Simple Phenylpropanols

Simple Phenylpropanols (143):

Cat. No.	Product Name	CAS No.	Purity	Chemical Structure

Chlorogenic acid	327-97-9	99.55%
Chlorogenic acid is a major phenolic compound in Lonicera japonica Thunb.. It plays several important and therapeutic roles such as antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension.

Echinacoside	82854-37-3	99.65%
Echinacoside, one of the phenylethanoids isolated from the stems of Cistanche deserticola, effectively inhibits Wnt/β-catenin signaling. Echinacoside elicits neuroprotection by activating Trk receptors and their downstream signal pathways. Antiosteoporotic activity.

HY-N0274

Caffeic acid phenethyl ester 104594-70-9 99.96%

Caffeic acid phenethyl ester is a NF-κB inhibitor.
HY-N0060

Ferulic acid 1135-24-6 99.87%

Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC₅₀s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.
HY-N0172

Caffeic acid 331-39-5 99.33%

Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase (5-LO).
HY-138073

Cryptomoscatone D2 276856-55-4

Cryptomoscatone D2 is a potent G2 checkpoint inhibitor.
HY-N8579

Eugenyl benzoate 531-26-0

Eugenyl benzoate has the potency for scavenging of DPPH radical. Eugenyl Benzoate Derivatives can be used for development of BCL-2 inhibitors.
HY-N3597

Clerodenoside A 164022-75-7

Clerodenoside A is a phenolic glycoside that can be extracted from the stem of Clerodendrum inerme.
HY-N0337

Eugenol 97-53-0 99.30%

Eugenol is an essential oil found in cloves with antibacterial, anthelmintic and antioxidant activity. Eugenol is shown to inhibit lipid peroxidation.

Caffeic acid phenethyl ester	104594-70-9	99.96%
Caffeic acid phenethyl ester is a NF-κB inhibitor.

Ferulic acid	1135-24-6	99.87%
Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC₅₀s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.

Caffeic acid	331-39-5	99.33%
Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase (5-LO).

Cryptomoscatone D2	276856-55-4
Cryptomoscatone D2 is a potent G2 checkpoint inhibitor.

Eugenyl benzoate	531-26-0
Eugenyl benzoate has the potency for scavenging of DPPH radical. Eugenyl Benzoate Derivatives can be used for development of BCL-2 inhibitors.

Clerodenoside A	164022-75-7
Clerodenoside A is a phenolic glycoside that can be extracted from the stem of Clerodendrum inerme.

Eugenol	97-53-0	99.30%
Eugenol is an essential oil found in cloves with antibacterial, anthelmintic and antioxidant activity. Eugenol is shown to inhibit lipid peroxidation.

Forsythoside B	81525-13-5	99.99%
Forsythoside B is a phenylethanoid glycoside isolated from Forsythia suspensa (Thunb.) Vahl, a Chinese folk medicinal plant for treating inflammatory diseases and promoting blood circulation. Forsythoside B could inhibit TNF-alpha, IL-6, IκB and modulate NF-κB.

HY-N1913

Danshensu 76822-21-4 ≥98.0%

Danshensu, an active ingredient of Salvia miltiorrhiza, shows wide cardiovascular benefit by activating Nrf2 signaling pathway.
HY-N0028

Forsythiaside A 79916-77-1 99.43%

Forsythiaside A, a phenylethanoside product isolated from air-dried fruits of Forsythia suspense, has anti-inflammatory and antioxidant effects.

Danshensu	76822-21-4	≥98.0%
Danshensu, an active ingredient of Salvia miltiorrhiza, shows wide cardiovascular benefit by activating Nrf2 signaling pathway.

Forsythiaside A	79916-77-1	99.43%
Forsythiaside A, a phenylethanoside product isolated from air-dried fruits of Forsythia suspense, has anti-inflammatory and antioxidant effects.

Sinapinic acid	530-59-6	99.95%
Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC₅₀ of 2.27 mM, and also inhibits ACE-I activity. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells. Sinapinic acid shows antioxidant and antidiabetic activities. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats.

HY-N0787

Cryptochlorogenic acid 905-99-7 99.88%

Cryptochlorogenic acid is a natural product.

Cryptochlorogenic acid	905-99-7	99.88%
Cryptochlorogenic acid is a natural product.

trans-Cinnamaldehyde	14371-10-9	99.41%
trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits.

HY-N0610A

Cinnamic acid 621-82-9 99.99%

Cinnamic acid has potential use in cancer intervention, with IC₅₀s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells.

Cinnamic acid	621-82-9	99.99%
Cinnamic acid has potential use in cancer intervention, with IC₅₀s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells.

Syringin	118-34-3	99.05%
Syringin is a main bioactive phenolic glycoside in Acanthopanax senticosus, with anti-osteoporosis activity. Syringin prevents cardiac hypertrophy induced by pressure overload through the attenuation of autophagy.

HY-N0351

p-Coumaric acid 501-98-4 99.44%

p-Coumaric acid is the abundant isomer of cinnamic acid which has antitumor and anti-mutagenic activities.

p-Coumaric acid	501-98-4	99.44%
p-Coumaric acid is the abundant isomer of cinnamic acid which has antitumor and anti-mutagenic activities.

Ferulic acid sodium	24276-84-4	≥99.0%
Ferulic acid sodium is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC₅₀s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.

Poliumoside	94079-81-9	99.80%
Poliumoside, a caffeoylated phenylpropanoid glycoside, is isolated from Brandisia hancei stems and leaves. Poliumoside is an advanced glycation end product (AGE) formation and rat lens aldose reductase (RLAR) inhibitor, with IC₅₀s of 19.69 and 8.47 μM, respectively. Poliumoside also has antiinflammatory and antioxidant activity.

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