat. No.: HY-B0371
CAS No.: 63590-64-7
Terazosin is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin works by relaxing blood vessels and the opening of the bladder. Terazosin has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment .
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8
8 Publications Verification
Cat. No.: HY-B0371A
CAS No.: 70024-40-7
Terazosin hydrochloride dihydrate is a quinazoline derivative and a competitive and orally active α1-adrenoceptor antagonist. Terazosin hydrochloride dihydrate works by relaxing blood vessels and the opening of the bladder. Terazosin hydrochloride dihydrate has the potential for benign prostatic hyperplasia (BPH) and high blood pressure treatment .
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3
3 Cited Publications
Cat. No.: HY-B0098
CAS No.: 74191-85-8
Synonyms: UK 33274
Doxazosin (UK 33274) is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors.
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3
3 Cited Publications
Cat. No.: HY-B0098A
CAS No.: 77883-43-3
Synonyms: UK 33274 mesylate
Doxazosin mesylate (UK 33274 mesylate) is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors.
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3
3 Cited Publications
Cat. No.: HY-13427
CAS No.: 1050500-29-2
Purity:  99.83%
Synonyms: AST-1306 (TsOH)
Target:  

EGFR

Research Areas:  

Cancer

Allitinib tosylate (AST-1306 (TsOH)) is an orally active and irreversible EGFR and ErbB2 inhibitor with IC50s of 0.5 and 3 nM, respectively. Allitinib tosylate also inhibits ErbB4 with an IC50 of 0.8 nM. Allitinib tosylate is an anilino-quinazoline compound and has anti-cancer activity
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3
3 Cited Publications
Cat. No.: HY-107364
CAS No.: 1952236-05-3
Purity:  99.81%
Synonyms: Mol 211
Target:  

EGFR PI3K

Research Areas:  

Cancer

MTX-211 (Mol 211) is a dual inhibitor of EGFR and PI3K with IC50 values of <100 nM. MTX-211 can be used for the research of cancer and other diseases .
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3
3 Cited Publications
Cat. No.: HY-15375
CAS No.: 897383-62-9
Purity:  99.36%
Synonyms: AST-1306; ALS 1306
Target:  

EGFR

Research Areas:  

Cancer

Allitinib (AST-1306) is an orally active and irreversible EGFR and ErbB2 inhibitor with IC50s of 0.5 and 3 nM, respectively. Allitinib also inhibits ErbB4 with an IC50 of 0.8 nM. Allitinib is an anilino-quinazoline compound and has anti-cancer activity .
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3
3 Cited Publications
Cat. No.: HY-N2106
CAS No.: 67909-49-3
Dehydroevodiamine is a major bioactive quinazoline alkaloid isolated from Evodiae Fructus, has an antiarrhythmic effect in guinea-pig ventricular myocytes . Dehydroevodiamine inhibits LPS-induced iNOS, COX-2, prostaglandin E2 (PGE2) and nuclear factor-kappa B (NF-κB) expression in murine macrophage cells .
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2
2 Cited Publications
Cat. No.: HY-10929
CAS No.: 1197196-48-7
Purity:  98.85%
Research Areas:  

Cancer

UNC0224 is a potent and selective histone methyltransferase G9a inhibitor with a Ki of 2.6 nM, an IC50 of 15 nM and a Kd of 23 nM. UNC0224 also potently inhibits b>GLP with assay-dependent IC50 values of 20-58 nM. UNC0224 is inactive against SET7/9, SET8/PreSET7, PRMT3 and JMJD2E .
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2
2 Cited Publications
Cat. No.: HY-N1103
CAS No.: 6159-55-3
Synonyms: Peganine
Vasicine (peganine) is a quinazoline alkaloid isolated from Justicia adhatoda. Vasicine activates PI3K/Akt signaling pathway, exhibits antioxidant, anti-inflammatory and antibacterial activities .
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2
2 Cited Publications
Cat. No.: HY-10930
CAS No.: 1238673-32-9
Purity:  99.91%
Research Areas:  

Cancer

UNC0321 is a potent and selective histone methyltransferase G9a inhibitor with a Ki of 63 pM and with assay-dependent IC50 values of 6-9 nM. UNC0321 also inhibits GLP with assay-dependent IC50 values of 15-23 nM. UNC0321 has anti-apoptotic activity and has potential application in diabetic vascular complications .
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2
2 Cited Publications
Cat. No.: HY-N1103A
CAS No.: 7174-27-8
Synonyms: Peganine hydrochloride
Vasicine hydrochloride (peganine hydrochloride) is a quinazoline alkaloid isolated from Justicia adhatoda. Vasicine hydrochloride activates PI3K/Akt signaling pathway, exhibits antioxidant, anti-inflammatory and antibacterial activities .
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1
1 Cited Publications
Cat. No.: HY-W749874
CAS No.: 97457-31-3
Qingdainone is a quinazoline alkaloid and also a TMPRSS2 inhibitor. Qingdainone can be isolated from Strobilanthes cusia. Qingdainone exhibits anti-tumor and anti-inflammatory activities. Qingdainone can be used in studies related to chronic myeloid leukemia .
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Cat. No.: HY-N1100
CAS No.: 486-64-6
Synonyms: (-)-Vasicinone
Vasicinone is a quinazoline alkaloid isolated from the Adhatoda vasica. Vasicinone is a potential agent for Parkinson's disease and possibly other oxidative stress-related neurodegenerative disorders .
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Cat. No.: HY-155107
CAS No.: 2446880-46-0
Purity:  98.26%
Research Areas:  

Infection

ND-011992 is a reversible, selective quinazoline-type inhibitor targeting quinone reductases and quinol oxidases. ND-011992 inhibits respiratory complex I and bo3 oxidase in addition to bd-I and bd-II oxidases in E. coli strain BL21*Δcyo with the IC50 of 0.12, 2.47, 0.63 and 1.3 μM, respectively. ND-011992 can be used for tuberculosis study .
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Cat. No.: HY-108419
CAS No.: 21561-09-1
Purity:  99.91%
Target:  

JNK

Research Areas:  

Cancer

WHI-P258, a quinazoline compound, binds to the active site of JAK3 with an estimated Ki of 72 µM. WHI-P258 does not inhibit JAK3 and does not affect the thrombin-induced aggregation of platelets even at 100 μM .
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Cat. No.: HY-117397
CAS No.: 120928-09-8
Purity:  99.78%
Synonyms: XDE-436; EL-436
Research Areas:  

Infection

Fenazaquin (XDE-436; EL-436) is a quinazoline acaricide .
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Cat. No.: HY-N6607R
CAS No.: 13220-57-0
Tryptanthrin (Standard) is the analytical standard of Tryptanthrin. This product is intended for research and analytical applications. Tryptanthrin is an indole quinazoline that could be an alkaloid from indigo-bearing plants. Tryptanthrin is a potent and orally active cellular Leukotriene (LT) biosynthesis inhibitor. Tryptanthrin has anticancer activity. Tryptanthrin suppresses the expression levels of NOS1, COX-2, and NF-κB and regulates the expression levels of IL-2, IL-10, and TNF-α .
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