JERVINE
Synonym(s):(3β, 23β)-17,23-Epoxy-3-hydroxyveratraman-11-one;(3β, 23β)-17,23-Epoxy-3-hydroxyveratraman-11-one, 11-Ketocyclopamine, Shh Signaling Antagonist III;11-Ketocyclopamine;Jervine - CAS 469-59-0 - Calbiochem
- CAS NO.:469-59-0
- Empirical Formula: C27H39NO3
- Molecular Weight: 425.6
- MDL number: MFCD01684066
- EINECS: 207-417-9
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-19 20:33:22
What is JERVINE?
Description
First obtained from Veratrum grandiflorum by Wright and Luff, this alkaloid is
also present in V. album. It was originally given the formula C26H3703N. 2H20,
subsequently altered to that given above by Jacobs and Craig. The base crystallizes from aqueous EtOH in stellate groups of colourless prisms and has [α]D -
147° (EtOH). The hydrochloride (dihydrate) has m.p. 208°C (Wright and Luff)
or 330-334°C (dec.) according to Jacobs and Craig, the latter finding a change
in crystalline form at 280°C. The hydriodide has m.p. 302-5°C; the nitrate and
aurichloride are both crystalline and the picrate melts at 278-284°C. TheN-nitroso derivative has m.p. 246-7°C; the N-acety1 compound, m.p. 161-2°C
and the O,N-diacetyl derivative, m.p. 17 6-7°C.
Treatment with aluminium tert-butoxide gives Δ4-jervone, m.p. 193-4°C;
[α]28D + 28.3° (EtOH), giving an oxime, m.p. 287-9°C and reduced by aluminium isopropoxide to Δ4-jervine, m.p. 203- 2 11°C. Catalytic hydrogenation
with Pd-C yields the dihydro derivative, m.p. 248-251°C; [α]26D - 82° (EtOH).
On further hydrogenation, the tetrahydro compound is formed, m.p. 216-
221°C; [α]28D - 18° (EtOH). Jervine may be reduced by sodium in butanol to
a:-dihydrojervinol, m.p. 223-5°C; [α]27D - 107° (EtOH). The similar reduction
of dihydrojervine yields (3-dihydrojervino1, m.p. 286-9°C; [α]28D-4 C(EtOH). On
Se dehydrogenation, the alkaloid behaves like cevine (q.v.) giving a mixture of
bases and hydrocarbons from which the following have been isolated; 5-methyl-
2-ethylpyridine; 5-methyl-2-ethyl-3-hydroxypyridine; C2oH22 , m.p. 79°C;
C24H30, m.p. 100- 1°C; C2l H24 , m.p. 70-8 1°C; C2oH 16 , m.p. I 25-7°C and
C22H20 , m.p. I 54-5℃。
In large doses, the alkaloid produces vasodilatation and a fall in blood
pressure
Chemical properties
White Crystalline Solid
The Uses of JERVINE
Has antibacterial properties. Jervine demonstrates teratogenic properties. It is the starting material for C-nor-D-homosteroids. Jervine induces holoprosencephaly and blocks endogenous Sonic hedgehog signaling
What are the applications of Application
Jervine is a naturally occuring steroidal alkaloid that can inhibit the sonic hedgehog pathway
Definition
ChEBI: Jervine is a member of piperidines.
storage
-20°C
Purification Methods
4 Crystallise Jervine from MeOH/H2O or Me2O. The hydrochloride has m 300-302o (from MeOH/Et2O), and the picrate has m 26
References
Wright, Luff., J. Chern. Soc., 35,405 (1879)
Saltzberger., Arch. Pharrn., 228,462 (1890)
Bredemann., Apoth. Zeit., 21,41,53 (1906)
Saito, Suginome, Takaoka., Bull. Chern. Soc. Japan, 9, 15(1934)
Saito, Suginome, Takaoka., ibid, 11, 168, 172 (I936)
Poethke., Arch. Pharrn., 357,571 (I937)
Poethke., ibid, 276, 170 (1938)
Jacobs, Craig., J. BioI. Chern., 148, 51 (1943)
Seiferle.,J. Econ. Entorn., 35,35 (1942)
Jacobs et al., J. Bioi. Chern., 170, 635 (1947)
Wintersteiner et al., J. A mer. Chern. Soc., 73, 2970 (1951)
Wintersteiner, Hosansky., ibid, 74,4474 (1952)
Stereochemistry:
Kupchan, Suffness., J. A mer. Chern. Soc., 90, 2730 (1968)
Masamune et al., Tetrahedron, 24, 3461 (1968)
Properties of JERVINE
Melting point: | 242- 244°C |
Boiling point: | 541.31°C (rough estimate) |
alpha | D20 -150° (ethanol) (Saito); D20 -167.6° (chloroform) (Poethke) |
Density | 1.18±0.1 g/cm3 (20 ºC 760 Torr) |
refractive index | 1.6400 (estimate) |
storage temp. | −20°C |
solubility | methanol: >2 mg/mL |
form | solid |
pka | 14.98±0.70(Predicted) |
color | White |
λmax | 250nm(lit.) |
Merck | 14,5264 |
Stability: | Store in Freezer at - 20°C |
Safety information for JERVINE
Signal word | Danger |
Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 Health Hazard GHS08 |
GHS Hazard Statements |
H301:Acute toxicity,oral |
Precautionary Statement Codes |
P201:Obtain special instructions before use. |
Computed Descriptors for JERVINE
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Mefenamic Acid IP/BP/EP/USP Diclofenac Sodium IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
You may like
-
Jervine CAS 469-59-0View Details
469-59-0 -
Jervine 95% CAS 469-59-0View Details
469-59-0 -
Jervine CAS 469-59-0View Details
469-59-0 -
1823368-42-8 98%View Details
1823368-42-8 -
2-(3-(tert-butyl)phenoxy)-2-methylpropanoic acid 1307449-08-6 98%View Details
1307449-08-6 -
Ethyl 3-(furan-2-yl)-3-hydroxypropanoate 25408-95-1 98%View Details
25408-95-1 -
2-Chloro-5-fluoro-1-methoxy-3-methylbenzene 98%View Details
1805639-70-6 -
Lithium ClavulanateView Details
61177-44-4