Bifidenone is an effective tubulin polymerization inhibitor.

Bifidenone is an effective tubulin polymerization inhibitor.

Biflorin is an o-naphthoquinone of clinical significance.

Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic hyperplasia (BPH).

Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic hyperplasia (BPH).

Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic hyperplasia (BPH).

Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic hyperplasia (BPH).

Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic hyperplasia (BPH).

Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic hyperplasia (BPH).

Bifonazole acts to destabilize the fungal cytochrome p450 51 enzyme (also known as Lanosterol 14-alpha-demethylase). It works by inhibiting the production of a substance called ergosterol, which is an essential component of fungal cell membranes. This is vital in the cell membrane structure of the fungus. Its inhibition leads to cell lysis. The disruption in […]

Bifonazole acts to destabilize the fungal cytochrome p450 51 enzyme (also known as Lanosterol 14-alpha-demethylase). It works by inhibiting the production of a substance called ergosterol, which is an essential component of fungal cell membranes. This is vital in the cell membrane structure of the fungus. Its inhibition leads to cell lysis. The disruption in […]

Human Big ET-1 comprises residues 53-90 of the endothelin precursor (preproendothelin). Compared to the mature endothelin-1 (hET-1), the peptide show less vasoconstrictor activity in vitro, but similar pressor effects in vivo. Former CAS-number 121014-53-7.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

Bigelovin is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation.It is also known as a potent cytotoxic sesquiterpene lactone from Inula sp.

BigLEN (mouse) acetate is a potent and selective agonist of orphan G protein-coupled receptor 171 (GPR171), with a Kd of ∼0.5 nM.

Biguanide can reduce oxidative stress in rats with hyperglycemia.

Biguanide can reduce oxidative stress in rats with hyperglycemia.

Imidodicarbonimidic diamide, N-​[4-​(10,​15,​20-​triphenyl-​21H,​23H-​porphin-​5-​yl)​phenyl]​-​, hydrochloride (1:1) is a phototoxic agent with anti-proliferative activity.

Imidodicarbonimidic diamide, N-​[4-​(10,​15,​20-​triphenyl-​21H,​23H-​porphin-​5-​yl)​phenyl]​-​, hydrochloride (1:1) is a phototoxic agent with anti-proliferative activity.

Imidodicarbonimidic diamide, N-​[4-​(10,​15,​20-​triphenyl-​21H,​23H-​porphin-​5-​yl)​phenyl]​-​, hydrochloride (1:1) is a phototoxic agent with anti-proliferative activity.

Imidodicarbonimidic diamide, N-​[4-​(10,​15,​20-​triphenyl-​21H,​23H-​porphin-​5-​yl)​phenyl]​-​, hydrochloride (1:1) is a phototoxic agent with anti-proliferative activity.

Imidodicarbonimidic diamide, N-​[4-​(10,​15,​20-​triphenyl-​21H,​23H-​porphin-​5-​yl)​phenyl]​-​, hydrochloride (1:1) is a phototoxic agent with anti-proliferative activity.

BIIB-057 is a selective Syk inhibitor.

BIIB-057 is a selective Syk inhibitor.

BIIB-057 is a selective Syk inhibitor.

BIIB-513 is an inhibitor of Na+/H+ exchange.

BIIB-513 is an inhibitor of Na+/H+ exchange.

BIIB-513 is an inhibitor of Na+/H+ exchange.

BIIB021 is an orally-available, fully synthetic inhibitor of HSP90(Ki=1.7 nM, EC50=38 nM).

BIIB021 is an orally-available, fully synthetic inhibitor of HSP90(Ki=1.7 nM, EC50=38 nM).